Patent Application
20230120021
The present invention relates to a nanoparticle comprising a drug dimer and a use thereof.
Hydrophobic drugs have difficulty in drug delivery despite their excellent pharmacological effects. Therefore, in order to increase the utility of hydrophobic drugs, many studies have been conducted on drug delivery. In particular, polymeric nanoparticles have been used for drug delivery systems to increase the low solubility of hydrophobic drugs and increase the circulation rate in vivo, but there are limitations in that methods of preparing them are complex and the drug content is low. In order to overcome these limitations, a dimer compound is synthesized by attaching hydrophobic drug monomers to both sides of a linker, and nanoparticles having a high drug content are prepared through self-assembly (Milena Menozzi et al., JPharmSci, Jun. 1, 1984). However, the nanoparticles comprising the dimer compounds have a disadvantage in that stability and particle size are not homogenous.
Accordingly, as a result of studying to develop various drug dimers, the present inventors prepared a novel drug dimer. In addition, the present inventors developed a method of preparing a nanoparticle comprising a drug dimer, in which the nanoparticle has an increased stability and a homogenous particle size. In addition, when using a linker that decomposes in a specific environment, such as in the presence of GSH (Glutathione) or hydrogen peroxide, it was confirmed that it exhibits a more effective effect of treating a disease by releasing a drug monomer under a specific condition. Based on the above, the present inventors completed the present invention.
In order to achieve the above object, in an aspect of the present invention, there is provided a novel drug dimer and a nanoparticle comprising the same.
In another aspect of the present invention, there is provided a nanoparticle comprising the drug dimer and fucoidan.
In another aspect of the present invention, there is provided a pharmaceutical composition comprising the nanoparticles as an active ingredient.
A nanoparticle comprising a drug dimer and fucoidan, which is one embodiment of the present invention, can increase the drug content and improve the dispersibility of the drug. In addition, the nanoparticle has increased targeting efficiency. Therefore, an effective pharmacological effect can be obtained by using a drug in a less amount, and thus the toxicity of the drug can be significantly reduced. Therefore, the nanoparticle has excellent commercial applicability.
As used herein, the term “solvate” refers to a compound solvated in an organic or inorganic solvent. The solvate is, for example, a hydrate.
As used herein, the term “salt” refers to an inorganic and organic acid addition salt of a compound. The pharmaceutically acceptable salt may be a salt that does not cause serious irritation to the organism to which the compound is administered, and does not impair the biological activity and physical properties of the compound. The inorganic acid salt may be hydrochloride, bromate, phosphate, sulfate, or disulfate. The organic acid salt may be formate, acetate, propionate, lactate, oxalate, tartrate, malate, maleate, citrate, fumarate, besylate, camsylate, edisylate, trichloroacetate, trifluoroacetate, benzoate, gluconate, methanesulfonate, glycolate, succinate, 4-toluenesulfonate, galacturonate, embonate, glutamate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, or aspartate. The metal salt may be a calcium salt, a sodium salt, a magnesium salt, a strontium salt, or a potassium salt.
As used herein, the term “fucoidan” is a sulfated polysaccharide having a sticky viscous structure, and is a component generally contained in brown algae such as seaweed and kelp, and has a molecular weight of 20 kDa on average, and is a substance in which fucose, which is a basic sugar, and sulfuric acid groups are bound. Fucoidan is known to have various physiological and biological activities such as antioxidants, anticoagulants, anticancer agents, and antibiotics.
As used herein, the term “nanoparticle comprising fucoidan” refers to the presence of fucoidan in the nanoparticle. The term may be expressed as a nanoparticle coated with fucoidan. In addition, the term “nanoparticle comprising a drug dimer and fucoidan” refers to a nanoparticle formed by aggregation of fucoidan and a drug dimer, and fucoidan may be present inside and/or outside the nanoparticle.
As used herein, the term “retinoid” refers to a natural or synthetic derivative of vitamin A, and is classified into retinol, which is retinoid that is naturally present in the human body, vitamin A, retinaldehyde, retinal, vitamin A aldehyde, and retinoic acid. Retinoid is activated in the form of retinoic acid in vivo, and is used in the treatment of several skin diseases through various actions. Retinoic acid activated in vivo not only regulates the proliferation and differentiation of keratinocytes, but also inhibits sebaceous glands and regulates immunity. Therefore, it is widely used in the treatment of diseases such as acne and psoriasis or malignant tumors such as skin cancer and T cell lymphoma.
As used herein, the term “ursodeoxycholic acid (UDCA)” is a major component of Bear's gall, which is gall bladder of a bear, and has strong detoxification ability. Therefore, the UDCA is used as a therapeutic agent for liver diseases by activating liver detoxification and metabolic functions and preventing cholesterol from accumulating in the liver. Currently, the UDCA is reported to be effective in treating colorectal cancer, liver cancer, pancreatic cancer and the like in addition to bile or bile duct disease.
As used herein, the term “4-(hydroxymethyl)phenyl benzoate” is also referred to as PB, and is decomposed in vivo to generate quinone methide (QM). The quinone methide is known to have anticancer activity.
As used herein, the term “paclitaxel (PTX)” is an anticancer substance that is most often used for the treatment of breast cancer, ovarian cancer, head and neck cancer, kaposi's sarcoma, non-small cell lung cancer and the like.
As used herein, the term “doxorubicin (DOX)” is an anthracycline-based anticancer agent that is widely used in breast cancer, lung cancer, lymphoma, gastrointestinal cancer and sarcoma, and causes immunological death i.e., immunogenic cell death (ICD) against cancer cells.
As used herein, the term “camptothecin (CPT)” is an alkaloid component isolated from the bark and stem of a tree called Camptotheca acuminata, and is a topoisomerase inhibitor. It has a wide range of anticancer activity and is well known as a first-line drug used in the treatment of metastatic rectal cancer. In addition, it is also used in the treatment of lung cancer, ovarian cancer, mammary cancer, gastric cancer, pancreatic cancer and the like.
Hereinafter, the present invention will be described in more detail.
Retinoid Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a retinoid dimer compound represented by formula 1a below, a solvate or a pharmaceutically acceptable salt thereof:
in formula 1a above,
L1 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L1 may be
m1, m2, p1 and p2 are each an integer of 1 to 10. Specifically, m1, m2, p1 and p2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which any one or two monomers of the compounds represented by formulas 1b to 1d below are bound to each other:
One embodiment of the dimer compound may be represented by formula 1e below:
Another aspect of the present invention provides a nanoparticle comprising the retinoid dimer compound.
Here, the size of the nanoparticle may range from 200 nm to 1,500 nm. Specifically, the size of the nanoparticle may range from 200 nm to 500 nm.
Another aspect of the present invention provides a nanoparticle comprising the retinoid dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 200 nm to 300 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the retinoid dimer compound, or a nanoparticle comprising the retinoid dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer or skin disease.
Ursodeoxycholic Acid Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a ursodeoxycholic acid dimer compound represented by formula 2a below, a solvate or a pharmaceutically acceptable salt thereof:
in formula 2a above,
L2 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L2 may be
m1, m2, p1 and p2 are each an integer of 1 to 10. Specifically, m1, m2, p1 and p2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 2b below is bound to each other:
in formula 2b above, n is each an integer of 1 to 10.
One embodiment of the dimer compound may be represented by formula 2c below:
Another aspect of the present invention provides a nanoparticle comprising the ursodeoxycholic acid dimer compound.
Here, the size of the nanoparticle may range from 200 nm to 500 nm.
Another aspect of the present invention provides a nanoparticle comprising the ursodeoxycholic acid dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 200 nm to 500 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the ursodeoxycholic acid dimer compound, or a nanoparticle comprising the ursodeoxycholic acid dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of liver disease, cancer, or cardiovascular disease.
4-(Hydroxymethyl)Phenyl Benzoate Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a 4-(hydroxymethyl)phenyl benzoate dimer compound represented by formula 3a below, a solvate, or a pharmaceutically acceptable salt thereof:
in formula 3a above,
L3 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L3 may be
s1, s2, t1 and t2 are each an integer of 1 to 10. Specifically, s1, s2, t1 and t2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 3b below is bound to each other:
One embodiment of the dimer compound may be represented by formula 3c below:
Another aspect of the present invention provides a nanoparticle comprising the 4-(hydroxymethyl)phenyl benzoate dimer compound.
Here, the size of the nanoparticle may range from 200 nm to 600 nm.
Another aspect of the present invention provides a nanoparticle comprising the 4-(hydroxymethyl)phenyl benzoate dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 100 nm to 500 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the 4-(hydroxymethyl)phenyl benzoate dimer compound, or a nanoparticle comprising the 4-(hydroxymethyl)phenyl benzoate dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer.
4-(Hydroxymethyl)Phenylboronic Acid Pinacol Ester Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a 4-(hydroxymethyl)phenylboronic acid pinacol ester dimer compound represented by formula 4a below, a solvate or a pharmaceutically acceptable salt thereof:
in formula 4a above, L4 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L4 may be any one selected from the group consisting of
s1, s2, t1, t2, q1, q2, r1 and r2 are each an integer of 1 to 10. s1, s2, t1, t2, q1, q2, r1 and r2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 4b below is bound to each other:
One embodiment of the dimer compound may be represented by formula 4c or formula 4d below:
Another aspect of the present invention provides a nanoparticle comprising the 4-(hydroxymethyl)phenylboronic acid pinacol ester dimer compound.
Here, the size of the nanoparticle may range from 100 nm to 800 nm.
Another aspect of the present invention provides a nanoparticle comprising the 4-(hydroxymethyl)phenylboronic acid pinacol ester dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 200 nm to 500 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the 4-(hydroxymethyl)phenylboronic acid pinacol ester dimer compound, or a nanoparticle comprising the 4-(hydroxymethyl)phenylboronic acid pinacol ester dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer.
Paclitaxel Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a paclitaxel dimer compound represented by formula 5a below, a solvate or a pharmaceutically acceptable salt thereof:
in formula 5a above, L5 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L5 may be
x1, x2, y1 and y2 are each an integer of 1 to 10. Specifically, x1, x2, y1 and y2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 5b below is bound to each other:
One embodiment of the dimer compound may be represented by formula 5c below:
Another aspect of the present invention provides a nanoparticle comprising the paclitaxel dimer compound.
Here, the size of the nanoparticle may range from 100 nm to 400 nm.
Another aspect of the present invention provides a nanoparticle comprising the paclitaxel dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 100 nm to 300 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticle. Here, the nanoparticle may be a nanoparticle comprising the paclitaxel dimer compound, or a nanoparticle comprising the paclitaxel dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer.
Doxorubicin Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a doxorubicin dimer compound represented by formula 6a below, a solvate or a pharmaceutically acceptable salt thereof:
[Formula 6a]
in formula 6a above, L6 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L6 may be
x1, x2, y1 and y2 are each an integer of 1 to 10. Specifically, x1, x2, y1 and y2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 6b below is bound to each other:
One embodiment of the dimer compound may be represented by formula 6c below:
Another aspect of the present invention provides a nanoparticle comprising the doxorubicin dimer compound.
Here, the size of the nanoparticle may range from 150 nm to 200 nm.
Another aspect of the present invention provides a nanoparticle comprising the doxorubicin dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 100 nm to 200 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the doxorubicin dimer compound, or a nanoparticle comprising the doxorubicin dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer.
Camptothecin Dimer and Nanoparticle Comprising the Same
One aspect of the present invention provides a camptothecin dimer compound represented by formula 7a below, a solvate or a pharmaceutically acceptable salt thereof:
in formula 7a above, L7 may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—.
The linker may be any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each an integer of 1 to 10.
In one embodiment, L7 may be
q1, q2, r1 and r2 are each an integer of 1 to 10. Specifically, q1, q2, r1 and r2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
Here, the dimer compound may be one in which a compound represented by formula 7b below is bound to each other:
One embodiment of the dimer compound may be represented by formula 7c below:
Another aspect of the present invention provides a nanoparticle comprising the camptothecin dimer compound.
Here, the size of the nanoparticle may range from 100 nm to 600 nm.
Another aspect of the present invention provides a nanoparticle comprising the camptothecin dimer compound and fucoidan.
Here, the size of the nanoparticle may range from 100 nm to 300 nm. Here, the fucoidan may be comprised in an amount of 10 to 30 parts by weight based on 100 parts by weight of the dimer compound.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles. Here, the nanoparticle may be a nanoparticle comprising the camptothecin dimer compound, or a nanoparticle comprising the camptothecin dimer compound and fucoidan.
The pharmaceutical composition may be for the prevention or treatment of cancer.
Nanoparticle Comprising Drug Dimer and Fucoidan and Use Thereof
One aspect of the present invention provides a nanoparticle comprising a dimer compound consisting of structural formula (I) below:
A-L-A (I)
in structural formula (I) above, A may be a drug containing two or more aromatic rings, in which —OH, —NH, and/or —COOH is present. Specifically, the drug may be any one selected from the group consisting of retinoid, ursodeoxycholic acid, 4-(hydroxymethyl)phenyl benzoate, 4-(hydroxymethyl)phenylboronic acid pinacol ester, paclitaxel, doxorubicin, and camptothecin.
L may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—. Specifically, L may be any one selected from the group consisting of
Here, m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 are each an integer of 1 to 10. Specifically, m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
The linking site between the drug and the linker may consist of a structure capable of hydrolysis such as ester, amide, carbonate, carbamate, urea and the like. Specifically, the linker may be decomposed by glutathione or reactive oxygen species.
As used herein, the term “nanoparticle comprising a drug dimer” may be expressed in various ways. For example, when —SS— is included as a linker, it may be described as a nanoparticle comprising a retinoid-SS-retinoid dimer or a retinoid-SS-retinoid dimer nanoparticle.
In addition, when —S— is included as a linker, it may be described as a nanoparticle comprising a retinoid-S-retinoid dimer or a retinoid-S-retinoid dimer nanoparticle.
Here, the nanoparticle may further comprise fucoidan. Here, the fucoidan may be included in an amount of 30% or less of the total content of the nanoparticles. Specifically, the drug dimer and fucoidan may have a weight ratio of 70:30 to 95:5. In one embodiment, the drug dimer and fucoidan may have a weight ratio of 70:30, 75:25, 80:20, 85:15, 90:10, or 95:5.
Here, the nanoparticle comprising fucoidan may have an excellent effect of targeting to p-Selectin by fucoidan.
Another aspect of the present invention provides a pharmaceutical composition comprising the nanoparticles.
As used herein, the term “prevention” refers to any action that inhibits or delays the onset of cancer, skin disease, liver disease, or cardiovascular disease by the administration of the pharmaceutical composition. As used herein, the term “treatment” refers to any action that improves or beneficially modifies symptoms of a disease related to cancer, skin disease, liver disease, or cardiovascular disease by the administration of the pharmaceutical composition.
The pharmaceutical composition may comprise a pharmaceutically acceptable carrier. The carrier is used in the sense of including an excipient, diluent or adjuvant. The carrier may be selected from the group consisting of, for example, lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, gum acacia, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, polyvinylpyrrolidone, water, physiological saline, a buffer such as PBS, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, and mineral oil. The composition may comprise a filler, an anti-aggregating agent, a lubricant, a wetting agent, a flavoring agent, an emulsifying agent, a preservative, or a combination thereof.
The pharmaceutical composition may be prepared in any formulation according to conventional methods. The composition may be formulated, for example, in an oral formulation (for example, a powder, a tablet, a capsule, a syrup, a pill, or a granule), or parenteral formulation (for example, an injection). In addition, the composition may be prepared as a systemic formulation or a topical formulation.
In the pharmaceutical composition, the solid preparation for oral administration may be a tablet, a pill, a powder, a granule, or a capsule. The solid preparation may further comprise an excipient. The excipient may be, for example, starch, calcium carbonate, sucrose, lactose, or gelatin. In addition, the solid preparation may further comprise a lubricant such as magnesium stearate or talc. In the pharmaceutical composition, the liquid preparation for oral administration may be a suspension, an internal solution, an emulsion, or a syrup. The liquid preparation may comprise water or liquid paraffin. The liquid preparation may comprise an excipient, for example, a wetting agent, a sweetening agent, a flavoring agent, or a preservative. In the pharmaceutical composition, the preparation for parenteral administration may be a sterile aqueous solution, a non-aqueous solvent, a suspension, an emulsion, a freeze-dried preparation and/or a suppository. The non-aqueous solvent or suspension may comprise a vegetable oil or an ester. The vegetable oil may be, for example, propylene glycol, polyethylene glycol, or olive oil. The ester may be, for example, ethyl oleate. The base of the suppository may be witepsol, macrogol, tween 61, cacao butter, laurin butter, or glycerogelatin.
The pharmaceutical composition comprises nanoparticles comprising a drug dimer compound according to one aspect or nanoparticles comprising a drug dimer compound and fucoidan as an active ingredient of the pharmaceutical composition. The “active ingredient” refers to a physiologically active substance used to achieve pharmacological activity (for example, cancer treatment).
The pharmaceutical composition may comprise nanoparticles comprising a drug dimer compound according to one aspect or nanoparticles comprising a drug dimer compound and fucoidan in an effective amount. As used herein, the term “effective amount” refers to an amount sufficient to exhibit the effect of preventing or treating a disease when administered to a subject in need of prevention or treatment. The effective amount can be appropriately selected by a person skilled in the art according to the selected cell or subject. The preferred dosage of the pharmaceutical composition may vary depending on the condition and body weight of the subject, the severity of disease, the drug formulation, the route and duration of administration, but may be appropriately selected by a person skilled in the art. However, the nanoparticles comprising a drug dimer compound or the nanoparticles comprising a drug dimer compound and fucoidan may be administered, for example, in an amount of about 0.0001 mg/kg to about 100 mg/kg, or about 0.001 mg/kg to about 100 mg/kg, which may be divided into once to 24 times a day, 1 to 7 times every 2 days to 1 week, or once to 24 times every 1 month to 12 months. In the pharmaceutical composition, the compound, solvate or pharmaceutically acceptable salt thereof may be included in an amount of about 0.0001% by weight to about 10% by weight, or about 0.001% by weight to about 1% by weight based on the total weight of the entire composition.
The method of administration may be oral or parenteral administration. The method of administration may be, for example, oral, transdermal, subcutaneous, rectal, intravenous, intraarterial, intraperitoneal, intramuscular, intrasternal, topical, intranasal, intratracheal, or intradermal route. The composition may be administered systemically or topically, and may be administered alone or in combination with other pharmaceutically active compounds.
The pharmaceutical composition may be for the prevention or treatment of a disease selected from the group consisting of cancer, skin disease, liver disease, and cardiovascular disease.
Specifically, the pharmaceutical composition may be applied to the prevention or treatment of gastric cancer, liver cancer, lung cancer, colorectal cancer, breast cancer, prostate cancer, ovarian cancer, pancreatic cancer, cervical cancer, thyroid cancer, laryngeal cancer, acute myelogenous leukemia, brain tumor, neuroblastoma, retinoblastoma, head and neck cancer, salivary gland cancer, and lymphoma.
Another aspect of the present invention provides a use of a pharmaceutical composition comprising nanoparticles comprising a dimer compound consisting of structural formula (I) according to one aspect; or nanoparticles comprising a dimer compound consisting of structural formula (I) and fucoidan for the prevention or treatment of a disease related to cancer, skin disease, liver disease, or cardiovascular disease.
The compound of structural formula (I) above is as described above. In addition, the content of fucoidan and the disease are as described above.
Method for Preventing and Treating Disease Using Nanoparticles
Another aspect of the present invention provides a method for preventing or treating a disease related to cancer, skin disease, liver disease, or cardiovascular disease, comprising: administering to a subject nanoparticles comprising a dimer compound consisting of structural formula (I) according to one aspect; or nanoparticles comprising a dimer compound consisting of structural formula (I) and fucoidan.
The compound of structural formula (I) is as described above. In addition, the subject may be a mammal, for example, a human, a mouse, a rat, a cow, a horse, a pig, a dog, a monkey, a sheep, a goat, an ape, or a cat. The subject may be a subject who suffers from or is likely to suffer from symptoms associated with the disease.
The method of administration may be oral or parenteral administration. The method of administration may be, for example, oral, transdermal, subcutaneous, rectal, intravenous, intraarterial, intraperitoneal, intramuscular, intrasternal, topical, intranasal, intratracheal, or intradermal route. The pharmaceutical composition may be administered systemically or topically, and may be administered alone or in combination with other pharmaceutically active compounds.
The preferred dosage of the pharmaceutical composition may vary depending on the condition and body weight of the patient, the severity of disease, the drug formulation, the route and duration of administration, but may be appropriately selected by a person skilled in the art. The dosage may be, for example, in the range of about 0.001 mg/kg to about 100 mg/kg, about 0.01 mg/kg to about 10 mg/kg, or about 0.1 mg/kg to about 1 mg/kg based on the adult dosage. The dosage may be administered once a day, multiple times a day, or once a week, once every two weeks, once every three weeks, or once every four weeks to once a year.
Method of Preparing Nanoparticle Comprising Drug Dimer and Fucoidan
One aspect of the present invention provides a method of preparing a nanoparticle comprising a drug dimer and fucoidan, comprising: mixing a dimer compound consisting of structural formula (I) below and fucoidan at a weight ratio of 80:20 to 95:5:
A-L-A (I)
in structural formula (I) above,
A is any one selected from the group consisting of retinoid, ursodeoxycholic acid, 4-(hydroxymethyl)phenyl benzoate, 4-(hydroxymethyl)phenylboronic acid pinacol ester, paclitaxel, doxorubicin, and camptothecin.
L may be a linker of C2-10 and include —S—, —SS—, —SSS—, —SeSe—, or —Se—. Specifically, L is any one selected from the group consisting of
and m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 are each an integer of 1 to 10. Specifically, m1, m2, p1, p2, s1, s2, t1, t2, q1, q2, r1, r2, x1, x2, y1 and y2 may be each 1, 2, 3, 4, 5, 6, 7, 8 or 10.
In the present specification, a nanoparticle refers to a compound formed through self-assembly of a dimer compound. In one embodiment of the present invention, the nanoparticle has a nano-unit size, and may be specifically formed in a size of 1 to 999 nm, 100 to 900 nm, 100 to 800 nm, 100 to 700 nm, 100 to 600 nm, 100 to 500 nm, 100 to 400 nm, or 100 to 300 nm. More specifically, it may be formed in a size of 200 to 300 nm. However, it is not limited thereto, and may vary depending on the type of drug.
In the present specification, a linker is a structure that connects drug monomers. For example, there are a sulfide bond-based linker, a thioketal-based linker, a selenide-based linker and the like. However, it is not limited thereto. In one embodiment of the present invention, the sulfide bond-based linker may include a sulfide bond or a disulfide bond.
In one embodiment of the present invention, the linker may be decomposed by glutathione or reactive oxygen species. However, it is not limited thereto.
In the present specification, a target cell refers to a cell having a membrane protein to which fucoidan is capable of binding. In one embodiment of the present invention, a target cell may be a cancer cell, a cardiovascular cell, or a liver cell. However, it is not limited thereto.
The weight ratio of a drug dimer and fucoidan may be 80:20 to 95:5. In one embodiment of the present invention, a dispersant may be added to the fucoidan solution in order to increase the dispersibility of the nanoparticles. Specifically, the dispersant includes polyvinyl alcohol (PVA). However, it is not limited thereto.
In one embodiment of the present invention, after preparing the nanoparticles, it may be performed by further comprising a step of freeze-drying. However, it is not limited thereto.
Hereinafter, the present invention will be described in more detail by way of the following examples. However, the following examples are only for illustrating the present invention, and the scope of the present invention is not limited thereto.
Retinoic acid (2 g) and 1,1′-carbonyldiimidazole (1.08 g) were dissolved in dichloromethane (20 mL) and then reacted at room temperature for 30 minutes. The mixture was separated and purified by silica gel chromatography (ethyl acetate/hexane, 1:1) to synthesize Compound 1.
Compound 1 (2 g) and cystamine dihydrochloride (1.74 g) were dissolved in 5 mL of dimethyl sulfoxide under nitrogen filling. After raising the temperature to 47° C., the reaction was carried out while stirring for 12 hours. Dimethyl sulfoxide and water were removed through water precipitation, centrifugation, and freeze-drying processes, and then separated and purified by silica gel chromatography (ethyl acetate/hexane, 1:1) to synthesize a retinoid dimer compound (RASS) (
1H NMR (400 MHz, DMSO-d6): δ 1.16 (12H, s), 1.33 (4H, m), 1.55 (4H, m), 1.72 (6H, s), 1.97 (6H, s), 2.06-2.16 (10H, m), 3.31-3.35 (8H, m), 6.10 (2H, s), 6.30-6.47 (6H, m), 6.65 (2H, d), 6.81 (2H, dd).
The nanoparticles were prepared by dispersing a RASS solution, which 50 mg of RASS prepared in Example 1 above was dissolved in 0.2 mL of methanol, using a syringe. Thereafter, methanol was removed using a rotary evaporator. The solution in which the nanoparticles were produced was centrifuged at 4° C. for 5 minutes under a condition of 15,000×g. After centrifugation, the supernatant was removed, and the resulting pellet was dispersed in PBS, and then centrifuged once more under the same conditions. The resulting pellet was dispersed in about 2 mL of PBS, frozen with liquid nitrogen, and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the RASS nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed.
100 mg of RASS was dissolved in 1 mL of methanol, and then the mixture was stirred while slowly adding to 20 mL of PBS in which 20 mg to 50 mg of BSA was dissolved. The mixture was sonicated for 3 minutes and homogenized for 2 minutes using a homogenizer. After removing methanol while stirring at room temperature for 5 hours, the RASS emulsion was centrifuged for 4 minutes at a rate of 11,000×g. The precipitated RASS nanoparticles were washed with water and then freeze-dried to obtain the RASS nanoparticles.
50 mg of RASS prepared in Example 1 above was dissolved in 0.2 mL of methanol, and 10 mg of fucoidan was dissolved in 1 mL of PBS. The RASS solution dissolved in methanol was added dropwise to a fucoidan solution (10 mL) dissolved in PBS using a syringe, and the nanoparticles formed during sonication were dispersed. Thereafter, methanol was removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution in which the nanoparticles were produced was centrifuged at 4° C. for 5 minutes under a condition of 15,000×g. After centrifugation, the supernatant was removed, and the resulting pellet was dispersed in PBS, and then centrifuged once more under the same conditions. The resulting pellet was dispersed in about 2 mL of PBS and then frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the RASS nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed (
In addition, in order to anaylize physical properties when preparing nanoparticles using a biologically derived polymer (albumin) other than fucoidan, the RASS nanoparticles comprising albumin were prepared as in Comparative Example 1 and compared and analyzed (
As a result, when albumin was used, nanoparticles were formed when treated at a higher concentration. When fucoidan was used, nanoparticles were formed even when treated at a low concentration. Therefore, it was confirmed that nanoparticles are well formed when fucoidan is used compared to albumin.
The retinoid dimer nanoparticles comprising fucoidan prepared in Example 3 above and retinoic acid were dispersed in PBS, and each of lung cancer A549 and prostate cancer DU145 cells was treated therewith. After 24 hours treatment, 100 μL of MTT solution was added on the cells. After 3 hours, 1 mL of DMSO was added to dissolve the crystal. After 10 minutes, the absorbance was measured at 570 nm to analyze the cell viability. As a result, it was confirmed that cell death appeared when the cells were treated with the nanoparticles at a high level (
The cancer targeting ability of each of the nanoparticles (RASS, Fu-RASS) prepared in Examples 2 and 3 above was examined. Tumorigenesis was induced by injecting about 2×106 A549 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected through the tail vein. For the tumor target image, nanoparticles carrying a fluorescent substance IR780 were used, and the targeting of the tumor was confirmed by comparative analysis for about 2 days. As a result, it was confirmed that the nanoparticles comprising fucoidan accumulate in cancer at a high concentration over time (
The cancer therapeutic efficacy of each of the nanoparticles (RASS, Fu-RASS) prepared in Examples 2 and 3 above was confirmed. Tumorigenesis was induced by injecting about 2×106 A549 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected daily for 3 days through the tail vein. For 30 days, the cancer size and the weight of the mice were monitored, and the therapeutic effect was compared and analyzed. As a result, the nanoparticles comprising fucoidan showed excellent cancer scavenging ability (
In order to evaluate liver toxicity, the retinoid (Fu-RASS) nanoparticles comprising fucoidan were intravascularly injected into normal mice at a concentration of 20 mg/kg. After 5 injections once every 3 days, blood was collected and analyzed for alanine transaminase (ALT). The liver, heart, lung, spleen, and kidney were excised, and the tissues were stained by H&E and analyzed for safety in vivo through histological analysis. It was confirmed that the toxicity of the substance was less because inflammation was not expressed in other organs including liver toxicity (
Ursodeoxycholic acid (2.54 mmol), 1-ethyl-3-(dimethylaminophenyl) carbonyldiimide (5.089 mmol), and hydroxybenzotriazole (5.089 mmol) were added to a round flask, and 20 mL DMSO was added. After completely dissolving, the flask was placed in ice water, and cystamine dihydrochloride (1.211 mmol) dissolved in 1 mL of DMSO was added dropwise while stirring. Trimethylamine (6.539 mmol) was slowly added to the reaction mixture and reacted at a temperature of 40° C. for 48 hours. Trimethylamine was removed using a rotary evaporator and added to 250 ml of distilled water, and the precipitate was obtained by centrifugation at a rate of 12,000×g for 10 minutes. All water was removed through freeze-drying to obtain ssUDCA (
1H NMR (400 MHz, DMSO-d6): δ 0.71 (6H, s), 0.98 (12H, d), 1.00-1.31 (10H, m), 1.36-2.18 (38H, m), 2.58 (4H, s), 2.82 (4H, s), 3.32-3.51 (4H, m), 3.84 (2H, s), 4.49 (2H, s), 8.42 (2H, s).
30 mg of ssUDCA was dissolved in 1 mL of tetrahydrofuran and then added dropwise to 10 mL of distilled water while stirring. The mixed solution was sonicated for 1 minute to homogenize. Tetrahydrofuran was removed while stirring at room temperature for 3 hours and then centrifuged at a rate of 12,000×g for 8 minutes. The ssUDCA nanoparticles forming a precipitate were washed three times with water and freeze-dried. The dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the UDCA nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed (
30 mg of ssUDCA was dissolved in 1 mL of tetrahydrofuran, and then 3 mg of fucoidan was dissolved in 10 mL of distilled water to prepare each solution. The ssUDCA solution was added dropwise using an injection needle while stirring rapidly the fucoidan solution. The mixed solution was sonicated for 1 minute to homogenize. Tetrahydrofuran was removed while stirring at room temperature for 3 hours and then centrifuged at a rate of 12,000×g for 8 minutes. The ssUDCA nanoparticles forming a precipitate were washed three times with water and freeze-dried. The dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the UDCA nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed (
The cancer targeting ability of each of the nanoparticles prepared in Examples 5 and 6 above was examined. Tumorigenesis was induced by injecting about 2×106 SW620 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected through the tail vein.
For the tumor target image, nanoparticles carrying a fluorescent substance IR780 were used, and the targeting of the tumor was confirmed by comparative analysis based on 12 hours. As a result, it was confirmed that the nanoparticles comprising fucoidan have excellent cancer targeting ability (
Hydroxybenzyl alcohol (6.0 g) and triethylamine (6.73 mL) were dissolved in 250 mL of dichloromethane and stirred at 0° C. for 30 minutes. Benzoyl chloride (6 mL) was dissolved in 50 mL of dichloromethane, and then added to a hydroxybenzyl alcohol solution, and then reacted at room temperature for 12 hours. The prepared compound (PB) was obtained through a silica column using ethyl acetate/hexane (1:3).
The prepared PB (3.0 g) and 1,1′-carbonyldiimidazole (3.0 g) were dissolved in 15 mL of dichloromethane and then reacted for 1 hour at room temperature. The synthesized substance (PB-CDI) was obtained through a silica column using ethyl acetate/hexane (1:2).
Cystamine dihydrochloride (0.47 g) was dissolved in 9 mL of dimethyl sulfoxide under a nitrogen environment. The prepared PB-CDI (2.0 g) was dissolved in 1 mL of dimethyl sulfoxide and then mixed with a cystamine dihydrochloride solution. It was reacted for 12 hours at a temperature of 40° C. Water and dichloromethane were added to the reaction solution to extract the product, and then dichloromethane was removed using a rotary evaporator. The product was precipitated by adding 10 mL of methanol to the concentrated product solution, and then separated through a silica column (
1H NMR (400 MHz, DMSO-d6): δ 2.82 (4H, t), 3.27 (4H, t), 5.02 (4H, s), 7.24 (4H, d), 7.43 (4H, d), 7.58 (4H, t), 7.73 (2H, t), 8.11 (4H, t).
30 mg of ssPB was dissolved in 1 mL of tetrahydrofuran and then added dropwise to 15 mL of distilled water using an injection needle while stirring rapidly. The mixed solution was sonicated for 1 minute to homogenize. Tetrahydrofuran was removed while stirring at room temperature for 3 hours and then centrifuged at a rate of 12,000×g for 8 minutes. The ssUDCA nanoparticles forming a precipitate were washed three times with water and freeze-dried. The dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the UDCA nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed.
30 mg of ssPB was dissolved in 1 mL of tetrahydrofuran, and then 3 mg of fucoidan was dissolved in 15 mL of distilled water to prepare each solution. The ssUDCA solution was added dropwise using an injection needle while stirring rapidly the fucoidan solution. The mixed solution was sonicated for 1 minute to homogenize. Tetrahydrofuran was removed while stirring at room temperature for 3 hours and then centrifuged at a rate of 12,000×g for 8 minutes. The ssUDCA nanoparticles forming a precipitate were washed three times with water and freeze-dried. The dried nanoparticles were used by dispersing in PBS immediately before use. On the other hand, the UDCA nanoparticles were excellent in re-dispersibility, so the use of PVA was not needed (
The cytotoxicity of the ssPB nanoparticles was analyzed by the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) method. SW620 and DU145 cells were treated with the ssPB nanoparticles. After 24 hours treatment, 100 μL of MTT solution was added. After 3 hours, 1 mL of DMSO was added to dissolve the crystal. After 10 minutes, the absorbance was measured at 570 nm to analyze the cell viability. In addition, the cell viability was analyzed according to the presence or absence of N-acetylcysteine (NAC), which is an antioxidant (
In order to confirm the cell apoptosis induction of the ssPB nanoparticles, a cell apoptosis marker Annexin V-FITC and a viability marker propidium iodide were used and the cells were analyzed by flow cytometer. It was confirmed that the cell death rate increased as the concentration increased (
The cancer targeting ability of each of the nanoparticles prepared in Examples 8 and 9 above was examined. Tumorigenesis was induced by injecting about 2×106 SW620 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected through the tail vein.
For the tumor target image, nanoparticles carrying a fluorescent substance IR780 were used, and the targeting of the tumor was confirmed by comparative analysis based on 24 hours. The ssPB nanoparticles to which fucoidan was added continued to accumulate into the tumor for up to 24 hours, but most of the nanoparticles to which fucoidan was not added were accumulated into the liver or excreted (
Since a high concentration of accumulation occurs in the tumor site or liver site, in order to evaluate liver toxicity, the ssPB nanoparticles comprising fucoidan were injected into normal mice through the tail vein at a concentration of 10 mg/kg or 20 mg/kg. After 5 injections once every 3 days, blood was collected and analyzed for alanine transaminase (ALT). As a result, there was a tendency to increase little by little, but all of the values were within the normal range, and the toxicity was not shown (
4-(hydroxymethyl)phenylboronic acid pinacol ester (2.0 g) and 1,1′-carbonyldiimidazole (2.07 g) were dissolved in 25 mL of dichloromethane and then reacted for 2 hours at room temperature. The synthesized substance BR-CDI was obtained through a silica column using ethyl acetate/hexane (1:1).
2,2-thiobis(ethylamine) (1 g) and BR-CDI (5.46 g) were dissolved in 9 mL of dimethyl sulfoxide under a nitrogen environment. It was reacted at room temperature for 12 hours. The resulting sBR was separated through a silica column using ethyl acetate/hexane (1:1).
1H NMR (400 MHz, DMSO-d6): δ 1.28 (24H, s), 2.58 (4H, t), 3.18 (4H, t), 5.09 (4H, s), 7.36 (4H, d), 7.41 (2H, t), 7.66 (4H, d).
1 mL of tetrahydrofuran in which 10 mg of sBR was dissolved was slowly added dropwise to distilled water while stirring rapidly. The mixture was sonicated for 1 minute and homogenized for 1 minute using a homogenizer. Tetrahydrofuran was removed using a rotary evaporator, a solution in which sBR was emulsified was centrifuged at a rate of 11,000×g for 4 minutes. The precipitated sBR nanoparticles were washed with water, and then freeze-dried to obtain the sBR nanoparticles.
1 mL of tetrahydrofuran in which 10 mg of sBR was dissolved was slowly added to 20 mL of PBS in which 1 mg of fucoidan was dissolved while stirring slowly. The mixture was sonicated for 1 minute and homogenized for 1 minute using a homogenizer. Tetrahydrofuran was removed using a rotary evaporator, and then a solution in which sBR was emulsified was centrifuged at a rate of 11,000×g for 4 minutes. The precipitated sBR nanoparticles were washed with water, and then freeze-dried to obtain the sBR nanoparticles.
The size and shape of the prepared nanoparticles were analyzed through a particle size analyzer and an electron microscope, and the surface potential of the nanoparticles was also compared and analyzed. It was determined that 10% of fucoidan showed the optimum concentration, and it was difficult to exhibit the properties of nanoparticles as the concentration of fucoidan increased. It was determined to be most appropriate when the concentration of fucoidan was 10 to 30% (
In order to evaluate liver toxicity, the sBR nanoparticles comprising fucoidan were intravascularly injected into normal mice at a concentration of 10 mg/kg. After 5 injections once every 3 days, blood was collected and analyzed for alanine transaminase (ALT). The liver, heart, lung, spleen, and kidney were excised, and the tissues were stained by H&E and analyzed for safety in vivo through histological analysis. As a result, it was confirmed that a significant toxicity was not shown (
4-(hydroxymethyl) phenylboronic acid pinacol ester (2.0 g) and 1,1′-carbonyldiimidazole (2.07 g) were dissolved in 25 mL of dichloromethane and then reacted for 2 hours at room temperature. The synthesized substance BR-CDI was obtained through a silica column using ethyl acetate/hexane (1:1).
Dithiodiethanol (1 g) and BR-CDI (4.26 g) were dissolved in 9 mL of dimethyl sulfoxide under a nitrogen environment. It was reacted at room temperature for 12 hours. The resulting sBR was separated through a silica column using ethyl acetate/hexane (1:1) (
1H NMR (400 MHz, DMSO-d6): δ 1.28 (24H, s), 3.03 (4H, t), 4.44 (4H, t), 5.18 (4H, s), 7.38 (4H, d), 7.68 (4H, d).
1 mL of tetrahydrofuran in which 10 mg of ssBR was dissolved was slowly added dropwise to distilled water while stirring rapidly. The mixture was sonicated for 1 minute and homogenized for 1 minute using a homogenizer. Tetrahydrofuran was removed using a rotary evaporator, and then a solution in which ssBR was emulsified was centrifuged at a rate of 11,000×g for 4 minutes, and the precipitated ssBR nanoparticles were washed with water, and then freeze-dried to obtain the ssBR nanoparticles.
1 mL of tetrahydrofuran in which 10 mg of ssBR was dissolved was slowly added to 20 mL of PBS in which 1 mg of fucoidan was dissolved while stirring slowly. The mixture was sonicated for 1 minute and homogenized for 1 minute using a homogenizer. Tetrahydrofuran was removed using a rotary evaporator, and then a solution in which ssBR was emulsified was centrifuged at a rate of 11,000×g for 4 minutes, and the precipitated ssBR nanoparticles were washed with water, and then freeze-dried to obtain the ssBR nanoparticles. The size and distribution of the nanoparticles according to the content of fucoidan were evaluated through a particle size analyzer and a transmission electron microscope (
The ssBR nanoparticles dispersed in PBS were added to the colorectal cancer SW620 cells. After 1 hour, the cells were separated, lysed on ice, and then centrifuged at a rate of 9,800×g. The supernatant was mixed with 50 μL of Ellman's reagent, and then the absorbance was measured at 405 nm to measure the concentration of GSH in cells (
It was confirmed that GSH is easily reduced, which is the pharmacological activity effect of BR. The cytotoxicity of the ssBR nanoparticles was analyzed by the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) method. SW620 cells were treated with the ssBR nanoparticles. After 24 hours treatment, 100 μL of MTT solution was added. After 3 hours, 1 mL of DMSO was added to dissolve the crystal. After 10 minutes, the absorbance was measured at 570 nm to analyze the cell viability. It was confirmed that the cell death rate increased as the concentration of the nanoparticles increased (
The cancer targeting ability of each of the nanoparticles prepared in Examples 14 and 15 above was confirmed. Tumorigenesis was induced by injecting about 2×106 SW620 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected through the tail vein.
For the tumor target image, nanoparticles carrying a fluorescent substance IR780 were used, and the targeting of the tumor was confirmed by comparative analysis based on 24 hours. The ssPB nanoparticles to which fucoidan was added continued to accumulate into the tumor for up to 24 hours, but most of the nanoparticles to which fucoidan was not added were accumulated into the liver or excreted (
In order to evaluate liver toxicity, the ssBR nanoparticles to which fucoidan was added were intravascularly injected into normal mice at a concentration of 20 mg/kg. After 5 injections once every 3 days, blood was collected and analyzed for alanine transaminase (ALT). The liver, heart, lung, spleen, and kidney were excised, and the tissues were stained by H&E and analyzed for safety in vivo through histological analysis. As a result, it was confirmed that a significant toxicity was not shown (
Paclitaxel (PTX) (2 g) and dithiodipropionic acid (0.25 g) were dissolved in 10 mL of dimethylformamide and then stirred for about 10 minutes. Thereafter, 1-ethyl-3-(dimethylaminophenyl) carbonyldiimide (0.90 g) and 4-dimethylaminopyridine (0.29 g) were added and further stirred for 16 hours. The reactivity was confirmed by TLC, and when all of the reaction proceeded, a solid produced by adding an excess of water was obtained by centrifugation. The obtained solid was dried, and then passed through ethyl acetate mobile phase column, and purified through recrystallization (
1H NMR (400 MHz, DMSO-d6): δ 1.10 (6H, s), 1.29 (2H, t), 1.58 (6H, s), 1.66 (6H, s), 1.68 (2H, d), 1.72 (6H, s), 2.00 (6H, s), 2.13 (2H, q), 2.28 (2H, q), 2.58 (6H, d), 2.72 (2H, t), 2.82 (4H, t) 3.46-3.72 (2H, dd), 3.93 (2H, d), 4.11 (4H, t), 4.32 (2H, m), 4.60-4.68 (4H, m), 5.04 (2H, t), 5.45 (2H, d), 5.83 (2H, m), 5.98 (2H, m), 6.89 (2H, s), 7.20 (2H, s), 7.28 (4H, t), 7.38 (4H, t), 7.42 (4H, m), 7.5-7.53 (4H, m), 7.60-7.65 (8H, m), 7.87 (4H, d).
10 mg of PTX-SS-PTX was dissolved in 5 mL of THF, added dropwise to 30 mL of PBS using a syringe, and subjected to ultrasonic irradiation to disperse the nanoparticles. Thereafter, THF was removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which THF was removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use.
10 mg of PTX-SS-PTX was dissolved in 5 mL of THF, and 2 mg of fucoidan was dissolved in 30 mL of PBS. The PTX-SS-PTX solution was added dropwise to the fucoidan solution that was subjected to ultrasonic irradiation to form and disperse the nanoparticles. Thereafter, THF was removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which THF was removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use (
The cancer targeting ability of each of the nanoparticles prepared in Examples 17 and 18 above was confirmed. Tumorigenesis was induced by injecting about 2×106 SW620 cells subcutaneously into the left leg of nude mice (average body weight of about 20 g, 8 weeks old). After about 10 days, when the size of the tumor was greater than 3×3 mm, each of the nanoparticles was intravascularly injected through the tail vein. For the tumor target image, nanoparticles carrying a fluorescent substance IR780 were used, and the targeting of the tumor was confirmed by comparative analysis based on 24 hours. It was confirmed that the ssPB nanoparticles to which fucoidan was added continued to accumulate into the tumor for up to 21 hours, but the nanoparticles to which fucoidan was not added were accumulated into the tumor in a small amount (
Doxorubicin (DOX) (1 g) and dithiodipropionic acid (0.157 g) were dissolved in 20 mL of dimethyl sulfoxide, and then triethylamine (0.24 μL) was added, and stirred for about 10 minutes while blocking the light. Thereafter, 1-ethyl-3-(dimethylaminophenyl) carbonyldiimide (0.5 g) and N-hydroxysuccinamide (0.198 g) were added and stirred for 16 hours while blocking the light. The reactivity was confirmed by TLC, and when all of the reaction proceeded, a solid produced by adding an excess of water was obtained by centrifugation. The obtained solid was dried, and then passed through ethyl acetate mobile phase column, and purified through recrystallization (
1H NMR (400 MHz, DMSO-d6): δ 1.12 (6H, s), 1.43 (2H, s), 1.84 (2H, t), 2.16 (2H, s), 2.23 (2H, s), 2.58 (4H, s), 2.89 (4H, d), 3.39 (6H, s), 3.89-3.95 (8H, m), 4.13 (2H, s), 4.53 (4H, s), 4.67 (4H, d) 4.70 (2H, s), 4.81 (2H, s), 5.21 (2H, s), 7.56 (2H, t), 7.65 (2H, d), 7.73 (2H, d), 7.83 (2H, d), 13.14 (2H, s), 13.87 (2H, s).
10 mg of DOX-SS-DOX was dissolved in 5 mL of THF and added dropwise to distilled water that was subjected to ultrasonic irradiation to form and then disperse the nanoparticles. Thereafter, THF was removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which THF was removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use (
10 mg of DOX-SS-DOX was dissolved in 5 mL of THF, and 2 mg of fucoidan was dissolved in 30 mL of PBS. The DOX-SS-DOX solution was added dropwise to the fucoidan solution that was subjected to ultrasonic irradiation to form and then disperse the nanoparticles. Thereafter, THF was removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which THF was removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use. As a result of comparative analysis by a particle size analyzer and a scanning electron microscope, the nanoparticles comprising fucoidan showed excellent physical properties in terms of the size, shape, and distribution compared to the nanoparticles without fucoidan (
An in vivo experiment was performed to confirm the toxicity of the doxorubicin dimer nanoparticles comprising fucoidan. The experiment schedule is as shown in
Specifically, the doxorubicin dimer nanoparticles comprising doxorubicin and fucoidan (hereinafter, ROD-101) were administered to the caudal vein once a day for 3 days, respectively. The drug was administered a total of three times. The tumor volume and the mouse body weight were measured on the day before drug administration, and then group separation was performed (first measurement). After the drug was administered a total of three times, on the next day, the tumor volume and the mouse body weight were measured (second measurement). After 4 days, the tumor volume and the mouse body weight were measured (third measurement).
On the other hand, as a control in this experiment, PBS-treated group (G5) and doxorubicin-treated group (G6) were used. Thereafter, the growth of the tumor was monitored every day by measuring the vertical diameter of the tumor with a caliper, and the change in viability over time was monitored to evaluate the anticancer effect using an animal model. On the other hand, the tumor volume was calculated by the following formula:
volume=0.523L (W)2 [Equation 1]
in which, L denotes for length, and W denotes for width.
As a result, it was confirmed that the anticancer effect of the doxorubicin dimer nanoparticles comprising fucoidan was superior to that of doxorubicin (
Camptothecin (CPT) (1 g) and 4-dimethylaminopyridine (0.35 g) were dispersed and dissolved in 50 mL of dichloromethane, and then stirred at a temperature of 4° C. or less using an ice water bath. Triphosgene (0.34 g) was added to change a solution state. Thereafter, the reaction was maintained while stirring for 16 hours at a temperature of 4° C. or less. Dithiodiethanol (0.18 g) was dissolved in a THF solution and then added dropwise to the reaction solution. The reactivity was confirmed by TLC, and when all of the reaction proceeded, it was dried and then purified through a column (
1H NMR (400 MHz, DMSO-d6): δ 0.77 (6H, t), 2.14 (4H, q), 2.92 (4H, t), 4.17 (4H, t), 5.16 (4H, s), 5.46 (4H, s), 7.00 (2H, s), 7.66 (2H, t), 7.77 (2H, t), 8.06 (4H, dd), 8.61 (2H, s).
10 mg of CPT-SS-CPT was dissolved in 5 mL of THF:MeOH (10:1) and added dropwise to distilled water that was subjected to ultrasonic irradiation to form and disperse the nanoparticles. Thereafter, THF and MeOH were removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which the organic solvents were removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use.
10 mg of CPT-SS-CPT was dissolved in 5 mL of THF:MeOH (10:1), and 2 mg of fucoidan was dissolved in 30 mL of PBS. The CPT-SS-CPT solution was added dropwise to the fucoidan solution that was subjected to ultrasonic irradiation to form and then disperse the nanoparticles. Thereafter, THF and MeOH were removed for 15 minutes under a condition of room temperature using a rotary evaporator. The solution from which the organic solvents were removed was frozen with liquid nitrogen and then freeze-dried. The completely dried nanoparticles were used by dispersing in PBS immediately before use. As a result of comparative analysis by a particle size analyzer and a scanning electron microscope, it was shown that the size, shape, and distribution of the nanoparticles comprising fucoidan were improved (
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2021/003765 | 3/26/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62994932 | Mar 2020 | US |
