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扑麻滴鼻液
相关语句
  puma nasal drops
     Chlorphenamine maleate and ephe drine hydrochloride in Puma nasal drops were determined simultaneous by CPA Matrix UV spectrophotometry.
     用CPA矩阵紫外分光光度法测定扑麻滴鼻液中扑尔敏和麻黄素的含量。
短句来源
  “扑麻滴鼻液”译为未确定词的双语例句
     DETERMINATION OF CHLORPHENAMINE MALEATE AND EPHEDRINE HYDROCHLORIDE IN PUMA NASAL DROPS BY CPA MATRIX UV SPECTROPHOTOMETRY
     CPA矩阵紫外分光光度法测定扑麻滴鼻液中扑尔敏和麻黄素的含量
短句来源
     Determination of Chlorophniramine in Chlorophniramine and Ephedrine Nasal Drops by Differential Spectrophotometry
     差示分光光度法测定扑麻滴鼻液中马来酸氯苯那敏的含量
短句来源
     Aim To determine chlorophniramine in chlorophniramine and ephedrine nasal drops and provide the method of quality control.
     目的 :测定扑麻滴鼻液中马来酸氯苯那敏的含量 ,为该药提供质量控制方法。
短句来源
     Methods Differential spectrophotometry was applied without prior separation.
     方法 :应用差示分光光度法测定扑麻滴鼻液中马来酸氯苯那敏的含量。
短句来源
  相似匹配句对
     Determination of Chlorophniramine in Chlorophniramine and Ephedrine Nasal Drops by Differential Spectrophotometry
     差示分光光度法测定滴鼻液中马来酸氯苯那敏的含量
短句来源
     Determination of ephedrine and dexamethasone nasal drops
     滴鼻液的含量测定研究
短句来源
     Simultaneously Determination of 3 Components in Pudima Nasal Drops by HPLC
     高效液相色谱法同时测定滴鼻液中3组分的含量
短句来源
     Methods Differential spectrophotometry was applied without prior separation.
     方法 :应用差示分光光度法测定滴鼻液中马来酸氯苯那敏的含量。
短句来源
     DETERMINATION OF CHLORPHENAMINE MALEATE AND EPHEDRINE HYDROCHLORIDE IN PUMA NASAL DROPS BY CPA MATRIX UV SPECTROPHOTOMETRY
     CPA矩阵紫外分光光度法测定滴鼻液尔敏和黄素的含量
短句来源
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Chlorphenamine maleate and ephe drine hydrochloride in Puma nasal drops were determined simultaneous by CPA Matrix UV spectrophotometry. The analytical wavelengths were 261.5nm, 257.5nm and 295nm. Average recoveries of chlorphenmine maleate and ephadrine hydrochloride are 100.7% and 100.3%; RSD were 2 05% and 0.82 respectively. This method was accurate, simple and rapid.

用CPA矩阵紫外分光光度法测定扑麻滴鼻液中扑尔敏和麻黄素的含量。测定波长分别为257.5、261.5、295nm;扑尔敏的平均回率为100.70%,RSD为2.05%;盐酸麻黄素的回收率为100.30%,RSD为0.82%。方法操作简便,快速、准确。

Aim To determine chlorophniramine in chlorophniramine and ephedrine nasal drops and provide the method of quality control.Methods Differential spectrophotometry was applied without prior separation.Results The corresponding average recovery and the relative standard deviation of chlorophniramine was 100.13%;0.76%.Conclusion This method is simple, quick and accurate.

目的 :测定扑麻滴鼻液中马来酸氯苯那敏的含量 ,为该药提供质量控制方法。方法 :应用差示分光光度法测定扑麻滴鼻液中马来酸氯苯那敏的含量。结果 :马来酸氯苯那敏的线性范围 15~ 75 μg·ml-1,回归方程Y =0 .0 10 18+ 0 .0 0 5 9(r =0 .9999) ,平均回收率和 RSD 分别为 10 0 .13% ;0 .76 %。结论 :方法简便、快速、准确 ,可作为该制剂的质量控制方法

OBJECTIVE:To establish a HPLC method for the determination of ephedrine hydrochloride,chlorphenamine maleate and dexamethasone sodium phosphate simultaneously in pudima nasal drops.METHODS:The determination was performed on Shimpack ODS column at room temperature,the mobile phase consisted of methanol-50mmol· L-1 KH2PO4 phosphate buffer solution(45∶ 55)with a flow rate at 1.0mL· min-1 and detective wavelength at 240nm.RESULTS:Linear ranges of ephedrine hydrochloride,chlorphenamine maleate and dexamethasone sodium...

OBJECTIVE:To establish a HPLC method for the determination of ephedrine hydrochloride,chlorphenamine maleate and dexamethasone sodium phosphate simultaneously in pudima nasal drops.METHODS:The determination was performed on Shimpack ODS column at room temperature,the mobile phase consisted of methanol-50mmol· L-1 KH2PO4 phosphate buffer solution(45∶ 55)with a flow rate at 1.0mL· min-1 and detective wavelength at 240nm.RESULTS:Linear ranges of ephedrine hydrochloride,chlorphenamine maleate and dexamethasone sodium phosphate were 100~ 400μ g· mL-1(r=0.999 3),50~ 200μ g· mL-1(r=0.999 7)and 10~ 40μ g· mL-1(r=0.999 8),respectively,the average recoveries were(99.59± 0.41)%,(100.25± 0.61)% and(100.70± 1.66)%,respectively.CONCLUSION:By this method,3 compositions and the supplemental agents are well separated,and the precision and recovery are high,therefore,the established method is suitable for the determination of 3 compositions in pudima nasal drops.

目的:建立以高效液相色谱法同时测定扑地麻滴鼻液中盐酸麻黄碱、马来酸氯苯那敏、地塞米松磷酸钠含量的方法。方法:色谱柱为ShimpackODS,流动相为甲醇-50mmol.L-1磷酸二氢钾缓冲液(45∶55),检测波长为240nm,流速为1.0mL.min-1,柱温为室温。结果:盐酸麻黄碱、马来酸氯苯那敏、地塞米松磷酸钠检测浓度分别在100~400(r=0.9993)、50~200(r=0.9997)、10~40(r=0.9998)μg.mL-1范围内与峰面积积分值线性关系良好,平均回收率分别为(99.59±0.41)%、(100.25±0.61)%、(100.70±1.66)%。结论:本方法对3组分和附加剂分离效果好,精密度和回收率高,可用于该药的含量测定。

 
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