Choi Hoo-Kyun, Chun Myung-Kwan, Lee Se Hee, Jang Mee Hee, Kim Hee Doo, Jung Chun Sik, Oh Seaung Youl
BK21 Project Team, School of Pharmacy, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759, Republic of Korea.
Int J Pharm. 2007 Aug 16;341(1-2):50-7. doi: 10.1016/j.ijpharm.2007.03.045. Epub 2007 Apr 5.
Ketoprofen-polyethylene glycol (PEG) conjugates (KPEG) were prepared and their potential as a prolonged release system was investigated. Three KPEG conjugates were synthesized from ketoprofen and methoxy PEG with three different molecular weights by esterification in the presence of DCC. The KPEG conjugates were characterized by FT-IR and (1)H NMR spectroscopy. The rate of hydrolysis profile showed a specific acid-base catalysis pattern with a minimum at pH 4-5. The pharmacokinetic study after the intravenous and intramuscular administration of KPEG750 showed that the plasma levels of KP increased slowly and reached a maximum concentration at later time. The AUC of KPEG750 was higher than that after administering an equivalent dose of ketoprofen except 40mg/kg dose of intramuscular administration. The tail-flick experiment and paw edema test after intramuscular administration showed that KPEG750 had extended analgesic and anti-inflammatory effects compared with ketoprofen. These results suggest that KPEG could be a promising NSAID prodrug with an extended pharmacological effect owing to delayed-release of parent drug.
制备了酮洛芬-聚乙二醇(PEG)缀合物(KPEG),并研究了其作为缓释系统的潜力。通过在二环己基碳二亚胺(DCC)存在下的酯化反应,由酮洛芬和三种不同分子量的甲氧基PEG合成了三种KPEG缀合物。通过傅里叶变换红外光谱(FT-IR)和氢核磁共振光谱(¹H NMR)对KPEG缀合物进行了表征。水解速率曲线显示出特定的酸碱催化模式,在pH 4-5时达到最小值。静脉注射和肌肉注射KPEG750后的药代动力学研究表明,酮洛芬(KP)的血浆水平缓慢上升,并在较晚时间达到最大浓度。除了40mg/kg剂量的肌肉注射外,KPEG750的曲线下面积(AUC)高于给予等效剂量酮洛芬后的AUC。肌肉注射后的甩尾实验和足爪水肿试验表明,与酮洛芬相比,KPEG750具有延长的镇痛和抗炎作用。这些结果表明,由于母体药物的延迟释放,KPEG可能是一种具有延长药理作用的有前景的非甾体抗炎药前体药物。