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盐酸雷尼替丁口腔速溶片的制备及质量检查

Preparation and Quality Inspection of Ranitidine Hydrochloride Fast Dissolving Tablets
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摘要 采用紫外分光光度法在314nm处测定盐酸雷尼替丁的含量及溶出度。盐酸雷尼替丁检测浓度在4~16μg/mL范围内与吸收度呈线性关系(r=0.9994,n=5),日内、日间精密度分别为0.88%、1.16%,平均回收率为99.59%,RSD=0.22%。该制剂制备工艺简单易行,质量检查方法准确可靠。 The content of ranitidine hydrochloride was determined by UV-spectrophotometry at the wavelength of 314 nm. The detected concentration of ranitidine hydrochloride was in linear relation to absorptivity in the range of 4-16 μg/mL (r=0. 999 4,n=5). The intra-day and inter-day precision were 0.88% and 1.16% .The average recovery was 99. 59% (RSD=0.22%).The preparation of technique is simple and the method for quality inspection is accurate and reliable.
出处 《河北化工》 2008年第7期38-39,56,共3页 Hebei Chemical Industry
关键词 盐酸雷尼替丁 制备 质量检查 ranitidine hydrochloride preparation quality inspection
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