体内
稳定器(航空)
塞来昔布
化学
控制释放
纳米晶
纳米技术
材料科学
生物化学
机械工程
生物
工程类
生物技术
作者
Mengdi Qin,Jinghan Xin,Han Wen,Mo Li,Xiaofan Sui,Haitao Dong,Qiang Fu,Zhonggui He
标识
DOI:10.1016/j.ijpharm.2022.122298
摘要
Nanocrystals (NCs) have been widely recognized as an available policy for the formulation of long-acting injections for insoluble drugs. Stabilizers are extremely important for the physical stability of NCs because they can reduce the surface free energy of the system. However, whether stabilizers can affect the in vivo performances of long-acting injectable NCs is unclear. In this study, three celecoxib (CXB) NCs formulated with different stabilizers (PVP K17, TPGS, and F68) were successfully developed by the wet milling method. Among the formulations, CXB-NCs/PVP K17 had a lower dissolution rate. More importantly, CXB-NCs/PVP K17 did not show burst release after intramuscular (i.m.) injection to rats, and it had a strong analgesic effect. These results showed that the stabilizers played a key role in the in vivo behaviors of long-acting injectable NCs. This strongly suggested that the burst release could be avoided by alteration of stabilizers of NCs by i.m. injection.
科研通智能强力驱动
Strongly Powered by AbleSci AI