章越, 丁陈陈, 温露, 陈钢. 核壳型聚乳酸-羟基乙酸共聚物磁性纳米系统用于中药复方多组分的时空递释J. 药学学报, 2018,53(12): 1968-1975. doi: 10.16438/j.0513-4870.2018-0333
引用本文: 章越, 丁陈陈, 温露, 陈钢. 核壳型聚乳酸-羟基乙酸共聚物磁性纳米系统用于中药复方多组分的时空递释J. 药学学报, 2018,53(12): 1968-1975. doi: 10.16438/j.0513-4870.2018-0333
ZHANG Yue, DING Chen-chen, WEN Lu, CHEN Gang. Core-shell magnetic poly (lactic-co-glycolic acid) nanosystem for tem-po-spatially controlled release kinetics of multiple components of traditional Chinese medicine formulaJ. Acta Pharmaceutica Sinica, 2018,53(12): 1968-1975. doi: 10.16438/j.0513-4870.2018-0333
Citation: ZHANG Yue, DING Chen-chen, WEN Lu, CHEN Gang. Core-shell magnetic poly (lactic-co-glycolic acid) nanosystem for tem-po-spatially controlled release kinetics of multiple components of traditional Chinese medicine formulaJ. Acta Pharmaceutica Sinica, 2018,53(12): 1968-1975. doi: 10.16438/j.0513-4870.2018-0333

核壳型聚乳酸-羟基乙酸共聚物磁性纳米系统用于中药复方多组分的时空递释

Core-shell magnetic poly (lactic-co-glycolic acid) nanosystem for tem-po-spatially controlled release kinetics of multiple components of traditional Chinese medicine formula

  • 摘要: 本研究的目的是构建可共载丹参-三七复方多组分且在特定部位能实现程序性释药的羟丙基-β-环糊精-聚乳酸-羟基乙酸共聚物(PLGA)磁性纳米递药系统,旨在为中药复方多组分制剂的设计提供参考。以不饱和醇溶液法制备羟丙基-β-环糊精包合物,以复乳法制备PLGA磁性纳米粒,再将两者共孵育制备成核壳型磁性纳米体系。应用激光共聚焦显微镜、透射电镜及激光粒度仪表征纳米粒的形貌特征及粒径分布;磁滞回线和磁铁吸附实验表征纳米粒的磁学性质;体外细胞摄取实验考察纳米粒的靶向分布行为;荧光纳米粒的细胞内分布实验考察其释药次序;共载丹参-三七复方多组分纳米粒的体外释放实验考察内核药物和外壳药物的释放差异。结果表明,该纳米系统具有核壳结构;饱和磁化强度约为3.0×10-4 emu·g-1,具有超顺磁性;在外置磁铁下,L929细胞可实现对磁性纳米粒的靶向摄取;包载罗丹明B和香豆素-6两种荧光物质的纳米粒在L929细胞内可呈现程序性释放行为;纳米粒中丹参-三七复方多组分的体外释放具有外壳速释-内核缓释的双相释放动力学特征。综上,本研究所制备的羟丙基-β-环糊精-PLGA纳米系统具有时空递释功能,有望在剂型设计层面上实现中药多组分的作用最优化。

     

    Abstract: Traditional Chinese medicine (TCM) formula is one of the unique cultural treasures of Chinese. However, only a few studies have been carried out to deliver TCM formula with utilization of nanocarriers. The purpose of this study was to prepare the hydroxypropyl-β-cyclodextrin complex-over-a-poly(lactic-co-glycolic acid) nanoparticle (HP-β-CD-PLGA NP) for co-delivery and sequential release of five main effective ingredients of Danshen and Sanqi to a specific target, which can provide strategies for design of intelligent drug delivery system of TCM formula. PLGA can be employed as scaffolds for sustained release of both hydrophobic and hydrophilic drugs. HP-β-CD could encapsulate the hydrophobic drugs by forming inclusion complexes. Superparamagnetic iron oxide nanoparticles (SPION) embedded inside PLGA nanoparticles that allow a spatio-specific targeting. HP-β-CD inclusion complex was prepared by an unsaturated alcohol solution method. PLGA NP loaded with SPION was obtained through double emulsion-organic solvents evaporation. Then core-shell PLGA nanosystem was formed by co-incubation of the above two materials. The nanoparticulate system was characterized by confocal laser scanning microscopy (CLSM), laser particle size instrument and transmission electron microscope. Magnetic property was determined by magnet adsorption and vibrating sample magnetometer (VSM). Targeted distribution was investigated by cell uptake and sequential release of multiple components was observed by intracellular distribution of fluorescent probes. Release difference of five components between core and shell of HP-β-CD-PLGA NP was measured by high performance liquid chromatography. The results demonstrated that NP had a unique core-shell structure and possessed superpara-magnetism. Magnetic NP could be ingested site-specifically by L929 cells with the aid of magnetic field, and coumarin-6 and rhodamine B were released from NP sequentially in the L929 cells. In vitro release of multiple components of Danshen and Sanqi from NP exhibited double phase time-controlled release kinetics of quick-release shell and sustained-release core. Therefore, the spatio-temporal nanoplatform has a great capacity for unlocking the full therapeutic potential of displaying synergistic efficacy of TCM formula in the formulation design.

     

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