TABLE 1

LC-MS-MS analytical parameters of 1-hydroxymidazolam and time-dependent inactivators


Analyte

1-Hydroxymidazolam

Amprenavir

Diclofenac

Diltiazem

Erythromycin

Raloxifene

Troleandomycin
Mobile phase gradient program: %B (min) 2(0) → 25 (0.6) → 55 2(0) → 40 2(0) → 25 2(0) → 25 2(0) → 30 2(0) → 2 2(0) → 25
(3.3) → 55 (3.5) → 98 (0.6) → 57 (0.6) → 55 (0.6) → 55 (0.6) → 55 (0.2) → 55 (0.6) → 55
(4.2) → 2 (4.25) (3.1) → 98 (3.3) → 55 (3.3) → 55 (3.3) → 55 (0.8) → 57 (3.1) → 55
(4.2) → 98 (3.5) → 98 (3.5) → 98 (3.4) → 98 (3.1) → 98 (3.5) → 98
(5) → 2 (5.2) (4.2) → 2 (4.25) (4.2) → 2 (4.25) (4.2) → 2 (4.25) (4.2) → 98 (4.2) → 2 (4.25)
(5) → 2 (5.2)
Analyte m/z transition 342 → 324 506 → 245 296 → 214 415 → 370 716 → 558 474 → 112 772 → 586
Mode Positive Positive Positive Positive Positive Positive Positive
Capillary voltage (kV) 2.50 2.52 2.52 2.52 2.52 2.52 2.52
Cone voltage (V) 40 32 50 36 35 30 17
Desolvation temperature (°C) 300 300 300 300 300 300 300
Collision energy (eV) 20 17 40 18 15 27 25
Retention time (min)
6.2
5.6
5.7
6.7
5.4
5.3
6.6