Preparation of donepezil sustained release microspheres and pharmacokinetic research in rabbits
- Author:
Jia-Xin PI
1
Author Information
- Publication Type:Journal Article
- Keywords: Donepezil; Poly(lactide-co-glycolide); Sustained-release microsphere; Ultrasound technique
- From: Chinese Pharmaceutical Journal 2013;48(15):1284-1288
- CountryChina
- Language:Chinese
- Abstract: OBJECTIVE: To prepare and evaluate donepezil sustained-release microspheres by ultrasound technique. METHODS: Preparation technology of donepezil biodegradable microspheres by ultrasound technique was established and optimized. In vitro evaluation of donepezil microspheres was carried out. The pharmacokinetics of donepezil microspheres was investigated by LC-MS/MS after subcutaneous injection in rabbits at a dose of 30.0 mg · kg. RESULTS: Donepezil microspheres with drug loading of 12.1% and mean particle size between 40 to 130 μm were successfully prepared by ultrasound technique. The donepezil microspheres displayed a one-month sustained-release character in vitro. The pharmacokinetic parameters were as follows: pmax 40.63 μg · L-1, tmax 2.47 d, MRT 14.81 d, and AUC0→∞ 646.96 μg · d · L-1. CONCLUSION: Ultrasound technique is successfully applied in the preparation of donepezil sustained-release microspheres.
