| Literature DB >> 29707870 |
Peng Zhang1, Priyesh Jain1, Caroline Tsao1, Zhefan Yuan1, Wenchen Li1, Bowen Li2, Kan Wu1, Hsiang-Chieh Hung1, Xiaojie Lin1, Shaoyi Jiang1,2.
Abstract
The commonly used "stealth material" poly(ethylene glycol) (PEG) effectively promotes the pharmacokinetics of therapeutic cargos while reducing their immune response. However, recent studies have suggested that PEG could induce adverse reactions, including the emergence of anti-PEG antibodies and tissue histologic changes. An alternative stealth material with no or less immunogenicity and organ toxicity is thus urgently needed. We designed a polypeptide with high zwitterion density (PepCB) as a stealth material for therapeutics. Neither tissue histological changes in liver, kidney, or spleen, nor abnormal behavior, sickness or death was induced by the synthesized polymer after high-dosage administration for three months in rats. When conjugated to a therapeutic protein uricase, the uricase-PepCB bioconjugate showed significantly improved pharmacokinetics and immunological properties compared with uricase-PEG conjugates.Entities:
Keywords: drug delivery; immune response; polypeptides; protein modification; zwitterions
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Year: 2018 PMID: 29707870 DOI: 10.1002/anie.201802452
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336