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首页> 外文期刊>Brazilian Journal of Pharmaceutical Sciences >Validation of a UV-spectrophotometric analytical method for determination of LPSF/AC04 from inclusion complex and liposomes
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Validation of a UV-spectrophotometric analytical method for determination of LPSF/AC04 from inclusion complex and liposomes

机译:紫外分光光度分析方法从包合物和脂质体中测定LPSF / AC04的验证

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The aim of this study was to develop and validate a UV spectrophotometric method for determination of LPSF/AC04 from inclusion complex and encapsulated into liposomes. The validation parameters were determined according to the International Conference on Harmonisation (ICH) and National Health Surveillance Agency (ANVISA) guidelines. LPSF/AC04 was determined at 250 nm in methanol by a UV spectrophotometric method, exhibiting linearity in the range from 0.3 to 2 µg.mL−1 (Absorbance=0.18068 x [LPSF/AC04 µg.mL-1] + 0.00348), (r2=0.9995). The limits of detection and quantification were 0.047µg.mL−1 and 0.143µg.mL−1, respectively. The method was accurate, precise, reproducible and robust since all the samples analyzed had coefficient of variation of less than 5% and no statistically significant difference between theoretical and practical concentrations was detected. Thus, a rapid, simple, low cost and sensitive spectrophotometric method was developed and validated for determining the content of inclusion complex and liposomes containing LPSF/AC04.
机译:这项研究的目的是开发和验证一种紫外分光光度法,该方法用于从包合物和包裹入脂质体中测定LPSF / AC04。验证参数是根据国际协调会议(ICH)和国家卫生监督局(ANVISA)指南确定的。 LPSF / AC04通过紫外分光光度法在甲醇中于250 nm处测定,线性范围为0.3至2μg.mL-1(吸光度= 0.18068 x [LPSF / AC04μg.mL-1] + 0.00348),( r2 = 0.9995)。检测限和定量限分别为0.047μg.mL-1和0.143μg.mL-1。该方法准确,精确,可重现且可靠,因为所有分析样品的变异系数均小于5%,并且理论浓度与实际浓度之间没有统计学上的显着差异。因此,开发了一种快速,简单,低成本且灵敏的分光光度法,并用于确定包含LPSF / AC04的包合物和脂质体的含量。

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