USE OF BUTYLPHTHALIDE AND DERIVATIVE THEREOF

CROSS-REFERENCE TO RELATED APPLICATIONS

The present disclosure claims priority and rights to three Chinese invention applications submitted to the China National Intellectual Property Administration as follows: a prior application No. 202010202588.4 titled “USE OF BUTYLPHTHALIDE AND DERIVATIVE THEREOF” and filed on 20 Mar. 2020, a prior application No. 202010790778.2 titled “USE OF BUTYLPHTHALIDE AND DERIVATIVE THEREOF” and filed on 7 Aug. 2020, and a prior application No. 202011233563.7 titled “USE OF BUTYLPHTHALIDE AND DERIVATIVE THEREOF” and filed on 6 Nov. 2020. The three prior applications are entirely incorporated herein by reference.

TECHNICAL FIELD

The present disclosure refers to the pharmaceutical field, and specifically refers to use of butylphthalide and a derivative thereof in the preparation of a drug for preventing, relieving, or treating peripheral neuropathy, and particularly in the preparation of a drug for preventing, relieving, or treating chemotherapy-induced peripheral neuropathy, as well as a method for preventing, relieving, or treating peripheral neuropathy, and particularly for preventing, relieving, or treating chemotherapy-induced peripheral neuropathy by using butylphthalide and a derivative thereof.

BACKGROUND OF THE INVENTION

Peripheral neuropathy is a syndrome consisting of sensory loss, muscle weakness and atrophy, tendon hyporeflexia, and vasomotion symptom alone or in any combination. There are many clinical peripheral neuropathies, including metabolic neuropathy such as diabetic neuropathy; traumatic neuropathy such as carpal tunnel syndrome; immune neuropathy, and the like. Chemotherapy-induced peripheral neuropathy (CIPN) is a common dose-limiting adverse reaction during chemotherapy of a cancer patient. The CIPN may be the most common type of toxic neuropathy, affecting between 58% and 78% of patients who receive neurotoxic chemotherapies (Seretny M, Currie G L, Sena E S, et al. (2014). Incidence, prevalence, and predictors of chemotherapy-induced peripheral neuropathy: a systemic review and meta-analysis. Pain 155: 2461-2470), and has particularly important clinical consequences. In most instances, it is the dose-limiting toxicity that restricts the use of chemotherapeutic agents in the treatment of malignant tumors. The presence of toxic neuropathy often leads to dose reduction, and sometimes results in the discontinuation of potentially life-saving therapy (Gadgil S, Ergun M, van den Heuval S A, et al. (2019) A systematic summary and comparison of animal models for chemotherapy induced peripheral neuropathy (CIPN). PLOS ONE https://doi.org/10.1371/journal.pone.0221787). Among patients who are administered potentially neurotoxic chemotherapeutic agents, it is estimated that by 6 months following the start of treatment, 30% to 71% continue to experience symptoms related to CIPN.

The CIPN is mainly induced by a chemotherapeutic drug, such as platinum (e.g., cisplatin, carboplatin, or oxaliplatin), paclitaxels (e.g., paclitaxel or docetaxel), vinca alkaloids (e.g., vincristine or vinblastine), a protease inhibitor (e.g., bortezomib), immunomodulator (thalidomide or lenalidomide), or epothilone (e.g., ixabepilone). The most common symptoms with CIPN are paresthesias of hands and feet, such as: pain (burning pain, sharp shooting pains, dysesthesias, allodynia, and hyperalgesia), tingling (paresthesias), and numbness (Ewertz M, Qvortrup C, Eckhoff L. (2015) Chemotherapy-induced peripheral neuropathy in patients treated with taxanes and platinum derivatives. ActaOncologica 54: 587-591); other common clinical findings include diminished or absent deep tendon reflexes, loss of temperature or vibratory sensation, orthostatic hypotension, and sensory ataxia (especially with the platinum based drugs). Less frequent are motion symptoms (e.g., distal or proximal weakness, muscle cramps and gait dysfunction), as well as autonomic symptoms (e.g., constipation or diarrhea, sweating, and lightheadedness with positional changes).

The clinical course of CIPN varies with different individual chemotherapeutic agents. With most chemotherapeutic agent symptoms of neuropathy begin to appear after a cumulative threshold dose has been reached and continue to progress with additional dosing. Depending on the specific agent, adjusting the dosing regimen, the frequency of dosing, and even the rate of infusion may impact the frequency of neuropathy that develops in a given population, but no adjustment to the regimen apart from discontinuing the chemotherapy will completely prevent CIPN in a treatment cohort. With some chemotherapeutic agents, symptoms will continue to progress for some time even after discontinuing the responsible agent, a phenomenon known as coasting. Even if the symptoms are relatively stable, they may persist for months, years, or indefinitely.

Two members of the taxane chemical family are commonly used therapeutically to treat a variety of cancers; paclitaxel and docetaxel. Taxanes, inhibit cancer growth by disassembling microtubules necessary for mitotic activity, and by the same mechanism disrupt microtubule based axonal transport, inhibiting trophic support for sensory neurons. Taxanes are commonly used to treat breast cancer, ovarian cancer, non-small cell lung cancer, gastric cancer, head and neck cancer and prostate cancer. Moderate or severe (grade 2-4) sensory neuropathy affecting both small diameter and large fiber sensory neurons occurs in 20-35% of patients who receive paclitaxel at a cumulative dose of 715-1500 mg/m2 or docetaxel at a cumulative dose of 371-600 mg/m². Sensory symptoms (numbness, tingling and pain) typically begin in the distal extremities, first the legs then the hands which is consistent with a mechanism of action targeting axonal transport. In 40% of these patients, symptoms may persist for 3 years or more (Park S B, Goldstein D, Krishnan A V, et al. (2013) Chemotherapy-induced peripheral neurotoxicity: A critical analysis. CA Cancer J Clin 63: 419-437), while 50% recover within 9 months. While sensory neuropathy is more common and more severe in patients with taxane neuropathy, some patients also develop a deficit in fine motor control.

Cisplatin, carboplatin and oxaliplatin are platinum based drugs used to treat cancer of the testes, ovary, cervix, head and neck, colon and rectum. Their mechanism of action is to cross link DNA limiting the ability of cancer cells to engage in DNA synthesis. When cumulative doses of 600 mg/m²or more are administered, it often results in a severe sensory ataxia secondary to injury of large diameter proprioceptive neurons. 50% who receive cumulative doses of 1170 mg/m²develop a debilitating grade 3 sensory neuropathy associated with degeneration of the sensory dorsal root ganglia. The most prominent findings are tingling, numbness, loss of proprioception and diminished or absent deep tendon reflexes, all indicative of predominantly large sensory fiber loss (Park S B, Goldstein D, Krishnan A V, et al. (2013) Chemotherapy-induced peripheral neurotoxicity: A critical analysis. CA Cancer J Clin 63: 419-437). Reduced sensory nerve conduction velocity and amplitudes are also seen. In addition to this chronic form of neuropathy, oxaliplatin is also associated with an acute type of neuropathy that immediately follows the infusion and affects the face in addition to the extremities. Coasting is common.

Vincristine and vinblastine are the most clinically important vinca alkaloids, and are used to treat leukemia, Hodgkin disease, malignant lymphoma, neuroblastoma, Wilms tumor, Kaposi sarcoma, melanoma, lung cancer, and uterine cancers. Their mechanism of action targets microtubule aggregation and results in a loss of cell division leading to cell death. 35% to 45% of patients treated with vincristine experience abnormal fine motor function and abnormal walking in addition to sensory deficits. 30% experience coasting when the chemotherapy is stopped (Park S B, Goldstein D, Krishnan A V, et al. (2013) Chemotherapy-induced peripheral neurotoxicity: A critical analysis. CA Cancer J Clin 63: 419-437).

Bortezomib is a relatively new chemotherapeutic agent that is highly effective at treating patients with multiple myeloma and some other hematological malignancies. Bortezomib administration results in a severe painful sensory neuropathy in 50% and about an additional 30% experience moderate to severe neurotoxicity. Symptoms include paresthesias and numbness in the distal extremities, especially in the lower limbs, sharp burning pain. The CIPN associated with Bortezomib is a predominantly small fiber sensory neuropathy, however, some patients also develop autonomic involvement and may present with orthostatic hypotension, suppressed heart rate variability, and delayed gastric emptying. Motor involvement is rare but does occur on occasion. The neuropathy has its onset with administration of cumulative doses of 16-26 mg/m², and increases in incidence with higher doses until a dose of 40-45 mg/m²is administered, when the incidence plateaus. The neuropathy is slow to recover, and 2-3 months after treatment 60-85% of patients still have clinically significant neuropathy.

Thalidomide and lenalidomide are synthetic glutamic acid derivatives used for treating relapsed and refractory multiple myeloma. CIPN is a major adverse reaction of this type of drug therapy, and the remission is slow or even irreversible. Thalidomide-induced neuropathy is mainly alliesthesia, which first occurs in the feet, then extends to the hands, often in a sock-like distribution, i.e., severe in the distal end without extending to above the knees and elbows. It includes hypoesthesia, hyperesthesia, disesthesia, muscle pain, haphalgesia, numbness, tingling, burning pain, tenseness, coldness in hands and feet, pallor, itchy legs, and anthurium (Bkl D, de Souza S M, Costa-Lima C, et al. Thalidomide for the treatment of gastrointestinal bleeding due to angiodysplasia in a patient with Glanzmann's thrombasthenia [J]. Hematol Rep, 2017, 9(2): 6961). Some literatures show that when the cumulative dose of thalidomide exceeds 20 g, there is a positive correlation between the occurrence and severity of neuropathy and the cumulative dose (Rui Gui et al., Medical Recapitulate, P1739-1742, Vol 18 No 11, June 2012).

Ixabepilone is a semi-synthetic epothilone lactam analog, and the first epothilone antitumor drug in the world. Compared with paclitaxel, the two drugs have different structures, but have a similar mechanism of action, i.e., causing tumor cell apoptosis by interfering with the cancer cell fission. Ixabepilone can induce peripheral lesions, causing abnormal sensory nerves. Such adverse reaction will generally disappear after 1 to 2 months of drug withdrawal. The degree of sensory neuropathy is related with the administration dose and the administration rate (Burotto M, Edgerly M, Velarde M, et al. A phase II multi-center study of bevacizumab in combination with ixabepilone in subjects with advanced renal cell carcinoma [J]. Oncologist, 2017, 22(8): 888-e84.)

Despite the fact that CIPN is considered as the most common severe side effect associated with chemotherapy, the American Society of Clinical Oncology clinical practice guidelines has concluded that there is currently no effective treatment available to prevent or reverse CIPN, and only recommends one drug (duloxetine) (see Table 1 (prevention) and Table 2 (treatment), Hershman D L, Lacchetti C, Dworkin R H, et al. (2014). Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers: American society of clinical oncology clinical practice guideline. J Clin Oncol 32:1941-67). The treatment is only limited to the treatment with drugs for neuropathic pain, the supportive care, and the chemotherapeutic dose adjustment (Kolb N, and Burns T (2018) Clinical Research in chemotherapy-induced peripheral neuropathy. Neurology 91: 379-380). Therefore, effective prevention and treatment of CIPN is a clinical problem to be urgently solved.

TABLE 1

Strength of
Strength of

Interventions
Recommendation
Evidence
Efficacy
Safety

Acetyl L-carnitine
Strong against
High
Low
Low

Diethyldithio-carbamate
Strong against
Low
No evidence
High

Nimodipine
Strong against
Low
No evidence
Moderate

Amifostine
Moderate against
Intermediate
Low
Moderate

Amitriptyline
Moderate against
Intermediate
No evidence
Moderate

Glutathione for patients receiving
Moderate against
Intermediate
Low
Low

paclitaxel/carboplatin chemotherapy

Org2766
Moderate against
Intermediate
Low
Low

All-trans retinoic acid
Moderate against
Low
Low
Moderate

rhuLIF
Moderate against
Low
No evidence
Low

Vitamin E
Moderate against
Intermediate
Low
Low

Calcium and magnesium for patients
Moderate against
Low
Low
Low

receiving oxaliplatin-based

chemotherapy

Glutathione for patients receiving
Inconclusive
Low
Low
Low

cisplatin/oxaliplatin-based chemotherapy

Acetylcysteine
Inconclusive
Low
Low
Low

Carbamazepine
Inconclusive
Low
Low
Low

Glutamate
Inconclusive
Low
Low
Low

Goshajinkigan
Inconclusive
Low
Low
Low

Omega-3-fatty acid for patients
Inconclusive
Low
Low
Low

receiving oxaliplatin treatment

Venlafaxine
Insufficient
Low
Low
Low

TABLE 2

Strength of
Strength of

Interventions
Recommendation
Evidence
Efficacy
Safety

Duloxetine
Moderate for
Intermediate
Moderate
Low

Lamotrigine
Moderate against
Intermediate
No evidence
Low

Acetyl L-carnitine
Inconclusive
Low
Low
Moderate

Amitriptyline/nortriptyline
Inconclusive
Intermediate
Low
Low

Gabapentin
Inconclusive
Intermediate
Low
Low

Baclofen, amitriptyline, and
Inconclusive
Intermediate
Moderate
Low

ketamine gels for external use

Butylphthalide (3-n-butylphathlide, NBP) (chemical name: 3-n-butylphthalide, and trade name: NBP) has a structure as shown in formula (I), and is a drug for treating mild to moderate ischemic apoplexy.

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At present, no report is available on use of butylphthalide in the prevention or treatment of peripheral neuropathy, and particularly chemotherapy-induced peripheral neuropathy.

BRIEF SUMMARY OF THE INVENTION

An object of the present disclosure is to provide use of butylphthalide or an optical isomer, a prodrug, a deuterated product, a metabolite, a ring-opening product, or a salt of the ring-opening product thereof in the preparation of a drug for preventing, relieving, or treating peripheral neuropathy. The peripheral neuropathy is preferably a drug-induced peripheral neuropathy, and more preferably a chemotherapeutic drug-induced peripheral neuropathy. The preventing, relieving, or treating peripheral neuropathy includes, but is not limited to, preventing, relieving, or treating chemotherapeutic drug-induced paresthesia and dyskinesia, such as paresthesia of pain and heat, or impaired motor coordination.

In some embodiments, the drug is in a single dose form or a divided dose form.

In some embodiments, the drug is prepared into a clinically acceptable formulation, such as an oral formulation, an injectable formulation, a topical formulation, or an external formulation, and preferably an oral formulation and an injectable formulation.

In some embodiments, the drug is an oral formulation. The oral formulation comprises from about 1 mg to about 1,000 mg, preferably from about 1 mg to about 500 mg, or from about 1 mg to about 300 mg, or from about 1 mg to about 200 mg, or from about 5 mg to about 180 mg, or from about 10 mg to about 150 mg, or from about 30 mg to about 120 mg, or from about 50 mg to about 120 mg, or from about 80 mg to about 120 mg, or from about 90 mg to about 110 mg, or about 100 mg, of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof, on the basis of butylphthalide.

In some embodiments, a daily dose of the oral formulation is from about 1 mg to about 10,000 mg, preferably from about 10 mg to about 5,000 mg, or from about 20 mg to about 3,000 mg, or from about 30 mg to about 2,000 mg, or from about 50 mg to about 1,500 mg, or from about 70 mg to about 1,200 mg, or from about 100 mg to about 1,000 mg, or from about 200 mg to about 900 mg, or from about 300 mg to about 800 mg, or from about 400 mg to about 700 mg, or from about 500 mg to about 600 mg, or from about 60 mg to about 800 mg, or from about 60 mg to about 600 mg, or from about 100 mg to about 800 mg, or from about 100 mg to about 600 mg, or from about 200 mg to about 600 mg, or from about 200 mg to about 800 mg, or from about 300 mg to about 600 mg, or from about 400 mg to about 600 mg, or from about 400 mg to about 800 mg, on the basis of butylphthalide.

In some embodiments, the oral formulation is administered once per day by administering from about 60 mg to about 800 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 60 mg, about 100 mg, about 200 mg, about 300 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, or about 800 mg of the oral formulation each time, on the basis of butylphthalide; or, the oral formulation is administered twice per day by administering from about 30 mg to about 400 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 30 mg, about 50 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, about 300 mg, about 350 mg, or about 400 mg of the oral formulation each time, on the basis of butylphthalide; or, the oral formulation is administered thrice per day by administering from about 20 mg to about 300 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 20 mg, about 50 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, or about 300 mg of the oral formulation each time, on the basis of butylphthalide.

In some embodiments, the drug is an injectable formulation. The injectable formulation comprises from about 0.001 mg/mL to about 100 mg/mL, preferably from about 0.005 mg/mL to about 50 mg/mL, or from about 0.01 mg/mL to about 10 mg/mL, or from about 0.1 mg/mL to about 5 mg/mL, or from about 0.1 mg/mL to about 3 mg/mL, or from about 0.1 mg/mL to about 1 mg/mL, or from about 0.12 mg/mL to about 0.80 mg/mL, or from about 0.15 mg/mL to about 0.50 mg/mL, more preferably from about 0.20 mg/mL to about 0.40 mg/mL, or from about 0.20 mg/mL to about 0.30 mg/mL, or about 0.25 mg/mL, of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof, on the basis of butylphthalide.

In some embodiments, a daily dose of the injectable formulation is from about 1 mg to about 1,000 mg, preferably from about 5 mg to about 500 mg, or from about 10 mg to about 300 mg, or from about 15 mg to about 200 mg, or from about 20 mg to about 150 mg, or from about 25 mg to about 120 mg, or from about 30 mg to about 100 mg, or from about 35 mg to about 90 mg, or from about 40 mg to about 80 mg, or from about 45 mg to about 70 mg, or from about 50 mg to about 60 mg, or from about 1 mg to about 100 mg, or from about 2 mg to about 80 mg, or from about 5 mg to about 75 mg, or from about 10 mg to about 50 mg, or from about 15 mg to about 50 mg, or from about 20 mg to about 50 mg, or from about 25 mg to about 75 mg, or from about 25 mg to about 50 mg, on the basis of butylphthalide.

In some embodiments, the injectable formulation is administered once per day by administering from about 1 mg to about 100 mg, preferably about 1 mg, about 2 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, or about 100 mg, of the injectable formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide; or, the injectable formulation is administered twice per day by administering from about 1 mg to about 50 mg, preferably about 1 mg, about 2 mg, about 2.5 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, or about 50 mg, of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time.

In some embodiments, the chemotherapeutic drug includes, but is not limited to, one of or the combination of more of the followings: (1) a chemotherapeutic drug acting on a microtubule system or an anti-mitotic chemotherapeutic drug, including: a taxane drug, such as paclitaxel, docetaxel or the like; or a vinca alkaloid drug, such as vincristine, vinblastine or the like; or an epothilone drug, such as ixabepilone or the like; or a protease inhibitor drug, such as bortezomib or the like; or (2) a chemotherapeutic drug that interferes with DNA synthesis, including a platinum drug, such as cisplatin, carboplatin, oxaliplatin or the like; or (3) an immunomodulator drug, such as thalidomide, lenalidomide or the like.

In some embodiments, the butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof may be used in the preparation of the drug in combination with one or more of other drugs for treating peripheral neuropathy, wherein the other drugs for treating peripheral neuropathy are preferably duloxetine or a salt thereof, or monosialotetrahexosyl ganglioside sodium.

Another object of the present disclosure further includes providing a method for preventing, relieving, or treating peripheral neuropathy, including administering to a subject or patient a therapeutically effective amount of butylphthalide or an optical isomer, a prodrug, a deuterated product, a metabolite, a ring-opening product, or a salt of the ring-opening product thereof, wherein the peripheral neuropathy is preferably a drug-induced peripheral neuropathy, more preferably a chemotherapeutic drug-induced peripheral neuropathy.

In some embodiments, the administration may be oral administration, injection administration, topical administration, or in vitro administration, preferably oral administration or injection administration. The therapeutically effective amount can prevent, treat, or relieve the peripheral neuropathy in the subject or patient.

In some embodiments, the administration may be oral administration. The therapeutically effective amount refers to a daily dose from about 1 mg to about 10,000 mg, preferably from about 10 mg to about 5,000 mg, or from about 20 mg to about 3,000 mg, or from about 30 mg to about 2,000 mg, or from about 50 mg to about 1,500 mg, or from about 70 mg to about 1,200 mg, or from about 100 mg to about 1,000 mg, or from about 200 mg to about 900 mg, or from about 300 mg to about 800 mg, or from about 400 mg to about 700 mg, or from about 500 mg to about 600 mg, or from about 60 mg to about 800 mg, or from about 60 mg to about 600 mg, or from about 100 mg to about 800 mg, or from about 100 mg to about 600 mg, or from about 200 mg to about 600 mg, or from about 200 mg to about 800 mg, or from about 300 mg to about 600 mg, or from about 400 mg to about 600 mg, or from about 400 mg to about 800 mg, on the basis of butylphthalide.

In some embodiments, the administration may be injection administration. The therapeutically effective amount refers to a daily dose from about 1 mg to about 1,000 mg, preferably from about 5 mg to about 500 mg, or from about 10 mg to about 300 mg, or from about 15 mg to about 200 mg, or from about 20 mg to about 150 mg, or from about 25 mg to about 120 mg, or from about 30 mg to about 100 mg, or from about 35 mg to about 90 mg, or from about 40 mg to about 80 mg, or from about 45 mg to about 70 mg, or from about 50 mg to about 60 mg, or from about 1 mg to about 100 mg, or from about 2 mg to about 80 mg, or from about 5 mg to about 75 mg, or from about 10 mg to about 50 mg, or from about 15 mg to about 50 mg, or from about 20 mg to about 50 mg, or from about 25 mg to about 75 mg, or from about 25 mg to about 50 mg, on the basis of butylphthalide.

In some embodiments, the method for preventing, relieving, or treating comprising administration once per day by administering from about 60 mg to about 800 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 60 mg, about 100 mg, about 200 mg, about 300 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, or about 800 mg of the oral formulation each time, on the basis of butylphthalide; or, administration twice per day by administering from about 30 mg to about 400 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 30 mg, about 50 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, about 300 mg, about 350 mg, or about 400 mg of the oral formulation each time, on the basis of butylphthalide; or, administration thrice per day by administering from about 20 mg to about 300 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 20 mg, about 50 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, or about 300 mg of the oral formulation each time, on the basis of butylphthalide; or administration once per day by administering from about 1 mg to about 100 mg, preferably about 1 mg, about 2 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, or about 100 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on basis of butylphthalide; or, administration twice per day by administering from about 1 mg to about 50 mg, preferably about 1 mg, about 2 mg, about 2.5 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, or about 50 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide.

In some embodiments, the chemotherapeutic drug includes, but is not limited to, one or the combination of more of the followings: (1) a chemotherapeutic drug acting on a microtubule system or an anti-mitotic chemotherapeutic drug, including: a taxane drug, such as paclitaxel, docetaxel or the like; or a vinca alkaloid drug, such as vincristine, vinblastine or the like; or an epothilone drug, such as ixabepilone or the like; or a protease inhibitor drug, such as bortezomib or the like; or (2) a chemotherapeutic drug that interferes with DNA synthesis, including a platinum drug, such as cisplatin, carboplatin, oxaliplatin or the like; or (3) an immunomodulator drug, such as thalidomide, lenalidomide or the like.

In some embodiments, the butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof may be used in combination with one or more of other drugs for treating peripheral neuropathy, wherein the other drugs for treating peripheral neuropathy are preferably duloxetine or a salt thereof, monosialotetrahexosyl ganglioside sodium.

Another object of the present disclosure further includes providing butylphthalide or an optical isomer, a prodrug, a deuterated product, a metabolite, a ring-opening product, or a salt of the ring-opening product thereof for use in preventing, relieving, or treating peripheral neuropathy. The peripheral neuropathy is preferably a drug-induced peripheral neuropathy, more preferably a chemotherapeutic drug-induced peripheral neuropathy.

In some embodiments, the preventing, relieving, or treating includes administering to a subject or patient a therapeutically effective amount of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof.

In some embodiments, the administration is selected from oral administration, injection administration, topical administration, or in vitro administration, and preferably oral administration or injection administration. The therapeutically effective amount can prevent, relieve, or treat the peripheral neuropathy in the subject or patient.

In some embodiments, the administration is oral administration. The therapeutically effective amount refers to a daily dose from about 1 mg to about 10,000 mg, preferably from about 10 mg to about 5,000 mg, or from about 20 mg to about 3,000 mg, or from about 30 mg to about 2,000 mg, or from about 50 mg to about 1,500 mg, or from about 70 mg to about 1,200 mg, or from about 100 mg to about 1,000 mg, or from about 200 mg to about 900 mg, or from about 300 mg to about 800 mg, or from about 400 mg to about 700 mg, or from about 500 mg to about 600 mg, or from about 60 mg to about 800 mg, or from about 60 mg to about 600 mg, or from about 100 mg to about 800 mg, or from about 100 mg to about 600 mg, or from about 200 mg to about 600 mg, or from about 200 mg to about 800 mg, or from about 300 mg to about 600 mg, or from about 400 mg to about 600 mg, or from about 400 mg to about 800 mg, on the basis of butylphthalide.

In some embodiments, the administration is injection administration. The therapeutically effective amount refers to a daily dose from about 1 mg to about 1,000 mg, preferably from about 5 mg to about 500 mg, or from about 10 mg to about 300 mg, or from about 15 mg to about 200 mg, or from about 20 mg to about 150 mg, or from about 25 mg to about 120 mg, or from about 30 mg to about 100 mg, or from about 35 mg to about 90 mg, or from about 40 mg to about 80 mg, or from about 45 mg to about 70 mg, or from about 50 mg to about 60 mg, or from about 1 mg to about 100 mg, or from about 2 mg to about 80 mg, or from about 5 mg to about 75 mg, or from about 10 mg to about 50 mg, or from about 15 mg to about 50 mg, or from about 20 mg to about 50 mg, or from about 25 mg to about 75 mg, or from about 25 mg to about 50 mg, on the basis of butylphthalide.

In some embodiments, the method for preventing, relieving, or treating includes: administration once per day by administering from about 60 mg to about 800 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 60 mg, about 100 mg, about 200 mg, about 300 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, or about 800 mg of the oral formulation each time, on the basis of butylphthalide; or, administration twice per day by administering from about 30 mg to about 400 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 30 mg, about 100 mg, about 200 mg, about 300 mg, or about 400 mg of the oral formulation each time, on basis of butylphthalide; or, administration thrice per day by administering from about 20 mg to about 300 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 20 mg, about 100 mg, about 200 mg, or about 300 mg of the oral formulation each time, on the basis of butylphthalide; or administration once per day by administering from about 1 mg to about 100 mg, preferably about 1 mg, about 2 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, or about 100 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide; or, administration twice per day by administering from about 1 mg to about 50 mg, preferably about 1 mg, about 2 mg, about 2.5 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, or about 50 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide.

In some embodiments, the chemotherapeutic drug includes, but is not limited to, one or more of the followings: (1) a chemotherapeutic drug acting on a microtubule system or an anti-mitotic chemotherapeutic drug, including: a taxane drug, such as paclitaxel, docetaxel or the like; or a vinca alkaloid drug, such as vincristine, vinblastine or the like; or an epothilone drug, such as ixabepilone or the like; or a protease inhibitor drug, such as bortezomib or the like; or (2) a chemotherapeutic drug that interferes with DNA synthesis, including a platinum drug, such as cisplatin, carboplatin, oxaliplatin or the like; or (3) an immunomodulator drug, such as thalidomide, lenalidomide or the like.

In some embodiments, the butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof may be used in combination with one or more of other drugs for treating peripheral neuropathy, wherein the other drugs for treating peripheral neuropathy are preferably duloxetine or a salt thereof, monosialotetrahexosyl ganglioside sodium.

Another object of the present disclosure further includes providing a pharmaceutical composition that comprises butylphthalide or an optical isomer, a prodrug, a deuterated product, a metabolite, a ring-opening product, or a salt of the ring-opening product thereof, and that is used for preventing, relieving, or treating peripheral neuropathy. The peripheral neuropathy is preferably a drug-induced peripheral neuropathy, more preferably a chemotherapeutic drug-induced peripheral neuropathy.

In some embodiments, the method for preventing, relieving, or treating peripheral neuropathy comprises: administration once per day by administering from about 60 mg to about 800 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 60 mg, about 100 mg, about 200 mg, about 300 mg, about 400 mg, about 500 mg, about 600 mg, about 700 mg, or about 800 mg of the oral formulation each time, on the basis of butylphthalide; or, administration twice per day by administering from about 30 mg to about 400 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 30 mg, about 100 mg, about 200 mg, about 300 mg, or about 400 mg of the oral formulation each time, on the basis of butylphthalide; or, administration thrice per day by administering from about 20 mg to about 300 mg of the oral formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, e.g., administering about 20 mg, about 100 mg, about 200 mg, or about 300 mg of the oral formulation each time, on the basis of butylphthalide; or administration once per day by administering from about 1 mg to about 100 mg, preferably about 1 mg, about 2 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, or about 100 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide; or, administration twice per day by administering from about 1 mg to about 50 mg, preferably about 1 mg, about 2 mg, about 2.5 mg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, or about 50 mg, of the injection formulation of butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof each time, on the basis of butylphthalide.

In some embodiments, the butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof may be used in combination with one or more of other drugs for treating peripheral neuropathy, wherein the other drugs for treating peripheral neuropathy are preferably duloxetine or a salt thereof, and monosialotetrahexosyl ganglioside sodium.

The optical isomer of the butylphthalide according to the present disclosure is L-butylphthalide, D-butylphthalide, or a mixture of the two isomers in any ratio.

The prodrug of the butylphthalide according to the present disclosure refers to a compound that is designed according to the prodrug principle. Such compound may be metabolized into butylphthalide in vivo to realize the same or similar pharmacological effects as butylphthalide.

The deuterated product of the butylphthalide according to the present disclosure means that one or some hydrogen atoms in the structure of the butylphthalide compound is/are substituted with isotopic atom deuterium. Such deuterated product has the same or similar pharmacological effects as butylphthalide, such as deuterated derivatives of butylphthalide and its derivatives disclosed in WO2019242765A1, and particularly deuterated derivatives of butylphthalide having the following structures:

embedded image

The metabolite of the butylphthalide according to the present disclosure refers to in vivo metabolite of butylphthalide or a derivative thereof. Such metabolite can realize the same or similar pharmacological effects as butylphthalide, such as derivatives MI and MII of butylphthalide disclosed in CN1689563A, as well as esters or salts of MI disclosed in CN102503919A or CN101289438A:

embedded image

The ring-opening product or the salt of the ring-opening product of the butylphthalide according to the present disclosure refers to the product or salt that is obtained by ring-opening the lactone in the structure of butylphthalide. Such ring-opening product can synthesize butylphthalide in vivo by ring closure, to realize the same or similar pharmacological effects as butylphthalide, such as the ring-opening product of butylphthalide or the salt of the ring-opening product disclosed in CN1382682A, CN1523003A, and CN104974050A:

embedded image

wherein M is a monovalent metal ion, which is a potassium ion, a sodium ion, or a lithium ion; or a divalent metal ion, which is a calcium ion, a magnesium ion, or a zinc ion, where n=1, or n=2; and M is preferably a potassium ion;

embedded image

and an optical isomer thereof;

and a ring-opening derivative of glycosyl-modified butylphthalide disclosed in CN108084233A, a ring-opening derivative of butylphthalide disclosed in CN109503548A, an organic amine ester derivative of 2-(α-hydroxypentyl)benzoic acid disclosed in CN108715579A, and the like.

The dose for butylphthalide or the optical isomer, the prodrug, the deuterated product, the metabolite, the ring-opening product, or the salt of the ring-opening product thereof according to the present disclosure is based on butylphthalide.

Those skilled in the art can understand that other butylphthalide analogs or optical isomers, prodrugs, deuterated products, metabolites, ring-opening products, or salts of the ring-opening products thereof, such as 7-hydroxybutylphthalide disclosed in CN106214674A, halobutylphthalide (particularly 5-bromobutylphthalide) disclosed in CN101029037A, halogenated 2-(α-hydroxypentyl)benzoate disclosed in CN101402565A, and sodium 5-bromo (α-hydroxypentyl)benzoate disclosed in CN104086399A, will also realize similar pharmacological effects as butylphthalide.

In the embodiments of the present disclosure, the word “about” before a numerical value refers to ±10%, preferably ±5%, of the numerical value, e.g., ±10%, ±9%, ±8%, ±7%, ±6%, ±5%, ±4%, ±3%, ±2%, or ±1% of the numerical value.

Technical Effects

1. The representative drug butylphthalide according to the present disclosure can significantly improve the peripheral neuropathy induced by paclitaxel or bortezomib, and can obviously reverse the symptoms of abnormal thermal pain threshold and mechanical pain threshold caused by the two chemotherapeutic drugs.

2. The representative drug butylphthalide according to the present disclosure neither will weaken the activity of bortezomib and paclitaxel in inhibiting the proliferation of tumor cells cultured in vitro, nor has significant influences on the in vivo tumor-inhibiting effect and pharmacokinetic properties of bortezomib and paclitaxel.

3. In vitro and in vivo experiments show that the drug according to the present disclosure can prevent or alleviate peripheral neuropathy caused by a chemotherapeutic drug without affecting the anti-tumor efficacy and pharmacokinetic properties of the chemotherapeutic drug.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

FIG. 1 shows a schematic diagram of a modeling method in Example 1.

FIG. 2 shows a diagram of the change in body weight of rats in each group from 0 to 16 days (D0-16) in Example 1. Compared with a model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 3 shows a diagram of the change in thermal pain threshold of rats in each group from 0 to 13 days (D0-13) in Example 1. Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 4 shows the comparison of thermal pain thresholds of rats in each group on days 7/10/13 (D7/D10/D13) in Example 1. Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 5 shows a time axis of modeling and administration in Example 2.

FIG. 6 shows a curve diagram of the changing values of body weight of rats in Example 2 (mean±SD, n=12). Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 7 shows the change of thermal pain threshold of rats on days −1/7/14 in Example 2 (mean±SD, n=12). Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 8 shows the change of mechanical pain threshold of rats on days 0/6/13 in Example 2 (mean±SD, n=12). Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 9 shows the change of body weight of rats in each group in Example 3. Compared with a solvent group, *P≤0.05, **P≤0.01, and ***P≤0.001; and compared with an ab-PTX group, ##P<0.01.

FIG. 10 shows the change of body weight of rats in each group in Example 4. According to statistical analysis, compared with the solvent group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 11 shows a time axis of modeling and administration in Example 6.

FIG. 12 shows the change of body weight of rats in each group on DO-D20 in Example 6. Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 13 shows the change of thermal pain threshold of rats in Example 6. Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 14 shows the change of mechanical pain threshold of rats in Example 6. Compared with the model group, *P≤0.05, **P≤0.01, and ***P≤0.001.

FIG. 15 shows a curve diagram of the changing values of body weight of mice in each group in Example 8 (mean±SD, n=6).

FIG. 16 shows a curve diagram of the change of xenograft tumor volume of tumor-bearing mice in Example 8 (mean±SD, n=6; and compared with the solvent group, *P≤0.05, **P≤0.01, and ***P≤0.001).

Note: mpk in the figures is equivalent to mg/kg.

DETAILED DESCRIPTION OF THE INVENTION

The examples listed below are provided to better illustrate the embodiments of the present disclosure, but the present disclosure is not limited to the listed examples. Those skilled in the art can make non-essential improvements and adjustments to the embodiments according to the above content of the disclosure, and the improved and adjusted embodiments still belong to the scope of the present disclosure.

Example 1

Study on in vivo efficacy of butylphthalide (intraperitoneal injection) on paclitaxel (albumin bound) chemotherapy-induced peripheral neuropathy in rats

1. Experimental Animals

59 male SD (Sprague Dawley) rats, 180-200 g.

2. Drugs

Lyophilized powder of paclitaxel (albumin bound, ab-PTX), 100 mg/bottle, made by CSPC Ouyi Pharmaceutical Co., Ltd, batch number: B041909121, dissolved in normal saline immediately prior to use.

Butylphthalide (NBP) injection, 25 mg/5 mL, made by CSPC NBP Pharmaceutical Co., Ltd, batch number: Q27190401, diluted in normal saline to a target concentration immediately prior to use.

3. Experimental Process

(1) Model Preparation and Administration Method

Male SD rats, ab-PTX 5 mg/kg, administration volume: 5 mL/kg, intraperitoneally injected (i.p.) on days 0, 2, 4, 6, 8, and 11 for modeling. NBP was administered at three doses (1.5, 5, and 15 mg/kg bid), starting on 1 day prior to the ab-PTX modeling, and during the ab-PTX administration and modeling, the first dose of NBP was administered by intraperitoneal injection 1 h prior to the ab-PTX administration. The second dose of NBP was administered with an interval of 4 h from the first dose, with an administration volume of 5 mL/kg, and was administered every day for 17 consecutive days. The normal group was administered with 0.9% normal saline (0.9% INJ NS) at the same frequency. The modeling method is shown in FIG. 1. The animal grouping, the administration method, and the doses are detailed in Table 3.

TABLE 3

Animal Grouping and Dose List in Example 1

Number of

Dose
Administration

Group
animals
Drug
(mg/kg)
route

Normal group
11
0.9% INJ NS
—
i.p.

Model group
12
0.9% INJ NS/ab-PTX
—/5
i.p./i.p.

NBP 1.5 mg/kg/bid
12
NBP/ab-PTX
1.5/5
i.p./i.p.

NBP 5 mg/kg/bid
12
NBP/ab-PTX
5/5
i.p./i.p.

NBP 15 mg/kg/bid
12
NBP/ab-PTX
15/5
i.p./i.p.

Note:

(1) bid: twice per day; and (2) the three doses of NBP were converted into adult daily doses (based on 60 kg, oral administration) of 60 mg/d, 200 mg/d, and 600 mg/d, respectively.

(2) Grouping

Based on the thermal pain threshold baselines and the body weights of the rats, the rats with the baseline values ranging from 3 to 6 s were selected, and were equally grouped in accordance with the above Table 3.

(3) Observation Indexes

{circle around (1)} Body weight: all animals were weighed once prior to the experiment, and were weighed at set time every day after the commencement of administration, but only the body weight data on days −1, 0, 2, 4, 6, 8, 10, 12, 14, and 16 were statistically recorded.

{circle around (2)} Thermal pain threshold: IITC Life Science Electronic Von Frey Anesthesio meter was used and the intensity of the light source was adjusted to obtain a baseline of thermal pain threshold of about 3-6 s. In this case, the light intensity was 58%, and the cutoff value was set as 10 s. The rats were placed in a plastic compartment on a glass plate, to make the planta centers of the rats be exposed to the light source. The time of reflexive withdrawal, i.e., the thermal pain threshold, of the rat was recorded, and measured once for each of the left foot and the right foot of each rat, and the measurement was repeated three times with each interval therebetween ≥15 min, to compute a mean value of the 6 thermal pain thresholds of each rat.

4. Experimental Results

(1) Body Weight

On days 4-16 (D4-16) of modeling, compared with the normal group, the body weights of the rats in the model group were significantly decreased (P<0.01); and compared with the model group, the body weights of the rats in the three dose groups of NBP (1.5, 5, and 15 mg/kg bid) were not significantly changed, as detailed in FIG. 2.

(2) Thermal Pain Threshold

Measurements were performed on days 7, 10, 13, and 17. On days 7-13 (D7-13), compared with the normal group, the thermal pain threshold of the model group was significantly increased (P<0.01); and compared with the model group, the increase of the thermal pain threshold of the model rats in the groups of NBP (1.5, 5, and 15 mg/kg bid) can be significantly decreased (P<0.05 or P<0.01), as detailed in FIG. 3 and FIG. 4.

On day 17 (D17), compared with the normal group, there was no statistical difference in the thermal pain threshold of the rats in the model group (D17 data was not shown), therefore the thermal pain threshold of the NBP therapy group was not detected, and the experiment was terminated.

5. Conclusions

Butylphthalide can effectively alleviate paclitaxel (albumin bound)-induced abnormal thermal pain symptoms of peripheral neuropathy in rats.

Example 2

Study on in vivo efficacy of butylphthalide (intragastric administration) on paclitaxel (albumin bound) chemotherapy-induced peripheral neuropathy in rats

1. Experimental animals

72 male SD (Sprague Dawley) rats, 160-180 g.

2. Drugs

Lyophilized powder of paclitaxel (albumin bound, ab-PTX), 100 mg/bottle, made by CSPC Ouyi Pharmaceutical Co., Ltd, batch number: B041909121, dissolved in normal saline immediately prior to use.

Butylphthalide (oral administration grade), 10 kg/bottle, made by CSPC NBP Pharmaceutical Co., Ltd, batch number: 518180803, diluted in a vegetable oil to a target concentration immediately prior to use.

Duloxetine hydrochloride, batch number: QRQYD-JN, TCI (Shanghai) Development Co., Ltd, prepared with normal saline containing 2% DMSO immediately prior to use.

3. Experimental Process

3.1 Model Preparation and Administration Method

In this experiment, male SD rats were administered with 5 mg/kg of ab-PTX with an administration volume of 5 mL/kg, and intraperitoneally injected (i.p.) on days 0, 2, 4, 6, 9, and 13 (the first dose of ab-PTX was administered on day 0 of the experiment) for modeling.

Three doses of NBP (3, 10, and 30 mg/kg bid) were used, and the positive control drug (duloxetine hydrochloride) was 15 mg/kg qd. Both NBP and duloxetine hydrochloride were administered 1 day prior to the ab-PTX modeling. During the ab-PTX administration and modeling, both NBP (first dose) and duloxetine hydrochloride were administered 1 h prior to intraperitoneal injection of ab-PTX. The second dose of NBP was administered with an interval of ≥4 h from the first dose, with an administration volume of 5 mL/kg, and was administered by intragastric administration for 14 consecutive days.

The model group was given vegetable oil at the same frequency and with the same administration method as NBP.

The normal group was given normal saline at the same frequency and with the same administration method as ab-PTX, and was given vegetable oil at the same frequency and with the same administration method as NBP.

The modeling method and the administration time are shown in FIG. 5. The animal grouping, the administration method, and the doses are detailed in Table 4.

TABLE 4

Animal Grouping and Dose List

Number of

Dose
Administration

Group
animals
Drug
(mg/kg)
route

Normal group
12
Vegetable oil/normal saline
—
p.o./i.p.

Model group
12
Vegetable oil/ab-PTX
5
p.o./i.p.

NBP 3 mg/kg bid
12
NBP/ab-PTX
3/5
p.o./i.p.

NBP 10 mg/kg bid
12
NBP/ab-PTX
10/5
p.o./i.p.

NBP 30 mg/kg bid
12
NBP/ab-PTX
30/5
p.o./i.p.

Duloxetine hydro-
12
Duloxetine hydrochloride/ab-
15/5
p.o./i.p.

chloride 15 mg/kg qd

PTX

Note:

(1) p.o.: intragastric administration; (2) i.p.: intraperitoneal injection; (3) the three doses of NBP were converted into adult daily doses (based on 60 kg, oral administration) of 60 mg/d, 200 mg/d, and 600 mg/d, respectively.

3.2 Grouping

Based on the thermal pain threshold baseline values and the body weights of the rats, the rats with the baseline values ranging from 3 to 6 s were selected, and were equally grouped in accordance with Table 4 in 3.1.

3.3 Observation Indexes

(1) Body weight: all animals were weighed once prior to the experiment, and were weighed at set time every day after the commencement of administration, but only the body weight data on days −1, 0, 2, 4, 6, 8, 10, 12, and 14 were statistically recorded.

(2) Thermal pain threshold: measurements were performed on days −1, 7, and 14.

Method: IITC Life Science Electronic Von Frey Anesthesio meter was used and the intensity of the light source was adjusted to obtain a baseline of thermal pain threshold of about 3-6 s. In this case, the light intensity was 58%, and the cutoff value was set as 10 s. The rats were placed in a plastic compartment on a glass plate, to make the planta centers of the rats be exposed to the light source. The time of reflexive withdrawal, i.e., the thermal pain threshold, of the rat was recorded, and was measured once for each of the left foot and the right foot of each rat, and the measurement was repeated three times with each interval therebetween ≥15 min, to compute a mean value of the 6 thermal pain thresholds of each rat.

(3) Mechanical stimulus pain threshold: measurements were performed on days 0, 6, and 13.

Method: the rats were placed in a plastic compartment on a wire mesh, left to stand still for 15 min, stimulated using a stimulation probe with a diameter of 0.4 mm of the IITC Life Science Electronic Von Frey Anesthesio meter at the planta centers of the rats by gradually increasing the force until reflexive withdrawal of the rats. The maximum value displayed by the instrument at this time, i.e., the mechanical pain threshold, was recorded. In each experiment, the left and right feet of each rat were measured three times with each interval therebetween ≥5 min, to compute a mean value of the 6 mechanical pain thresholds of each rat.

4. Results

4.1 Influence on Body Weight

On days 4-14 of the experiment, compared with the normal group, the body weights of the rats in the model group were obviously decreased (P<0.05); and throughout the administration period, compared with the model group, the body weights of the rats in the three dose groups of NBP (3, 10, and 30 mg/kg bid) were not obviously changed, and the positive drug duloxetine hydrochloride can significantly increase the body weights of the model rats (P<0.05), as detailed in FIG. 6.

4.2 Influence on Thermal Pain Threshold

On day 7 of the experiment, compared with the normal group, the thermal pain threshold of the rats in the model group was significantly increased (P<0.01); and compared with the model group, the thermal pain threshold of the rats in the group of NBP (30 mg/kg bid) was significantly decreased (P<0.05).

On day 14 of the experiment, compared with the normal group, the thermal pain threshold of the rats in the model group was significantly increased (P<0.001); and compared with the model group, the thermal pain thresholds of the rats in the three dose groups of NBP (3, 10, and 30 mg/kg bid) and the group of positive drug duloxetine hydrochloride (15 mg/kg qd) were significantly decreased (P<0.05), as detailed in FIG. 7.

4.3 Influence on Mechanical Pain Threshold

On day 6 of the experiment, compared with the normal group, the mechanical pain threshold of the rats in the model group was significantly increased (P<0.05); and compared with the model group, the mechanical pain threshold of the rats in the group of NBP (30 mg/kg bid) was significantly decreased (P<0.05).

On day 13 of the experiment, compared with the normal group, the mechanical pain threshold of the rats in the model group was significantly increased (P<0.001); and compared with the model group, the mechanical pain thresholds of the rats in the dose groups of NBP (10 and 30 mg/kg bid) and the group of positive drug duloxetine hydrochloride (15 mg/kg qd) were significantly decreased (P<0.05), and the mechanical pain threshold of the rats in the dose group of NBP (3 mg/kg bid) had a decreasing trend, but did not have statistical difference, as detailed in FIG. 8.

6. Conclusions

Under the conditions of this experiment, NBP can dose-dependently effectively relieve the symptoms of peripheral neuropathy in an ab-PTX-induced PIPN (Paclitaxel-Induced Peripheral Neuropathy) model of rats.

Example 3

Influence of NBP on antitumor efficacy and PK of ab-PTX against B16/F10 xenograft tumor

1. Experimental System

1.1 Experimental Animals

40 female C57BL/6N mice, 15-17 g.

1.2 Cell strains

B16/F10 cells (mice melanoma cells): purchased from Shanghai Genechem Co., Ltd.

2. Drugs

Lyophilized powder of paclitaxel (albumin bound), 100 mg/bottle, made by CSPC Ouyi Pharmaceutical Co., Ltd, batch number: B041909121, dissolved in normal saline immediately prior to use.

Butylphthalide, 25 mg/5 mL/bottle, made by CSPC NBP Pharmaceutical Co., Ltd, batch number: Q27190401, diluted in normal saline to a target concentration immediately prior to use.

3. Experimental Process

3.1 Model Preparation

After in vitro resuscitation and passage of B16/F10 cells to a sufficient amount, the cells were counted by a microscope, and diluted with a serum-free medium to adjust the cell count to about 1×10⁷cells/mL. The cell suspension was kept in an ice-water bath.

The B16/F10 cell suspension was extracted by a sterile syringe, and inoculated into the subcutaneous tissue of the forelimb axilla of the C57BL/6N mice, with the inoculation volume of 0.1 mL/mouse containing about 1.0×10⁶tumor cells, to prepare B16/F10 xenograft tumor model of the C57BL/6N mice.

3.2 Administration Method

Therapy Group:

Monotherapy group of ab-PTX: intraperitoneal injection of ab-PTX at 25 mg/kg, biw (on days 1, 4, 8, 11, and 15). Administration volume: 10 mL/kg.

NBP/ab-PTX group: ab-PTX was administered by intraperitoneal injection at 25 mg/kg, biw (on days 1, 4, 8, 11, and 15); NBP was administered by intraperitoneal injection at 3 mg/kg, 10 mg/kg, or 30 mg/kg twice per day, bid (administration was commenced on day 0); and during the ab-PTX modeling, the first dose of NBP was administered by intraperitoneal injection 1 h prior to the ab-PTX administration, and the second dose of NBP was administered with an interval of more than 4 h from the first dose. The administration was performed for 15 consecutive days. The administration volume was 10 mL/kg.

Solvent group: the solvent (normal saline) was intraperitoneally injected at the same frequency and with the same administration volume as ab-PTX and NBP.

Note: the three doses of NBP were converted into adult daily doses (based on 60 kg, oral administration) of 60 mg/d, 200 mg/d, and 600 mg/d, respectively.

3.3 Observation Indexes and Evaluation Indexes

3.3.1 General Observation Indexes

(1) General state observation: all animals were observed once per day during the experimental period, and the abnormality and behavioral changes of their body parts were recorded.

(2) Body weight: all animals were weighed once prior to the experiment, and animals having suitable body weights were selected for the experiment. Animals were weighed at set time once per day after the commencement of administration.

(3) Death and near death: the death time of dead animal was recorded, and dying animal should be observed more frequently to determine the death time.

3.3.2 Tumor Weight

At the end of the experiment, after the animals were euthanized by CO₂asphyxiation, the tumors were excised and weighed.

Tumor weight inhibition rate %=(1-tumor weight in therapy group/tumor weight in solvent group)×100%

3.3.3 PK Blood Sampling and Detection

Before the administration of the last dose of ab-PTX (0 h), and 5 min, 0.5 h, 1 h, 4 h, 8 h, 12 h, 24 h after the administration, blood was sampled (as detailed in Table 5), anticoagulated with heparin, and centrifuged to separate plasma, which was stored at −80° C. for later use. The total amount of paclitaxel in the plasma was determined by protein precipitation-LC/MS/MS.

TABLE 5

List of Blood Sampling Time of Mice in Each Group

Group
Animal No.
Blood sampling time

Solvent group
1-8
0 h

Therapy groups
1-4
0 h, 0.5 h, 8 h, 12 h

Therapy groups
5-8
5 min, 1 h, 8 h, 24 h

4. Results

4.1 Influence on Body Weight

Compared with the solvent group, the body weight gain rate of mice in each therapy group was significantly decreased (P<0.01). Compared with the ab-PTX group, the body weight gain rate of the dose group of NBP/ab-PTX (10/25 mg/kg) was significantly decreased (P<0.01). Based on analysis of the tumor weight data, the decrease in the body weight gain rate of each therapy group should be caused by inhibition of the drug on the tumor weight, as detailed in FIG. 9.

4.2 Influence on Tumor Weight

Compared with the solvent group, the tumor growth of each therapy group can be significantly inhibited (P<0.001); and compared with the ab-PTX group, the combined therapy of different doses of NBP and ab-PTX did not have statistical difference in tumor inhibition (P>0.05). The tumor weight of each group is detailed in Table 6.

TABLE 6

Influence on Tumor Weights of Mice (mean ± SD, n = 8)

Number of animals
Tumor weight
Inhibition rate

Group
(surviving/total)
(g)
(%)

Solvent group
8/8
5.2178 ± 1.5146
—

NBP/ab-PTX 3/25 mg/kg
8/8
1.9635 ± 0.7882***
62.4

NBP/ab-PTX 10/25 mg/kg
8/8
1.7374 ± 0.5333***
66.7

NBP/ab-PTX 30/25 mg/kg
8/8
1.8226 ± 0.9578***
65.1

ab-PTX 25 mg/kg
8/8
2.5024 ± 0.8133***
52.0

Note:

Compared with the solvent group: ***P < 0.001.

4.3 Influence on PK

The total amount of paclitaxel in the plasma was determined by protein precipitation-LC/MS/MS. The results showed that there was no significant statistical difference in C_max, AUC_0-t, and other indexes in each therapy group, indicating that NBP did not affect the PK behavior of ab-PTX in mice, as detailed in FIG. 7.

TABLE 7

Influence on Pharmacokinetic Parameters

C_max
AUC_0-t
AUC_0-∞
T_max
t_1/2

Group
(ng/ml)
(h*ng/ml)
(h*ng/ml)
(h)
(h)

NBP/ab-PTX 3/25 mg/kg
3157
8012
8065
0.5
1.55

NBP/ab-PTX 10/25 mg/kg
2315
7178
7226
0.5
1.72

NBP/ab-PTX 30/25 mg/kg
2210
6973
7130
1.0
2.31

ab-PTX 25 mg/kg
2443
8126
8178
0.5
1.55

5. Conclusions

In this experiment, NBP did not have obvious influence on the antitumor efficacy of ab-PTX and the PK behavior of ab-PTX.

Example 4

Influence of NBP on antitumor efficacy and PK of ab-PTX against JIMT-1 xenograft tumor

1. Experimental System

1.1 Experimental Animals

48 female Nu/Nu mice, 15-17 g.

1.2 Cell Strains

JIMT-1 cells (human breast cancer cells): purchased from Nanjing Cobioer Biosciences Co., Ltd.

2. Experimental Objective

JIMT-1 cell xenograft model of the Nu/Nu mice was used in this experiment to validate the influence of NBP on the antitumor efficacy and PK behavior of ab-PTX.

3. Drugs

Lyophilized powder of paclitaxel (albumin bound), 100 mg/bottle, batch number: B042007410, made by CSPC Ouyi Pharmaceutical Co., Ltd, dissolved in normal saline immediately prior to use.

Butylphthalide (oral administration grade), 10 kg/bottle, batch number: 518180803, made by CSPC NBP Pharmaceutical Co., Ltd, diluted with vegetable oil to a target concentration immediately prior to use.

4. Experimental Process

4.1 Model Preparation

After in vitro resuscitation and passage of JIMT-1 cells to a sufficient amount, the cells were counted by a microscope, and diluted with a serum-free medium to adjust the cell count to about 1×10⁸cells/mL. The cell suspension was kept in an ice-water bath.

The JIMT-1 cell suspension was extracted by a sterile syringe and inoculated into the subcutaneous tissue of the forelimb axilla of the Nu/Nu mice, with the inoculation volume of 0.1 mL/mouse containing about 1.0×10⁷tumor cells, to prepare JIMT-1 xenograft tumor model of the Nu/Nu mice.

4.2 Administration Method

Therapy Groups:

Monotherapy group of ab-PTX: intravenous injection of ab-PTX at 15 mg/kg once every week, qw (on days 0, 7, 14, 21, and 28). Administration period: 28 days. Administration volume: 10 mL/kg.

Monotherapy group of NBP: NBP was administered by transoral gavage at 60 mg/kg, bid (administration was commenced on day 0), the dosing interval should be longer than 4 h; and the administration period was 28 days. The administration volume was 10 mL/kg.

NBP/ab-PTX group: intravenous injection of ab-PTX at 15 mg/kg, qw (on days 0, 7, 14, 21, and 28). NBP was administered by transoral gavage at 6 mg/kg, 20 mg/kg, or 60 mg/kg twice per day, bid (administration was commenced on day 0), the dosing interval should be longer than 4 h; the first dose of NBP was administered 1 h prior to the ab-PTX administration. The administration period was 28 days. The administration volume was 10 mL/kg.

The solvent group was given normal saline at the same frequency and with the same method as ab-PTX, and was given vegetable oil at the same frequency and with the same method as NBP.

Note: The administration doses of NBP were converted into adult daily doses (based on 60 kg, oral administration) of 60 mg/d, 200 mg/d, and 600 mg/d, respectively.

4.3 Observation Indexes and Evaluation Indexes

4.3.1 General Observation Indexes

(1) General state observation: all animals were observed once per day during the experimental period, and the abnormality and behavioral changes of their body parts were recorded.

(3) Death and near death: the death time of dead animals was recorded, and dying animals should be observed more frequently to determine the death time.

4.3.2 Tumor weight

At the end of the experiment, after the animals were euthanized by CO₂asphyxiation, the tumors were excised and weighed.

Tumor weight inhibition rate %=(1-tumor weight in therapy group/tumor weight in solvent group)×100%

4.3.3 PK Blood Sampling and Detection

Before administration of the last dose of ab-PTX (0 h), and 5 min, 15 min, 0.5 h, 1 h, 4 h, 8 h, 24 h after the administration, blood was sampled (as detailed in Table 8), anticoagulated with heparin, and centrifuged to separate plasma, which was stored at −80° C. for later use. The total amount of paclitaxel in the plasma was determined by protein precipitation-LC/MS/MS.

TABLE 8

List of Blood Sampling Time of Mice in Each Group

Group
Animal No.
Blood sampling time

Solvent group
1-8
0 h

Therapy groups
1-8
0 h, 5 min, 15 min, 0.5 h,

1 h, 4 h, 8 h, 24 h

5. Results

5.1 Influence on Body Weight

As can be seen from the body weight data, there was no significant difference in the body weights of the mice in each group, indicating that neither ab-PTX nor NBP had significant influence on the body weights of the mice, as detailed in FIG. 10.

5.2 Influence on Tumor Weight

The tumor weight results showed that, compared with the solvent group, the tumor growth of the ab-PTX therapy group can be significantly inhibited (P<0.001), and the tumor growth of the mice in the NBP dose group of 60 mg/kg was not obviously affected; compared with the ab-PTX group of 15 mg/kg, the combined therapy of different doses of NBP and ab-PTX did not have statistical difference in tumor inhibition (P>0.05), as detailed in Table 9.

TABLE 9

Influence on Tumor Weights of Mice (mean ± SD, n = 8)

Number of animals
Tumor weight
Inhibition rate

Group
(surviving/total)
(g)
(%)

Solvent group
8/8
0.9969 ± 0.2426
—

ab-PTX 15 mg/kg
8/8
0.2789 ± 0.0858***
72.0

NBP/ab-PTX 6/15 mg/kg
8/8
0.2466 ± 0.1651***
75.3

NBP/ab-PTX 20/15 mg/kg
8/8
0.2807 ± 0.1309***
71.8

NBP/ab-PTX 60/15 mg/kg
8/8
0.3140 ± 0.1724***
68.5

NBP 60 mg/kg
8/8
0.9570 ± 0.2529
4.0

Note:

Compared with the solvent group: ***P < 0.001.

5.4 Influence on PK

The results showed that the main pharmacokinetic parameters of paclitaxel in the plasma of the monotherapy group of ab-PTX and the combined therapy group of NBP and ab-PTX were substantially consistent without significant difference, indicating that combined therapy of butylphthalide and ab-PTX did not affect the pharmacokinetic behavior of paclitaxel in the plasma, as detailed in Table 10.

TABLE 10

Main Pharmacokinetic Parameters of Total

Amount of Paclitaxel in Therapy Groups

Mean ± SD (n = 8)

NBP/ab-PTX
NBP/ab-PTX
NBP/ab-PTX

Parameters (unit)
ab-PTX
6/15 mg/kg
20/15 mg/kg
60/15 mg/kg

C_max(ng/mL)
2981 ± 718
2510 ± 290
2208 ± 382
3083 ± 498

AUC_0-t(h*ng/mL)
2526 ± 963
2565 ± 371
2467 ± 633
2732 ± 376

AUC_0-∞(h*ng/mL)
2575 ± 992
2600 ± 369
2491 ± 659
2762 ± 383

t_1/2(h)
1.28 ± 0.28
1.16 ± 0.14
1.08 ± 0.13
1.09 ± 0.21

Vss (L/kg)
7.39 ± 1.64
6.64 ± 0.63
6.91 ± 1.73
5.70 ± 0.94

CI(L/h/kg)
6.61 ± 2.40
5.87 ± 0.81
6.43 ± 1.84
5.53 ± 0.82

MRT_0-t(h)
1.05 ± 0.24
1.04 ± 0.13
1.01 ± 0.14
0.956 ± 0.140

6. Conclusions

In this experiment, NBP did not have obvious influence on the antitumor efficacy of ab-PTX and the PK behavior of ab-PTX.

Example 5

Influence of NBP on in vitro efficacy of ab-PTX

1. Cell and Culture Conditions

TABLE 11

Cell and Essential Culture Medium

Histological

Cell strains
Source
source
Culture medium

MDA-MB-231
Cell Culture Center, Peking Union
Human breast
RPMI Medium 1640

Medical College
cancer cells
containing 10% FBS

JIMT-1
Nanjing Cobioer Biosciences Co.,
Human breast
DMEM containing 10%

Ltd
cancer cells
FBS

SK-OV-3
Shanghai Institutes for Biological
Human ovarian
McCoy's 5A containing

Sciences, Chinese Academy of
cancer cells
10% FBS

Sciences

HT29
Shanghai Institutes for Biological
Human colon
McCoy's 5A containing

Sciences, Chinese Academy of
cancer cells
10% FBS

Sciences

A549
ATCC
Human lung
RPMI Medium 1640

cancer cells
containing 10% FBS

A375
Cell Culture Center, Peking Union
Human
DMEM containing 10%

Medical College
melanoma cells
FBS

The above cell culture conditions were 37° C. and 5% CO₂.

2. Experimental Objective

To investigate whether NBP affects the function of ab-PTX in the in vitro inhibition of tumor cell proliferation.

3. Drugs

Lyophilized powder of paclitaxel (albumin bound), 100 mg/bottle, batch number: B041909121, made by CSPC Ouyi Pharmaceutical Co., Ltd.

Butylphthalide (oral administration), 10 kg/bottle, batch number: 518180803, made by CSPC NBP Pharmaceutical Co., Ltd.

4. Experimental Design

This experiment includes a monotherapy group of ab-PTX, a combined therapy group (ab-PTX/NBP), and an NBP group. Different drug concentration gradients were set for each group.

Monotherapy group of ab-PTX: {circle around (1)} MDA-MB-231, JIMT-1, SK-OV-3, and A549 cell strains: ab-PTX was 3× serially diluted from an initial concentration of 200 nM to 8 concentrations: 200, 66.67, 22.22, 7.41, 2.47, 0.82, 0.27, and 0.09 nM, respectively. {circle around (2)} A375 and HT29 cell strains: in the first experiment, ab-PTX was 3× serially diluted from an initial concentration of 100 nM to 8 concentrations: 100, 33.33, 11.11, 3.70, 1.24, 0.41, 0.14, and 0.05 nM, respectively; and in the repeated experiment, ab-PTX was 2× serially diluted from an initial concentration of 100 nM to 8 concentrations: 100, 50, 25, 12.5, 6.25, 3.13, 1.56, and 0.78 nM, respectively.

ab-PTX/NBP group: the final concentration of NBP was 30 μM, and the concentration gradient of ab-PTX was the same as that of the monotherapy group.

Monotherapy group of NBP: NBP was 2× serially diluted from an initial concentration of 480 μM to 8 concentrations: 480, 240, 120, 60, 30, 15, 7.5, and 3.75 μM, respectively.

The action time of the drug was 72 h.

5. Experimental Process

A certain number of conventionally cultured cells in logarithmic growth phase were inoculated in a 96-well plate with 100 μL per well. 24 h after adherence, 100 μL of the culture solution containing different concentration gradients of ab-PTX was added to each well of the monotherapy group of ab-PTX; 100 μL of the culture solution containing different concentration gradients of ab-PTX and 30 μM NBP was added to each well of the combined therapy group of ab-PTX/NBP; 100 μL of the culture solution containing different concentration gradients of NBP was added to each well of the monotherapy group of NBP; 3 repeated wells were provided for each concentration of each drug, and the blank wells (only culture medium was present) and the normal wells (drug concentration was 0) were provided. The drugs functioned for 72 h, then MTT working solution (5 mg/mL) was added at 20 μL per well; after functioning at 37° C. for 4 h, the supernatant was removed, 150 μL of DMSO (analytically pure) was added; the mixture was fully mixed using a microplate oscillator, the plate was wiped clean, and the optical density (OD) at 550 nm was measured using a microplate reader.

The cell growth inhibition rate was computed using the following equation:

Inhibition rate (%)=(OD value_{normal well}−OD value_{administration well})/(OD value_{normal well}−OD value_{blank well})×100%

Based on the inhibition rate of each concentration, the median inhibitory concentration IC₅₀of the drug was computed using SPSS19.0.

The experiment was repeated three times, and the IC₅₀value was expressed as the mean±SD of the results of the 3 experiments.

6. Results

6.1 Influence of NBP on IC₅₀Value of Ab-PTX

The results of the monotherapy group of ab-PTX showed that ab-PTX had obvious inhibitory effect on the in vitro proliferation of human breast cancer cells (MDA-MB-231, JIMT-1), human ovarian cancer cells (SK-OV-3), human colon cancer cells (HT29), human lung cancer cells (A549), and human melanoma (A375), and the mean IC₅₀value was in the range of 5-50 nM. NBP at a particular concentration (30 μM) was added for the combined therapy. Compared with the monotherapy of ab-PTX, the mean IC₅₀of ab-PTX of cells in the combined therapy group was not obviously changed, and remained in the range of 5-50 nM. The result showed that NBP did not significantly affect the function of ab-PTX in the in vitro inhibition of tumor cell proliferation.

IC₅₀values of the monotherapy of ab-PTX and the combined therapy of ab-PTX and NBP in inhibiting the in vitro proliferation of 6 tumor cell strains are shown in Table 12.

TABLE 12

IC₅₀Values (nM) of Monotherapy of ab-PTX and Combined

Therapy of ab-PTX and NBP in Inhibiting the in

vitro Proliferation of 6 Tumor Cell Strains

IC₅₀(nM)

Monotherapy of
Combined therapy of

Cell type
ab-PTX
ab-PTX/NBP

MDA-MB-231
37.11 ± 11.78
47.60 ± 9.05

JIMT-1
5.61 ± 2.40
7.24 ± 0.96

SK-OV-3
20.82 ± 8.20
27.66 ± 15.05

HT29
5.03 ± 1.39
5.95 ± 1.83

A549
31.20 ± 16.72
46.23 ± 21.37

A375
12.18 ± 7.49
17.89 ± 7.51

6.2 Influence of NBP on the In Vitro Proliferation of Tumor Cells

The NBP alone did not have obvious inhibitory effect on the in vitro proliferation of human breast cancer cells (MDA-MB-231, JIMT-1), human ovarian cancer cells (SK-OV-3), human colon cancer cells (HT29), human lung cancer cells (A549), and human melanoma (A375). The inhibition rate of 30 μM NBP on the proliferation of 6 cell strains is shown in Table 13.

TABLE 13

Inhibition Rate (%) of 30 μM NBP Alone on 6 Cell Strains

Cell type
Inhibition rate (%, 30 μM NBP)

MDA-MB-231
3.43 ± 3.95

JIMT-1
7.39 ± 13.23

SK-OV-3
12.37 ± 7.41

HT29
10.07 ± 7.94

A549
5.12 ± 7.36

A375
10.92 ± 0.57

7. Conclusions

NBP does not affect the inhibitory effect of ab-PTX on the in vitro proliferation of human breast cancer cells (MDA-MB-231, JIMT-1), human ovarian cancer cells (SK-OV-3), human colon cancer cells (HT29), human lung cancer cells (A549), and human melanoma cells (A375); and the NBP alone did not have obvious inhibitory effect on the in vitro proliferation of human breast cancer cells (MDA-MB-231, JIMT-1), human ovarian cancer cells (SK-OV-3), human colon cancer cells (HT29), human lung cancer cells (A549), and human melanoma (A375).

Example 6

Study on in vivo efficacy of butylphthalide on bortezomib chemotherapy-induced peripheral neuropathy

1. Experimental Animals

72 male SD (Sprague Dawley) rats, 180-200 g.

2. Drugs

Bortezomib: batch number: 20191102, made by CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd, dissolved in normal saline containing 2% DMSO immediately prior to use.

Butylphthalide (oral administration grade), 10 kg/bottle, batch number: 518180803, made by CSPC NBP Pharmaceutical Co., Ltd, diluted in vegetable oil to a target concentration immediately prior to use.

Duloxetine hydrochloride, batch number: QRQYD-JN, made by TCI (Shanghai) Development Co., Ltd, prepared with normal saline containing 2% DMSO immediately prior to use.

3. Experimental Process

3.1 Model Preparation and Administration Method

In this experiment, male SD rats were administered with bortezomib at a dose of 0.3 mg/kg with an administration volume of 5 mL/kg, and were intraperitoneally injected on days 0, 2, 4, 6, 8, 10, and 13 for modeling.

Three doses (3, 10, and 30 mg/kg bid) of NBP were used. The first dose of NBP was administered by transoral gavage 1 day prior to the Bortezomib modeling. During the Bortezomib administration and modeling, the first dose of NBP was administered 1 h prior to the Bortezomib administration every day. The second dose of NBP was administered with an interval of ≥4 h from the first dose, with an administration volume of 10 mL/kg, and was administered for 21 consecutive days.

The normal group was given normal saline containing 2% DMSO at the same frequency and with the same administration method as Bortezomib, and was given vegetable oil at the same frequency and with the same administration method as NBP. (The modeling and administration time are shown in FIG. 11. The animal grouping, the administration method, and the doses are detailed in Table 14).

TABLE 14

Animal Grouping and Dose List

Number of

Dose
Administration

Group
animals
Drug
(mg/kg)
route

Normal control
12
Vegetable oil/normal
0/0
p.o./i.p.

group

saline containing 2%

DMSO

Model group
12
Vegetable
0/0.3
p.o./i.p.

Oil/Bortezomib

Low-dose group of
12
NBP/Bortezomib
3/0.3
p.o./i.p.

NBP

Moderate-dose
12
NBP/Bortezomib
10/0.3
p.o./i.p.

group of NBP

High-dose group of
12
NBP/Bortezomib
30/0.3
p.o./i.p.

NBP

Positive drug
12
Duloxetin/Bortezomib
15/0.3
p.o./i.p.

duloxetine group

3.2 Grouping

3.3 Observation Indexes

(1) Body weight: all animals were weighed once prior to the experiment, and were weighed at set time every day after the commencement of administration.

(2) Thermal pain threshold: measurements were performed on days 0, 7, 14, and 21.

Method: IITC Life Science Electronic Von Frey Anesthesio meter was used and the intensity of the light source was adjusted to obtain a thermal pain threshold baseline of about 3-6 s. In this case, the light intensity was 58%, and the cutoff value was set as 10 s. The rats were placed in a plastic compartment on a glass plate, to make the planta centers of the rats be exposed to the light source. The time of reflexive withdrawal, i.e., the thermal pain threshold, of the rats was recorded, and was measured once for each of the left foot and the right foot of each rat, the measurement was repeated three times with each interval therebetween ≥15 min, to compute a mean value of the 6 thermal pain thresholds of each rat.

(3) Mechanical Stimulus Pain Threshold: Measurements were Performed on Days −1, 6, 13, and 20.

4. Results

4.1 Influence on Body Weight

On day 21 of the experiment, compared with the normal control group, the body weights of the rats in the model group were significantly decreased (P<0.05); and compared with the model group, the body weights of the rats in the three dose groups of NBP (3, 10, and 30 mg/kg bid) were not obviously changed, as detailed in FIG. 12.

4.2 Influence on Thermal Pain Threshold

On day 21 of the experiment, compared with the normal control group, the thermal pain threshold of the model group was significantly decreased; and compared with the model group, the decrease of the thermal pain threshold of the model rats in the group of NBP 3, 10, and 30 mg/kg bid can be significantly reversed, as detailed in FIG. 13.

4.3 Influence on Mechanical Stimulus Pain Threshold

On day 20 of the experiment, compared with the normal control group, the mechanical stimulus pain threshold of the model group was significantly decreased; and compared with the model group, the decrease of the mechanical stimulus pain threshold of the model rats in the group of NBP 10 and 30 mg/kg bid can be significantly reversed, as detailed in FIG. 14.

5. Conclusions

Under the conditions of this experiment, NBP can dose-dependently effectively relieve the symptoms of Bortezomib-induced peripheral neuropathy in the CIPN model of rat.

Example 7

Experiment for influence of NBP on in vitro anti-tumor activity of Bortezomib

1. Cell and Culture Conditions

TABLE 15

Cell and Essential Culture Medium

Cell strains
Source
Histological source
Culture medium

MM.1S
Nanjing Cobioer Biosciences
Human multiple
RPMI Medium 1640

Co., Ltd
myeloma cells
containing 10% FBS

Jeko-1
Shanghai Institutes for
Human mantle cell
RPMI Medium 1640

Biological Sciences, Chinese
lymphoma cells
containing 20% FBS

Academy of Sciences

HT29
Shanghai Institutes for
Human colon cancer
McCoy's 5A

Biological Sciences, Chinese
cells
containing 10%

Academy of Sciences

FBS

A549
ATCC
Human non-small cell
RPMI Medium 1640

lung cancer cells
containing 10% FBS

DU145
Institute of Basic Medical
Human prostate cancer
RPMI Medium 1640

Sciences, Chinese Academy of
cells
containing 10% FBS

Medical Sciences

The above cell culture conditions were 37° C. and 5% CO₂.

2. Experimental Objective

To investigate whether NBP affects the function of Bortezomib in the in vitro inhibition of tumor cell proliferation.

3. Drugs

Bortezomib (bulk drug), made by CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd., batch number: 20190802

Butylphthalide (oral administration grade), 10 kg/bottle, made by CSPC NBP Pharmaceutical Co., Ltd., batch number: 518180803

4. Experimental Design

This experiment includes a monotherapy group of Bortezomib, a combined therapy group (Bortezomib/NBP), and a monotherapy group of NBP. Different drug concentration gradients were set for each group.

Monotherapy group of Bortezomib: {circle around (1)} MM.1S, Jeko-1, and HT29 cells: Bortezomib was 1.5× serially diluted from an initial concentration of 20 nM to 8 concentrations: 20, 13.33, 8.89, 5.93, 3.95, 2.63, 1.76, and 1.17 nM, respectively; {circle around (2)} A549 cells: Bortezomib was 2×serially diluted from an initial concentration of 200 nM to 8 concentrations: 200, 100, 50, 25, 12.5, 6.25, 3.13, and 1.56 nM, respectively; and {circle around (3)} DU145 cells: Bortezomib was 2× serially diluted from an initial concentration of 100 nM to 8 concentrations: 100, 50, 25, 12.5, 6.25, 3.13, 1.56, and 0.78 nM, respectively.

Bortezomib/NBP group: the final concentration of NBP was 30 μM, and the concentration gradient of Bortezomib was the same as the final concentration of the monotherapy group of Bortezomib.

Monotherapy group of NBP: NBP was 2× serially diluted from an initial concentration of 480 μM to 8 concentrations: 480, 240, 120, 60, 30, 15, 7.5, and 3.75 μM, respectively.

The action time of the drug was 72 h.

5. Experimental Process

A certain number of conventionally cultured cells in logarithmic growth phase were inoculated in a 96-well plate with 100 μL per well. For suspension cells MM.1S and Jeko-1, on the day of inoculation, 100 μL of a culture solution containing different concentration gradients of Bortezomib was added into each well of the Bortezomib group, 100 μL of a culture solution containing different concentration gradients of Bortezomib and 30 μM NBP was added into each well of the combined therapy group of Bortezomib/NBP, and 100 μL of a culture solution containing different concentration gradients of NBP was added into each well of the monotherapy group of NBP. For adherent cells HT29, A549, and DU145, the above drugs were added 24 h after adherence. 3 replicate wells were set for each concentration of each drug, and blank wells (only culture medium was present, and no tumor cells were inoculated) and normal wells (a culture medium inoculated with tumor cells, drug concentration was 0) were set. The drugs functioned for 72 h, then MTT working solution (5 mg/mL) was added at 20 μL per well; after functioning at 37° C. for 4 h, the supernatant was removed, 150 μL of DMSO (analytically pure) was added; the mixture was fully mixed using a microplate oscillator, the plate was wiped clean, and the optical density (OD) at 550 nm was measured using a microplate reader.

The cell growth inhibition rate was computed using the following equation:

Inhibition rate (%)=(OD value_{normal well}−OD value_{administration well})/(OD value_{normal well}−OD value_{blank well})×100%

Based on the inhibition rate of each concentration, the median inhibitory concentration IC₅₀of the drug was computed using SPSS19.0.

The experiment was repeated three times, and the IC₅₀value was expressed as the mean±standard deviation of the results of the 3 experiments.

6. Results

The results showed that both the monotherapy group of Bortezomib and the combined therapy group of Bortezomib/NBP had obvious inhibitory effect on the in vitro proliferation of MM.1S, Jeko-1, HT29, A549, and DU145, and mean IC₅₀values thereof were in the range from 1 to 20 nM, suggesting that NBP did not affect the function of Bortezomib in the in vitro inhibition of tumor cell proliferation, as detailed in FIG. 16.

TABLE 16

IC₅₀Values (nM) of Bortezomib and Combined Therapy of Bortezomib/NBP for 5 Cell

Strains

Bortezomib/NBP

Bortezomib
1st
2nd
3rd

1st dose
2nd dose
3rd dose
Mean ± SD
dose
dose
dose
Mean ± SD

MM.1S
2.55
2.94
2.99
2.83 ± 0.24
2.55
3.25
2.99
2.93 ± 0.35

Jeko-l
4.83
3.51
4.47
4.27 ± 0.68
5.82
3.45
4.60
4.62 ± 1.19

HT29
4.43
4.97
5.65
5.02 ± 0.61
4.67
5.56
5.72
5.32 ± 0.56

A549
11.82
13.31
10.56
11.89 ± 1.38
9.01
11.60
10.92
10.51 ± 1.34

DU145
12.79
11.88
17.13
13.94 ± 2.80
9.59
10.39
15.32
11.77 ± 3.10

The monotherapy of NBP does not have obvious inhibitory effect on the in vitro proliferation of human multiple myeloma cells (MM.1S), human mantle cell lymphoma cells (Jeko-1), human colon cancer cells (HT29), human lung cancer cells (A549), and human prostate cancer cells (DU145). The inhibition rate of 30 μM NBP alone on the proliferation of 5 cell strains is detailed in Table 17.

TABLE 17

Inhibition Rate (%) of 30 μM NBP

Alone on Proliferation of 5 Cell Strains

Inhibition rate (%, 30 μM NBP)

Cell type
First dose
Second dose
Third dose
Mean ± SD

MM.1S
0.16
14.08
22.08
12.11 ± 11.09

Jeko-1
−7.67
−18.83
−8.11
−11.54 ± 6.32

HT29
9.98
8.27
13.73
10.66 ± 2.79

A549
−11.08
9.68
4.74
1.11 ± 10.84

DU145
−2.22
9.44
4.87
4.03 ± 5.88

Conclusions: NBP does not affect the inhibitory effect of Bortezomib on the in vitro proliferation of human multiple myeloma cells (MM.1S), human mantle cell lymphoma cells (Jeko-1), human colon cancer cells (HT29), human lung cancer cells (A549), and human prostate cancer cells (DU145).

Example 8

Experiment for influence of NBP on in vivo anti-tumor efficacy of Bortezomib

1. Experimental System

1.1 Experimental Animals

42 female Nu/Nu mice, 18-20 g.

1.2 Cell Strains

MM.1S cells (human multiple myeloma cells), purchased from Nanjing Cobioer Biosciences Co., Ltd.

2. Experimental Objective

A xenograft model of MM.1S cells of the Nu/Nu mice was used in this experiment to validate the influence of NBP on the antitumor efficacy and PK behavior of Bortezomib.

3. Drugs

Bortezomib (bulk drug): manufacturer: CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd, batch number: 20191102; dissolved in normal saline containing 2% DMSO immediately prior to use.

Butylphthalide (oral administration grade), 10 kg/bottle, manufacturer: CSPC NBP Pharmaceutical Co., Ltd, batch number: 518180803, diluted in vegetable oil to a target concentration immediately prior to use.

Palbociclib (bulk drug), manufacturer: Shanghai Fangnan Biotechnology Co., Ltd, batch number: AL-0127-API-1811001; prepared with a solution of propylene glycol and 20% hydroxypropyl-β-cyclodextrin at a ratio of 5:95 to a solution having a target concentration immediately prior to use.

4. Experimental Process

4.1 Model Preparation

After in vitro resuscitation and passage of MM.1S cells to a sufficient amount, the cells were counted by a microscope, and diluted with a serum-free medium to adjust the cell count to about 1×10⁸cells/mL. The cell suspension was kept in an ice-water bath.

The MM.1S cell suspension was extracted by a sterile syringe and inoculated into the subcutaneous tissue of the forelimb axilla of the Nu/Nu mice. The inoculation volume was 0.1 mL/mouse, containing about 1.0×10⁷tumor cells, to prepare MM.1S xenograft tumor model of the Nu/Nu mice.

4.2 Administration Method

Monotherapy group of Bortezomib: administered by intraperitoneal injection at 0.5 mg/kg, biw (on days 0, 3, 7, 10, and 15);

Monotherapy group of NBP: administered by transoral gavage at 60 mg/kg, bid (the administration was commenced on day 0), and the second dose of NBP was administered with an interval from the first dose of ≥4 h;

Monotherapy group of Palbociclib: intragastric administration at 70 mg/kg, qd (the administration was commenced on day 0);

Combined therapy group of NBP/Bortezomib: the administration frequency and dose were the same as the frequency and dose of the monotherapy group of NBP and the monotherapy group of Bortezomib, respectively.

Combined therapy group of Bortezomib/Palbociclib: the administration frequency and dose were the same as the frequency and dose of the monotherapy group of Bortezomib and the monotherapy group of Palbociclib, respectively.

Combined therapy group of NBP/Bortezomib/Palbociclib: the administration frequency and dose were the same as the frequency and dose of the monotherapy group of NBP, the monotherapy group of Bortezomib, and the monotherapy group of Palbociclib, respectively.

The solvent group was given the solvent at the same frequency and with the same administration method as Bortezomib and NBP.

The administration period was 16 days, and the administration volume was 10 mL/kg.

4.3 Observation Indexes and Evaluation Indexes

4.3.1 Observation Indexes

(1) General state observation: all animals were observed once per day during the experimental period, and the abnormality and behavioral changes of their body parts were recorded.

(3) Death and near death: the death time of dead animals was recorded, and dying animals should be observed more frequently to determine the death time.

4.3.2 Tumor Volume Evaluation

After animals were grouped, the long diameter and the short diameter of the tumor were measured twice every week.

(1) Tumor volume: V=½×A×B²

(2) Relative tumor volume:

$RTV = \frac{TVn}{TV 0 d}$

(3) Relative tumor volume proliferation rate:

$T / C % = \frac{Therapy group RTVxnd}{Solvent group RTVxnd} \times 100 %$

(4) Tumor growth inhibition rate:

$TGI % = [1 - \frac{({TV}_{xn} - {TV}_{x 0}}{({TV}_{Mn} - {TV}_{M 0})}] \times 100 %$

Note: V: tumor volume; A: tumor length; B: tumor width; RTV: relative tumor volume; TV_nd: tumor volume on day n; TV_0d: tumor volume on day 0; RTV_xnd: mean relative tumor volume on day n; TV_Xn: mean tumor volume of the therapy group on day n; TV_X0: mean tumor volume of the therapy group on day 0; TV_Mn: mean tumor volume of the solvent group on day n; and TV_M0: mean tumor volume of the solvent group on day 0

4.3.3 Tumor Weight

At the end of the experiment, after the animals were euthanized by CO₂asphyxiation, the tumors were excised and weighed.

Tumor weight inhibition rate %=(1-tumor weight in therapy group/tumor weight in solvent group)×100%

4.3.4 PK Blood Sampling and Detection

Before administration of the last dose of Bortezomib (0 h), and 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, 24 h after the administration, blood was sampled (as detailed in Table 8) (except that blood was sampled from the mice in the solvent group only at 0 h), anticoagulated with heparin, and centrifuged to separate plasma, which was stored at −80° C. for later use. Bortezomib and butyphthalide in the plasma were determined by protein precipitation-LC/MS/MS.

TABLE 18

List of Blood Sampling Time of Mice in Each Group

Group
Animal No.
Blood sampling time

Solvent group
1-6
0 h

Therapy groups
1-6
0, 5 min, 15 min, 30 min, 1 h,

2 h, 4 h, 8 h, 24 h

5. Experimental Results

5.1 Influence on Body Weight

As can be seen from the body weight data, there was no significant difference in the body weights of the mice in each group (P>0.05), indicating that none of Bortezomib, Palbociclib, and NBP had influence on the body weights of the mice, as detailed in FIG. 15.

5.2 Influence on Tumor Volume

At the end of the experiment, compared with the monotherapy group of Bortezomib, during the combined therapy of NBP/Bortezomib, NBP did not have obvious negative influence on the tumor inhibition efficacy of Bortezomib; and compared with the combined therapy group of Bortezomib/Palbociclib, in the combined therapy group of NBP/Bortezomib/Palbociclib, NBP did not have obvious negative influence on the antitumor efficacy of combined therapy of Bortezomib/Palbociclib, either. The tumor volume of each group is detailed in FIG. 16, and the body weight, TV, RTV, TGI %, T/C %, tumor weight, etc. at the end of the experiment (day 14) are detailed in Table 19.

TABLE 19

Summary of Various Index Parameters of NU/NU Mice on Day 14 of the Experiment

(mean ± SD, n = 6)

Bor/Pal
NBP/Bor/Pa
NBP/Bor

Bor
Pal
0.5/70
1 60/0.5/70
60/0.5
NBP 60

Index
Solvent
0.5 mg/kg
70 mg/kg
mg/kg
mg/kg
mg/kg
mg/kg

Body
24.4 ±
24.7 ±
23.9 ±
24.0 ±
24.1 ±
23.8 ±
24.9 ±

weight(g)
1.8
1.2
1.7
0.9
2.1
1.3
1.2

TV (mm³)
1220.4 ±
1124.8 ±
605.4 ±
436.7 ±
420.6 ±
876.9 ±
938.1 ±

625.3
260.5
388.7
178.3
178.9
300.8
451.9

RTV
9.8 ±
9.6 ±
4.3 ±
3.4 ±
3.3 ±
7.2 ±
7.2 ±

2.1
2.8
1.5
0.9
0.6
2.8
2.0

TGI %
—
8.7
56.3
71.7
73.1
31.3
25.8

T/C %

98.0
44.4
34.9
34.2
73.9
73.8

Tumor weight
1.648 ±
1.282 ±
0.550 ±
0.391 ±
0.413 ±
1.086 ±
1.040 ±

0.678
0.206
0.392
0.176
0.227
0.341
0.398

Tumor weight
—
22.2
66.6
76.3
75.0
34.1
36.9

inhibition rate

(%)

Note:

Bor represents Bortezomib, and Pal represents Palbociclib.

Conclusions: in this experiment, NBP did not have obvious influence on the antitumor efficacy of Bortezomib and of the combined therapy of Bortezomib/Palbociclib.

5.3 Influence on PK

The results showed that the Bortezomib exposure doses in the bodies of the mice in the Bortezomib group, the NBP/Bortezomib group, the Bortezomib/Palbociclib group, and the NBP/Bortezomib/Palbociclib group were substantially consistent, suggesting that NBP did not have obvious influence on the in vivo pharmacokinetic behaviors of the monotherapy of Bortezomib and the combined therapy of Bortezomib/Palbociclib. The main pharmacokinetic parameters are detailed in Table 20, Table 21, and Table 22.

TABLE 20

Summary of Main Pharmacokinetic Parameters of Bortezomib in

Plasma of NU/NU Mice (mean ± SD, n = 6)

Bor
Bor/Pal
NBP/Bor/Pal
NBP/Bor

Parameters (unit)
0.5 mg/kg
0.5/70 mg/kg
60/0.5/70 mg/kg
60/0.5 mg/kg

C_max(ng/mL)
113 ± 8
114 ± 17
128 ± 16
126 ± 37

AUC_0-t(h*ng/mL)
290 ± 104
322 ± 57
234 ± 66
264 ± 75

t_1/2(h)
56.6 ± 1.16
40.2 ± 14.8
65.6 ± 66.2
59.1 ± 63.5

Vd (L/kg)
14.2 ± 3.2
24.2 ± 6.4
37.2 ± 11.6
24.2 ± 7.1

CI(L/h/kg)
1.81 ± 0.56
0.44 ± 0.09
0.86 ± 0.67
0.97 ± 0.91

MRT_0-t(h)
5.9 ± 0.8
12.7 ± 2.2
10.5 ± 0.9
9.5 ± 4.2

TABLE 21

Summary of Main Pharmacokinetic Parameters of NBP in Plasma

of NU/NU Mice (mean ± SD, n = 6)

NBP/Bor/Pal
NBP/Bor
NBP

Parameters (unit)
60/0.5/70 mg/kg
60/0.5 mg/kg
60 mg/kg

C_max(ng/mL)
145 ± 108
125 ± 74
117 ± 88

AUC_0-t(h*ng/mL)
242 ± 259
433 ± 166
236 ± 100

t_1/2(h)
4.91 ± 2.52
10.9 ± 3.2
10.1 ± 9.7

Vd (L/kg)
1979 ± 1486
1723 ± 699
1445 ± 298

CI(L/h/kg)
258 ± 124
112 ± 36
173 ± 104

MRT_0-t(h)
2.1 ± 0.7
7.5 ± 1.2
3.1 ± 0.6

Note: In Tables 20 and 21, Bor represents Bortezomib, Pal represents Palbociclib, C_maxrepresents a maximum blood concentration, AUC_0-trepresents the area under the drug-time curve from 0 to t, t_1/2represents the half-life, Vd represents the apparent volume of distribution, CI represents the clearance rate, and MRT_0-trepresents the mean residence time from 0 to t.

TABLE 22

Results of Comparison between Mean Plasma Exposures of Bortezomib

and NBP in Combined Therapy Group and Monotherapy Group

Group
C_max
AUC_0-t
LN(C_max)
LN(AUC_0-t)

Ratio to monotherapy group of Bortezomib

Bor/Pal 0.5/70 mg/kg
1.01
1.11
1.00
1.02

NBP/Bor/Pal 60/0.5/70 mg/kg
1.13
0.81
1.05
0.96

NBP/Bor 60/0.5 mg/kg
1.12
0.91
1.02
0.98

Ratio to monotherapy group of NBP

NBP/Bor/Pal 60/0.5/70 mg/kg
1.24
1.03
1.05
1.00

NBP/Bor 60/0.5 mg/kg
1.08
1.83
1.02
1.11

Note:

Bor represents Bortezomib, and Pal represents Palbociclib.

The ratios of C_maxand AUC_0-tof Bortezomib in the combined therapy groups of Bortezomib/Palbociclib, the combined therapy groups of NBP/Bortezomib/Palbociclib, and the combined therapy groups of NBP/Bortezomib to those in the monotherapy group of Bortezomib were 1.01-1.13 and 0.81-1.11, respectively. Upon logarithmic transformation of C_maxand AUC_0-t, the ratios of the combined therapy groups of Bortezomib/Palbociclib, the combined therapy groups of NBP/Bortezomib/Palbociclib, and the combined therapy groups of NBP/Bortezomib to the monotherapy group of Bortezomib were 1.00-1.05 (LNC_max) and 0.96-1.02 (LNAUC_0-t), respectively, therefore the in vivo exposures of Bortezomib in the monotherapy group and the combined therapy groups were substantially consistent.

The ratios of C_maxand AUC_0-tof NBP in the combined therapy groups of NBP/Bortezomib/Palbociclib and the combined therapy groups of NBP/Bortezomib to those in the monotherapy group of NBP were 1.08-1.24 and 1.03-1.83, respectively. Upon logarithmic transformation of C_maxand AUC_0-t, the ratios of the combined therapy groups of NBP/Bortezomib/Palbociclib and the combined therapy groups of NBP/Bortezomib to the monotherapy group of NBP were 1.02-1.05 (LNC_max) and 1.00-1.11 (LNAUC_0-t), respectively. Due to the obvious individual differences in mice after intragastric administration of NBP, a small number of mice were arranged in each experimental group. The ratio of the exposure level of the combined therapy group to the exposure level of the monotherapy group after logarithmic transformation showed that the in vivo exposure of the monotherapy group of NBP was not obviously different from the in vivo exposure of the combined therapy group.

Conclusions: in this experiment, NBP substantially did not affect the pharmacokinetic behavior of Bortezomib in mice, and Bortezomib substantially did not affect the pharmacokinetic behavior of NBP in mice.

Number	Date	Country	Kind
202010202588.4	Mar 2020	CN	national
202010790778.2	Aug 2020	CN	national
202011233563.7	Nov 2020	CN	national

USE OF BUTYLPHTHALIDE AND DERIVATIVE THEREOF

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