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XU Xue-jun, TAO Qing, XU De-qin. Determination of fluoxetine hydrochloride in plasma by HPLC[J]. Journal of Pharmaceutical Practice and Service, 2012, 30(3): 222-225. doi: 10.3969/j.issn.1006-0111.2012.03.019
Citation: XU Xue-jun, TAO Qing, XU De-qin. Determination of fluoxetine hydrochloride in plasma by HPLC[J]. Journal of Pharmaceutical Practice and Service, 2012, 30(3): 222-225. doi: 10.3969/j.issn.1006-0111.2012.03.019

Determination of fluoxetine hydrochloride in plasma by HPLC

doi: 10.3969/j.issn.1006-0111.2012.03.019
  • Received Date: 2012-02-10
  • Rev Recd Date: 2012-03-27
  • Objective To establish and optimize a simple, rapid, reliable, high sensitive and high selective method for the determination of fluoxetine hydrochloride in plasma by high-performance liquid chromatographic (HPLC) so as to monitor the clinical drug use. Methods The plasma samples were deproteined by acetonitrile. Separation was performed on a Hypersil ODS2 column(5 μm, 4.6 mm×200 mm). The mobile phase contained acetonitrile-25 mmol/ L phosphate buffer(pH6.5)(34:66). The flow rate and sample volume injected were 1.2 ml/min and 20 μl, respectively. Detection wavelength was 227 nm. Results The calibration curve of fluoxetine hydrochloride in plasma was linear in the concentration range of 0.5~50 ng/ml and coefficient was 0.996 9. The intra-assay precision did not exceed 8.06% and inter-assay precision did not exceed 10.46% for low, medium and high quality samples, respectively. The average recovery of the described method was 91.7%,97.06% and 100.75%, respectively. Conclusion In comparison with previous work, the improved chromatographic method was more economical, less polluted and better protected column, besides simple preparation of plasma samples, high reproducibility, and high selectivity.
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Determination of fluoxetine hydrochloride in plasma by HPLC

doi: 10.3969/j.issn.1006-0111.2012.03.019

Abstract: Objective To establish and optimize a simple, rapid, reliable, high sensitive and high selective method for the determination of fluoxetine hydrochloride in plasma by high-performance liquid chromatographic (HPLC) so as to monitor the clinical drug use. Methods The plasma samples were deproteined by acetonitrile. Separation was performed on a Hypersil ODS2 column(5 μm, 4.6 mm×200 mm). The mobile phase contained acetonitrile-25 mmol/ L phosphate buffer(pH6.5)(34:66). The flow rate and sample volume injected were 1.2 ml/min and 20 μl, respectively. Detection wavelength was 227 nm. Results The calibration curve of fluoxetine hydrochloride in plasma was linear in the concentration range of 0.5~50 ng/ml and coefficient was 0.996 9. The intra-assay precision did not exceed 8.06% and inter-assay precision did not exceed 10.46% for low, medium and high quality samples, respectively. The average recovery of the described method was 91.7%,97.06% and 100.75%, respectively. Conclusion In comparison with previous work, the improved chromatographic method was more economical, less polluted and better protected column, besides simple preparation of plasma samples, high reproducibility, and high selectivity.

XU Xue-jun, TAO Qing, XU De-qin. Determination of fluoxetine hydrochloride in plasma by HPLC[J]. Journal of Pharmaceutical Practice and Service, 2012, 30(3): 222-225. doi: 10.3969/j.issn.1006-0111.2012.03.019
Citation: XU Xue-jun, TAO Qing, XU De-qin. Determination of fluoxetine hydrochloride in plasma by HPLC[J]. Journal of Pharmaceutical Practice and Service, 2012, 30(3): 222-225. doi: 10.3969/j.issn.1006-0111.2012.03.019
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