吡噻旺钠的制备及处方设计

常志初;蒋勤;徐炳祥;马振赢

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.
	Chang zhi-chun et al.The Prescription Design and Clinical Trall of MPO-Na[J].Chin J Mod Appl Pharm(中国现代应用药学),1997,(2):46-47.

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吡噻旺钠的制备及处方设计
常志初;蒋勤;徐炳祥;马振赢

作者	单位
常志初;蒋勤;徐炳祥;马振赢

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。

关键词: 吡噻旺钠制备稳定性

DOI：

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The Prescription Design and Clinical Trall of MPO-Na

Chang zhi-chun et al

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 ofalco

Key words: MPO-Na stability MIC effective rate