DIRECT DETERMINATION OF THEOPHYLLINE IN HUMAN SERUM BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING ZWITTERIONIC MICELLAR MOBILE-PHASE - COMPARISON WITH AN ENZYME-MULTIPLIED IMMUNOASSAY TECHNIQUE

Citation
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
Citations number
21
Categorie Soggetti
Chemistry Analytical
Journal title
ISSN journal
00032654
Volume
118
Issue
12
Year of publication
1993
Pages
1511 - 1513
Database
ISI
SICI code
0003-2654(1993)118:12<1511:DDOTIH>2.0.ZU;2-G
Abstract
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.