Preparation and In Vitro Release of Curcumin Nanoparticles with A Novel Codendrimer as Stabilizer
10.3870/j.issn.1004-0781.2017.05.018
- VernacularTitle:基于新型树枝状大分子姜黄素纳米粒的制备及体外释放
- Author:
Ran LI
;
Yanna ZHAO
;
Ting WANG
;
Meihua HAN
;
Xiangtao WANG
;
Xueying YAN
;
Yifei GUO
- Keywords:
Curcumin;
nanoparticles;
Codendrimer;
Release,in vitro
- From:
Herald of Medicine
2017;36(5):538-543
- CountryChina
- Language:Chinese
-
Abstract:
Objective To enhance the solubility and bioavailability of curcumin (CUR).Methods A novel curcumin nanoparticles were prepared.The CUR-PGD nanoparticles were prepared by the method of ultrasound precipitation combined with high-pressure homogenization using codendrimer PAMAM-co-0.25OEG (PGD) as stabilizer.The stability of CUR-PGD nanoparticles was measured in 0.9% sodium chloride solution,5% glucose, PBS and plasma.Results The drug loading capacity (DL%) of CUR-PGD nanoparticles was 41.2%, the solubility of CUR was increased to 1.5 mg·mL-1 (50 times of CUR bulk powder).The mean diameter of the nanoparticles was 438.0 nm with spherical morphology and the zeta potential was 41.4 mV.The nanoparticles was stable in 0.9% sodium chloride solution,5% glucose, PBS and plasma and there was no hemolytic phenomenon, which meant they were suitable for intravenous administration.The DSC and XRD spectra of CUR-PGD nanoparticles showed that the CUR was presented as crystal morphology in the nanoparticles.The CUR released from nanoparticles was detected in different releasing medium and presented obvious controlled release behavior.Conclusion PGD may be an effective stabilizer for the preparation of CUR-PGD nanoparticles and CUR-PGD nanoparticles are a promising drug delivery system for CUR application in clinic.
