Characterization of alkyl-cobalamins formed on trapping of epoxide metabolites of 1,3-butadiene
✍ Scribed by Charlotta Fred; Johanna Haglund; Tomas Alsberg; Per Rydberg; Johanna Minten; Margareta Törnqvist
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 279 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Analytical methods facilitating studies of electrophilically reactive and genotoxic compounds in vitro and in vivo are needed. The strong nucleophile, cob(I)alamin, formed by reduction of Vitamin B~12~ [cob(III)alamin], may be used for trapping and analysis of 1,2‐epoxides and other electrophiles. In the present study, cob(I)alamin is evaluated as an analytical tool for 1,2‐epoxide metabolites (oxiranes) of 1,3‐butadiene. Products of reaction of cob(I)alamin with 1,2‐epoxy‐3‐butene (EB), 1,2:3,4‐diepoxybutane (DEB), and 1,2‐epoxy‐3,4‐butanediol (EBdiol) have been analyzed by reversed phase high performance liquid chromatography (HPLC) coupled on‐line to electrospray ionization mass spectrometry (ESI‐MS) and ultraviolet diode array detection (UV‐DAD). It was shown that a specific alkyl‐Cbl complex is formed for each metabolite and that it was possible to discriminate between the products by HPLC‐UV and by LC‐MS. Quantification of DEB with the method by use of another 1,2‐epoxide as an internal standard was successfully performed. The possibility of using cob(I)alamin for trapping and analysis of the three oxirane metabolites of 1,3‐butadiene will facilitate quantitative comparisons of species in vitro with regard to metabolism of 1,3‐butadiene.
📜 SIMILAR VOLUMES
## Abstract The conformational equilibrium of 1‐alkyl‐3‐hydroxypiperidines in __n__‐heptane and aqueous solution is investigated. Several methods, e.g. IR and NMR spectroscopy, are discussed. The conformation trapping in D~2~SO~4~‐D~2~O mixtures, and subsequent analysis of the ^1^H and ^13^C NMR sp
MSBSM five-block copolymers where B stands for butadiene, S for styrene, and M for either methyl methacrylate (MMA) or tert-butyl methacrylate (tBMA) have been synthesized by sequential anionic polymerization in a n apolar solvent by using a difunctional anionic initiator derived from 1,3-diisoprope