Validated ultra HPLC method for the simultaneous determination of atorvastatin, aspirin, and their degradation products in capsules

Journal of Liquid Chromatography and Related Technologies

Volumn 31, Issue 18, 2008, Pages 2821-2837

  Vora, D N ^a,b   Kadav, A A ^a  

^a Mithibai College Of Arts Chauhan Institute Of Science & Amrutben Jivanlal College of Commerce and Economics   (India)

^b INSTITUTE OF SCIENCE   (India)

Author keywords

Aspirin; Atorvastatin; Capsules; Degradation products; Stability indicating method; UHPLC

Indexed keywords

ACETONITRILE; BIODEGRADATION; HIGH PRESSURE LIQUID CHROMATOGRAPHY; ISOMERS; LIQUID CHROMATOGRAPHY; SEPARATION; SULFATE MINERALS;

ASPIRIN; ATORVASTATIN; C18 COLUMN; CAPSULES; CHROMATOGRAPHIC SEPARATIONS; DEGRADATION PRODUCTS; FLOW-RATE; FORCED DEGRADATION; GRADIENT ELUTION; HPLC METHODS; PHOSPHATE BUFFER; REPRODUCIBILITY; SALICYLIC ACID; SIMULTANEOUS DETERMINATIONS; STABILITY INDICATING METHOD; UHPLC; UV DETECTION;

DEGRADATION;

ACETONITRILE; ACETYLSALICYLIC ACID; ACETYLSALICYLSALICYLIC ACID; ATORVASTATIN; CARBON; LACTONE; SALICYLIC ACID; SALICYLIC ACID DERIVATIVE; SALSALATE; UNCLASSIFIED DRUG;

ARTICLE; CHROMATOGRAPHY; DRUG CAPSULE; DRUG DEGRADATION; DRUG DETERMINATION; DRUG FORMULATION; DRUG STABILITY; ELUTION; FLOW RATE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; REPRODUCIBILITY; SEPARATION TECHNIQUE; VALIDATION PROCESS;

EID: 52449131097     PISSN: 10826076     EISSN: 1520572X     Source Type: Journal    
DOI: 10.1080/10826070802388482     Document Type: Article

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