| 吡噻旺钠的制备及处方设计 |
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| 引用本文： | 常志初, 蒋勤, 徐炳祥, 马振赢. 吡噻旺钠的制备及处方设计[J]. 中国现代应用药学, 1997, (2): 46-47. |
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| 作者姓名： | 常志初 蒋勤 徐炳祥 马振赢 |
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| 作者单位： | 解放军第一○二医院!常州，213003(常志初，蒋勤)，第二军医大学药学院!上海，213003(徐炳祥)，上海工业微生物研究所!上海，213003(马振赢) |
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| 摘 要： | 合成了吡噻旺钠,并将其配成1%的稀醇液,考察了其在该溶液中的稳定性,测得该处方中吡噻旺钠的t0.9为1.81a。
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| 关 键 词： | 吡噻旺钠 制备 稳定性 |
The Prescription Design and Clinical Trall of MPO-Na |
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| Chang zhi-chun et al. The Prescription Design and Clinical Trall of MPO-Na[J]. The Chinese Journal of Modern Applied Pharmacy, 1997, 0(2): 46-47 |
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| Authors: | Chang zhi-chun et al |
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| Abstract: | To cbtain more potent and wide-spectrum agent, 2-mercaptopyridinai 1-oxidesodium (MPO-Na,I) was, synthesized, the minimum inhibitory concentrations of this compoundagainst 12 mycotic stiams were 0.25-10 pprn. The t0.9 of MPO-Na (1%) in the solution ofalcohol (40%) was 1.81 year. 56 patients were involved in the trail of MPO-Na (1%) solution,the total effective rate was 94. 64%. |
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| Keywords: | MPO-Na stability MIC effective rate |
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