分散性
药剂学
化学
多酚类酚
活性成分
色谱法
PEG比率
纳米技术
药理学
有机化学
材料科学
外科
医学
硬化疗法
财务
经济
作者
Zeqiong Yu,Shaowei Bo,Huiyuan Wang,Li Yu,Zhigang Yang,Yongzhuo Huang,Zhong‐Xing Jiang
标识
DOI:10.1021/acs.molpharmaceut.7b00496
摘要
Polydisperse PEGs are ubiquitously used in pharmaceutical industry and biomedical research. However, the monodispersity in PEGs may play a role in the development of safe and effective PEGylated small molecular drugs. Here, to avoid the polydispersity in polidocanol, the active ingredient in a clinically used drug, a macrocyclic sulfate-based strategy for the efficient and scalable synthesis of monodisperse polidocanols, their sulfates, and their methylated derivatives, was developed. TLC and HPLC analysis indicated a complex mixture in regular polidocanol and high purities in monodisperse polidocanols and their derivatives. Assay on HUVEC, L929, and HePG2 cells showed that monodisperse polidocanols have much higher cytotoxicity and safety than that of regular polidocanol. It was found that the monodispersity of PEGs in polidocanols is crucial for achieving the optimal therapeutic results. Therefore, based on this case study, it would be beneficial to optimize PEGylated small molecular drugs with monodisperse PEGs in pharmaceutical research and development.
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