Preparation of rosiglitazone maleate sustained-release floating microspheres for improved bioavailability

Hu Lian-Dong; Xing Qian-Bin; Shang Chuang; Liu Wei; Liu Ci; Luo Zhao-Liang; Xu Hong-Xin

HERO ID

4936470

Reference Type

Journal Article

Year

2010

HERO ID 4936470
In Press No
Year 2010
Title Preparation of rosiglitazone maleate sustained-release floating microspheres for improved bioavailability
Authors Hu Lian-Dong; Xing Qian-Bin; Shang Chuang; Liu Wei; Liu Ci; Luo Zhao-Liang; Xu Hong-Xin
Journal Die Pharmazie
Volume 65
Issue 7
Page Numbers 477-480
Abstract The object of this study was to prepare rosiglitazone maleate (RM) sustained-release floating microspheres and investigate their pharmacokinetics. AM microspheres were prepared with ethyl cellulose (EC) and octadecyl alcohol as the carrier materials by an emulsion-solvent diffusion method, and the properties of morphology in vitro floating capability, drug loading (DL), entrapment efficiency (EE), in vitro release and in vivo pharmacokinetics were investigated. The prepared microspheres had a completely spherical shape. The percentage of microspheres floating after 12h was (91.45 +/- 1.62)%, and the DL and EE were (9.31 +/- 0.31)% and (89.55 +/- 1.65)% respectively. Pharmacokinetic studies demonstrated that the RM floating microspheres were superior to commercial tablets in terms of the decrease in peak plasma concentration and maintenance of AM concentration in plasma. The area under the curve of plasma concentration time (AUC) of the floating microspheres was equivalent to that of reference tablets. The results showed that floating microspheres are a feasible approach for the sustained-release preparation of drugs which have limited absorption sites in the upper small intestine.
Doi 10.1691/ph.2010.9828
Wosid WOS:000279891200006
Is Certified Translation No
Dupe Override No
Is Public Yes