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用于眼部给药的新型纳米胶束姜黄素制剂:提高稳定性、溶解度及眼部抗炎治疗效果

New nanomicelle curcumin formulation for ocular delivery: improved stability, solubility, and ocular anti-inflammatory treatment.

作者信息

Li Mengshuang, Xin Meng, Guo Chuanlong, Lin Guiming, Wu Xianggen

机构信息

a Department of Pharmacy, College of Chemical Engineering , Qingdao University of Science and Technology , Qingdao , China.

b School of Medicine and Life Sciences , University of Jinan-Shandong Academy of Medical Sciences , Jinan , China.

出版信息

Drug Dev Ind Pharm. 2017 Nov;43(11):1846-1857. doi: 10.1080/03639045.2017.1349787. Epub 2017 Jul 11.

Abstract

CONTEXT

A stable topical ophthalmic curcumin formulation with high solubility, stability, and efficacy is needed for pharmaceutical use in clinics.

OBJECTIVES

The objective of this article was to describe a novel curcumin containing a nanomicelle formulation using a polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol (PVCL-PVA-PEG) graft copolymer.

METHODS

Nanomicelle curcumin was formulated and optimized and then further evaluated for in vitro cytotoxicity/in vivo ocular irritation, in vitro cellular uptake/in vivo corneal permeation, and in vitro antioxidant activity/in vivo anti-inflammatory efficacy.

RESULTS

The solubility, chemical stability, and antioxidant activity were greatly improved after the encapsulation of the PVCL-PVA-PEG nanomicelles. The nanomicelle curcumin ophthalmic solution was simple to prepare and the nanomicelles are stable to the storage conditions, and it had good cellular tolerance. Nanomicelle curcumin also had excellent ocular tolerance in rabbits. The use of nanomicelles significantly improved in vitro cellular uptake and in vivo corneal permeation as well as improved anti-inflammatory efficacy when compared with a free curcumin solution.

CONCLUSIONS

These findings indicate that nanomicelles could be promising topical delivery systems for the ocular administration of curcumin.

摘要

背景

临床上药物应用需要一种具有高溶解性、稳定性和疗效的稳定的局部用眼科姜黄素制剂。

目的

本文的目的是描述一种使用聚乙烯己内酰胺-聚醋酸乙烯酯-聚乙二醇(PVCL-PVA-PEG)接枝共聚物的新型含姜黄素纳米胶束制剂。

方法

制备并优化纳米胶束姜黄素,然后进一步评估其体外细胞毒性/体内眼刺激性、体外细胞摄取/体内角膜渗透性以及体外抗氧化活性/体内抗炎疗效。

结果

PVCL-PVA-PEG纳米胶束包封后,姜黄素的溶解度、化学稳定性和抗氧化活性大大提高。纳米胶束姜黄素眼用溶液制备简单,纳米胶束在储存条件下稳定,且具有良好的细胞耐受性。纳米胶束姜黄素在兔体内也具有优异的眼耐受性。与游离姜黄素溶液相比,纳米胶束的使用显著提高了体外细胞摄取和体内角膜渗透性,并提高了抗炎疗效。

结论

这些发现表明,纳米胶束可能是用于眼部给药姜黄素的有前景的局部递送系统。

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