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. 2012 Feb 16;4(1):51–59. doi: 10.1016/j.jare.2012.01.003

Table 2.

Determination of Ezetimibe and Atorvastatin calcium in laboratory prepared mixtures by the proposed spectrophotometric methods and the reported method.

Mixture no. Ezetimibe recovery %a
Atorvastatin calcium recovery %a
Claimed taken (μg mL−1)
IS
Atorvastatin Ezetimibe D1 224.6 nm 238.6 nm Reported methodb D1 D2 Reported methodb
1 10 10 98.88 99.67 100.86 100.85 100.33 98.77 100.4
2 10 15 100.43 101.82 99.86 99.91 98.67 100.77 100.07
3 10 20 98.27 101.7 101.61 101.68 98.67 101.06 98.6
4 15 10 100.65 100.7 100.45 100.1 99.11 100.23 99.4
5 20 10 100.06 100.58 99.59 100.57 100.17 101.53 98.18
Mean ± S.D. 99.66 ± 1.03 100.89 ± 0.89 100.47 ± 0.81 100.62 ± 0.70 99.39 ± 0.81 100.47 ± 1.06 99.33 ± 0.94
a

Average of three determinations.

b

Absorbance ratio method (Q-analysis) at 238.6 nm (iso-absorptive point) and 232.6 nm (λmax of Ezetimibe) [3].