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Stability indicating validated RP-HPLC technique for the analysis of multicomponent anti-diabetic drug combos in pharmaceutical dosage forms

机译：经稳定性验证的RP-HPLC技术可用于分析药物剂型中的多组分抗糖尿病药组合

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Konari Sarif Niroush; Jacob Jane T.;
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年度 2015
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1. Stability indicating validated RP-HPLC technique for the analysis of multicomponent anti-diabetic drug combos in pharmaceutical dosage forms [J] . Sarif Niroush Konari, Jane T. Jacob Karbala International Journal of Modern Science . 2015,第1期

机译：稳定性表明经验证的RP-HPLC技术可用于分析药物剂型中的多组分抗糖尿病药组合
2. Application of Analytical Validated High-Performance Thin-Layer Chromatographic Technique for the Multicomponent Analysis of Cardiovascular Drug Combos in Pharmaceutical Dosage Form [J] . Konari Sarif Niroush, Jacob Jane T. Journal of Planar Chromatography-Modern TLC: JPC . 2015,第5期

机译：经分析验证的高性能薄层色谱技术在药物剂型心血管药物组合多组分分析中的应用
3. 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
4. ADDITIVE MANUFACTURING IN PHARMACEUTICAL FORMULATION - DEVELOPMENT OF BIODEGRADABLE PRINTED DOSAGE FORMS FOR ORAL DRUG DELIVERY [C] . Matej Novak, Frantisek Stepanek, Pavel Kovacik Conference on Innovative Materials For Additive Manufacturing . 2020

机译：药物制剂中的添加剂制造 - 用于口服药物递送的可生物降解印刷剂型的发育
5. Part I. Rapid analysis of pharmaceutical compounds using high-speed HPLC columns. Part II. Simulataneous determination of drugs in tablet dosage forms using packed column supercritical fluid chromatography. Part III. Pharmaceutical analysis of selected drugs using capillary electrophoresis. [D] . Zhou, Meng. 2001

机译：第一部分：使用高速HPLC色谱柱对药物化合物进行快速分析。第二部分使用填充柱超临界流体色谱法同时测定片剂剂型中的药物。第三部分使用毛细管电泳对选定药物进行药物分析。
6. Validated Stability-Indicating RP-HPLC Method for the Estimation of Degradation Behaviour of Organic Peroxide and Third-Generation Synthetic Retinoids in Topical Pharmaceutical Dosage Formulation [O] . Chinmoy Roy, Lalatendu Panigrahi, Jitamanyu Chakrabarty 2015

机译：用于评估局部用药剂量配方中有机过氧化物和第三代合成类维生素A降解行为的经验证的稳定性指示RP-HPLC方法
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

Stability indicating validated RP-HPLC technique for the analysis of multicomponent anti-diabetic drug combos in pharmaceutical dosage forms

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