A rapid and specific HPLC assay for quantitative determination of bupivacaine in human serum is described. The technique incorporates an on-line sample clean-up system followed by reversed-phase chromatography with UV detection. The proposed method uses a column-switching technique and protein-coat
Enantioselective high performance liquid chromatographic assay of acebutolol and its active metabolite diacetolol in human serum
β Scribed by Joanna Szymura-Oleksiak; Maria Walczak; Jacek Bojarski; Hassan Y. Aboul-Enein
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 112 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0899-0042
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β¦ Synopsis
A stereoselective direct liquid chromatographic method for assay of the enantiomers of the β€-adrenergic blocker acebutolol (AC) and its active metabolite, diacetolol (DC), in human serum was developed. The assay is based on extraction with ethyl acetate and separation of enantiomers on an amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase (Chiralpak AD) column. The method was validated and proved useful for the determination of the enantiomers in serum samples of patients suffering from hypertension and chronically treated with racemic AC. The results were compared and found similar with an indirect assay based on derivatization of the enantiomers with (+)-(S)-1-(1-naphthyl)ethyl isocyanate (NEIC).
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## Abstract A simple and sensitive assay for glucuronidation activity of 7βethylβ10βhydroxycamptothecin (SNβ38), the active metabolite of irinotecan (CPTβ11), in human liver microsomes by highβperformance liquid chromatography (HPLC) with fluorescence detection is reported. The method was validated