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    Effect of various absorption enhancers based on tight junctions on the intestinal absorption of forsythoside A in Shuang-Huang-Lian, application to its antivirus activity

    Wei Zhou2,3,4, Xuan Xuan Zhu5, Ai Ling Yin2, Bao Chang Cai2, Hai Dan Wang5, Liuqing Di2,3,4★, Jin Jun Shan6★ Corresponding author

    1. 1College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, PR China.
    2. 2Jiangsu Engineering Research Center for Effi cient Delivery System of TCM, Nanjing, PR China.
    3. 3Nanjing Engineering Research Center for Industrialization of Chinese Medicine Pellets, Nanjing, PR China.
    4. 4Department of Pharmacology, Affi liated Hospital of Nanjing University of Chinese Medicine, Nanjing, PR China.
    5. 5First Medicine College, Nanjing University of Chinese Medicine, Nanjing, PR, China.

    CORRESPONDENCE

    Liuqing Di

    Jiangsu Engineering Research Center for Effi cient Delivery System of TCM, Nanjing, PR China.

    diliuqing@hotmail.com

    Received: 05-03-2013; Revised: 15-04-2013.

    Volume 10, Issue 37 · pp. 9–17 · PUBLISHED 7 February 2014 · DOI: 10.4103/0973-1296.126651

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: Forsythoside A (FTA), one of the main active ingredients in Shuang-Huang-Lian (SHL), possesses strong antibacterial, antioxidant and antiviral effects, and its pharmacological effects was higher than that of other ingredients, but the absolute bioavailability orally was approximately 0.72%, which was signifi cantly low, infl uencing clinical effi cacies of its oral preparations seriously. Materials and Methods: In vitro Caco-2 cell and in vivo pharmacokinetics study were simultaneously performed to investigate the effects of absorption enhancers based on tight junctions: sodium caprate and water-soluble chitosan on the intestinal absorption of FTA, and the eventual mucosal epithelial damage resulted from absorption enhancers was evaluated by MTT test and morphology observation, respectively. The pharmacological effects such as antivirus activity improvement by absorption enhancers were verifi ed by MDCK damage inhibition rate after infl uenza virus propagation. Results: The observations from in vitro Caco-2 cell showed that the absorption of FTA in SHL could be improved by absorption enhancers. Meanwhile, the absorption enhancing effect of water-soluble chitosan may be almost saturable up to 0.0032% (w/v), and sodium caprate at concentrations up to 0.64 mg/mL was safe, but water-soluble chitosan at different concentrations was all safe for these cells. In pharmacokinetics study, water-soluble chitosan at dosage of 50 mg/kg improved the bioavailability of FTA in SHL to the greatest extent, and was safe for gastrointestine from morphological observation. Besides, treatment with SHL with water-soluble chitosan at dosage of 50 mg/kg prevented MDCK damage after infl uenza virus propagation better signifi cantly than that of control. Conclusion: Water-soluble chitosan at dosage of 50 mg/kg might be safe and effective absorption enhancer for improving the bioavailability of FTA and the antivirus activity in vitro in SHL.

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      Zhou, W., Zhu, X. X., Yin, A. L., Cai, B. C., Wang, H. D., Di, L., & Shan, J. J. (2014). Effect of various absorption enhancers based on tight junctions on the intestinal absorption of forsythoside A in Shuang-Huang-Lian, application to its antivirus activity. Pharmacognosy Magazine, 10(37), 9–17. https://doi.org/10.4103/0973-1296.126651