Study on preparation and in vitro release of poly (lactide-co-glycolide) nanoparticle loaded with ropivacaine
- VernacularTitle:罗哌卡因乳酸羟基乙酸共聚物纳米粒的制备及体外释药研究
- Author:
Jianteng YANG
;
Guozhong CHEN
;
Aiwen HUANG
;
Hongtao SONG
;
Liping WANG
- Publication Type:Journal Article
- Keywords:
Ropivacaine;
Nanoparticle;
PLGA;
CCD-RSM;
In vitro release
- From:
Journal of Medical Postgraduates
2015;(4):411-415
- CountryChina
- Language:Chinese
-
Abstract:
Objective The biological half-life in vivo of local anesthesia is short, high concentration in local tissue is in-clined to cause central nerve and cardiovascular toxicity due to the drug absorption into blood by blood vessels.The research was to pre-pare the poly ( lactide-co-glycolide) nanoparticle loaded with ropivacaine ( RVC-PLGA-NPS) , optimize its process, and determine its characteristics in vitro. Methods An oil-in-water emulsion solvent evaporation technique was adopted to prepare the RVC-PLGA-NPS.The formulation was optimized by central composite design/response surface method(CCD-RSM), with the encapsulation effi-ciency( EE) , drug loading( DL) and particle size as the indexes.Research was also made on itsin vitro release by fitting different model equations. Results The acquired nanoparticals were smooth, with the mean particle size (331.21±2.11) nm, DL (13.81±1.35)%and EE (74.82±2.53)%.The accumulative release rate of the nanoparticals was about 73%in 96 h, which showed that Higuchi func-tion fitted the release curve. Conclusion The RVC-PLGA-NPS made by emulsion solvent evaporation technique have obvious drug-release behaviour in vitro.
