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分子印迹聚合物纳米粒子:癌症治疗的新兴多功能平台。

Molecularly Imprinted Polymer Nanoparticles: An Emerging Versatile Platform for Cancer Therapy.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, Nanjing, 210023, China.

Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, K1H 8M5, Canada.

出版信息

Angew Chem Int Ed Engl. 2021 Feb 19;60(8):3858-3869. doi: 10.1002/anie.202005309. Epub 2020 Nov 23.

Abstract

Molecularly imprinted polymers (MIPs) are chemically synthesized affinity materials with tailor-made binding cavities complementary to the template molecules in shape, size, and functionality. Recently, engineering MIP-based nanomedicines to improve cancer therapy has become a rapidly growing field and future research direction. Because of the unique properties and functions of MIPs, MIP-based nanoparticles (nanoMIPs) are not only alternatives to current nanomaterials for cancer therapy, but also hold the potential to fill gaps associated with biological ligand-based nanomedicines, such as immunogenicity, stability, applicability, and economic viability. Here, we survey recent advances in the design and fabrication of nanoMIPs for cancer therapy and highlight their distinct features. In addition, how to use these features to achieve desired performance, including extended circulation, active targeting, controlled drug release and anti-tumor efficacy, is discussed and summarized. We expect that this minireview will inspire more advanced studies in MIP-based nanomedicines for cancer therapy.

摘要

分子印迹聚合物(MIPs)是一种化学合成的亲和材料,具有与模板分子形状、大小和功能互补的定制结合腔。最近,工程化基于 MIP 的纳米药物以改善癌症治疗已成为一个快速发展的领域和未来的研究方向。由于 MIPs 的独特性质和功能,基于 MIP 的纳米颗粒(nanoMIPs)不仅是当前癌症治疗用纳米材料的替代品,而且还有可能填补基于生物配体的纳米药物相关的空白,例如免疫原性、稳定性、适用性和经济可行性。在这里,我们综述了用于癌症治疗的 nanoMIPs 的设计和制备方面的最新进展,并强调了它们的独特特征。此外,还讨论和总结了如何利用这些特征来实现预期的性能,包括延长循环时间、主动靶向、控制药物释放和抗肿瘤疗效。我们期望这篇简评将激发更多关于基于 MIP 的癌症治疗纳米药物的先进研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df71/7894159/72141a17185c/ANIE-60-3858-g004.jpg

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