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PLGA 微/纳米颗粒在生物大分子治疗药物传递中的最新进展。

Recent advances of PLGA micro/nanoparticles for the delivery of biomacromolecular therapeutics.

机构信息

BioSystems and Micromechanics (BioSyM) IRG, Singapore-MIT Alliance for Research and Technology (SMART) Centre, 1 CREATE Way, Enterprise Wing, Singapore 138602, Singapore.

BioSystems and Micromechanics (BioSyM) IRG, Singapore-MIT Alliance for Research and Technology (SMART) Centre, 1 CREATE Way, Enterprise Wing, Singapore 138602, Singapore.

出版信息

Mater Sci Eng C Mater Biol Appl. 2018 Nov 1;92:1041-1060. doi: 10.1016/j.msec.2017.12.036. Epub 2018 Jan 5.

Abstract

Recent advancements in biopharmaceutical industry have facilitated the development of novel bioactive macromolecular therapeutics. One of the challenges towards the clinical use of these biomacromolecules lies in the selection of appropriate carriers to protect, deliver and release them in vivo to maximize their pharmacological effects. Micro/nanoparticles made from biodegradable poly (d,l-lactic-co-glycolic acid) (PLGA) have been explored as delivery vehicles for therapeutics. Due to their excellent biocompatibility and controllable biodegradability, PLGA micro/nanoparticles could protect macromolecules from instant degradation in vivo while allowing tunable release rate and profile. In this review, recent progress in the design, fabrication/formulation and application of PLGA based micro/nanoparticles for the controlled delivery of biomacromolecules are discussed. Special focuses will be on the novel loading methods and releasing mechanisms of macromolecules as well as the in vivo applications of therapeutic macromolecule-loaded PLGA micro/nanoparticles.

摘要

近年来,生物制药行业的发展促进了新型生物活性大分子治疗药物的研发。这些生物大分子在临床应用中面临的挑战之一在于选择合适的载体,以保护它们、将它们递送到体内并释放,从而最大限度地发挥它们的药效。由可生物降解的聚(D,L-丙交酯-共-乙交酯)(PLGA)制成的微/纳米颗粒已被探索作为治疗药物的递送载体。由于其出色的生物相容性和可控制的生物降解性,PLGA 微/纳米颗粒可以保护大分子在体内免受即时降解,同时允许可调的释放速率和模式。本文综述了基于 PLGA 的微/纳米颗粒在控制生物大分子递送上的设计、制备/配方和应用的最新进展。特别关注大分子的新型负载方法和释放机制以及治疗性大分子负载的 PLGA 微/纳米颗粒的体内应用。

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