雷公藤醇
炎症
急性胰腺炎
胰腺
髓过氧化物酶
胰腺炎
PEG比率
化学
医学
药理学
内科学
生物化学
细胞凋亡
财务
经济
作者
Zhou Xu,Xi Cao,He Tu,Zhirong Zhang,Li Deng
标识
DOI:10.1021/acs.molpharmaceut.8b01342
摘要
Celastrol (CLT)-loaded PEG–PLGA nanoparticles (NPs/CLT) coated with neutrophil membranes (NNPs/CLT) were explored for the management of acute pancreatitis (AP). PEG–PLGA nanoparticles sized around 150 nm were proven to selectively accumulate in the pancreas in rats with AP. NNPs were found to overcome the blood–pancreas barrier and specifically distributed to the pancreatic tissues. Moreover, NNPs showed more selective accumulation in the pancreas than nanoparticles without any membrane coating in AP rats. Compared to CLT solution and the NPs/CLT group, NNPs/CLT significantly downregulated the levels of serum amylase and pancreatic myeloperoxidase in AP rats. Also, using NNPs as the delivery vehicle significantly reduced the systemic toxicity of CLT in AP rats. Together, these results suggest that NNPs/CLT represent a highly promising delivery vehicle for the targeted therapy of AP.
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