Gold nanoparticles generated and stabilized by water soluble curcumin–polymer conjugate: Blood compatibility evaluation and targeted drug delivery onto cancer cells

姜黄素 细胞毒性 化学 共轭体系 药物输送 结合 共焦显微镜 胶体金 纳米载体 内化 癌细胞 流式细胞术 生物物理学 氯金酸 赫拉 阿霉素 生物利用度 纳米颗粒 纳米技术 材料科学 生物化学 体外 药理学 细胞 聚合物 有机化学 分子生物学 癌症 细胞生物学 生物 数学 数学分析 遗传学 化疗
作者
S. Manju,K. Sreenivasan
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:368 (1): 144-151 被引量:171
标识
DOI:10.1016/j.jcis.2011.11.024
摘要

Curcumin (Cur) shows low anticancer activity in vivo due to its reduced systemic bioavailability stemmed from its poor aqueous solubility and instability. Suitably functionalized nanocarriers designed to empty the drug specifically at tumor sites can potentially enhance the antitumor activity of Cur. We devised a simple method for the fabrication of water soluble Cur conjugated gold nanoparticles to target various cancer cell lines. Cur was conjugated to hyaluronic acid (HA) to get a water soluble conjugate (HA-Cur). We generated gold nanoparticles (AuNPs) by reducing chloroauric acid using HA-Cur, which played the dual role of a reducing and stabilizing agent and subsequently anchored folate conjugated PEG. These entities were probed using different analytical techniques, assayed the blood compatibility and cytotoxicity. Their interaction with cancer cell lines (HeLa cells, glyoma cells and Caco 2 cells) was followed by flow cytometry and confocal microscopy. Blood-materials interactions studies showed that the nanoparticles are highly hemocompatible. Flow cytometry and confocal microscopy results showed significant cellular uptake and internalization of the particles by cells. HA-Cur@AuNPs exhibited more cytotoxicity comparing to free Cur. The strategy, we adopted here, resulted the formation blood compatible Cur conjugated AuNPs with enhanced targeting and improved efficacy.

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