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Development and validation of UV-spectrophotometric methods for quantitative estimation of Drotaverine HCl injection

机译:紫外分光光度法定量估计盐酸盐酸屈他维林的研制与验证

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Introduction: The objective of this study is to develop and validate spectrophotometric method for Drotaverine HCl injection analysis. A very simple, unique, novel, protective, secured, reliable and quick method of spectrophotometric estimation in UV-region has been developed for the assay of Drotaverine HCl injection formulation. Method: Methanol and water were used as diluents for the assay of Drotaverine HCl. Results: However no interference was observed in spectrophotometric determinations. ICH guidelines were followed during selection of parameters and these were then validated statistically using neat chromate grams by RSD and %RSD. The Beer’s law was followed when 8-40 mcg/ml concentration was used. Accuracy, linearity, precision and ruggedness were used for the validation of this method. Recovery studies were used to statistically validate the proposed method. Conclusion: UV spectrophotometer was used to scan the standard solution at wavelength between 200 nm to 400 nm on spectrum mode. Maximum absorbance was found at 242 nm.
机译:简介:这项研究的目的是开发和验证用于盐酸盐酸屈他维林注射液分析的分光光度法。已经开发了一种非常简单,独特,新颖,保护,安全,可靠和快速的紫外区域分光光度估计方法,用于测定盐酸盐酸屈他维林的制剂。方法:使用甲醇和水作为稀释剂,测定盐酸屈花碱。结果:但是在分光光度法测定中未观察到干扰。在选择参数的过程中遵循ICH指南,然后通过RSD和%RSD使用纯铬酸盐克对它们进行统计学验证。当使用8-40 mcg / ml的浓度时,遵循比尔定律。准确性,线性,精度和坚固性均用于验证该方法。回收率研究用于统计验证所提出的方法。结论:使用紫外分光光度计以光谱模式扫描标准溶液,波长在200 nm至400 nm之间。在242nm处发现最大吸光度。

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    《Pharmaceutical Methods》 |2017年第1期|共5页
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  • 中图分类 药学;
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