Research Article
Development and Validation of a High-Performance Liquid Chromatographic Method for the Determination of Cinitapride in Human Plasma
| Stability | Spiked final concentration (g/mL) | Mean ± SD | %CV | %nominal | %RE |
| BT | 3 | 2.79 ± 0.10 | 3.47 | 93.05 | −6.95 | 15 | 14.52 ± 0.22 | 1.51 | 96.79 | −3.20 | 35 | 33.83 ± 0.49 | 1.45 | 96.65 | −3.35 | ST | 35 | 32.82 ± 0.68 | 3.61 | 93.78 | −6.22 | LT | 35 | 33.22 | 2.52 | 94.90 | −5.10 | FT | 3 | 2.78 ± 0.08 | 3.09 | 2.78 | −7.22 | 10 | 9.59 ± 0.25 | 2.63 | 95.90 | −4.10 | 25 | 24.46 ± 0.18 | 0.73 | 97.84 | −2.16 | DI | 14 | 13.55 ± 0.28 | 2.04 | 96.80 | −3.20 | 7 | 6.82 ± 0.11 | 1.65 | 97.38 | −2.62 |
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BT: bench-top stability, 6 hrs; ST: short-term stability, 6 hrs; LT: long-term stability, 35 days; FT: freeze-thaw stability, 3 cycles; DI: dilution integrity.
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