Patent Application
20200156951
The present invention refers to a process of obtaining an inorganic nanostructured complex (CFI-1), a protein-associated nanostructured complex (MRB-CFI-1) and use.
The main technology application is the treatment of urinary bladder cancer, both in animals and in humans, its antitumor activity is unique and a potentially substitute for other commercial antineoplastic drugs.
All organs of the urogenital tract are potential spots for malignant tumors. The incidence and type vary from organ to organ. Urinary bladder cancer (CB) represents the second most common malignant disease of the urinary tract (Siegel et al., 2012; American Cancer Society, 2016).
The American Cancer Society estimated about 76,960 new cases of CB in 2016 in the United States, being 58,950 in men and 18,010 in women. The estimate also predicted 16,390 deaths due to CB, being 11,820 in men and 4,570 in women (American Cancer Society, 2016). According to data from the National Cancer Institute (INCA, 2016), the estimate for Brazil in 2016 was 9,670 new cases of CB, being 7,200 in men and 2,470 in women. In 2013, 3,642 deaths were reported due to CB, being 2,542 in men and 1,099 in women, thus demonstrating a drastic increase in the prevalence of this type of tumor.
More than 70% of the incidence of CS is superficial (pTis, pTa and pT1), of non-invasive tumor (CBNMI), and the occurrence of an invasive disease is occasional (Askeland et al., 2012). However, 50% of invasive non-muscle tumors recurrence to 4 years after treatment and 11% evolve to the invasive phenotype (Askeland et al., 2012).
The histological staging of CE is determined by the depth of tumor invasion of the bladder wall and will depend on the transurethral resection (RTU) of the tumor, by endoscopic approach, for a correct diagnosis. Fragments of superficial and deep resection should be analyzed separately (Epstein et al., 1998; Epstein, 2003). The Tumour Node Metastasis (TNM) classification 2009 (UICC—Union for Cancer Control) is used for staging.
A significant number of risk factors have been related to the development of CB. According to record data from the INCA population database, the greatest risk factor for the development of CB is smoking, accounting for about 66% of new cases in men and 30% in women (INCA, 2016), in the meta-analysis of epidemiological studies of Zeegers et al, (2000) on the impact of smoking characteristics on the risk of urinary tract cancer, smoking was appointed as a factor that substantially increases the risk for the development of bladder cancer. Cigarettes have dozens of toxic substances, including aromatic amines and N-nitrous analogues of MNU (N-methyl-N-nitrosourea), a potent carcinogen.
Another potential risk factor for the development of CB is occupational exposure to aromatic amines by workers from rubber, textile and ink industries, and infection by Schistosoma Haematobiun, that is endemic in Mediterranean countries, such as Egypt (Zeegers et al., 2000; Poon et al., 2015; Rosenquist & Grollman, 2016). Exposure to certain substances such as arsenic, which may be present in water supplies, aristolochic acid present in many medicinal plants and pioglitazone present in drugs for the treatment of diabetes are associated as a risk factor (Poon et al., 2015; Rosenquist & Grollman, 2016).
According to the American Cancer Society, the reduced intake of liquids can be a risk factor, since an individual who ingests high amounts of liquids, mainly water, tends to eliminate chemicals more quickly, taking into consideration that this will tend to deflate the bladder more frequently (American Cancer Society, 2016).
In general, CB is about 3 to 4 times more common in men than in women (News et al., 2009). On the other hand, women survival is worse with this type of tumor. It is speculated that the high aggressiveness of bladder cancer in women is due to hormonal imbalance, which arises from the fifth decade of life. Although the urinary bladder is secondarily regulated by steroid sex hormones, the normal urothelial and tumor urothelial are responsive to androgens and estrogens (Garcia et al., 2015), Garcia et at (2015) demonstrated for the first time in rats chemically induced to CBNMI that increased protein levels of ubiquitin ligase SIAH-2 upregulated the androgenic receptors and decreased levels of estrogen receptors, culminating in the escape of neoplastic urothelial cells from the immune system. These same authors found that the levels of immune system receptors, toll-like receptors (TLRs) were decreased in CBNMI and associated this effect with the increase of SIAH-2 levels and androgenic receptors.
The primary treatment of non-muscle invasive bladder cancer (NMIBC) is based on surgical treatment through transurethral resection (RTU), followed by intravesical immunotherapy with Bacillus Calmette-Guerin (BCG), for decreasing recurrence and preventing tumor progression. However, the use of living and attenuated organisms can cause side effects and difficulty in predicting the immune and antitumor response. The use of BCG is limited in NMIBC-due to treatment failure, adverse effects and intolerance occurring in more than two-thirds of patients. Although the use of RTU with chemotherapy or adjuvant immunotherapy represents an important breakthrough in the treatment of CBNMI, the management of this tumor, especially for high-grade tumors, remains a challenge due to the high recurrence rates and progression to invasive and/or metastatic muscle phenotypes. The surgical option for such cases, partial or total cystectomy, is often associated with high rates of morbidity and mortality. Furthermore, for some patients, cystectomy is not an available option due to the presence of concomitant comorbidities. Thus, the development of new therapeutic modalities that prevent disease progression, allow the preservation of the organ and the quality of life of patients and, finally, provide an option for those who are ineligible for cystectomy, is of utmost importance. Compounds that are able to act as agonists of the receptors of the immune system (toll-like receptors) can represent promising candidates to be developed as medicines against cancer.
In this context, the use of the biological response modifier—inorganic phosphate complex 1 (MRB-CFI-1) stands out, which has been proposed with promising results in the treatment of NMIBC. Moreover, the invention of this new nanodrug for the treatment of CBNMI presents great efficiency, low toxicity and is economically viable, with great reproducibility and yield. After experiments with laboratory animals and clinical-veterinary protocol in dogs with CBNMI, the invention presents great potential for use in humans.
The present invention refers to a process of obtaining an inorganic nanostructured complex (CFI-1), a protein-associated nanostructured complex (MRB-CFI-1) and use.
The nanostructured complex (CFI-1) comprises inorganic phosphate, with a size ranging from 190.0 to 310.3±36.4 nm, polydispersity of 0.563 and zeta potential of −22.6±4.15 mV.
The protein-associated nanostructured complex (MRB-CFI-1) comprises protein-associated phosphates, with a size ranging from 318.0 to 477.1±146 nm, polydispersity of 0.9 and zeta potential of −28.60±6.74 mV.
Further objects are the use of the complexes obtained (CFI-1) and (MRB-CFI-1) to treat cancer, preferably of prostate, bladder, colorectal, mastocytoma and lymphoma.
Although the compounds NH4MgPO4×6H2O, (NH4)2MgH2(PO4)2×4H2O, (NH4)2Mg3(HPO4)4×8H2O and NH4MgPO4×H2O are described in the literature, associated or not with hydrolytic proteins, they are objects to treat cancer in this invention. The present invention also discloses the mechanisms of the aforementioned complexes in activating the immune system, both epithelial (local) and systemic against tumors.
In order to achieve a full and complete view of the object of this invention, referenced figures are presented below, as follows.
In a first aspect, the present invention refers to processes of obtaining an inorganic nanostructured complex (CFI-1), a protein-associated nanostructured complex (MRB-CFI-1) and antitumor use.
Two examples of embodiments related to obtaining the inorganic nanostructured complex (CFI-1) and the protein-associated nanostructured complex (MRB-CRI-1) are described below.
The process of obtaining a nanostructured complex (CFI-1) by chemical synthesis comprises the following steps:
(a) Preparing dibasic ammonium phosphate [(NH4)2HP04] in situ in the presence of ammonia and orthophosphoric acid, in a mechanical homogenizer with minimum power of 500 W (for example, of the Ultra Turrax type), at a temperature between 25 and 55° C. for 20-30 min up to neutralization;
(b) Mixing two salts: Hexahydrate magnesium chloride, at 1-3% (by mass) and dibasic ammonium phosphate obtained in step (a) at 1-4% (by mass) between 22 and 30° C. and pH 5-7, in a mechanical homogenizer with minimum power of 500 W (e.g., of Ultra-Turrax type) in a variable rotation range between 7000 and 15000 rpm for 30-40 min;
(c): Applying a pressure level to the mixture obtained in step (b) in a high pressure homogenizer (e.g.; NIRO) with the homogenization valve with variable pressure between 400 and 700 bar, preferably 600 bar, and in the second stage, the homogenizing valve with variable pressure between 50 and 70 bar, preferably 60 bar, for up to 1 to 3 cycles, preferably 2 cycles;
(d) Cooling the suspension obtained at step (c) in ice bath at a temperature range comprised between 0 and 20° C., preferably 15° C.;
(e) Precipitating; and
(f) Washing the crystals with distilled and sterile water and drying at 30 to 40° C., preferably at 37° C. for 24 to 72 h, preferably 48 h.
After step (f), the CFI-1 crystals were dried and weighed, showing a mass yield of 45-50%.
The nanostructured complex (CFI-1), obtained as defined in the embodiment example (I) (PRODUCT 1), comprises inorganic phosphate with size varying from 190.0 to 310.3±36.4 nm, polydispersity of 0.563 and zeta potential of −22.6+4.5 mV.
The process of obtaining a protein-associated nanostructured complex (MRB-CFI-1) by chemical synthesis comprises the following steps:
(a) Preparing dibasic ammonium phosphate [(NH4)2HP04] in situ in the presence of ammonia and orthophosphoric acid, in a mechanical homogenizer with minimum power of 500 W (for example, of the Ultra Turrax type), at a temperature between 25 and 55° C. for 20-30 min up to neutralization;
(b) Mixing two salts: Hexahydrate magnesium chloride, at 1-3% (by mass) and dibasic ammonium phosphate obtained in step (a) at 1-4% (by mass) between 22 and 30° C. and pH 5-7, in a mechanical homogenizer in a variable rotation range between 7000 and 15000 rpm for 30-40 min;
(c) Adding protein in a concentration of 0.5-1.5% (mass/mass), preferably 1%, to the complex obtained in step (b), wherein the aforementioned protein comprises the hydrolytic proteins selected from the group comprised by chitinase of Bacillus Subtilis (14 kDa) and lysozyme from egg whites (14 kDa), preferably lysozyme, which have immunomodulatory activity.
(d) Applying a pressure level to the mixture obtained in step (c) in a high pressure homogenizer (NIRO) with the homogenization valve with variable pressure between 400 and 700 bar, preferably 600 bar, and in the second stage, the homogenizing valve with variable pressure between 50 and 70 bar, preferably 60 bar, for up to 1 to 3 cycles, preferably 2 cycles;
(e) Cooling the suspension obtained at step (c) in ice bath at a temperature range comprised between 0 and 20° C., preferable 15° C.;
(f) Precpitating; and
(g) Washing the crystals with distilled and sterile water and drying at 30 to 40° C., preferably 37° C. for 24 to 72 h, preferably 48 h.
The protein added in step (c) preferably comprises a concentration of 0.7%.
The protein-associated nanostructured complex (MRB-CFI-1), obtained as defined in the example of embodiment (I), said PRODUCT 2, comprises inorganic phosphate associated with protein, with size varying from 318.0 to 477.1±146 nm, polydispersity of 0.9 and zeta potential of −28.60±6.74 mV.
The process of obtaining a nanostructured complex (CFI-1) by chemical synthesis comprises the following steps:
(a) Preparing an ultrapure (99.99%) dibasic ammonium phosphate [(NH4)2HPO4] solution (molar mass: 132.6 g/mol) with concentration comprised in the range of 1 and 4% (by mass), preferably 1%, diluted in 1,000-2,000 mL of distilled water, under magnetic stirring with controlled speed and rotation between 200 and 400 rpm, preferably 300 rpm, at temperature between 22° C. and 30° C. and pH 8.26-8.57 for 5 minutes;
(b) Adding from 0.5 to 2.0% of an amine selected from the group comprised by monoethanolamine; diethanolamine and triethanolamine, preferably monoethanolamine (2-aminoethanol; C2H7NO; molar mass: 61.08 g/mol), in the solution of ammonium phosphate dibasic [(NH4)2HP04] obtained in step (a) under stirring, with rotation between 200 and 400 rpm, at a temperature range between 22° C. and 30° C., and pH between 9.72 and 9.80 for 5 minutes, until completing homogenization.
(c) Maintaining the solution of ammonium phosphate dibasic [(NH4)2HP04] and monoethalonamine, obtained in step (b), under mechanical stirring, rotation between 200 and 400 rpm, at temperature between 22° C. and 30° C. and pH 9.72-9.80;
(d) Preparing an ultrapure (99.99%) solution of hexahydrate magnesium chloride (MgCl2.6H2O) (molar mass: 203.3 g/mol), in a concentration comprised in the range of 1-3% (by mass), preferably 2%, under stirring with rotation comprised between 200 and 400 rpm, preferably 300 rpm, at the temperature range between 22 and 30° C., and pH between 7.38 and 7.56, for 5 min until completing homogenization; the solution is subsequently transferred into a 200-600 mL separation funnel or to a Titrette® Bottletop Burette apparatus with appropriate volume;
(e) Slow and controlled drip of the denser liquid obtained in step (d) in the resulting solution obtained in step (b) under stirring, with rotation between 200 and 400 rpm, at temperature between 22° C. and 30° C., and pH 9.72-9.80;
(f) Maintaining the solution resulting from step (e) under stirring for 2 hours with rotation between 200 and 400 rpm, at temperature between 22° C. and 30° C., and pH 8.10-8.20 until complete dissolution;
(g) Cooling the suspension obtained at step (f) in ice bath at a temperature range comprised between 0 and 20° C., preferably 15° C.;
(h) Precipitating;
(i) Washing the CFI-1 crystals with distilled and sterile water, and drying at 30 to 40° C., preferably at 37° C. for 24 to 72 h, preferably 48 h.
Drip control in step (e) is performed at the speed between 26 and 33 drops per minute, in a time interval between 3-4 hours.
The pH in step (e) is controlled so that 30 minutes after the start of dripping, the pH is comprised between 9.12 and 9.32; 1 hour after the start of dripping, the pH is comprised between 8.81 and 8.89; 2 hours after the start of dripping, the pH is comprised between 8.25 and 8.43; and 3 hours after the start of dripping, the pH is comprised between 8.10 and 8.20; the pH must be kept constant throughout the reaction.
After step (i), the CFI-1 crystals were dried and weighed, showing a mass yield of 98-100%.
The nanostructured complex (CFI-1) in the presence of a compound with an amine group that acts as pH stabilizer, obtained as defined in the embodiment of example (II), said PRODUCT 3, comprises inorganic phosphate with an average size of 449.6±116.6 nm, polydispersity of 0.55 and zeta potential of −20.0±5.1 mV.
The process of obtaining a nanostructured complex (CFI-1) associated with protein (MRB-CFI-1) in the presence of a compound with an amine group acting as a pH stabilizer comprises the addition of the CFI-1, obtained as defined in the example of embodiment (II), to a solid state protein, at 1:1, 1:2, 1:3 and preferably 1:2 weight/weight ratios, wherein the aforementioned protein is selected from the group comprised by P14-16, Bacillus subtilis chitinase (14 kDa) or egg white lysozyme (14 kDa), which are known to have immunomodulatory activities.
The protein-associated nanostructured complex P14-16 (MRB-CFI-1) comprises inorganic phosphate mixed with protein, by simple addition of protein crystals to CFI-1 at appropriate concentrations for the study of bladder cancer; with a mean size of 509.6±92.6 nm and zeta potential of −26.3±6.7 mV.
Further objects are the use of the complexes obtained (CFM) and (MRB-CFI-1) to treat cancer, preferably of prostate, bladder, colorectal, mastocytoma and lymphoma. Additionally, the complexes (CFI-1) and (MRB-CFI-1) can be used as adjuvants to commercial chemotherapeutic drugs to treat prostate, bladder, colorectal, mastocytoma and lymphoma cancers.
Although the compounds NH4MgPO4×6H2O, (NH4)2MgH2(PO4)2×4H2O, (NH4)2Mg3(HPO4)4×8H2O and NH4MgPO4×H2O are described in the literature, associated or not with hydrolytic proteins, they are objects to treat cancer in this invention.
Results—Embodiment Example (I)
Characterization of the nanostructured magnesium and ammonium phosphate complex (CFI-1):
Analysis of XFD shows the presence of ammonium, magnesium and phosphate: Table 1A (CRI-1) shows a ratio of phosphate to magnesium of 3.2 and shows only traces of metals, such as iron and calcium, and a value of the remaining structure, such as NH4+H2O (calculated by difference by weight of total mass). By this analysis, the approximate unit cell would be (NH4)6Mg3(PO4)4. P/Mg ratio=3.2. Table 1B (MRB-CRI-1) shows a phosphate to magnesium ratio of 2.86. By this analysis, the unit cell is (NH4)6Mg3(PO4)4, without considering the organic part.
Table 2 shows the components of the CFI-1 and MRB-CFI-1 complex on the surface of the crystals, such as magnesium, nitrogen, phosphorus and oxygen, and Metal absence of carbon by XPS. Therefore, this technique shows, on the crystal surface, nitrogen (NH4), phosphate and magnesium as the only components of compound C19-1. In the case of MRB-CFI-1, the protein components are shown. Therefore, for CFI-1 it would be NO6Mg3(PO)2 and for MRB-CFI-1 it would be C14NO8Mg2(PO4)2.
The minimum chemical formula of the crystal surface was as follows: for CFI-1: NO6Mg3(PO4)2 and for MRB-CFI-1: C14NO8Mg2(PO4)2.
The crystal surface has the following values: CFI-1 ratio: P/Mg=0.86; MRB-CRI-1 ratio=P/Mg=1.68.
X-ray refraction pattern:
In
Fourier transform infrared spectrum (FIR):
The bands observed for CFI-1 (spectrum not shown in figure) around 3600, 3500, 3260 and 3115 cm−1, in the FTIR spectrum, probably belong to the stretching vibrations of group OH and the antisymmetric stretching vibration of NH4 groups. The water-PO4—H bond appears around 2500 and 2200 cm−1. Water deformation appears at 1680 cm−1 and the bands at 1600 to 1400 cm−1 were those of the deformation mode of the H—NH group of NH4. The PO4 group alone is observed at 1006 cm−1 (antisymmetric elongation), 571 cm−1 (P—O flexion), 463 and 438 cm−1 (PO4−3 mode). At 618 and 688 cm−1 (Mg—O bond), and at 894 cm−1 the deformation bond of the group with Mg). The water-water hydrogen bond was observed at 760 and 695 cm−1, while the bond between water hydrogen and NH4 group was observed at 890 cm−1. The MRB-CFI-1 FTIR spectrum presents the same bands with the addition of amide I 1640-1650 cm−1 and amide II 1574-1550 cm−1 bands.
Thermogravimetric analysis of CFI-1 and MRB-CFI-1:
Differential scanning calorimetry (DSC) analysis of CFI-1 and MR8-CFI-1:
Raman spectrum:
Solubility at different pHs:
Table 3 shows the solubility of the CFI-1-water system that was determined at 25 and 35° C. by means of crystal and solution balance in a container. An experimental solution of 100 ml of volume containing 0.45 g of CFI-1 was treated at venous pHs. The pH variation of the solution was made by the addition of HCl and NaOH solutions. The mixtures were continuously stirred for 24 h to ensure the solution saturation. The undissolved solid was settled without agitation and, after 2 additional hours, it was filtered through a 0.22 μm membrane filter. The residue was dried overnight in the oven at 35° C. The dry samples were weighed using an analytical balance. The difference between the residue and initial mass of CFI-1 provided the solubility. Table 3 shows that the solubility value at pH 7 was 80 mg/l. This value can change as a function of pH and ionic strength.
Characterization of MRB-CFI-1 complex:
X-ray diffraction pattern (XRD).
Circular dichroism of MRB-CFI-1.
Size (nm) and surface charge (zeta potential, mV) of CFI-1 (A) versus (B) MRB-CFI-1.
In vivo toxicological and biochemical analyses of MRB-CFI-1:
For the toxicological and biochemical analyses of the nanodrug MRB-CFI-1, 20 Fischer 344 female rats, 20 C57BL/6 female mice and 20 New Zealand female rabbits were used.
The animals were distributed into 4 groups for each species, namely: control group (n=5 animals for each species): received an intravesical dose of physiological solution 0.9%, for 6 consecutive weeks; group MRB-CFI-1 20 (n=5 animals for each species): received an intravesical dose of MRB-CFI-1 20 mg/Kg for 6 consecutive weeks; group MRB-CFI-1 50 (n=5 animals for each species): received an intravesical dose of MRB-CFI-1 50 mg/Kg for 6 consecutive weeks; group MRB-CFI-1 100 (n=5 animals for each species): received an intravesical dose of MRB-CFI-1 100 mg/Kg for 6 consecutive weeks.
The protocol for use of animals in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocols numbers: 4536-1/2017; 45794/2017; 4435-1).
After the 6-week experimental period, all animals from each group were euthanized. For the local and systemic toxicity analyses of the MRB-CFI-1 nanodrug, the organs of the urinary system (urinary bladder, ureters and kidneys), and other target organs such as liver, spleen, stomach and pancreas, were collected and subjected to histopathological analyses. The histopathology of these organs was evaluated and the toxicity correlated with the degrees of inflammation. The degree of inflammation was evaluated by a semi-quantitative scale: 0, absence of inflammation, 1, minimal inflammation (less than five lymphocytes in an area of 0.25 mm2), 2, moderate inflammation (mononuclear inflammatory cells scattered throughout the tissue, but still with visible stroma), 3, intense inflammation (mononuclear inflammatory cells densely infiltrating the tissues.
Also, biochemical analyses were performed to verify the systemic toxicity of this compound, namely: alanine aminotransferase (ALT), a specific marker for hepatic parenchymal lesion; aspartate aminotransferase (AST), a nonspecific marker for hepatic and/or cardiac injury; alkaline phosphatase; as well as circulating levels of creatinine and urea to verify renal function. Spectrophotometric determinations were performed on a Pharmacia Biotech spectrophotometer with a temperature-controlled cuvette chamber (UV/visible Ultrospec 5,000 with Swift II application software for computer control, 97-4213, Cambridge, England, UK). All chemical reagents were from company LaborLab (Guarulhos, Sao Paulo, Brazil).
In vivo assessment of peritoneal inflammatory response after administration of CFI-1, P14-16 protein and MRB-CFI-1 compound:
To verify whether compound MRB-CFI-1 and its constituents (CFI-1 and P14-16 protein) were able to deflate the peritoneal inflammatory response (activation of the immune system) when administered directly to the abdominal cavity, 8 7-week old Fischer 344 female rats were used, weighing 150 grams on average, which were obtained at the Vivarium Center of the State University of Campinas (CEMIB/UNICAMP).
The animals were divided into 4 groups (n=2 animals per group): Control group: received an intraperitoneal dose of 0.3 mL of physiological solution 0.9% every 72 hours, totaling 3 doses; group CFI-1: received an intraperitoneal dose of 20 mg/kg of CFI-1 suspended in physiological solution 0.9% every 72 hours, totaling 3 doses; group P14-16: received an intraperitoneal dose of 20 mg/Kg of protein P14-16 suspended in physiological solution 0.9% every 72 hours, totaling 3 doses; group MRB-CFI-1: received an intraperitoneal dose of 20 mg/kg of compound MRB-CFI-1 suspended in physiological solution 0.9% every 72 hours, totaling 3 doses. After 24 hours from the last application of each compound, the animals were euthanized and the peritoneums were evaluated macroscopically and collected for further histological assessment.
The protocol for use of animals in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocol number: 4536-1/2017).
Pre-clinical trial: induction and treatment of non-muscle invasive urinary bladder cancer (NMIBC) in Fischer 344 rats:
In the present invention, 100 7-week Fischer 344 rats were used, weighing 150 grams on average, which were obtained from the Vivarium Center of the State University of Campinas (CEMIB/UNICAMP). For NMIBC Induction, 80 animals were anaesthetized with xylazine hydrochloride 2% (5 mg/kg i.m.; Köig, Sao Paulo, Brazil) and ketamine hydrochloride 10% (60 mg/kg, i.m.; Fort Dodge, Iowa, USA), maintained in this state for 45 minutes to avoid spontaneous urination and a dose of 1.5 mg/kg of N-methyl-N-nitrosourea (MNU-Sigma, St. Louis, Mo., USA) dissolved in 0.3 ml of sodium citrate (1M pH 6.0) was instilled every 15 days (weeks 0, 2, 4 and 6), totaling 4 doses (Fávaro et al., 2014; Garcia et al., 2016). The other 20 animals that did not receive MNU were considered as the control group.
Two weeks after the last MNU dose, the animals were submitted to an ultrasound examination to evaluate tumor occurrence. Ultrasounds were evaluated using a portable software-controlled ultrasound system with a 10-5 MHz 38 mm linear transducer.
Ultrasound of the urinary bladder of the animals induced with MNU showed tumor masses infiltrating the cranial, ventral and dorsal walls of the organ, measuring 0.32 cm×0.21 cm; 0.32 cm×0.24 cm; and 0.27 cm×0.21 cm (
After NMIBC induction with MNU, the animals were distributed into 5 groups (20 animals per group): control group (group 1): received an intravesical dose of 0.3 ml of physiological solution 0.9% for 6 consecutive weeks; group MNU (cancer, group 2): received the same treatment as group 1; group MNU+CFI-1 (group 3): received an intravesical dose of 20 mg/kg of CFI-1 suspended in physiological solution 0.9% for 6 consecutive weeks; group MNU+P14-16 (group 4): received an intravesical dose of 20 mg/kg of protein P14-16 suspended in physiological solution 0.9% for 6 consecutive weeks; group MNU+MRB-CFI-1 (group 5): received an intravesical dose of 20 mg/Kg of compound MRB-CFI-1 suspended in physiological solution 0.9% for 6 consecutive weeks,
The intravesical doses in the different experimental groups were instillated using a 20 gauge flexible catheter (Abocath, Sao Paulo, Brazil). The animals from all experimental groups received water and the same solid diet ad libitum (Nuvilab, Colombo, PR, Brea). After 16 weeks of treatment, the animals were euthanized and the urinary bladders were collected and subjected to histopathological and immunohistochemical analyses. The protocol for use of animals in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocol number: 4536-1/2017).
Histopathologic analysis:
For histological analysis, samples of the urinary bladder from all anirnais of each experimental group (n=20 animals per group) were collected and fixed with Bouin for twelve hours. After fixation, tissues were washed in ethyl alcohol 70%, with subsequent dehydration in a growing series of alcohols, Subsequently, the fragments were cleared with xylene for 2 hours and included in plastic polymers (Paraplast Plus, ST, Louis, Mo., USA). Subsequently, the materials were sectioned using a Slee CUT5062 RM 2165 microtome (Slee Mainz Mainz, Germany) with 5 micrometer thickness, stained with hematoxylin-eosin and photographed using DM2500 photomicroscope (Leica, Munich, Germany).
The diagnosis of urothelial lesions was classified according to the staging proposed by the common understanding of the World Health Organization/International Society of Urological Pathology (Epstein et al., 1998).
Antigen immunostaining: TLR4, TR1F, IRF3, INF-γ, TLR2, IKK-α, MyD88, IL-6 and TNF-α:
Samples from the urinary bladder of all animals of each experimental group (n=20 animals per group), the same used for histopathological analyses, were used for immunostaining. Then, cuts with 5 μm thickness in the rotating microtome Slee CUT5062 RM 2165 (Slee Mainz, Mainz, Germany) were collected on silanized sections. The antigenic recovery was performed by incubation of the sections in citrate buffer (pH 6.0) at 100° C. in a microwave, or by treatment with proteinase K, depending on the characteristics of each antibody. The blockage of endogenous peroxidases was carried out with H2O2 (methanol 0.3%) with subsequent incubation in a blocking solution with bovine serum albumin (BSA) 3%, in TBS-T buffer for 1 hour at room temperature. Subsequently, the antigens TLR4, TRIF, IRF3, INF-γ, TLR2, IKK-α, MyD88, IL-6 and TNF-α were located through the specific primary antibodies (table 4), diluted in BSA 1% and stored overnight at 4° C. The Advance™ HRP kit (Dako Cytomation Inc., USA) was used for antigen detection according to the manufacturer instructions. After washing with TBS-T buffer, the cuts were incubated with conjugated secondary HRP antibody from the Advance™ HRP kit for 40 minutes, and were subsequently revealed with diaminobenzidine (DAB), counterstained with Harris hematoxylin and evaluated using a DM2500 photomicroscope (Leica, Munich, Germany).
To evaluate the immunoreactivity intensity of the antigens, the percentage of positive urothelial cells was examined in ten fields for each antibody with a 400× magnitude. The staining intensity was graded on a 0-3 scale, and expressed as 0 (absence of immunoreactivity), 0% of positive urothelial cells; 1 (weak immunoreactivity), 1-35% of positive urothelial cells; 2 (moderate immunoreactivity), 36-70% of positive urotheiial cells; and 3 (intense immunoreactivity), >70% of positive urothelial cells (Garcia et al., 2016).
Statistical analysis:
The histopathological and immunohistochemical analyses were evaluated using the ratio test. For these analyses, a 5% type I error was considered statistically significant.
Pre-clinical trial: induction and treatment of non-muscle invasive urinary bladder cancer (NMIBC) in C57BL/6 mice:
In the present invention, 100 7-week old C57BL/6J female mice were used, weighing 40 grams on average, which were obtained from the Vivarium Center of the State University of Campinas (CEMIB/UNICAMP). The animals from all experimental groups received water and the same solid diet ad libitum (Nuvilab, Colombo, PR, Brazil). For NMIBC induction, 80 animals were anaesthetized with xylazine hydrochloride 2% (5 mg/kg i.m.; König, Sao Paulo, Brazil) and ketamine hydrochloride 10% (60 mg/kg, i.m.; Fort Dodge, Iowa, USA), maintained in this state for 45 minutes to avoid spontaneous urination and a dose of 1.5 mg/kg of N-methyl-N-nitrosourea (MNU-Sigma, St. Louis, Mo., USA) dissolved in sodium citrate (1M pH 6.0) was instilled every 15 days (weeks 0, 2, 4 and 6), totaling 3 doses (Fávaro et al., 2012). The other 20 animals that did not receive MNU were considered as the control group.
One week after the last MNU dose, the animals were submitted to ultrasound examination to evaluate tumor occurrence and were subsequently divided into 5 groups (n=20 animals per group) for the respective treatments: a) control group (group 1): received a intravesical dose of 0.1 ml of physiological solution 0.9% for 6 consecutive weeks; b) MNU Group (cancer): received the same treatment as group 1; c) MNU+CFI-1 group (group 3): received an intravesical dose of 20 mg/Kg of inorganic phosphate (CFI-1) for 6 consecutive weeks; d) MNU+P14-16 group (group 4): received an intravesical dose of 20 mg/kg of P14-16 protein for 6 consecutive weeks; e) MNU+MRB-CFI-1 group (group 5): received an intravesical dose of 20 mg/kg of MRB-CFI-1 compound for 6 consecutive weeks.
The intravesical doses in the different experimental groups were instillated using a 22 gauge flexible catheter (Abocath, Sao Paulo, Brazil). Urine was collected weekly and, after treatment, the animals were euthanized and the urinary bladders were collected. The protocol for use of animals in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocol number: 4579-1/2017).
Histopathologic analysis:
For histological analysis, samples of the urinary bladder from all animals of each experimental group (n=20 animals per group) were collected and fixed with Bouin for twelve hours. After fixation, tissues were washed in ethyl alcohol 70%, with subsequent dehydration in a growing series of alcohols. Subsequently, the fragments were cleared with xylol for 2 hours and included in plastic polymers (Paraplast Plus, ST. Louis, Mo., USA). Subsequently, the materials were sectioned using a Slee CUT5062 RM 2165 microtome (Slee Mainz, Mainz, Germany) with 5 micrometer thickness, stained with hematoxylin-eosin and photographed using DM2500 photomicroscope (Leica, Munich, Germany). The diagnosis of urothelial lesions was classified according to the staging proposed by the common understanding of the World Health Organization/International Society of Urological Pathology (Epstein et al., 1998).
Cell Viability Assays
Cell viability of the MRB-CFI-1 nanodrug and its constituents was evaluated in grade II urinary bladder carcinoma cells (cell line 5637), with 24 hours of incubation. For this, two approaches (MTT and calcein/propidium iodide) were used, with different chemical agents to increase the robustness of the results and avoid artifacts. The 5637 cells were plated in a cell density of 2.0×104 and treated with serial dilutions of the compounds (12.5 mg, 6.25 mg, 3.13 mg, 1.56 mg and 0.39 mg) over 24 hours of incubation.
Statistical Analyses:
The histopathological analyses were evaluated using the ratio test. For these analyses, a 5% type I error was considered statistically significant.
Results:
In vivo toxicological and biochemical analyses of MRB-CFI-1:
Serum levels of ALT, AST, alkaline phosphatase, urea and creatinine in rats, mice and rabbits treated intravesically with MRB-CFI-1 at doses of 20 mg/kg, 50 mg/kg and 100 mg/kg did not differ statistically from their respective controls (tables 5, 6 and 7), indicating that this compound did not present systemic toxic effects.
The urinary bladder, ureter and kidneys from rats, mice and rabbits in the control group did not present inflammation and histopathological alterations (
Mice from MRB-CFI-1 20 group showed minimal inflammation in the urinary bladder (100.0%) and ureters (100.0%), and absence of inflammation in kidneys (
Absence of inflammation and histopathological alterations were verified hi the liver, spleen, stomach and pancreas of all animals from each species (tables 8, 9, 10).
Two means followed by the same lowercase letter do not differ statistically, according to the Turkey test (P<0.05).
Two means followed by the same lowercase letter do not differ statistically, according to the Turkey test (P<0.05).
Two means followed by the same lowercase letter do not differ statistically, according to the Turkey test (P<0.05).
Assessment of peritoneal inflammatory response after administration of CFI-1, P14-16 protein and MRB-CFI-1 compound:
The macroscopic analyses of the peritoneum disclosed that the animals from control groups (
Histopathological analysis: Treatment of non-muscle invasive urinary bladder cancer (NMIBC) in Fischer 344 rats:
The urinary tract of the control group did not present microscopic alterations (
In contrast, the urinary tract of the MNU Group (cancer) showed drastic histopathological alterations, such as: invasive urothelial carcinoma (pT1) (
The most frequent neoplastic lesions in the MNU group+inorganic phosphate complex were the flat carcinoma in situ (pTis) (
The histopathological analyses of the animals from MNU+P14-16 group had 40% of tumor regression, and 20% of them presented flat hyperplasia (
The microscopic aspects of the urinary bladder of MRB-CFI-1 group were similar to those found in the control group. Normal urothelium was found in 40% of the animals (
Antigen immunostaining: TLR4, TRIF, IRF3, INF-γ, TLR2, IKK-α, MyD88, IL-6 and TNF-α: treatment of non-muscle invasive urinary bladder cancer (NMIBC) in Fischer 344 rats:
Immunostainings for MyD88 and IKK-α were significantly moderated in the control, MNU+CFI-1, MNU+P14-16 and MRB-CFI-1 groups in relation to the MNU group, which presented weak immunoreactivity for these antigens (table 12). Also, the immunostaining for IL-6 and TNF-α were significantly moderate in the MNU group compared to the other experimental groups, indicating that the nanodrug MRB-CFI-1 and its constituents did not induce the pathway for producing inflammatory cytokines mediated by TLRs 2 and 4.
In contrast, the immunomarkers for TLR2, TLR4, TRIF, IRF3 and INF-γ were significantly intense in the urothelium of MRB-CFI-1 and control groups in comparison with the other experimental groups (table 12), indicating that the MRB CFI-1 nanodrug was able to stimulate the interferon pathway mediated by TLRs 2 and 4. Also, the immunomarkers for these antigens were moderated in the MNU CFI-1 and MNU+P14-16 groups in relation to the MNU Group (table 12).
Histopathological analysis—non-muscle invasive urinary bladder cancer (NMIBC) treatment in C57BL/6 mice:
The urinary tract of the control group did not present microscopic alterations (table 13). In contrast, the urinary tract of the MNU Group (cancer) showed drastic histopathological alterations, such as: pT1 carcinoma, pTa carcinoma and pTis carcinoma in 20%, 20% and 60% of the animals, respectively (table 13).
The most frequent neoplastic lesions in the MNU+CFI-1 group were pTis carcinoma and pTa carcinoma, which occurred in 20% and 40% of the animals, respectively (table 13). The other animals did not present malignant lesions, with 20% of them presenting flat hyperplasia and 20% a pre-malignant lesion called low-grade intraurothelial neoplasia (table 13), indicating that this treatment promoted regression and inhibited tumor progression in 40% of the animals.
The histopathological analyses of the animals from group MNU+P14-16 presented 20% of tumor regression, and 20% of them presented flat hyperplasia (table 13). The most frequent neoplastic lesions in this group were pTis, pTa and pT1 carcinomas, both in 20%, 40% and 60% of the animals, respectively (table 13).
The microscopic aspects of the urinary bladder of MRS-CFI-1 group were similar to those found in the control group. Normal urothelium was found in 40% of the animals (table 13). Benign lesions such as flat hyperplasia, and pre-malignant lesions such as low-grade intraurothelial neoplasia, were found in 20% and 20% of the animals, respectively (table 13), indicating that this treatment promoted regression and inhibited tumor progression in 80% of the animals. The most frequent neoplastic lesion in this group was pTis carcinoma in 20% of the animals (table 13).
Clinical-veterinary assay: treatment of spontaneous urinary bladder cancer in dogs:
Several animal models experimentally induced for bladder cancer have been established, including chemically induced tumors. Although such animal models are in use in the research of bladder cancer, animal models in which the disease occurs naturally, mimic as close as possible to humans and may be useful to assess new therapies (Wu et al., 2006; Arantes-Rodrigues et al., 2013), including therapy with MRB-CFI-1.
Naturally occurring bladder cancer in dogs can provide an excellent model as it approaches human invasive bladder cancer, specifically high-grade invasive urothelial carcinoma in terms of cell and molecular characteristics; biological behavior, including sites and frequency of metastases; and response to therapy (Knapp et al., 2014).
To this end, the effects of intravesical immunotherapy with MRB-CFI-1 in the progression of bladder cancer are being evaluated in 20 dogs, attended at the veterinary clinic “Dr. Ronaldo Tizziani” (Campinas, Sao Paulo, Brazil). After the diagnosis of urothelial carcinoma and the consent of the dog's owners, the treatment with MRS-CFI-1 was initiated. The protocol for use of dogs in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocol number: 4481-1/2017).
Dogs received 25 mg of MRB-CFI-1 dissolved in 2.0 mL of physiological saline solution 0.9% intravesically (probing) or bycystocentesis, depending on the conditions of access to the uirnary bladder of each dog. These animals received a weekly dose of MRB-CFI-1 for six consecutive weeks. For maintenance therapy, the animals received a dose of MRB-CFI-1 every 15 days for 6 months and a monthly dose for another 6 months.
The therapeutic effects of MRB-CFI-1 were evaluated by ultrasound during the treatment cycle. Ultrasound evaluations were performed at the following times: before the first instillation, after the first instillation and after 3, 6, 18 and 24 instillations of MRB-CFI-1.
Six dogs completed the full therapeutic regimen with MRB-CFI-1, while 12 were in the maintenance phase and 2 in the induction phase. The following are the results of the 6 dogs, who completed the full therapeutic regimen: Dog 1: Dachshund breed, gender: female, age: 9 years; Dog 2: undefined breed (SRD), gender: female, age: 16 years; Dog 3: Dachshund breed, gender: female, age: 9 years; Dog 4: Teckel breed, Gender: female, age: 1 year; Dog 5: Lhasa Apso breed, gender: female, age: 13 years; Dog 5: Dachshund breed, gender: female, age: 12 years; Dog 6: Poodle breed, gender: female, age: 16 years.
Results:
Biochemical analyses of dogs with urinary bladder cancer undergoing treatment with MRB-CFI-1:
Serum hemoglobin, leukocytes, platelets, hepatic function (ALT) and renal function (urea and creatinine) analyses indicated that the complete treatment with MRB-CFI-1 (24 applications) was not toxic to the 6 dogs, and many parameters such as hemoglobin, leukocytes and ALT reached normal values with the proposed treatment (table 14).
Therefore, these exams indicated that treatment with MRB-CFI-1 showed no signs of systemic toxicity at the proposed therapeutic dose.
Ultrasound analyses of dogs with urinary bladder cancer undergoing treatment with MRB-CFI-1:
a) Dog 1: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 3.08 cm×1.89 cm, and volume of 5.75 cm3 (
b) Dog 2: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 3.42 cm×2.75 cm, and volume of 13.53 cm3 (
c) Dog 3: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 4.22 cm×2.60 cm, and volume of 14.93 cm3 (
d) Dog 4: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 3.91 cm×1,84 cm, and volume of 6.92 cm3 (
a) Dog 5: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 2.25 cm×1.86 cm, and volume of 4.07 cm3 (
f) Dog 6: before the first instillation of MRB-CFI-1, it was observed the presence of tumor mass with irregular contours, mixed echogenicity and hyperechoic echotexture, measuring 2.84 cm×2.73 cm, and volume of 11.08 cm3 (
Thus, these results indicated that intravesical immunotherapy with MRS-CFI-1 was effective in reducing and preventing the progression of urothelial neoplastic lesions in spontaneous cancer of the canine urinary bladder.
Cell Viability Assays
Ceil viability of MRB-CFI-1 and its components, CFI-1 and protein P14-16, was 76.01%±12.39, 68.63%±9.47 and 75.71%±11.52, respectively, using the maximum concentration of 12.5 mg, as denoted in the MTT reduction assay (
Erythrocytes reference value (urine I): up to 6,000 p/ml
Analysis of therapeutic adjuvancy of intravesical immunotherapy with MRB-CFI-1 and systemic chemotherapy with cisplatin in non-muscle invasive bladder cancer (CBNMI)
The histopathological effects of intravesical iminunotherapy with MRB-CFI-1 combined with systemic chemotherapy with systemic cisplatin were verified in Fischer 344 female rats, chemically induced to non-muscle invasive bladder cancer (CBNMI), as per the method already described above. After inducing NMIBC with N-methyl-N-nitrosourea (MNU), the animals were distributed in four experimental groups (n=7 animals per group): group 1 (cancer): received an intravesical dose of 0.2 mL of physiological solution 0.9% for 6 consecutive weeks; group 2 (cancer+MRB-CFI-1): received an intravesical dose of 20 mg/kg of compound MRB-CFI-1 for 6 consecutive weeks; group 3 (cancer+cisplatin): received an intraperitoneal dose of 0.25 mg/kg cisplatin once a week for 4 consecutive weeks; group 4 (cancer+MRB-CFI-1+cisplatin): received simultaneous treatment with MRB-CFI-1 and cisplatin in the same concentrations and through the same administration pathways as groups 2 and 3. The protocol for use of animals in research was approved by the Ethics Committee on the Use of Animals (CEUA)—UNICAMP (protocol number: 4324-1).
The results showed urothelial carcinoma with invasion of lamina propria (pT1) and papillary carcinoma (pTa) in 100% of animals in the cancer group.
The animals treated systemically with cisplatin showed a decrease in the progression of urothelial neoplastic lesions in 14.28% of the animals, which presented a benign lesion characterized by papillary hyperplasia (table 16). The most frequent neoplastic lesions in this group were carcinoma in situ (pTis), pTa carcinoma and pT1 carcinoma in 14.28%, 57.14% and 14.28% of the animals, respectively (table 16).
The animals treated with intravesical MRB-CFI-1 showed a 42.85% decrease in the progression of urothelial neoplastic lesions, which presented normal urothelium (table 16). The most frequent neoplastic lesions in this group were pTis carcinoma and pTa carcinoma in 28.57% and 28.57% of the animals, respectively (table 16).
The treatment combined with intravesical immunotherapy with MRB-CFI-1 and systemic chemotherapy with cisplatin showed better histopathological recovery of the cancer state and decreased progression of urothelial neoplastic lesions in 71.42% of the animals, of which 42.85% had normal urothelium and 28.57% had a benign lesion characterized by flat hyperplasia (table 16). The most frequent neoplastic lesion in this group was pTis carcinoma in 28.57% of the animals (table 16).
Thus, it can be concluded that the combination of intravesical immunotherapy with MRB-CFI-1 and systemic cisplatin may be considered a valuable option for the treatment of patients who do not respond to standard treatment with BCG and/or who do not meet the criteria for early cystectomy.
Results—Exemplary Embodiments (I) and (II)
The characterization of CFI-1 with pH control in the absence (PIBR 10 2017 012768 0) (CFI-1-PIBR-2017) and the presence of monoethanolamine are as follows:
Elementary analysis:
(A) CFI-1 (obtained as defined in the exemplary embodiment (I)): C (0.05%), H (7.02%), N (5.35%). (B) CFI-1 (obtained as defined in the exemplary embodiment (II)); C (0.08%), H (6.92%), N (5.33%).
Analysis of XPS or X-ray-excited photoelectron spectroscopy:
(A) CFI-1 (obtained as defined in the exemplary embodiment (I)); P (16.4%), Mg (19.1%), N (4.2%), O (60.3%), P/Mg ratio=0.9. (B) CFI-1 (obtained as defined in the exemplary embodiment (II)): P (16.9%), Mg (16.7%), N (5.0%) and 0 (61.3%), P/Mg ratio=1,0.
Size (nm) and surface charge (zeta potential, mV):
(A) CFI-1 (obtained as defined in the exemplary embodiment (I)): shows a nanoparticle size value of 310.3, ±56.9 nm; and zeta potential of −21.8±5.8 mV. (B) CFI-1 (obtained as defined in the exemplary embodiment (II)): shows a nanoparticle size value of 449.6±116.6 nm; and zeta potential of −20.0±5.1 mV.
X-ray fluorescence spectroscopic analysis (XRF);
(A) CFI-1 (obtained as defined in the exemplary embodiment (I)): PO4 (55.06%), Mg (16.88%), NH4 (27.68), PO4/Mg ratio=3.36. (B) CFI-1 (obtained as defined in the exemplary embodiment (II)): PO4 (56.43%), Mg (17.61%), NH4 (25.13), PO4/Mg ratio=3.02.
Xray Diffraction Pattern (XRD)
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2017 012768 0 | Jun 2017 | BR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/BR2018/000031 | 6/14/2018 | WO | 00 |
