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PLA/PLGA nanoparticles for delivery of drugs across the blood-brain barrier

机译:PLA / PLGA纳米颗粒,可跨血脑屏障输送药物

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摘要

The blood-brain barrier (BBB), which protects the central nervous system (CNS) from unnecessary sub-stances, is a challenging obstacle in the treatment of CNS disease. Many therapeutic agents such as hydrophilic and macromolecular drugs cannot overcome the BBB. One promising solution is the employment of polymeric nanoparticles (NPs) such as poly (lactic-co-glycolic acid) (PLGA) NPs as drug carrier. Over the past few years, sig- nificant breakthroughs have been made in developing suitable PLGA and poly (lactic acid) (PLA) NPs for drug delivery across the BBB. Recent advances on PLGA/PLA NPs enhanced neural delivery of drugs are reviewed in this paper. Both in vitro and in vivo studies are included. In these papers, enhanced cellular uptake and therapeutic efficacy of drugs delivered with modified PLGA/PLA NPs compared with free drugs or drugs delivered by unmodified PLGA/ PLA NPs were shown; no significant in vitro cytotoxicity was observed for PLGA/PLA NPs. Surface modification of PLGA/PLA NPs by coating with surfactants/polymers or covalently conjugating the NPs with targeting ligands has been confirmed to enhance drug delivery across the BBB. Most unmodified PLGA NPs showed low brain uptake (<1%), which indirectly confirms the safety of PLGA/PLA NPs used for other purposes than treating CNS diseases
机译:保护中枢神经系统(CNS)免受不必要物质侵害的血脑屏障(BBB)是治疗CNS疾病的具有挑战性的障碍。许多治疗剂,例如亲水性和大分子药物不能克服血脑屏障。一种有希望的解决方案是采用聚合物纳米颗粒(NP)作为药物载体,例如聚(乳酸-乙醇酸)(PLGA)NP。在过去的几年中,在开发合适的PLGA和聚乳酸(PLA)NPs以便通过BBB进行药物输送方面取得了重大突破。本文综述了PLGA / PLA NPs增强药物神经传递的最新进展。包括体外和体内研究。在这些论文中,与游离药物或未经修饰的PLGA / PLA NP传递的药物相比,修饰的PLGA / PLA NP传递的药物具有更高的细胞摄取和治疗功效。对于PLGA / PLA NP,未观察到明显的体外细胞毒性。已经证实,通过用表面活性剂/聚合物包被或与靶向配体共价缀合NP,PLGA / PLA NP可以进行表面修饰,从而增强了BBB的药物传递。大多数未修饰的PLGA NPs表现出低的大脑摄取(<1%),这间接证实了用于治疗CNS疾病以外的其他目的的PLGA / PLA NPs的安全性

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