PEGylation for enhancing nanoparticle diffusion in mucus

被引:306
作者
Huckaby, Justin T. [2 ]
Lai, Samuel K. [1 ,2 ,3 ]
机构
[1] Univ North Carolina Chapel Hill, Eshelman Sch Pharm, Div Pharmacoengn & Mol Pharmaceut, 125 Mason Farm Rd, Chapel Hill, NC 27599 USA
[2] Univ North Carolina Chapel Hill, UNC NCSU Joint Dept Biomed Engn, 125 Mason Farm Rd, Chapel Hill, NC 27599 USA
[3] Univ North Carolina Chapel Hill, Dept Microbiol & Immunol, 125 Mason Farm Rd, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
Mucus; Mucus barrier; PEG; Nanoparticle; Mucus-penetrating; Muco-inert; Diffusivity; POLYETHYLENE-GLYCOL PEG; ORAL-DRUG DELIVERY; HUMAN CERVICOVAGINAL MUCUS; CYSTIC-FIBROSIS PATIENTS; IN-VITRO; GENE DELIVERY; EX-VIVO; POLYMERIC NANOPARTICLES; GASTROINTESTINAL MUCUS; POLY(ETHYLENE GLYCOL);
D O I
10.1016/j.addr.2017.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The viscoelastic mucus secretions coating exposed organs such as the lung airways and the female reproductive tract can trap and quickly eliminate not only foreign pathogens and ultrafine particles but also particle-based drug delivery systems, thus limiting sustained and targeted drug delivery at mucosal surfaces. To improve particle distribution across the mucosa and enhance delivery to the underlying epithelium, many investigators have sought to develop nanoparticles capable of readily traversing mucus. The first synthetic nanoparticles shown capable of rapidly penetrating physiological mucus secretions utilized a dense coating of polyethylene glycol (PEG) covalently grafted onto the surface of preformed polymeric nanoparticles. In the decade since, PEG has become the gold standard in engineering mucus-penetrating drug carriers for sustained and targeted drug delivery to the lungs, gastrointestinal tract, eyes, and female reproductive tract. This review summarizes the history of the development of various PEG-based mucus-penetrating particles, and highlights the key physicochemical properties of PEG coatings and PEGylation strategies to achieve muco-inert PEG coatings on nanoparticle drug carriers for improved drug and gene delivery at mucosal surfaces. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 139
页数:15
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