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Development and validation of stability-indicating RP-HPLC method for determination of Olmesartan medoxomile in pharmaceutical dosage form and identification, characterization of alkaline degradation impurity of Olmesartan medoxomile drug substance as well as drug product

机译：用于测定药物剂型中奥美沙坦酯的稳定性指示Rp-HpLC方法的开发和验证，以及奥美沙坦酯药物的碱性降解杂质的鉴定，表征以及药物产品

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Jain P.S.; Chaudhari A.J.; Surana S.J.;
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年度 2012
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1. Development and validation of stability-indicating RP-HPLC method for determination of Olmesartan medoxomile in pharmaceutical dosage form and identification, characterization of alkaline degradation impurity of Olmesartan medoxomile drug substance as well as drug product [J] . Jain P.S., Chaudhari A.J., Surana S.J. Chemical Industry Chemical Engineering Quarterly . 2012,第4a1期

机译：稳定剂型RP-HPLC法测定奥美沙坦片中奥美沙坦的质量，鉴定和表征奥美沙坦片中的碱性降解杂质及药物的开发与验证
2. Development of a stability-indicating UPLC method for determination of olmesartan medoxomil and its degradation products in active pharmaceutical ingredient and dosage forms [J] . RajS., SivaKumariK., NarasimhaRaoA., Journal of liquid chromatography and related technologies . 2012,第5a8期

机译：建立用于指示奥美沙坦美多美及其活性成分和剂型中降解产物的指示稳定性的UPLC方法的开发
3. DEVELOPMENT OF A STABILITY-INDICATING UPLC METHOD FOR DETERMINATION OF OLMESARTAN MEDOXOMIL AND ITS DEGRADATION PRODUCTS IN ACTIVE PHARMACEUTICAL INGREDIENT AND DOSAGE FORMS [J] . Shiva Raja K. Siva Kumarib* A. Narasimha Raob I. Ugandhar Reddyb, M. Naga Rajub Journal of Liquid Chromatography & Related Technologies . 2012,第8期

机译：指示活性药物成分中奥美沙坦含量及其降解产物的稳定性指示UPLC方法的建立
4. Dissolution testing for prolonged-release solid dosage form containing drug substances degrading in test media.Application to polymeric delivery systems of paracetamol [C] . A A Rakina, T I Spriridonova, S I Tverdokhlebov International Scientific and Technical Youth Conference Perspective Materials of Constructional and Medical Purpose . 2019

机译：延长释放固体剂型的溶解试验含有药物物质的试验介质降解。扑热酰胺的聚合物输送系统中的应用
5. Development and Validation of Analytical Methods for the Estimation of Some CNS Acting Drugs in their Pharmaceutical Dosage Forms. [D] . Chhalotiya, Usmangani K. 2013

机译：估计某些中枢神经系统作用药物的药物剂量形式的分析方法的开发和验证。
6. Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation [O] . Navneet Kumar, Dhanaraj Sangeetha 2013

机译：测定药物中雷贝拉唑钠的工艺相关杂质和降解产物的稳定性指示RP-HPLC方法的开发和验证
7. Development and validation of stability-indicating RP-HPLC method for determination of Olmesartan medoxomile in pharmaceutical dosage form and identification, characterization of alkaline degradation impurity of Olmesartan medoxomile drug substance as well as drug product [O] . Jain P.S., Chaudhari A.J., Surana S.J. 2012

机译：用于测定药物剂型中奥美沙坦酯的稳定性指示Rp-HpLC方法的开发和验证，以及奥美沙坦酯药物的碱性降解杂质的鉴定，表征以及药物产品

Development and validation of stability-indicating RP-HPLC method for determination of Olmesartan medoxomile in pharmaceutical dosage form and identification, characterization of alkaline degradation impurity of Olmesartan medoxomile drug substance as well as drug product

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