分析分光光度法测定咪达唑仑的含量

Saad انطكلي, Raghad قباني, Haya بابنسي
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引用次数: 0

摘要

建立了咪达唑仑原料药和片剂制剂中咪达唑仑(MDZ)快速、简便的定量分析方法。该方法是基于咪达唑仑和溴甲酚紫在乙腈介质中形成黄色(离子对络合物)。对溶剂、试剂浓度、相关比、时间等因素对反应的影响进行了优化。所形成的配合物在402 nm处以分光光度法定量。线性范围为3.26 ~ 26.06µg/mL,回归分析相关系数R2 = 0.9998。检测限(LOD)和定量限(LOQ)分别为0.89µg/mL和2.71µg/mL。咪达唑仑的平均回收率为99.46 ~ 100.92 %。本研究应用于叙利亚医药产品(DOMID-Oubari 7.5 mg)。该方法可用于片剂中咪达唑仑的含量测定。该方法具有直接、灵敏、简便、不需要任何提取过程等特点。因此,该方法可用于常规分析和质量控制。
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Determination of Midazolam by analytical spectrophotometry
Rapid useful and easy spectrophotometric method for the quantitative analysis of (Midazolam) (MDZ) in raw material and tablet pharmaceutical formulation has described. This method is based on the formation of yellow (ion-pair complex) between (Midazolam) and Bromocresol purple in Acetonitrile medium. Different parameters affecting the reaction such as: effect of solvents, the concentration of reagent, correlation ratio, time etc. were optimized. The formed complex was quantified spectrophotometrically at absorption maximum at 402 nm. The range of linearity was 3.26 – 26.06 µg/mL, regression analysis had a good correlation coefficient R2 = 0.9998. The limit of detection (LOD) also limit of quantification (LOQ) were 0.89 µg/mL and 2.71 µg/mL respectively. The average percent recovery was (99.46 - 100.92)% for Midazolam. This study was applied on Syrian pharmaceutical products: (DOMID-Oubari 7.5 mg). This method was successfully applied for (Midazolam) determination in tablets pharmaceutical formulation. The proposed method is direct, sensitive, simple, and doesn’t require any (extraction) process. Thus, the method could be ready to apply in routine analysis and quality control.
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