Research Article

Validated Reverse-Phase High-Performance Liquid Chromatography for Quantification of Furosemide in Tablets and Nanoparticles

Table 6

Determination of the molar absorptivity by UV spectrophotometry and HPLC.

MethodCalibration range (ng/mL)Equation Slope ( )MeanRelative standard deviation (%)

UV1,000–25,000Abs = 36,745 0.99636,745
Abs = 36,506 0.99236,506
Abs = 36,495 0.99836,49536,5820.386

HPLC1,000–25,000Area = 37,023 0.99837,023
Area = 37,819 0.99537,819
Area = 37,379 0.99337,37937,407 1.065