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基于槲皮素-季铵化壳聚糖(Qu-QCS)轭合物的载姜黄素纳米胶束的制备及其与阿霉素协同抗乳腺癌作用的评价。

Fabrication of curcumin-loaded nano-micelles based on quercetin-quarternary ammonium-chitosan (Qu-QCS) conjugate and evaluation of synergistic effect with doxorubicin against breast cancer.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Drug Delivery System Excellent Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.

Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Drug Delivery System Excellent Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.

出版信息

Int J Biol Macromol. 2024 Nov;281(Pt 2):135904. doi: 10.1016/j.ijbiomac.2024.135904. Epub 2024 Oct 31.

Abstract

The applications of quarternized chitosans have achieved notable success in the development of drug-delivery systems. This study reported the preparation of quercetin-quarternized chitosan (Qu-QCS) conjugate and its application for the fabrication of stable and safe curcumin (cur) loaded nano-micelles with high targeting ability and selectivity towards the breast cancer cell lines. Moreover, doxorubicin (dox) was co-treated with the nanomicelles to enhance the efficacy and reduce the cardiotoxic effects of dox. Structural properties of Qu-QCS were evaluated by FTIR, DSC, and XRD analysis and the yield obtained was 48.82 %. The nano-micelles obtained showed spherical shape, <200 nm size, 48.38 % entrapment efficiency, prolonged stability at 4 °C and pH-responsive release pattern. The cur-loaded nano-micelles showed higher activity and selectivity against breast cancer (MCF-7 and MDA-MB-231) cell lines with enhanced internalization, lower toxicity to the normal cardiomyoctyes (H9C2), enhanced the cell cycle arrest at the G2/M phase of the breast cancer cell lines and induced apoptosis with high intensity compared to pure cur. Moreover, the co-treatment of dox with cur-loaded Qu-QCS nano-micelles showed increased anticancer activity and reduced cardiotoxicity. Overall, this study suggests the potential applications of cur-loaded Qu-QCS micelles in the delivery of chemotherapeutic agents and complementary support in combination with chemotherapeutic agents.

摘要

季铵化壳聚糖在药物传递系统的开发中得到了广泛的应用。本研究报道了槲皮素-季铵化壳聚糖(Qu-QCS)缀合物的制备及其在制备具有高靶向性和选择性的稳定、安全的姜黄素(cur)负载纳米胶束中的应用,该纳米胶束对乳腺癌细胞系具有靶向性和选择性。此外,还将阿霉素(dox)与纳米胶束共同处理,以提高疗效并降低 dox 的心脏毒性。通过 FTIR、DSC 和 XRD 分析对 Qu-QCS 的结构性质进行了评价,产率为 48.82%。所得纳米胶束呈球形,粒径<200nm,包封率为 48.38%,在 4°C 和 pH 响应性释放模式下具有良好的稳定性。载 cur 的纳米胶束对乳腺癌(MCF-7 和 MDA-MB-231)细胞系表现出更高的活性和选择性,具有增强的内化作用,对正常心肌细胞(H9C2)的毒性较低,增强了乳腺癌细胞系的细胞周期停滞在 G2/M 期,并诱导凋亡,强度高于纯 cur。此外, dox 与载 cur 的 Qu-QCS 纳米胶束共同处理显示出增强的抗癌活性和降低的心脏毒性。总的来说,本研究表明载 cur 的 Qu-QCS 胶束在递药系统和与化疗药物联合应用方面具有潜在的应用价值。

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