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纯药物纳米组装体:一种简便的无载体纳米平台用于高效癌症治疗

英文原题:Pure drug nano-assemblies: A facile carrier-free nanoplatform for efficient cancer therapy.

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Pure drug nano-assemblies: A facile carrier-free nanoplatform for efficient cancer therapy.

PubMed 2021/08/14(内容时间) Acta Pharm Sin B Q1 · IF 14.6(JCR 2025)

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中文摘要

纳米颗粒药物递送系统(Nano-DDSs)已成为解决抗癌药物递送障碍的可能方案。然而,其临床结局和转化受到若干缺点的限制,如低载药量、药物过早泄漏和载体相关毒性。近年来,由纯药物分子自组装或共组装制备的纯药物纳米组装体(PDNAs)引起了广泛关注。其简便且可重复的制备技术有助于消除纳米药物在质量控制、放大生产和临床转化方面的瓶颈。作为载体和货物,无载体的PDNAs具有超高甚至100%的载药量。此外,基于PDNAs的联合治疗可能解决癌症治疗中最棘手的问题,如肿瘤转移和耐药性。在本综述中,概述了PDNAs用于癌症治疗的最新进展。首先,根据药物分子的组成对PDNAs进行分类,并讨论其组装机制。此外,总结了PDNAs用于联合治疗的共递送,特别关注治疗结局的改善。最后,重点介绍了PDNAs用于高效癌症治疗的未来前景和挑战。

展开英文摘要原文

Nanoparticulate drug delivery systems (Nano-DDSs) have emerged as possible solution to the obstacles of anticancer drug delivery.

However, the clinical outcomes and translation are restricted by several drawbacks, such as low drug loading, premature drug leakage and carrier-related toxicity. Recently, pure drug nano-assemblies (PDNAs), fabricated by the self-assembly or co-assembly of pure drug molecules, have attracted considerable attention.

Their facile and reproducible preparation technique helps to remove the bottleneck of nanomedicines including quality control, scale-up production and clinical translation. Acting as both carriers and cargos, the carrier-free PDNAs have an ultra-high or even 100% drug loading.

In addition, combination therapies based on PDNAs could possibly address the most intractable problems in cancer treatment, such as tumor metastasis and drug resistance. In the present review, the latest development of PDNAs for cancer treatment is overviewed. First, PDNAs are classified according to the composition of drug molecules, and the assembly mechanisms are discussed.

Furthermore, the co-delivery of PDNAs for combination therapies is summarized, with special focus on the improvement of therapeutic outcomes.

Finally, future prospects and challenges of PDNAs for efficient cancer therapy are spotlighted.

论文信息

作者
Fu S、Li G、Zang W、Zhou X、Shi K、Zhai Y
第一作者单位
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.China
通讯作者单位
Department of Biomedical Engineering, School of Medical Device, Shenyang Pharmaceutical University, Shenyang 110016, China.China
文献类型
综述
期刊
Acta pharmaceutica Sinica. B2022 Jan
原文标识
PubMed 35127374 · DOI 10.1016/j.apsb.2021.08.012