释放环肽基纳米载体的治疗潜力,以增强结肠癌的治疗。

IF 1.4
Vedhapriya Souresh, M Srikayalsamyukktha, M Harini, Yudhesh Saravanan, Rupachandra Saravanakumar
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引用次数: 0

摘要

环肽因其结构稳定、生物利用度高、靶向特异性强而成为结肠癌的治疗药物。从植物、海洋和微生物中提取的天然环肽具有强大的抗癌特性。纳米技术的进步促进了基于环肽的纳米载体的使用,以改善药物传递,增强肿瘤渗透,并尽量减少不良反应。纳米载体包括脂质体、纳米小体、纳米海绵和纳米聚合物,通过促进环肽的局部分布、增强稳定性和控制释放,提供了一种革命性的方法。这种策略改善了药代动力学,降低了全身毒性,克服了传统治疗的局限性。基于环肽的纳米技术的最新进展表明,环肽和纳米载体在克服结肠癌耐药方面具有协同作用。本文综述了环肽的来源、作用机制以及在结肠癌治疗中的应用。进一步探讨了环肽功能化纳米载体在克服耐药和改善药物传递方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unlocking the Therapeutic Potential of Cyclic Peptide-Based Nanocarriers for Enhanced Colon Cancer Treatment.

Cyclic peptides have emerged as therapeutic agents for colon cancer due to their structural stability, enhanced bioavailability, and high target specificity. Natural cyclic peptides derived from plant, marine, and microbial sources exhibit potent anticancer properties. Advancements in nanotechnology have facilitated using cyclic peptide-based nanocarriers to improve drug delivery, enhance tumor penetration, and minimize adverse effects. Nanocarriers including liposomes, niosomes, nanosponges, and nanopolymers provide a revolutionary approach by facilitating localized distribution, enhanced stability, and controlled release of cyclic peptides. This strategy improves pharmacokinetics and lowers systemic toxicity to overcome the limitations of conventional treatments. Recent developments in cyclic peptide-based nanotechnology demonstrate the synergy between cyclic peptides and nanocarriers in overcoming drug resistance in colon cancer. This review provides a comprehensive overview of the sources, mechanisms of action, and therapeutic applications of cyclic peptides in colon cancer treatment. It further explores the role of cyclic peptide-functionalized nanocarriers in overcoming drug resistance and improving drug delivery.

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