DIRECT DETERMINATION OF THEOPHYLLINE IN HUMAN SERUM BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING ZWITTERIONIC MICELLAR MOBILE-PHASE - COMPARISON WITH AN ENZYME-MULTIPLIED IMMUNOASSAY TECHNIQUE
D. Habel et al., DIRECT DETERMINATION OF THEOPHYLLINE IN HUMAN SERUM BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING ZWITTERIONIC MICELLAR MOBILE-PHASE - COMPARISON WITH AN ENZYME-MULTIPLIED IMMUNOASSAY TECHNIQUE, Analyst, 118(12), 1993, pp. 1511-1513
A liquid chromatographic procedure is reported for the direct determin
ation of theophylline in human serum. It includes the use of a micella
r zwitterionic mobile phase [10(-3) mol l(-1) 3-(dimethyldodecylammoni
o) propanesulfonate (also known as C-12 DAPS)-propanol (97 + 3, v/v) a
nd a mu Bondapak phenyl column. Detection is based on ultraviolet abso
rption at a wavelength of 273 nm. After dilution with the mobile phase
, the serum is injected into the chromatography; no solvent extraction
or deproteinization is performed. The linearity of the method describ
ed was excellent over the range 0.5-20 mg l(-1). The within-run precis
ion was better than 2%, and the recovery of the theophylline approache
d 98%. Two hundred direct injections of serum samples did not affect t
he column life. The total analysis time, including chromatography, was
approximately 15 min. As little as 0.5 mg l(-1) of theophylline could
be detected, and the results were in good agreement with those of an
enzyme multiplied immunoassay technique.