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Fig 1.

Chemical structure of (a) ALP (b) OXP (c) LES and (d) IS.

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Fig 1 Expand

Fig 2.

Fragment ions spectra of (a) ALP (b) OXP (c) LES and (d) IS.

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Fig 2 Expand

Table 1.

Optimized compound specific parameters for ALP, OXP, LES and IS.

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Table 1 Expand

Fig 3.

The representative MRM chromatograms of ALP, OXP, LES and IS in (a) blank rat plasma and (b) plasma spiked at LLOQ concentrations.

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Fig 3 Expand

Table 2.

Inter and inter-day precision and accuracy data of ALP, OXP and LES in rat plasma.

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Table 2 Expand

Table 3.

Extraction recovery and matrix effects data of ALP, OXP, LES and IS in rat plasma (n = 5).

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Table 3 Expand

Fig 4.

The representative MRM chromatograms of ALP, OXP, LES and IS at one h after oral administration of ALP (20 mg/kg) and LES (15 mg/kg).

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Fig 4 Expand

Fig 5.

The plasma concentration-time profile of ALP, OXP, LES after oral administration of ALP (20 mg/kg) and LES (15 mg/kg).

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Fig 5 Expand

Table 4.

The non-compartmental pharmacokinetic parameters for ALP, OXP and LES in rat plasma after oral administration of mg/kg of ALP and 15 mg/kg of LES.

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Table 4 Expand