Research Article
Development and Validation of Spectrophotometric Methods for the Determination of Rasagiline in Pharmaceutical Preparations
Table 2
Results of recovery studies by standard addition method.
| Method | Amount taken μg mL−1a | Amount added μg mL−1 | Total amount foundb μg mL−1] Mean ± S.D.c | Recovery % | RSD % |
| Method A | | 25 | 125.247 ± 1.14 | 100.99 | 1.23 | 100 | 100 | 200.187 ± 1.58 | 100.19 | 0.93 | | 200 | 300.132 ± 2.58 | 100.07 | 0.96 |
| Method B | | 25 | 125.14 ± 1.34 | 100.56 | 1.49 | 100 | 100 | 200.36 ± 1.87 | 100.36 | 1.02 | | 250 | 351.49 ± 2.56 | 100.60 | 0.84 |
| Method C | | 50 | 150.24 ± 1.14 | 100.48 | 0.79 | 100 | 200 | 303.01 ± 1.58 | 101.51 | 0.76 | | 400 | 504.36 ± 3.87 | 101.09 | 0.81 |
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Rasalas tablet [1 mg].
bFive independent analyses.
cStandard deviation.
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