IN VITRO EVALUATION OF SOME BRANDS OF DICLOFENAC SODIUM INJECTION MARKETED IN GREATER NOIDA, UTTAR PRADESH, INDIA USING UV-VIS SPECTROPHOTOMETRIC METHOD

Pradyumna Ghosal, S. S
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Abstract

Quality is of principal subject to human beings in all perspective of life. When it comes to the quality of the pharmaceuticals which are consumed by humans, it is of most extreme significant as they are utilized for the prosperity of the humanity. In this study our objective was to evaluate the experimental in vitro study of the commercially obtainable Diclofenac Sodium injection brands which are available in Greater Noida. Ten different ampoules of 75mg/3ml diclofenac sodium injection products randomly collected from retail pharmacies and Govt. Hospital of targeted area in Greater Noida, Uttar Pradesh, India, twenty ampoules 75 mg/3ml have the same batch number of each brand were collected for the analysis. All the analytical methods were done in the quality control laboratories of JBJM Parenteral Pvt Ltd, Greater Noida, Uttar Pradesh, India. The study was carried out by performing various tests which is affiliated with the quality such asgeneral appearance of Diclofenac Sodium injection ampoule, Particulate matter, Average fill volume, pH and content assay through pH Meter (Spectra lab), UV-Vis Spectrophotometer (UV-1900i SHIMADZU). The assay was evaluated by UV-Vis Spectrophotometer at the wavelength of 276nm. The results show that diclofenac sodium injection following IP specification, it can be concluded that all of the 10 brands of the drug passed through UV-Vis spectroscopy method also in pH meter. The Spectroscopy method was successfully applied to evaluate of Diclofenac Sodium injection. KEYWORDS: In vitro evaluation, Diclofenac sodium injection, UV-Vis Spectroscopy, pH, Analytical method, Pharmaceutical analysis, SHIMADZU, Greater Noida, Spectroscopy, Quality evaluation
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紫外-可见分光光度法对在印度北方邦大诺伊达市销售的一些品牌双氯芬酸钠注射液进行体外评价
从生活的各个角度看,质量是人类的首要任务。当谈到人类所消费的药品的质量时,它是最重要的,因为它们被用于人类的繁荣。在这项研究中,我们的目的是评估大诺伊达市售双氯芬酸钠注射液品牌的体外实验研究。从印度北方邦大诺伊达地区的零售药店和政府医院随机抽取10瓶75mg/3ml双氯芬酸钠注射液,各品牌各有相同批号的20瓶75mg/3ml进行分析。所有分析方法均在印度北方邦大诺伊达JBJM静脉注射私人有限公司的质量控制实验室完成。本研究通过对双氯芬酸钠注射液安瓿的总体外观、颗粒物、平均填充体积、pH值和含量测定(光谱实验室)、紫外可见分光光度计(UV-1900i SHIMADZU)进行了各项质量检测。采用紫外可见分光光度计在276nm波长处对该方法进行评价。结果表明,双氯芬酸钠注射液符合IP规格,可以得出结论,所有10个品牌的药物都通过了紫外可见光谱法也在pH计中。应用光谱学方法对双氯芬酸钠注射液进行了评价。关键词:体外评价,双氯芬酸钠注射液,紫外可见光谱法,pH值,分析方法,药物分析,SHIMADZU, Greater Noida,光谱学,质量评价
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