2008
DOI: 10.1016/j.jchromb.2007.11.015
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Corrigendum to “HPLC–MS method for the simultaneous quantification of the new HIV protease inhibitor darunavir, and 11 other antiretroviral agents in plasma of HIV-infected patients” [J. Chromatogr. B 859 (2007) 234–240]

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Cited by 12 publications
(28 citation statements)
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“…Previous publications show DRV, ETV, MVC and RAL to be stable at room temperature, 4 • C and when frozen [36,40,45]. Furthermore, the stability of NNRTI and PI under different conditions has been assessed and reported by other articles [30,32,33,35]. The assay described combines a very short run time of 5 min per sample with a quick and simple sample pre-treatment procedure and is therefore, suitable for high-throughput TDM purposes whereby large numbers of samples are processed quickly and efficiently.…”
Section: Discussionmentioning
confidence: 93%
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“…Previous publications show DRV, ETV, MVC and RAL to be stable at room temperature, 4 • C and when frozen [36,40,45]. Furthermore, the stability of NNRTI and PI under different conditions has been assessed and reported by other articles [30,32,33,35]. The assay described combines a very short run time of 5 min per sample with a quick and simple sample pre-treatment procedure and is therefore, suitable for high-throughput TDM purposes whereby large numbers of samples are processed quickly and efficiently.…”
Section: Discussionmentioning
confidence: 93%
“…A number of previously published HPLC-UV and LC-MS/MS assays have quantified darunavir from human plasma either alone [34] or with other antiretroviral drugs [30,[35][36][37]. Raltegravir has been quantified separately using HPLC with fluorescent detection [38] and LC-MS/MS methods [39,40].…”
Section: Introductionmentioning
confidence: 99%
“…Chromatographic separation of several antiviral drugs using traditional LC columns requires a total analysis time of about 20 minutes as reported by D'Avoloi et al [5] for the analysis of eleven analytes with co-elution of several compounds. Compared to columns packed with 3.5 or 5.0 µm particles, sub 2.0 µm particles allow to greatly improve the column efficiency and peak capacity as well as to shorten the analysis time.…”
Section: Assay Development and Validationmentioning
confidence: 98%
“…Several assays have already been reported for the analysis of antiviral drugs based on liquid chromatography and mass spectrometric detection in the single ion monitoring mode [5] or in the multiple reaction monitoring mode [7]. Chromatographic separation of several antiviral drugs using traditional LC columns requires a total analysis time of about 20 minutes as reported by D'Avoloi et al [5] for the analysis of eleven analytes with co-elution of several compounds.…”
Section: Assay Development and Validationmentioning
confidence: 99%
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