Method Development, Validation and Stress Degradation Study of Teneligliptin by RP-HPLCRP-HPLCValidationMethanolTeneligliptinForce degradationTo develop and validate simple, rapid, linear, accurate, precise and economical reverse phase-highperformance liquid chromatography (RP-HPLC) method for of stress ...
Rapid Analytical Method Development and Validation of RP-HPLC Method for the Simultaneous Estimation of Exemestane and Genistein with Specific Application in Lipid-Based Nanoformulations Exemestane (EXE), an irreversible aromatase inhibitor, is employed as a therapy for hormone-dependent breast cancer. Sev...
Analytical method development and validation of Capecitabine in bulk by RP-HPLC method. Int Res J Pharm 2012;3:177-80.Macula A, Anjum F, Tangadpally R, Kondepudi RK, analytical method development and validation of Capecitabine in bulk by RP-HPLC method, International Research Journal of ...
An accurate, precise, simple and stability-indicating RP-HPLC method was developed and validated for the simultaneous quantitation of perindopril arginine (PA), amlodipine (AML) and glimepiride (GLM) in solution in accordance with the International Conference on Harmonisation (...
(2006) Intact protein RP-HPLC method development using minimal sample. LC-GC North America 16 (... Cheng,Hung-Yuan,Ervin,... - LC-GC North America 被引量: 4发表: 2006年 Development and validation of RP-HPLC method for the quantitative estimation of αs1-genetic variants in goat milk A...
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A novel and effective reversed-phase high-performance liquid chromatographic (RP-HPLC) technique has been developed to determine the tepotinib, an anti-cancer drug, in a tablet formulation. Furthermore, this method has been validated in accordance with the guidelines of the Inter...
RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF LINAGLIPTIN AND EMPAGLIFLOZIN A simple, accurate and precise RP-HPLC method was developed for the simultaneous estimation of the linagliptin and empagliflozin in tablet dosage form. Chr... LR A.,T, Prasanthi,A E. L. - 《In...
2.5. Validation of the HPLC method 2.5.1. System suitability The system suitability was assured by determining peak retention time, peak area, theoretical plates and tailing or asymmetry factor for DTX, CCM and PTX. The ideal values for system suitability are CV < 1%, asymmetry factor ...
A stability indicating RP-HPLC method was developed and validated for the simultaneous determination of Formoterol Fumarate (FF) 6g and Budesonide (Bude) 400g in metered dose inhaler formulation. The chromatographic separations was carried out with Waters alliance 2695 separation module, 2996 PDA detec...