叶酸共轭壳聚糖纳米粒子在靶向递送抗癌药物中的潜在应用

Prakash Nathaniel Kumar Sarella, Pavan Kumar Thammana
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摘要

叶酸共轭壳聚糖纳米粒子是一种很有前景的靶向递送抗癌药物的纳米平台。这种纳米颗粒载体能保护治疗药物不被降解,并能靶向过度表达叶酸受体的癌细胞。本综述总结了合成叶酸共轭壳聚糖纳米粒子的最新研究进展,并评估了其作为靶向给药系统的潜力。首先讨论了叶酸与壳聚糖的化学共轭,然后概述了制备尺寸小于 200 nm 的稳定叶酸共轭壳聚糖纳米粒子的不同技术。然后概述了将各种抗癌药物加入这些纳米颗粒并研究其对多种癌细胞系的体外细胞毒性的最新研究。结果表明,与非共轭纳米粒子相比,叶酸共轭纳米粒子由于受体介导的内吞作用而表现出更高的细胞毒性和靶向效率。最后,概述了未来的挑战和机遇,包括体内研究以确定叶酸共轭壳聚糖纳米粒子系统的有效性、毒性和药代动力学,以及其作为癌症化疗靶向药物载体的潜在临床应用。
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Potential applications of Folate-conjugated Chitosan Nanoparticles for Targeted delivery of Anticancer drugs
Folate-conjugated chitosan nanoparticles represent a promising nanoplatform for targeted delivery of anticancer drugs. The nanoparticle carrier can protect the therapeutic agents from degradation and offer the ability to target cancer cells overexpressing folate receptors. This review summarizes recent research progress in synthesizing folate-conjugated chitosan nanoparticles as well as evaluating their potential as targeted drug delivery systems. The chemical conjugation of folic acid to chitosan is first discussed followed by an overview of different techniques for preparation of stable folate-conjugated chitosan nanoparticles less than 200 nm in size. Recent studies loading various anticancer drugs into these nanoparticles and investigating their in vitro cytotoxicity against multiple cancer cell lines are then summarized. The results indicate that folate-conjugated nanoparticles exhibit higher cytotoxicity and targeting efficiency compared to non-conjugated nanoparticles due to receptor-mediated endocytosis. Lastly, future challenges and opportunities are outlined including in vivo investigations to determine the effectiveness, toxicity, and pharmacokinetics of folate-conjugated chitosan nanoparticle systems as well as their potential clinical translation as targeted drug carriers for cancer chemotherapy.
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