Block copolymer micelles as ocular drug delivery systems

被引:6
|
作者
Assiri, Ahmad A. [1 ,2 ]
Glover, Katie [1 ]
Mishra, Deepakkumar [1 ]
Waite, David [1 ]
Vora, Lalitkumar K. [1 ]
Thakur, Raghu Raj Singh [1 ]
机构
[1] Queens Univ Belfast, Med Biol Ctr, Sch Pharm, Belfast, North Ireland
[2] Najran Univ, Coll Pharm, Dept Pharmacognosy, Najran, Saudi Arabia
关键词
ocular drug delivery; block copolymer micelles; ocular barriers; characterization; anterior segment; posterior segment; POLYMERIC MICELLES; CYCLOSPORINE-A; PHASE-I; CELLULAR UPTAKE; CREMOPHOR-FREE; GENE DELIVERY; PEG; RELEASE; STABILITY; PLA;
D O I
10.1016/j.drudis.2024.104098
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Block copolymer micelles, formed by the self-assembly of amphiphilic polymers, address formulation challenges, such as poor drug solubility and permeability. These micelles offer advantages including a smaller size, easier preparation, sterilization, and superior solubilization, compared with other nanocarriers. Preclinical studies have shown promising results, advancing them toward clinical trials. Their mucoadhesive properties enhance and prolong contact with the ocular surface, and their small size allows deeper penetration through tissues, such as the cornea. Additionally, copolymeric micelles improve the solubility and stability of hydrophobic drugs, sustain drug release, and allow for surface modifications to enhance biocompatibility. Despite these benefits, long-term stability remains a challenge. In this review, we highlight the preclinical performance, structural frameworks, preparation techniques, physicochemical properties, current developments, and prospects of block copolymer micelles as ocular drug delivery systems.
引用
收藏
页数:21
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