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. 2012 Jan;40(1):25–31. doi: 10.1124/dmd.111.042283

TABLE 1.

Performance of the analytical method

Retention time, limit of detection, and linear range (R2 ≥ 0.99) for ESI-MS detection in SRM mode, and UV detection at 265 nm are shown.

Compound Retention Time LC-ESI(−)-MS/MS
UV
LOD LOQ Linear Range LOD LOQ Linear Range
min fmol nM fmol nM
DCC 4.36 ± 0.03 3 1–1000 300 100–10,000
TCC 5.10 ± 0.04 3 1–1000 300 100–10,000
2′-OH-TCC 6.81 ± 0.07 3 1–1000 300 100–10,000
6′-OH-TCC 7.45 ± 0.05 3 1–1000 300 100–10,000
3′-OH-TCC 4.61 ± 0.02 3 1–1000 300 100–10,000
2′-SO3-O-TCC 3.46 ± 0.02 3 1–1000 300 100–10,000
N-Gluc-TCC 1.97 ± 0.01 n.d. n.d. n.d. n.d.
N′-Gluc-TCC 2.07 ± 0.02 n.d. n.d. n.d. n.d.
2′-O-gluc-TCC 2.50 ± 0.02 10 3–1000 300 100–10,000
6′-O-gluc-TCC 2.51 ± 0.02 n.d. n.d. n.d. n.d.
3′-O-gluc-TCC 2.26 ± 0.02 n.d. n.d. n.d. n.d.

LOQ, limit of quantitation; n.d., not determined because no reference compound was available.