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设计超分子自组装纳米材料作为用于癌症治疗的刺激响应性药物递送平台。

Designing supramolecular self-assembly nanomaterials as stimuli-responsive drug delivery platforms for cancer therapy.

作者信息

Liu Yingqi, Wu Yunyun, Luo Zhong, Li Menghuan

机构信息

School of Life Science, Chongqing University, Chongqing 400044, P. R. China.

Chongqing Municipal Center for Disease Control and Prevention, Chongqing 400042, China.

出版信息

iScience. 2023 Feb 27;26(3):106279. doi: 10.1016/j.isci.2023.106279. eCollection 2023 Mar 17.

Abstract

Stimuli-responsive nanomaterials have attracted substantial interest in cancer therapy, as they hold promise to deliver anticancer agents to tumor sites in a precise and on-demand manner. Interestingly, supramolecular chemistry is a burgeoning discipline that entails the reversible bonding between components at the molecular and nanoscale levels, and the recent advances in this area offer the possibility to design nanotherapeutics with improved controllability and functionality for cancer therapy. Herein, we provide a comprehensive summary of typical non-covalent interaction modes, which primarily include hydrophobic interaction, hydrogel bonding, host-guest interaction, π-π stacking, and electrostatic interaction. Special emphasis is placed on the implications of these interaction modes to design novel stimuli-responsive drug delivery principles and concepts, aiming to enhance the spatial, temporal, and dosage precision of drug delivery to cancer cells. Finally, future perspectives are discussed to highlight current challenges and future opportunities in self-assembly-based stimuli-responsive drug delivery nanotechnologies for cancer therapy.

摘要

刺激响应性纳米材料在癌症治疗中引起了广泛关注,因为它们有望以精确且按需的方式将抗癌药物递送至肿瘤部位。有趣的是,超分子化学是一门新兴学科,涉及分子和纳米尺度上组分之间的可逆键合,该领域的最新进展为设计具有更高可控性和功能性的纳米治疗剂用于癌症治疗提供了可能性。在此,我们全面总结了典型的非共价相互作用模式,主要包括疏水相互作用、水凝胶键合、主客体相互作用、π-π堆积和静电相互作用。特别强调了这些相互作用模式对设计新型刺激响应性药物递送原理和概念的意义,旨在提高药物递送至癌细胞的空间、时间和剂量精度。最后,讨论了未来展望,以突出基于自组装的刺激响应性药物递送纳米技术在癌症治疗中的当前挑战和未来机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62b0/10014307/00be70bd9613/fx1.jpg

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