| Literature DB >> 26139127 |
Haiqing Dong1, Min Tang1, Yan Li1, Yongyong Li1, Dong Qian2, Donglu Shi1,3.
Abstract
PEGylation in polymeric nanomedicine has gained substantial predominance in biomedical applications due to its resistance to protein absorption, which is critically important for a therapeutic delivery system in blood circulation. The shielding layer of PEGylation, however, creates significant steric hindrance that negatively impacts cellular uptake and intracellular distribution at the target site. This unexpected effect compromises the biological efficacy of the encapsulated payload. To address this issue, one of the key strategies is to tether the disulfide bond to PEG for constructing a disulfide-bridged cleavable PEGylation. The reversible disulfide bond can be cleaved to enable selective PEG detachment. This article provides an overview on the strategy, method and progress of PEGylation nanosystem with the cleavable disulfide bond.Entities:
Keywords: cleavable PEGylation; disulfide bond; drug delivery; gene delivery; micelles; prodrug; vesicles
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Year: 2015 PMID: 26139127 DOI: 10.2217/nnm.15.38
Source DB: PubMed Journal: Nanomedicine (Lond) ISSN: 1743-5889 Impact factor: 5.307