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用于治疗耐药性软骨肉瘤的比率型药物递释的可注射温敏纳米复合水凝胶的研制。

Development of Injectable Thermosensitive Nanocomposite Hydrogel for Ratiometric Drug Delivery to Treat Drug Resistant Chondrosarcoma In Vivo.

机构信息

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, 100190, China.

School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China.

出版信息

Small. 2024 Aug;20(31):e2310340. doi: 10.1002/smll.202310340. Epub 2024 Mar 8.

Abstract

Chondrosarcoma(CS), a prevalent primary malignant bone tumor, frequently exhibits chemotherapy resistance attributed to upregulated anti-apoptosis pathways such as the Bcl-2 family. In this manuscript, a new strategy is presented to augment chemosensitivity and mitigate systemic toxicity by harnessing a nano-enabled drug delivery hydrogel platform. The platform utilizes "PLGA-PEG-PLGA", an amphiphilic triblock copolymer combining hydrophilic polyethylene glycol (PEG) and hydrophobic polylactide glycolide (PLGA) blocks, renowned for its properties conducive to crafting a biodegradable, temperature-sensitive hydrogel. This platform is tailored to encapsulate a ratiometrically designed dual-loaded liposomes containing a first-line chemo option for CS, Doxorubicin (Dox), plus a calculated amount of small molecule inhibitor for anti-apoptotic Bcl-2 pathway, ABT-737. In vitro and in vivo evaluations demonstrate successful Bcl-2 suppression, resulting in the restoration of Dox sensitivity, evident through impeded tumor growth and amplified necrosis rates at the tumor site. This delivery system showcases remarkable thermal responsiveness, injectability, and biodegradability, all finely aligned with the clinical demands of CS treatment. Collectively, this study introduces a transformative avenue for tackling drug resistance in CS chemotherapy, offering significant clinical potential.

摘要

软骨肉瘤(CS)是一种常见的原发性恶性骨肿瘤,由于抗凋亡途径如 Bcl-2 家族的上调,常表现出化疗耐药性。在本手稿中,提出了一种新策略,通过利用纳米使能的药物输送水凝胶平台来增强化疗敏感性和减轻全身毒性。该平台利用“PLGA-PEG-PLGA”,一种两亲性三嵌段共聚物,结合亲水性聚乙二醇(PEG)和疏水性聚乳酸-羟基乙酸(PLGA)链段,以其有利于制备可生物降解、温度敏感水凝胶的特性而闻名。该平台被定制用于封装一种比例设计的双重负载脂质体,其中包含 CS 的一线化疗药物多柔比星(Dox),以及计算量的抗凋亡 Bcl-2 途径小分子抑制剂 ABT-737。体内外评估表明成功抑制了 Bcl-2,从而恢复了 Dox 的敏感性,在肿瘤部位观察到肿瘤生长受阻和坏死率增加。该输送系统表现出显著的温度响应性、可注射性和生物降解性,完全符合 CS 治疗的临床需求。总的来说,这项研究为解决 CS 化疗中的耐药性提供了一种变革性的方法,具有重要的临床潜力。

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