2015
DOI: 10.1016/j.jpba.2014.12.042
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Development and validation of a liquid chromatography–tandem mass spectroscopy method for simultaneous determination of (+)-(13aS)-deoxytylophorinine and its pharmacologically active 3-O-desmethyl metabolite in rat plasma

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Cited by 5 publications
(5 citation statements)
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References 14 publications
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“…For comparison, the ions after only coarse isolation were fragmented. Figure d plots the MS/MS spectrum, where the isotope ion at m / z 135 corresponded to the fragment ion of rosiglitazone, and the isotope ions at m / z 165 and m / z 192 corresponded to the fragment ions of rotundine. In addition, the isotope ion at m / z 136 also appeared (blue line of the inset of Figure c), according to the fragmentation law, which can be considered that the ion was the fragmentation of the rosiglitazone isotope D+1. On the other hand, when the isotope ion D obtained after fine isolation was fragmented, as indicated by the red dashed line of the inset of Figure c, the fragment peak was only retained at m / z 135 and other fragment peaks disappeared.…”
Section: Resultsmentioning
confidence: 98%
“…For comparison, the ions after only coarse isolation were fragmented. Figure d plots the MS/MS spectrum, where the isotope ion at m / z 135 corresponded to the fragment ion of rosiglitazone, and the isotope ions at m / z 165 and m / z 192 corresponded to the fragment ions of rotundine. In addition, the isotope ion at m / z 136 also appeared (blue line of the inset of Figure c), according to the fragmentation law, which can be considered that the ion was the fragmentation of the rosiglitazone isotope D+1. On the other hand, when the isotope ion D obtained after fine isolation was fragmented, as indicated by the red dashed line of the inset of Figure c, the fragment peak was only retained at m / z 135 and other fragment peaks disappeared.…”
Section: Resultsmentioning
confidence: 98%
“…5d plots the secondary mass spectrum, where the isotope ion at m/z 135 corresponded to the fragment ion of rosiglitazone, and the isotope ions at m/z 165 and m/z 192 corresponded to the fragment ions of rotundine. [40][41][42][43] In addition, the isotope ion at m/z 136 also appeared (inside Figure 5e), according to the fragmentation law, which can be considered that the ion was the fragmentation of the rosiglitazone isotope. The D isotope ion obtained after fine isolation was fragmented, as in the interior of Figure 5e, only the fragment peak was retained at m/z 135 and other fragment peaks disappeared.…”
Section: Resultsmentioning
confidence: 99%
“…Figure 5d plots the MS/MS spectrum, where the isotope ion at m/z 135 corresponded to the fragment ion of rosiglitazone, and the isotope ions at m/z 165 and m/z 192 corresponded to the fragment ions of rotundine. [39][40][41][42] In addition, the isotope ion at m/z 136 also appeared (blue line of the inset of Figure 5c), according to the fragmentation law, which can be considered that the ion was the fragmentation of the rosiglitazone isotope D+1. On the other hand, when the \isotope ion D obtained after fine isolation was fragmented, as indicated by the red dashed line of the inset of Figure 5c, the fragment peak was only retained at m/z 135 and other fragment peaks disappeared.…”
Section: Resultsmentioning
confidence: 99%