Therapeutic drug monitoring of vancomycin and voriconazole by liquid chromatography-tandem mass spectrometric method

Yanyan Li , Lei Yin , Yanhua Li , Zhihui Sun , Xiaojun Zhao , Mingyue Gao , Hongliang Wang

Chemical Research in Chinese Universities ›› 2017, Vol. 33 ›› Issue (3) : 339 -342.

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Chemical Research in Chinese Universities ›› 2017, Vol. 33 ›› Issue (3) : 339 -342. DOI: 10.1007/s40242-017-7051-8
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Therapeutic drug monitoring of vancomycin and voriconazole by liquid chromatography-tandem mass spectrometric method

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Abstract

A reliable liquid chromatography-tandem mass spectrometric(LC-MS/MS) method was developed and validated for the simultaneous determination of vancomycin and voriconazole in human plasma. The analytes and internal standard 10-hydroxycarbazepine were separated at a flow rate of 0.9 mL/min using a Zorbax SB-C18 column (50 mm×4.6 mm, 2.7 μm). Positive ion electrospray ionization was used to detect vancomycin, voriconazole and intrenal standard(IS) 10-hydroxycarbazepine followed by multiple reaction monitoring(MRM) of the transition at m/z 725.5→144.2, 350.3→281.0 and 253.1→208.0, respectively. The total run time for both vancomycin and voriconazole samples was 5 min; 0.30 μg/mL was the lower limit of quantification. The precision of intraday and interday was no more than 12.4%. The method was successfully and resoundingly applied in therapeutic drug monitoring of 156 patients treated with vancomycin and voriconazole.

Keywords

Liquid chromatography-tandem mass spectrometry(LC-MS/MS) / Vancomycin / Voriconazole / Therapeutic drug monitoring

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Yanyan Li, Lei Yin, Yanhua Li, Zhihui Sun, Xiaojun Zhao, Mingyue Gao, Hongliang Wang. Therapeutic drug monitoring of vancomycin and voriconazole by liquid chromatography-tandem mass spectrometric method. Chemical Research in Chinese Universities, 2017, 33(3): 339-342 DOI:10.1007/s40242-017-7051-8

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References

[1]

Ye Z. K., Chen Y. L., Chen K., Zhang X. L., Du G. H., He B., Li D. K., Liu Y. N., Yang K. H., Zhang Y. Y., Zhai S. D. J. Antimicrob. Chemother., 2016, 71(11): 3020.

[2]

Lestner J. M., Hill L. F., Heath P. T., Sharland M. Curr. Opin. Infect. Dis., 2016, 29: 237.

[3]

Elyasi S., Khalili H. Eur.^J. Clin. Pharmacol., 2016, 72: 777.

[4]

van Wanrooy M. J., Rodgers M. G., Span L. F., Zijlstra J. G., Uges D. R., Kosterink J. G., van der Werf T. S., Alffenaar J. W. Ther. Drug Monit., 2016, 38: 313.

[5]

Sebaaly J. C., MacVane S. H., Hassig T. B. Am.^J. Health Syst. Pharm., 2016, 73: S14.

[6]

Chawla P. K., Nanday S. R., Dherai A. J., Soman R., Lokhande R. V., Naik P. R., Ashavaid T. F. Int.^J. Clin. Pharm., 2015, 37: 925.

[7]

Usman M., Hempel G. Springerplus, 2016, 5: 124.

[8]

Chawla P. K., Dherai A. J., Ashavaid T. F. Indian^J. Clin. Biochem., 2016, 31: 209.

[9]

Hagihara M., Sutherland C., Nicolau D. P. J. Chromatogr. Sci., 2013, 51: 201.

[10]

Jesus Valle M. J., Lopez F. G., Navarro A. S. J. Pharm. Biomed. Anal., 2008, 48: 835.

[11]

Burkin M. A., Burkin A. A. Prikl. Biokhim. Mikrobiol., 2009, 45: 232.

[12]

Smith A., Leung-Pineda V. J. Clin. Lab. Anal., 2016, 30: 411.

[13]

Prommas S., Puangpetch A., Jenjirattithigarn N., Chuwongwattana S., Jantararoungtong T., Koomdee N., Santon S., Chamnanphon M., Su-kasem C. J. Clin. Lab. Anal., 2016.

[14]

Oyaert M., Peersman N., Kieffer D., Deiteren K., Smits A., Allegaert K., Spriet I., van Eldere J., Verhaegen J., Vermeersch P., Pauwels S. Clin. Chim. Acta, 2015, 441: 63.

[15]

Lin D., Li G., Chen L. J. Chromatogr. Sci., 2013, 51: 485.

[16]

Konig K., Kobold U., Fink G., Leinenbach A., Dulffer T., Thiele R., Zander J., Vogeser M. Clin. Chem. Lab. Med., 2013, 51: 1761.

[17]

Pauwels S., Vermeersch P., van Eldere J., Desmet K. Clin. Chim. Acta, 2012, 413: 740.

[18]

Wang H., Wang J. Y., Wu X. P., Shen H. Y., Luo Y., Dai H. F., Mei W. L. Chem. Res. Chinese Universities, 2015, 31(1): 38.

[19]

Fda U. Guidance for Industry: Bioanalytical Method Validation, 2001.

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