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Research Article

Quantification of thonningianin a in rat plasma by liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study

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Pages 523-529 | Received 17 Nov 2020, Accepted 31 Mar 2021, Published online: 29 Apr 2021

Figures & data

Figure 1. Proposed MS/MS fragmentation pathway of thonningianin A (A) and IS (B).

Figure 1. Proposed MS/MS fragmentation pathway of thonningianin A (A) and IS (B).

Figure 2. Full scan product ion spectra of thonningianin A (A) and IS (B).

Figure 2. Full scan product ion spectra of thonningianin A (A) and IS (B).

Figure 3. SRM chromatograms of thonningianin A and IS in a blank plasma sample (A), a blank sample spiked the analyte (LLOQ) and IS (B), and a plasma sample at 0.083 h after oral administration of 20 mg/kg thonningianin A (C).

Figure 3. SRM chromatograms of thonningianin A and IS in a blank plasma sample (A), a blank sample spiked the analyte (LLOQ) and IS (B), and a plasma sample at 0.083 h after oral administration of 20 mg/kg thonningianin A (C).

Table 1. Precision and accuracy of the LC-MS/MS method (n = 5).

Table 2. Stability of the thonningianin A in rat plasma (n = 5).

Table 3. Recovery and matrix effect of the thonningianin A and IS in rat plasma (n = 5).

Figure 4. Mean plasma concentrations of thonningianin A after oral administration to rats orally (p.o., 10, 20, and 40 mg/kg).

Figure 4. Mean plasma concentrations of thonningianin A after oral administration to rats orally (p.o., 10, 20, and 40 mg/kg).

Table 4. Mean pharmacokinetic parameters of thonningianin A after oral administration to rats orally.