Malekhosseini Shifteh, Rezaie Aram, Khaledian Salar, Abdoli Mohadese, Zangeneh Mohammad Mahdi, Hosseini Amin, Behbood Leila
Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Nano Drug Delivery Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Heliyon. 2020 May 18;6(5):e03975. doi: 10.1016/j.heliyon.2020.e03975. eCollection 2020 May.
A nanomicelle based drug delivery systems is a formulation that can improve the bioavailability and dissolution rate of water-insoluble drugs. In this study, the Dextran-Poly Lactic-co-Glycolic Acid copolymer was synthesized with esterification reaction, confirmed using the fourier-transform infrared spectroscopy and nuclear magnetic resonance. The used method for nanomicelle preparation was nanoprecipitation and the critical micelle concentration value was obtained 10 μg/mL. The particle size of the nanomicelle was less than 100 nm ± 4 nm with narrow size distribution (Polydispersity index = 0.06). Hydrocortisone was loaded to this system. The obtained results for the encapsulation efficiency were 79%, and the drug release was adjusted to a first-order kinetic model with 90% release of drug within the 12 h. The MTT assay showed that even in the high concentration of micelle, the cell viability was remained higher than 90%. Considering the toxicity investigation findings, the Dextran-Poly Lactic-co-Glycolic Acid micellar systems can be suggested as a considerable drug delivery system in hydrocortisone pharmaceutical dosage forms.
基于纳米胶束的药物递送系统是一种能够提高水不溶性药物生物利用度和溶解速率的制剂。在本研究中,通过酯化反应合成了葡聚糖-聚乳酸-乙醇酸共聚物,并使用傅里叶变换红外光谱和核磁共振进行了确认。制备纳米胶束所采用的方法是纳米沉淀法,临界胶束浓度值为10μg/mL。纳米胶束的粒径小于100nm±4nm,粒径分布狭窄(多分散指数=0.06)。将氢化可的松负载到该系统中。所获得的包封率结果为79%,药物释放符合一级动力学模型,在12小时内药物释放率为90%。MTT试验表明,即使在高浓度胶束存在的情况下,细胞活力仍高于90%。考虑到毒性研究结果,葡聚糖-聚乳酸-乙醇酸胶束系统可被推荐为氢化可的松药物剂型中一种相当不错的药物递送系统。