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通过使用聚氰基丙烯酸正丁酯纳米球提高10-羟基喜树碱的口服生物利用度。

Enhanced oral bioavailability of 10-hydroxycamptothecin through the use of poly (n-butyl cyanoacrylate) nanospheres.

作者信息

Jin Xin, Asghar Sajid, Zhu Xieting, Chen Zhipeng, Liu Junhong, Li Yibo, Li Hongying, Ping Qineng, Xiao Yanyu

机构信息

a Department of Pharmaceutics, State Key Laboratory of Natural Medicines , China Pharmaceutical University , Nanjing , PR China.

b Faculty of Pharmaceutical Sciences , Government College University Faisalabad , Faisalabad , Pakistan.

出版信息

Drug Dev Ind Pharm. 2017 Oct;43(10):1637-1647. doi: 10.1080/03639045.2017.1328432. Epub 2017 May 19.

Abstract

The article describes the preparation, physicochemical characterization, drug release, and in vivo behavior of 10-hydroxycamptothecin-loaded poly (n-butyl cyanoacrylate) (PBCA) nanospheres (HCPT-PBCA-NSs). HCPT-PBCA-NSs were successfully prepared via emulsion polymerization of n-butyl cyanoacrylate (BCA) monomer in acidic medium with the aid of two colloidal stabilizers (Poloxamer 188 and Dextran 70). The influence of pH, the time of polymerization, and the dosage of the drug on particle size and encapsulation efficiency (EE) were studied. HCPT-PBCA-NSs were of spherical shape and uniformly dispersed with a particle size of 135.7 nm, and zeta potential of -18.18 mV. EE, drug loading (DL), and yield of HCPT-PBCA-NSs were 51.52, 0.63, and 88.25%, respectively. FTIR, H NMR, and DSC showed complete polymerization of BCA monomer and HCPT existed in the form of molecular or amorphous in NSs. In vitro release of the drug from HCPT-PBCA-NSs exhibited sustained-release behavior with an initial burst release and about 60% of HCPT was released from the formulation within 24 h of dialysis. The pharmacokinetic study in healthy rats after oral administration showed that encapsulation of HCPT into PBCA-NSs increased the C about 3.84 times and increased AUC about 5.40 times compared with that of HCPT suspension. It was concluded that PBCA-NSs could be a promising drug carrier to load HCPT for oral drug delivery if efforts are made in the future to improve its poor DL capacity.

摘要

本文描述了载有10-羟基喜树碱的聚氰基丙烯酸正丁酯(PBCA)纳米球(HCPT-PBCA-NSs)的制备、理化性质表征、药物释放及体内行为。通过在酸性介质中借助两种胶体稳定剂(泊洛沙姆188和葡聚糖70)对氰基丙烯酸正丁酯(BCA)单体进行乳液聚合,成功制备了HCPT-PBCA-NSs。研究了pH、聚合时间和药物用量对粒径和包封率(EE)的影响。HCPT-PBCA-NSs呈球形,均匀分散,粒径为135.7 nm,ζ电位为-18.18 mV。HCPT-PBCA-NSs的EE、载药量(DL)和产率分别为51.52%、0.63%和88.25%。傅里叶变换红外光谱(FTIR)、核磁共振氢谱(H NMR)和差示扫描量热法(DSC)表明BCA单体完全聚合,且HCPT以分子或无定形形式存在于纳米球中。HCPT-PBCA-NSs的体外药物释放呈现出缓释行为,有初始突释,在透析24小时内约60%的HCPT从制剂中释放。健康大鼠口服给药后的药代动力学研究表明,与HCPT混悬液相比,将HCPT包封于PBCA-NSs中使血药浓度(C)提高了约3.84倍,曲线下面积(AUC)提高了约5.40倍。结论是,如果未来努力改善其载药量低的问题,PBCA-NSs可能成为一种有前景的载药HCPT用于口服给药的载体。

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