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小分子前药纳米组装体:用于抗癌药物递送的新兴纳米平台。

Small-Molecule Prodrug Nanoassemblies: An Emerging Nanoplatform for Anticancer Drug Delivery.

机构信息

Department of Pharmaceutics, Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016, China.

出版信息

Small. 2021 Dec;17(52):e2101460. doi: 10.1002/smll.202101460. Epub 2021 Aug 3.

Abstract

The antitumor efficiency and clinical translation of traditional nanomedicines is mainly restricted by low drug loading, complex preparation technology, and potential toxicity caused by the overused carrier materials. In recent decades, small-molecule prodrug nanoassemblies (SMP-NAs), which are formed by the self-assembly of prodrugs themselves, have been widely investigated with distinct advantages of ultrahigh drug-loading and negligible excipients-trigged adverse reaction. Benefited from the simple preparation process, SMP-NAs are widely used for chemotherapy, phototherapy, immunotherapy, and tumor diagnosis. In addition, combination therapy based on the accurate co-delivery behavior of SMP-NAs can effectively address the challenges of tumor heterogeneity and multidrug resistance. Recent trends in SMP-NAs are outlined, and the corresponding self-assembly mechanisms are discussed in detail. Besides, the smart stimuli-responsive SMP-NAs and the combination therapy based on SMP-NAs are summarized, with special emphasis on the structure-function relationships. Finally, the outlooks and potential challenges of SMP-NAs in cancer therapy are highlighted.

摘要

传统纳米药物的抗肿瘤效率和临床转化主要受到载药量低、制备工艺复杂以及过度使用载体材料引起的潜在毒性等因素的限制。近几十年来,由前药自组装形成的小分子前药纳米组装体(SMP-NAs)受到了广泛的研究,具有超高载药量和可忽略不计的赋形剂触发不良反应的显著优势。得益于简单的制备工艺,SMP-NAs 被广泛应用于化疗、光疗、免疫治疗和肿瘤诊断。此外,基于 SMP-NAs 精确共递药行为的联合治疗可以有效解决肿瘤异质性和多药耐药性的挑战。本文概述了 SMP-NAs 的最新研究进展,并详细讨论了相应的自组装机制。此外,总结了智能刺激响应型 SMP-NAs 和基于 SMP-NAs 的联合治疗,并特别强调了结构-功能关系。最后,本文还强调了 SMP-NAs 在癌症治疗中的前景和潜在挑战。

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