Development and validation of a UPLC method for screening potentially counterfeit anti-hypertensive drugs using design of experiment

2014 ◽  
Vol 6 (13) ◽  
pp. 4610-4616 ◽  
Author(s):  
Chiguru Vishnuvardhan ◽  
R. Srinivas ◽  
N. Satheeshkumar

An isocratic reversed phase ultra performance liquid chromatography (RP-UPLC) method was developed for screening counterfeit medicines with UV detection at 210 nm.

2021 ◽  
Vol 11 (6) ◽  
pp. 86-91
Author(s):  
Sachin N. Kapase

For qualitative and quantitative analysis, various analytical techniques are available such as Ultraviolet (UV) Spectrophotometry, High-performance liquid chromatography (HPLC), High-performance thin layer chromatography (HPTLC). As per literature survey, there are some UV, HPLC, Ultra-Performance Liquid Chromatography (UPLC) and HPTLC analytical methods are developed for Montelukast and Doxofylline individually and in a combination with other drugs too, since yet there are no significant stability studies indicating HPLC method reported for Montelukast and Doxofylline combinations. In the current study, the HPLC method is developed and validated for simultaneous quantitative estimations of Montelukast and Doxofylline. These present techniques are more efficient and sensitive as compared to other analytical techniques.


2010 ◽  
Vol 93 (2) ◽  
pp. 389-399 ◽  
Author(s):  
Alaa Kamel ◽  
Yaorong Qian ◽  
Elizabeth Kolbe ◽  
Charles Stafford

Abstract A multiresidue method was developed and validated for the determination of 13 neonicotinoid pesticides and metabolites, and nine macrocyclic lactone pesticides and veterinary drugs using SPE and ultra-performance liquid chromatography/MS/MS. The method was validated in milk, orange, spinach, apple, plum, watermelon, green bean, zucchini, broccoli, strawberry, grape, and tomato by analyzing replicates of residue-free control samples fortified with a mixture of 22 target analytes at three concentration levels. The recoveries of the analytes from the fortified matrixes were mostly within 70120, except for some of the neonicotinoid metabolites. The LOD values varied by analyte and matrix and ranged between 0.0012 ng/g. The developed method was successful in combining two widely different classes of compounds into a single analysis.


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