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出 处:《中国药房》2007年第31期2477-2478,共2页China Pharmacy
摘 要:目的:了解我国药物配伍稳定性方面研究的总体情况。方法:通过中国医院知识仓库检索,将2005年52种期刊上发表的113篇药物配伍稳定性文章进行归纳分析。结果:涉及药物类别主要为抗生素(59%)、中药或中药成分(20%)及其它药物(21%) ;91篇文章进行了定量分析,主要方法为紫外分光光度法(79%)、高效液相色谱法(20%)。结论:紫外分析方法的大量采用及试验方案设计不够严谨,可能会严重影响结果的准确性,给临床安全配伍用药留下极大隐患。OBJECTIVE: To probe into the overall situation about the study on compatible stability of drugs. METHODS: The compatible stability of drugs reported in a total of 113 articles in 2005 in 52 kinds of periodicals were retrieved from CHKD and summarized analytically. RESULTS: The drug categories involved were chiefly antibiotics (59%), Chinese traditional medicines or Chinese drug components (20%) and other drugs (21%) . Quantitative analyses in 91 articles were chiefly conducted by ultraviolet spectrophotometry (79%) or HPLC (20%). CONCLUSION: Because the ultraviolet spectrophotometry was greatly used and some experimental designs were not well- knit enough, the reliability of experimental results of compatible stability of drugs might be seriously affected, which poses a great danger to the clinical compatible use of drugs.
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