1. New Poly(3-hydroxybutyrate) Microparticles with Paclitaxel Sustained Release for Intraperitoneal Administration
- Author
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V. L. Myshkina, Anton P. Bonartsev, S. G. Yakovlev, Natalia V. Andronova, T.K. Mahina, A.L. Zernov, Galina B. Smirnova, Mikhail S. Kalishjan, I. I. Zharkova, Juliya A. Borisova, Helena M. Treshalina, Konstantin V. Shaitan, and Garina A. Bonartseva
- Subjects
Drug ,Cancer Research ,Paclitaxel ,Biocompatibility ,Surface Properties ,Polyesters ,media_common.quotation_subject ,Hydroxybutyrates ,Antineoplastic Agents ,Breast Neoplasms ,02 engineering and technology ,Pharmacology ,010402 general chemistry ,01 natural sciences ,Carcinoma, Lewis Lung ,Mice ,Structure-Activity Relationship ,chemistry.chemical_compound ,In vivo ,Prohibitins ,Tumor Cells, Cultured ,medicine ,Animals ,Humans ,Particle Size ,Cell Proliferation ,media_common ,Dose-Response Relationship, Drug ,Molecular Structure ,Chemistry ,Cell growth ,Mammary Neoplasms, Experimental ,Lewis lung carcinoma ,Cancer ,021001 nanoscience & nanotechnology ,medicine.disease ,In vitro ,0104 chemical sciences ,Molecular Medicine ,Drug Screening Assays, Antitumor ,0210 nano-technology ,Injections, Intraperitoneal - Abstract
Background: Poly(hydroxyalkanoates) (PHA) have recently attracted increasing attention due to their biodegradability and high biocompatibility, which makes them suitable for the development of new prolong drug formulations. Objective: This study was conducted to develop new prolong paclitaxel (PTX) formulation based on poly(3- hydroxybutyrate) (PHB) microparticles. Method: PHB microparticles loaded with antitumor cytostatic drug PTX were obtained by spray-drying method using Nano Spray Dryer B-90. The PTX release kinetics in vitro from PHB microparticles and their cytotoxity on murine hepatoma cell line MH-22a were studied. Microparticles antitumor activity in vivo was studied using intraperitoneally (i.p.) transplanted tumor models: murine Lewis lung carcinoma and xenografts of human breast cancer RMG1. Results: Uniform PTX release from PHB-microparticles during 2 months was observed. PTX-loaded PHB microparticles have demonstrated a significant antitumor activity versus pure drug both in vitro in murine hepatoma cells and in vivo when administered i.p. to mice with murine Lewis lung carcinoma and xenografts of human breast cancer RMG1. Conclusion: The developed technique of PTX sustained delivery from PHB-microparticles has therapeutic potential as prolong anticancer drug formulation.
- Published
- 2017
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