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脂解模型在脂质给药系统体外评价中的应用研究进展

曾棋平 张晶 刘志宏 宋洪涛

曾棋平, 张晶, 刘志宏, 宋洪涛. 脂解模型在脂质给药系统体外评价中的应用研究进展[J]. 药学实践与服务, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
引用本文: 曾棋平, 张晶, 刘志宏, 宋洪涛. 脂解模型在脂质给药系统体外评价中的应用研究进展[J]. 药学实践与服务, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
ZENG Qiping, ZHANG Jing, LIU Zhihong, SONG Hongtao. In vitro evaluation of lipid drug delivery system by lipolysis model[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
Citation: ZENG Qiping, ZHANG Jing, LIU Zhihong, SONG Hongtao. In vitro evaluation of lipid drug delivery system by lipolysis model[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002

脂解模型在脂质给药系统体外评价中的应用研究进展

doi: 10.3969/j.issn.1006-0111.2014.02.002
基金项目: 福建省自然科学基金(2010J01218).

In vitro evaluation of lipid drug delivery system by lipolysis model

  • 摘要: 目的 综述脂解模型的组成及其在脂质制剂体外评价的应用,为推动脂质制剂的发展提供参考。 方法 通过查阅近年来国内外相关文献,归纳、分析和总结。 结果 体外脂解模型能准确反映脂质制剂在人体内的性质,建立良好的体内外相关性。 结论 脂解模型用于筛选和评价脂质制剂具有良好的应用前景。
  • [1] Stella VJ,Nti-Addae KW.Prodrug strategies to overcome poor water solubility[J]. Adv Drug Deliv Rev, 2007, 59(7):677-694.
    [2] Yu LX, Amidon GL, Polli JE, et al. Biopharmaceutics classification system:the scientific basis for biowaiver extensions[J]. Pharm Res, 2002,19(7):921-925.
    [3] Giliyar C, Fikstad DT, Tyavanagimatt S. Challenges and opportunities in oral delivery of poorly water-soluble drugs[J]. Drug Deliv Technol,2006,6(1):57-63.
    [4] Hauss DJ. Oral lipid-based formulations[J]. Adv Drug Deliv Rev, 2007,59(7):667-676.
    [5] Colin WP. Formulation of poorly water-soluble drugs for oral administration:physicochemical and physiological issues and the lipid formulation classification system[J]. Eur J Pharm,2006, 29(3-4):278-287.
    [6] Pouton CW. Formulation of poorly water soluble drugs for oral administration:physicochemical issues and the lipid formulation classification system[J]. Eur J Pharm, 2006(29):278-287.
    [7] Hamberstone AJ, Charman WN. Lipid-based vehicles for the oral delivery of poorly water soluble drugs[J]. Adv Drug Deliv Rev, 1997, 25:103-108.
    [8] Pouton CW, Porter CJH. Formulation of lipid-based delivery systems for oral administration:materials, methods and strategies[J]. Adv Drug Deliv Rev, 2008, 60:625-637.
    [9] Setbia S, Squillante E. Solid dispersion:revival with greater possibilities and application in oral drug delivery[J]. Crit Rev Ther Drug Carrier Syst, 2003,20(2-3):215-247.
    [10] 安富荣, 苏德森. 生物技术药物的脂质体给药系统研究进展[J]. 中国生化药物杂志, 2003, 24(4):207-209.
    [11] 张 宁, 王海学, 钱思源. 浅谈细胞毒类抗肿瘤药物脂质体制剂的研究思路[J]. 中国新药杂志, 2006,15(21):1805-1807.
    [12] Porter CJH, Pouton CW, Cuine JF, et al. Enhancing intestinal drug solubilisation using lipid based delivery systems[J]. Adv Drug Deliv Rev, 2008, 60:673-691.
    [13] Zangenberg NH, Mullertz A, Kristensen HG, et al. A dynamic in virto lipolysis model.Ⅰ:controlling the rate of lipolysis by continuous addition of calcium[J]. Eur J Pharm, 2001, 14:115-122.
    [14] Kaukonen AM, Boyd BJ, Porter CJH, et al. Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulation[J]. Pharm Res, 2004,21:245-253.
    [15] Zangenberg NH, Mullertz A, Kristensen HG, et al. A dynamic in virto lipolysis model. Ⅱ:evaluation of the model[J].Eur J Pharm, 2001, 14:237-244.
    [16] Larsen A, Sassene P, Mullertz A. In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems[J]. Int J Pharm, 2011, 417:245-255.
    [17] Dahan A, Hoffman A. Use of a dynamic in vitro lipolysis model to rationalize of poorly water soluble drugs:correlation with in vivo data and the relationship to intra enterocyte processes in rats[J]. Pharm Res, 2006, 23(9):2165-2174.
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    [19] Fatouros DG, Nielsen FS, Douroumis D, et al. In vitro-in vivo correlations of self emulsifying drug delivery systems combining the dynamic lipolysis model and neuro fuzzy networks[J]. Eur J Pharm, 2008, 69:887-898.
    [20] 宦 娣, 易 涛, 刘 颖, 等. 微粉硅胶对固体自微乳化给药系统小肠吸收的影响[J]. 药学学报, 2011, 46 (4):466-471.
    [21] 刘 颖, 肖 璐, 何吉奎, 等. 脂质制剂体外动态肠吸收模型的建立及评价[J]. 药学学报, 2011, 46(8):983-989.
    [22] 刘 颖, 易 涛, 宦 娣, 等. 利用体外脂解模型评价Ⅰ型脂质制剂[J]. 药学学报, 2010, 45 (10):1307-1311.
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出版历程
  • 收稿日期:  2013-04-25
  • 修回日期:  2013-11-04

脂解模型在脂质给药系统体外评价中的应用研究进展

doi: 10.3969/j.issn.1006-0111.2014.02.002
    基金项目:  福建省自然科学基金(2010J01218).

摘要: 目的 综述脂解模型的组成及其在脂质制剂体外评价的应用,为推动脂质制剂的发展提供参考。 方法 通过查阅近年来国内外相关文献,归纳、分析和总结。 结果 体外脂解模型能准确反映脂质制剂在人体内的性质,建立良好的体内外相关性。 结论 脂解模型用于筛选和评价脂质制剂具有良好的应用前景。

English Abstract

曾棋平, 张晶, 刘志宏, 宋洪涛. 脂解模型在脂质给药系统体外评价中的应用研究进展[J]. 药学实践与服务, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
引用本文: 曾棋平, 张晶, 刘志宏, 宋洪涛. 脂解模型在脂质给药系统体外评价中的应用研究进展[J]. 药学实践与服务, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
ZENG Qiping, ZHANG Jing, LIU Zhihong, SONG Hongtao. In vitro evaluation of lipid drug delivery system by lipolysis model[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
Citation: ZENG Qiping, ZHANG Jing, LIU Zhihong, SONG Hongtao. In vitro evaluation of lipid drug delivery system by lipolysis model[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(2): 85-87. doi: 10.3969/j.issn.1006-0111.2014.02.002
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