PENENTUAN DISOLUSI PADA OBAT SENYAWA KETOPROFEN SECARA SPEKTROFOTOMETRI

Renny Futeri, Pevi Riani
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Abstract

Research on dissolution determination of Ketoprofen compounds by Spectrophotometry. Ketoprofen is a non-steroidal anti-inflammatory drug compound (NSAID) that works as an anti-inflammatory. Anti-inflammatory here is a group of drugs used to reduce inflammation and relieve pain. The dissolution test is a method used to determine the content of active compounds that dissolve in drugs, where the time, temperature and media are set according to the human stomach and intestines, and can find out how much the content of active compounds dissolves in the human intestines and stomach. This dissolution test, then the ketoprofen drug is read by spectrophotometry. Test the dissolution by spectrophotometer at a wavelength of 260 nm using HCl 0.1 N and buffer pH 7.4. The results of the determination of the dissolution test of the active substance on ketoprofen at the acid stage obtained an average of 0.009% and at the pH 7.4 buffer stage obtained an average content of 86.4155%. It can be concluded that the determination of the ketoprofen dissolution test in the sample meets the requirements (MS), in accordance with the specifications of the Internal Standard of PT Novell Pharmaceutical Laboratories, namely at the acid stage not more than 10% of ketoprofen dissolved in 2 hours, and at the pH 7.4 buffer stage it has a requirement of 75%. ketoprofen dissolved in 45 minutes. In the dissolution of acidic media, 0.1 N HCl is used because its condition resembles that of the stomach.
光谱测定化合物KETOPROFEN的解药
分光光度法测定酮洛芬类化合物溶出度的研究。酮洛芬是一种非甾体抗炎药化合物(NSAID),具有抗炎作用。消炎在这里是指一组用于减少炎症和缓解疼痛的药物。溶出度试验是测定药物中溶解的活性化合物含量的一种方法,根据人体的肠胃设定时间、温度和介质,可以得知活性化合物的含量在人体的肠胃中溶解了多少。溶出度试验,然后用分光光度法读出酮洛芬药物。用盐酸0.1 N,缓冲液pH 7.4,分光光度计在260 nm波长下测定溶出度。酮洛芬在酸性阶段的活性物质溶出度测定结果平均为0.009%,pH 7.4缓冲阶段的平均含量为86.4155%。可以得出,样品中酮洛芬溶出度试验的测定符合要求(MS),按照PT Novell制药实验室内部标准的规定,即在酸阶段,酮洛芬在2小时内溶出量不超过10%,在pH 7.4缓冲阶段,酮洛芬溶出量要求为75%。酮洛芬在45分钟内就溶解了。在酸性介质的溶解中,使用0.1盐酸,因为它的情况类似于胃的情况。
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