聚乙二醇化
PEG比率
聚乙二醇
化学
部分
生物结合
组合化学
试剂
生物制药
高分子
小分子
纳米技术
有机化学
生物化学
材料科学
生物
生物技术
经济
财务
作者
Sachin Gundecha,Satish V. Shirolkar,Sanjivani Deshkar,Sohan S. Chitlange,Sunil Shewale,Rahul Arun Jagtap
出处
期刊:International Journal of Health Sciences (IJHS)
[Suryasa and Sons]
日期:2022-05-18
卷期号:: 6622-6634
被引量:2
标识
DOI:10.53730/ijhs.v6ns3.7477
摘要
Covalent conjugation of polyethylene glycol (PEG) molecules to biopharmaceutical molecules is known to increase the pharmacological and medicinal characteristics of proteins and other big molecules and has been utilized effectively in 12 authorized medications. PEG reagents with straight and branched chains up to 40 kDa were utilized with a variety of PEG derivatives with varied linker chemistries. This article discusses the characteristics of PEG, the history and evolution of PEGylation chemistry, and examples of PEGylated pharmaceuticals with a proven track record. They prefer to employ bigger PEG polymers and complicated PEG structures, although they use extremely pure and well-characterized PEG reagents. The preclinical toxicity data for PEG in PEGylated biologics that have been authorized are summarised. Microscopically detected cell vacuolization in phagocytes, which is connected to the biological function of absorption and elimination of particles and macromolecules from blood and tissues. It's possible. Side effects in toxicity tests typically relate to the active moiety of the medicine, not the PEG moiety, according to experience with commercially available PEGylated pharmaceuticals.
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