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. 2000 May;49(5):453–461. doi: 10.1046/j.1365-2125.2000.00193.x

Table 1.

H.p.l.c. conditions for drug assays.

Drug Mobile phase H.p.l.c. column Mobile phase flow rate (ml min−1) Detector wavelength (nm) Retention time of analyte (min)
Caffeine (internal standard) 95% Na acetate buffer (pH 4.0, 1.7 mm)/5% acetonitrile C-18 2 276 8.5 (10.2)
Amiodarone 58% distilled water with 0.01 m NH4CIO4/42% acetronitrile (adjusted to pH 3.0 with perchloric acid) C-8 2 242 8.75
Amitriptyline 60% distilled water with 3 mm octanesulphonic acid, and 0.5 mm NNN’N′-TMED/40% acetonitrile (adjusted to pH 2.5 with H3PO4) C-8 2 230 7.0
Nortriptyline As for amitriptyline 7.75
Naproxen 85% 20 mm phosphate buffer (pH 7.0)/15% acetonitrile C-18 1.8 254 5.5
Tolbutamide 70% 10 mm Na acetate/ 30% acetonitrile (adjusted to pH 4.3 with glacial acetic acid) C-18 2 254 6.75
Phenytoin As for tolbutamide C-18 2 254 5.2

C-18: Waters, Nova Pak, particle size 4 micron, 3.9 mm (id) × 150 mm C-8: Beckman Ultrasphere (Octyl), particle size 5 micron, 4.6 mm (id) × 25 cm.