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采用反相液相色谱法测定辛伐他汀和西替利嗪:应用于冻融(FT)稳定性研究。

Estimation of simvastatin and cetirizine by RP-LC method: Application to freeze and thaw (FT) stability studies.

作者信息

Naveed Safila, Usmanghani Khan, Sana Aisha, Ali Huma, Zafar Farya, Qamar Fatima, Sarwer Ghulam, Abbas Sarah, Alam M Tanweer, Shinwari Muhammad Ibrar

机构信息

Jinnah University for Women, Karachi, Pakistan.

Jinnah University for Women, Karachi, Pakistan / Herbion Pakistan (Pvt.) Ltd., Karachi, Pakistan.

出版信息

Pak J Pharm Sci. 2018 Jan;31(1):137-141.

Abstract

Sensitive, simple, reliable and rapid HPLC technique for the estimation of simvastatin (SMV) and cetirizine has been designed in this study. The chromatographic conditions were set using Shimadzu LC-10 AT VP pump, with UV detector (SPD-10 AV-VP). System integration was performed with CBM-102 (Bus Module). Partitioning of components was attained with pre-packed C-18 column of Purospher Star (5 μm, 250 x 4.6 mm) at ambient conditions. Injected volume of sample was 10 μl. Mobile phase was composed of 50:50 v/v ratio of Acetonitrile/water (pH 3.0 adjusted with ortho-phosphoric acid) having 2 ml/minutes rate of flow. Compounds were detected in UV region at 225 nm. Percent Recovery of simvastatin was observed in the range of 98-102%. All results were found in accept table range of specification. The projected method is consistent, specific, precise, and rapid, that can be employed to quantitate the SMV along with cetirizine HCl. It was estimated by 3 successive cycles of freeze and thaw stability. Results of FT samples were found within accept table limits the method was developed and validated in raw materials, bulk formulations and final drug products.

摘要

本研究设计了一种灵敏、简单、可靠且快速的高效液相色谱(HPLC)技术,用于测定辛伐他汀(SMV)和西替利嗪。使用岛津LC - 10 AT VP泵、紫外检测器(SPD - 10 AV - VP)设置色谱条件。通过CBM - 102(总线模块)进行系统整合。在环境条件下,使用Purospher Star预填充C - 18柱(5μm,250×4.6mm)实现组分的分离。样品进样体积为10μl。流动相由乙腈/水体积比为50:50(用正磷酸调节pH至3.0)组成,流速为2ml/分钟。在225nm的紫外区域检测化合物。辛伐他汀的回收率在98 - 102%范围内。所有结果均在可接受的规格范围内。所提出的方法具有一致性、特异性、精密度和快速性,可用于定量SMV以及盐酸西替利嗪。通过3个连续的冻融稳定性循环进行评估。冻融样品的结果在可接受的限度内,该方法已在原料、散装制剂和最终药品中开发并验证。

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