Preparation and biodistribution of paclitaxel-loaded nanoparticles after intravascular infusion
10.3760/cma.j.issn.1673-4181.2012.02.002
- VernacularTitle:紫杉醇纳米粒子制备及血管内局部灌注后的组织分布
- Author:
Jing YANG
;
Lifu MIAO
;
Wenling ZHU
;
Cunxian SONG
- Publication Type:Journal Article
- Keywords:
Paclitaxel;
Poly(lactic-co-glycolic acid);
Nanoparticles;
Intravascular local delivery
- From:
International Journal of Biomedical Engineering
2012;35(2):70-73,78
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo prepare paclitaxel-loaded nanoparticles (NPs),and to observe drug biodistribution after intravascular infusion of the NPs using a DispatchTM catheter into New Zealand rabbit abdominal aorta models.Methods Paclitaxel-loaded NPs were prepared by ultrasonication/emulsificcation/solvent evaporation technique using biodegradable poly (lactic-co-glycolic acid)(PLGA) as drug carrier.NP size and morphology was assessed by submicro-laser defractometer and scanning electron microscopy.In vitro release of paclitaxel from the NPs was performed by shaking in PBS at 37℃.The NPs was delivered into New Zealand rabbit abdominal aorta using a DispatchTM catheter.ResultsThe diameter of paclitaxel NPs was around 246 nm with very narrow size distribution.The NPs showed good spherical shape with smooth uniform surface.Paclitaxel loading in the NPs was about 19.06％ with encapsulation efficiency about 93.25％.The NPs maintained a sustained in vitro drug release for 30 days in PBS.After in vivo NP infusion,paclitaxel was detected in the vascular tissue around the infusion site and it retained in the site for 21 days.ConclusionPLGA nanoparticles as local drug delivery carrier showed great potential to maintain a high local drug concentration and prolonged drug resident time in animal model in vivo.
