药物输送
乙二醇
PLGA公司
前列腺癌
体内
靶向给药
纳米技术
药品
表面改性
适体
细胞毒性
纳米颗粒
生物相容性材料
材料科学
化学
纳米医学
谷氨酸羧肽酶Ⅱ
可生物降解聚合物
体外
药理学
癌症
生物医学工程
医学
聚合物
生物化学
分子生物学
有机化学
内科学
物理化学
生物
生物技术
作者
Juliana M. Chan,Pedro M. Valencia,Liangfang Zhang,Róbert Langer,Omid C. Farokhzad
出处
期刊:Methods in molecular biology
日期:2010-01-01
卷期号:: 163-175
被引量:296
标识
DOI:10.1007/978-1-60761-609-2_11
摘要
The use of biodegradable polymeric nanoparticles (NPs) for controlled drug delivery has shown significant therapeutic potential. Concurrently, targeted delivery technologies are becoming increasingly important as a scientific area of investigation. In cancer, targeted polymeric NPs can be used to deliver chemotherapies to tumor cells with greater efficacy and reduced cytotoxicity on peripheral healthy tissues. In this chapter, we describe the methods of (1) preparation and characterization of drug-encapsulated polymeric NPs formulated with biocompatible and biodegradable poly(D,L-lactic-co-glycolic acid)-poly(ethylene glycol) (PLGA-b-PEG) copolymers; (2) surface functionalization of the polymeric NPs with the A10 2'-fluoropyrimidine ribonucleic acid (RNA) aptamers that recognize the prostate-specific membrane antigen (PSMA) on prostate cancer cells; and (3) evaluation of the binding properties of these targeted polymeric NPs to PSMA-expressing prostate cancer cells in vitro and in vivo. These methods may contribute to the development of other useful polymeric NPs to deliver a spectrum of chemotherapeutic, diagnostic, and imaging agents for various applications.
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