Planta Med 2010; 76(8): 786-792
DOI: 10.1055/s-0029-1240705
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

The Mechanisms for Enhanced Oral Absorption of Hydroxysafflor Yellow A by Chuanxiong Volatile Oil

Jianping Qi1 , 2 [*] , Minjie Sun1 [*] , Qineng Ping1 , Jie Zhuang1 , Jiangran Li1 , Frank Peddie3 , Yunmei Song3
  • 1School of Pharmacy, China Pharmaceutical University, Nanjing, People's Republic of China
  • 2School of Pharmacy, Fudan University, Shanghai, People's Republic of China
  • 3School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia
Further Information

Publication History

received April 27, 2009 revised Nov. 15, 2009

accepted Nov. 23, 2009

Publication Date:
23 December 2009 (online)

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Abstract

The aims of this study were to investigate the effect of Ligusticum chuanxiong volatile oil (CVO) on the oral absorption of hydroxysafflor yellow A (HSYA). The effects were studied both in vitro and in vivo. The contents of CVO were measured by GC‐MS. The Caco-2 cell model was used to evaluate HSYA permeation with or without the presence of CVO. Transepithelial electrical resistance (TEER) of the Caco-2 cell monolayers was monitored and the alteration in the subcellular localization of claudin-1, the tight junction protein, was observed by immunofluorescence. The irritation of CVO on rat intestine was studied by paraffin slice technology. Our results demonstrated that CVO mainly contained ligustilide (47.82 %). The Papp of HSYA was improved by 5.34-fold and 4.62-fold in the presence of 0.02 mg/mL and 0.01 mg/mL of CVO, respectively. After opening of the tight junctions of the Caco-2 cell monolayer, TEER decreased, the position of claudin-1 changed, and its expression increased. CVO at different concentrations (10, 25, 100 and 200 mg/kg) caused no significant irritation on rat intestine. The bioavailability of HSYA in rats was increased by 6.48-fold and 4.91-fold when 100 and 25 mg/kg of CVO were co-administrated, respectively. CVO was an effective absorption enhancer for oral delivery of BCS III drugs. It can cause redistribution of claudin-1 proteins and open the tight junctions.

Abbreviations

References

1 Both authors contributed equally to this work

Prof. Qineng Ping

Department of Pharmaceutical Sciences
China Pharmaceutical University

No. 24 Tong jia xiang

210009 Nanjing

People's Republic of China

Phone: + 86 25 83 27 10 98

Fax: + 86 25 83 30 16 06

Email: pingqn2004@yahoo.com.cn