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同步激活治疗性纳米制剂:增强和追踪低氧诱导化疗。

Synchronized activating therapeutic nano-agent: Enhancement and tracing for hypoxia-induced chemotherapy.

机构信息

State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials, Dalian University of Technology, 2 Linggong Road, Dalian, 116024, China.

College of Chemistry and Chemical Engineering, Yantai University, Yantai, 264005, China.

出版信息

Biomaterials. 2023 Nov;302:122365. doi: 10.1016/j.biomaterials.2023.122365. Epub 2023 Oct 22.

DOI:10.1016/j.biomaterials.2023.122365
PMID:37890436
Abstract

Prodrug is a potential regime to overcome serious adverse events and off-target effects of chemotherapy agents. Among various prodrug activators, hypoxia stands out owing to the generalizability and prominence in tumor micro-environment. However, existing hypoxia activating prodrugs generally face the limitations of stringent structural requirements, the lack of feedback and the singularity of therapeutic modality, which is imputed to the traditional paradigm that recognition groups must be located at the terminus of prodrugs. Herein, a multifunctional nano-prodrug Mal@Cy-NTR-CB has been designed. In this nano-prodrug, a self-destructive tether is introduced to break the mindset, and achieves the activation by hypoxia of chemotherapy based on Chlorambucil (CB), whose efficacy can be augmented and traced by photodynamic therapy (PDT) and fluorescence from Cyanine dyes (Cy). In addition, Maleimide (Mal) carried by the nano-shells can regulate glutathione (GSH) content, preventing O scavenging, so as to realize PDT sensitization. Experiments demonstrate that Mal@Cy-NTR-CB specifically responds to hypoxic tumors, and achieve synchronous activation, enhancement and feedback of chemotherapy and PDT, inhibiting the tumor growth effectively. This study broadens the design ideas of activatable prodrugs and provides the possibility of multifunctional nano-prodrugs to improve the generalization and prognosis in precision oncology.

摘要

前药是克服化疗药物严重不良反应和脱靶效应的一种潜在策略。在各种前药激活剂中,缺氧因其在肿瘤微环境中的普遍性和突出性而脱颖而出。然而,现有的缺氧激活前药通常面临着严格的结构要求、缺乏反馈和治疗方式单一的限制,这归因于传统的观念,即识别基团必须位于前药的末端。在此,设计了一种多功能纳米前药 Mal@Cy-NTR-CB。在该纳米前药中,引入了自毁连接子来打破思维定式,并通过基于苯丁酸氮芥 (CB) 的缺氧实现化疗的激活,其疗效可以通过光动力疗法 (PDT) 和来自菁染料 (Cy) 的荧光来增强和跟踪。此外,纳米壳携带的马来酰亚胺 (Mal) 可以调节谷胱甘肽 (GSH) 含量,防止 O 清除,从而实现 PDT 敏化。实验表明,Mal@Cy-NTR-CB 特异性地响应缺氧肿瘤,并实现化疗和 PDT 的同步激活、增强和反馈,有效地抑制肿瘤生长。这项研究拓宽了可激活前药的设计思路,并为多功能纳米前药提供了可能性,以提高精准肿瘤学中的通用性和预后。

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