Katiyar Sameer S, Muntimadugu Eameema, Rafeeqi Towseef Amin, Domb Abraham J, Khan Wahid
a Department of Pharmaceutics , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , Telangana , India.
b Central Research Institute of Unani Medicine (CRIUM) , Hyderabad , Telangana , India , and.
Drug Deliv. 2016 Sep;23(7):2608-2616. doi: 10.3109/10717544.2015.1039667. Epub 2015 Jun 2.
P-glycoprotein (P-gp) efflux is the major cause of multidrug resistance (MDR) in tumors when using anticancer drugs, moreover, poor bioavailability of few drugs is also due to P-gp efflux in the gut. Rapamycin (RPM) is in the clinical trials for breast cancer treatment, but its P-gp substrate property leads to poor oral bioavailability and efficacy. The objective of this study is to formulate and evaluate nanoparticles of RPM, along with a chemosensitizer (piperine, PIP) for improved oral bioavailability and efficacy. Poly(d,l-lactide-co-glycolide) (PLGA) was selected as polymer as it has moderate MDR reversal activity, which may provide additional benefits. The nanoprecipitation method was used to prepare PLGA nanoparticles with particle size below 150 nm, loaded with both drugs (RPM and PIP). Prepared nanoparticles showed sustained in vitro drug release for weeks, with initial release kinetics of zero order with non-Fickian transport, subsequently followed by Higuchi kinetics with Fickian diffusion. An everted gut sac method was used to study the effect of P-gp efflux on drug transport. This reveals that the uptake of the RPM (P-gp substrate) has been increased in the presence of chemosensitizer. Pharmacokinetic studies showed better absorption profile of RPM from polymeric nanoparticles compared to its suspension counterpart and improved bioavailability of 4.8-folds in combination with a chemosensitizer. An in vitro cell line study indicates higher efficacy of nanoparticles compared to free drug solution. Results suggest that the use of a combination of PIP with RPM nanoparticles would be a promising approach in the treatment of breast cancer.
在使用抗癌药物时,P-糖蛋白(P-gp)外排是肿瘤多药耐药(MDR)的主要原因,此外,少数药物的低生物利用度也归因于肠道中的P-gp外排。雷帕霉素(RPM)正处于乳腺癌治疗的临床试验阶段,但其P-gp底物特性导致口服生物利用度和疗效不佳。本研究的目的是制备并评估RPM纳米颗粒,以及一种化学增敏剂(胡椒碱,PIP),以提高口服生物利用度和疗效。选择聚(d,l-丙交酯-共-乙交酯)(PLGA)作为聚合物,因为它具有适度的MDR逆转活性,这可能会带来额外的益处。采用纳米沉淀法制备粒径低于150 nm的负载两种药物(RPM和PIP)的PLGA纳米颗粒。制备的纳米颗粒在体外显示出数周的持续药物释放,初始释放动力学为零级非菲克转运,随后为具有菲克扩散的Higuchi动力学。采用外翻肠囊法研究P-gp外排对药物转运的影响。这表明在存在化学增敏剂的情况下,RPM(P-gp底物)的摄取增加。药代动力学研究表明,与悬浮剂相比,聚合物纳米颗粒中的RPM具有更好的吸收曲线,与化学增敏剂联合使用时生物利用度提高了4.8倍。体外细胞系研究表明纳米颗粒的疗效高于游离药物溶液。结果表明,PIP与RPM纳米颗粒联合使用可能是治疗乳腺癌的一种有前景的方法。