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用于载药纳米球的血小板介导递送系统的设计,以增强抗肿瘤治疗效果。

Design of a Platelet-Mediated Delivery System for Drug-Incorporated Nanospheres to Enhance Anti-Tumor Therapeutic Effect.

作者信息

Jo Jun-Ichiro, Emi Tsubasa, Tabata Yasuhiko

机构信息

Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Pharmaceutics. 2021 Oct 18;13(10):1724. doi: 10.3390/pharmaceutics13101724.

Abstract

The objective of this study is to construct a platelet-mediated delivery system for drug-incorporated nanospheres. Nanospheres of poly(lactic-co-glycolic acid) (PLGA-NS) with different sizes and surface properties were prepared by changing the preparation parameters, such as the type of polymer surfactant, the concentration of polymer surfactant and PLGA, and the stirring rate. When incubated with platelets, PLGA-NS prepared with poly(vinyl alcohol) suppressed the platelet activation. Scanning electron microscopic and flow cytometry examinations revealed that platelets associated with PLGA-NS (platelet hybrids, PH) had a similar appearance and biological properties to those of the original platelets. In addition, the PH with PLGA-NS specifically adhered onto the substrate pre-coated with fibrin to a significantly great extent compared with PLGA-NS alone. When applied in an in vitro model of tumor tissue which was composed of an upper chamber pre-coated with fibrin and a lower chamber culturing tumor cells, the PH with PLGA-NS incorporating an anti-tumor drug were delivered to the tumor cells through the specific adhesion onto the upper chamber and, consequently, drug release from the upper chamber took place, resulting in the growth suppression of tumor cells. It is concluded that the drug delivery system based on PH is promising for tumor treatment.

摘要

本研究的目的是构建一种用于载药纳米球的血小板介导递送系统。通过改变制备参数,如聚合物表面活性剂的类型、聚合物表面活性剂和聚乳酸-羟基乙酸共聚物(PLGA)的浓度以及搅拌速率,制备了具有不同尺寸和表面性质的PLGA纳米球(PLGA-NS)。当与血小板一起孵育时,用聚乙烯醇制备的PLGA-NS可抑制血小板活化。扫描电子显微镜和流式细胞术检查显示,与PLGA-NS相关的血小板(血小板杂合体,PH)与原始血小板具有相似的外观和生物学特性。此外,与单独的PLGA-NS相比,含有PLGA-NS的PH在很大程度上特异性地黏附于预先包被有纤维蛋白的底物上。当应用于由预先包被有纤维蛋白的上腔室和培养肿瘤细胞的下腔室组成的肿瘤组织体外模型时,含有抗肿瘤药物的PLGA-NS的PH通过特异性黏附于上腔室而被递送至肿瘤细胞,结果,药物从上腔室释放,导致肿瘤细胞生长受到抑制。结论是基于PH的药物递送系统在肿瘤治疗方面具有前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e02/8540062/12c3057938c5/pharmaceutics-13-01724-g001.jpg

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