Study on pharmacokinetics of geniposide in mice administrated by xingnaojing microemulsion and mPEG2000-PLA modified xingnaojing microemulsion.
- Author:
Ran WEN
;
Xiao-Lan CHEN
;
Hui-Yun LI
;
Qing-Li GUO
;
Yang LU
;
Shou-Ying DU
- Publication Type:Journal Article
- MeSH:
Animals;
Drugs, Chinese Herbal;
administration & dosage;
chemistry;
Emulsions;
Iridoids;
blood;
pharmacokinetics;
Lactic Acid;
chemistry;
Male;
Mice;
Polyesters;
Polyethylene Glycols;
chemistry;
Polymers;
chemistry
- From:
China Journal of Chinese Materia Medica
2014;39(6):1111-1114
- CountryChina
- Language:Chinese
-
Abstract:
An HPLC method for the determination of geniposide concentration in mouse plasma was developed and the pharmacokinetics after intranasal administration of Xingnaojing microemulsion (XNJ-M) and mPEG2000-PLA modified Xingnaojing microemulsion (XNJ-MM) were investigated. Eighty mice were treated by XNJ-M and XNJ-MM nasally. The plasma samples were collected at different times and the drug in samples was detected by HPLC. The pharmacokinetic parameters were calculated by the software of Kinetica. The pharmacokinetic parameters of geniposide of XNJ-M were C(max) (4.36 +/- 2.69) mg x L(-1), t(max) 1 min, MRT (29.73 +/- 4.54) min, AUC (53.63 +/- 14.03) mg x L(-1) x min. The pharmacokinetic parameters of geniposide of XNJ-MM were C(max) (9.75 +/- 4.14) mg x L(-1), t(max) 1 min, MRT(22.34 +/- 2.90) min, AUC (131.87 +/- 40.13) mg x L(-1) x min. Geniposide can be absorbed into blood in a higher degree after intranasal administration with XNJ-MM compared to XNJ-M, which maybe caused by its less irritating and more absorption.
