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紫外分光光度法测定尼美舒利栓的含量 被引量:2

Determination of Nimesulide in suppositories by UV Spectrophotometry
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摘要 目的 :建立用紫外分光光度法测定尼美舒利栓中尼美舒利的含量。方法 :用不同的有机溶剂萃取尼美舒利栓中的基质 ,用紫外分光光度法测定尼美舒利的含量。结果 :用正己烷作为萃取剂。用紫外分光光度法测定尼美舒利栓的含量 ,标准曲线线性好尼美舒利线性范围为 3~ 15 μg·ml-1(r =0 .9999)、回收率较好 (98.3% )。结论 :用紫外分光光度法测定尼美舒利栓剂的含量 ,方法简便、快速、结果准确 ,可作为尼美舒利含量测定的方法。 Objective: To establish a method for determination of nimesulide in suppositories. Methods: Screening different organic solution to extract the ground substrate in suppositories and determinating nimesulide by UV spectrophotometry. Results: N -Hexano was used as the solution of extraction. The method was very good for its good standard line( r = 0.9 999 ), high accuracy( RSD = 0.472% ) and high recovery( 98.3% ). Conclusion: This mehod is simple, rapid, and accurate.
出处 《中国药师》 CAS 2003年第5期277-278,285,共3页 China Pharmacist
基金 新疆特丰药业股份有限公司资助
关键词 尼美舒利栓 紫外分光光度法 含量测定 Nimesulide suppositories UV Spectrophotometry Content determination
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参考文献4

  • 1Famaey JP. In vitro and in vivo pharmacological evidence of selective cyclooxygermse-2 inhibition by Nimesulide: an overview [J ]. Inflamm-Res, 1997, 46(11) : 437-446.
  • 2Pochobradsky MG, Mele G, Beretta A, et al. Post-marketing survey of nimesulide in the short-term treatment of osteoarthrisis[J].Drugs-Exp-Clin-Res. 1991, 17(3) : 197-204.
  • 3Fusetti G, Magni E, Armandola, MC. Tolerability of Nimesulide.Epidemiological data[J]. Drugs. 1993, 46 Suppl 1277-1280.
  • 4Davis R, Brogden RN. Nimesulide. An update of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy [ J ].Drugs, 1994, 48(3) :431-454.

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