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基于pH敏感型星形共聚物的纳米载体用于药物控释

Nano-Carriers Based on pH-Sensitive Star-Shaped Copolymers for Drug-Controlled Release.

作者信息

Jiang Wenzhao, Guo Jianwei, Wen Weiqiu, Jia Yong-Guang, Liu Sa

机构信息

School of Chemical Engineering & Light Industry, Guangdong University of Technology, Guangzhou 510006, China.

School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China.

出版信息

Materials (Basel). 2019 May 16;12(10):1610. doi: 10.3390/ma12101610.

Abstract

Polymeric nano-carriers are considered as promising tools in biomedical applications due to multiple attractive characteristics including their low toxicity, high loading capacity, controlled drug release capabilities, and highly tunable chemical properties. Here, a series of pH-sensitive star-shaped copolymers, Ad-P[(EMA--MAA)--PPEGMA], was prepared via electron transfer atom radical polymerization (ARGETE ATRP) and selective hydrolysis. These star-shaped copolymers can be self-assembled into micelles ( = 150-160 nm) and their critical micelle concentrations (CMC) were estimated to be 3.9-5.0 mg/L. The pH-sensitiveness of the micelles was evidenced by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The maximal paclitaxel (PTX) loading efficiency (DLC) and entrapment efficiency (EE) were 18.9% and 36%, respectively. In vitro release studies revealed that about 19% of the PTX released at an acidic condition of pH 1.2 over 70 h, whereas more than 70% was released within the same time interval at pH 6.8. In vitro cytotoxicity suggested that the low cytotoxicity of the blank micelles, while the PTX-loaded micelles providing the cytotoxicity close to that of free PTX. These results indicated that this novel pH-sensitive nano-carriers have great potential applications for oral drug-controlled release.

摘要

由于具有低毒性、高载药量、可控药物释放能力和高度可调节化学性质等多种吸引人的特性,聚合物纳米载体被认为是生物医学应用中有前景的工具。在此,通过电子转移原子自由基聚合(ARGET ATRP)和选择性水解制备了一系列pH敏感的星形共聚物Ad-P[(EMA-MAA)-PPEGMA]。这些星形共聚物可自组装成胶束(粒径 = 150 - 160 nm),其临界胶束浓度(CMC)估计为3.9 - 5.0 mg/L。通过透射电子显微镜(TEM)和动态光散射(DLS)证明了胶束的pH敏感性。紫杉醇(PTX)的最大载药效率(DLC)和包封率(EE)分别为18.9%和36%。体外释放研究表明,在pH 1.2的酸性条件下,约19%的PTX在70小时内释放,而在pH 6.8时,在相同时间间隔内释放超过70%。体外细胞毒性表明空白胶束的细胞毒性较低,而载药胶束的细胞毒性接近游离PTX。这些结果表明,这种新型pH敏感纳米载体在口服药物控释方面具有巨大的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaab/6566147/4e538b985d77/materials-12-01610-sch001.jpg

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