Original ArticlePharmacognosy MagazineVol. 8 | Issue 32 | 2012 | pp. 256–262Open access
In vivo pharmacokinetic comparisons of ferulic acid and puerarin after oral administration of monomer, medicinal substance aqueous extract and Nao-De-Sheng to rats
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- 1 School of Pharmacy, Pharmacognosy Jiangsu University, Zhenjiang, 212013, PR, China.
Published in Pharmacognosy Magazine
Correspondence: Zhen Ouyang
School of Pharmacy, Pharmacognosy Jiangsu University, Zhenjiang, 212013, PR, China.
Email: zhenouyang@ujs.edu.cn
Copyright: © 2012 Manuscript Technomedia. This is an open access article.
- Published:
- Nov 22, 2012
- Received:
- Dec 17, 2011
How to cite
Ouyang, Z., Zhao, M., Tang, J., & Pan, L. (2012). In vivo pharmacokinetic comparisons of ferulic acid and puerarin after oral administration of monomer, medicinal substance aqueous extract and Nao-De-Sheng to rats. Pharmacognosy Magazine, 8(32), 256–262. https://doi.org/10.4103/0973-1296.103648
Abstract
Background: Nao-De-Sheng decoction (NDS), a traditional Chinese medicine (TCM) prescription containing Radix puerariae lobatae, Floscarthami, Radix et Rhizoma Notoginseng, Rhizoma chuanxiong and Fructus crataegi, is effective in the treatment of cerebral arteriosclerosis, ischemic cerebral stroke and apoplexy linger effect. Ferulic acid and puerarin are the main absorbed effective ingredients of NDS. Objective: To assess the affection of other components in medical material and compound recipe compatibility on the pharmacokinetics of ferulaic acid and puerarin, of ferulic acid from the monomer Rhizoma chuanxiong aqueous extract and NDS were studied. And pharmacokinetics comparisons of puerarin from the monomer Radix puerariae extract and NDS decoction were investigated simultaneously. Materials and Methods: At respective different time points after oral administration of the monomer, medicinal substance aqueous extract and NDS at the same dose in rats, plasma concentrations of ferulic acid and puerarin in rats were determined by RP-HPLC, and the main pharmacokinetic parameters were estimated with 3P97 software. Results: The plasma concentration-time curves of ferulaic acid and puerarin were both best fitted with a two-compartment model. AUC0−t, AUC0→∞, Tmax, and Cmax of ferulic acid in the monomer and NDS decoction were increased significantly (P < 0.05) compared with that in Rhizoma chuanxiong aqueous extract. And statistically significant increase (P < 0.05) in pharmacokinetic parameters of puerarin including AUC0−t, AUC0→∞, CL, Tmax and Cmax were obtained after oral administration of puerarin monomer compared with Radix puerariae extract. Although the changes of AUC0−t, AUC0→∞ and CL had no statistically significant, Cmax of puerarin in NDS was increased remarkably (P < 0.05) compared with that in single puerarin. Conclusions: Some ingredients of Rhizoma chuanxiong and Radix puerariae may be suggested to remarkably influence plasma concentrations of ferulaic acid and puerarin. Some ingredients in NDS may increase dissolution and absorption of ferulaic acid and puerarin, delay elimination, and subsequently enhance bioavailability of ferulaic acid and puerarin in rats after compatibility.
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Article metadata
| Title | In vivo pharmacokinetic comparisons of ferulic acid and puerarin after oral administration of monomer, medicinal substance aqueous extract and Nao-De-Sheng to rats |
|---|---|
| Authors | Zhen Ouyang; Ming Zhao; Jianming Tang; Lulin Pan |
| Affiliations | School of Pharmacy, Pharmacognosy Jiangsu University, Zhenjiang, 212013, PR, China. |
| Corresponding author | zhenouyang@ujs.edu.cn |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 8, Issue 32 (2012) |
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