max was 0.43 h and Cmax was 0.93 mg/L in SMEDDS group, which were 1/7 and 2.16 times of those in MGF group. Conclusion The SMEDDS could increase the drug dissolution in vitro significantly and improve the pharmacokinetic properties."/>

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首頁 > 過刊瀏覽>2013年第36卷第3期 >2013,36(3):166-170. DOI:10.7501/j.issn.1674-6376.2013.03.002
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芒果苷自微乳給藥系統(tǒng)的制備及其大鼠體內藥動學研究

Preparation of self-micro emulsifying drug delivery systems of mangiferin and its pharmacokinetic study in rats

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