Phosphoric acid esters of riboflavin can be easily separated by reverse-phase high-performance liquid chromatography using eluants of 0.1 M ammonium formate in aqueous methanol. Commercial FMN preparations contained seven different flavin phosphates; the content of riboflavin S-phosphate was 70-7590
Identification of FAD, FMN, and riboflavin in the retina by microextraction and high-performance liquid chromatography
✍ Scribed by David W. Batey; Curtis D. Eckhert
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 366 KB
- Volume
- 188
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
✦ Synopsis
The presence of flavins in the retina has been known for some time. However, the small size of the tissue has made it difficult to quantify the levels of the individual flavins, riboflavin (RB), FMN, and FAD without pooling large numbers of retinas. A procedure to extract and quantitate RB, FMN, and FAD in retinal tissue from as few as four rat retinas has been developed. The procedure resolves these three classes of flavins and provides a recovery near 100%. For the analysis, HPLC using a reverse-phase column with cyclohexyl functional groups was coupled to a fluorescence detector. The microextraction-HPLC procedure was reproducible for the quantitative analysis of flavins in the retina and equally applicable for analysis of flavins in liver and plasma.
📜 SIMILAR VOLUMES
Many preparations of flavin nucleotides contain nucleotide isomers of the natural compounds which are difficult to remove or separate. The method of dynamic complex-exchange (or pairedion) chromatography has been used with high-performance liquid chromatography to achieve resolution and purification
## Abstract A new, selective and sensitive method has been developed for the determination of tricyclic antidepressant drugs, amoxapine and nortriptyline, in human blood plasma and serum, involving their reaction with allyl isothiocyanate and extraction of thiourea derivatives with water‐miscible o
## Abstract A method termed liquid–liquid–liquid microextraction (LLLME) was utilized to extract 4‐t‐butylphenol, 4‐t‐octylphenol, 4‐n‐nonylphenol, and bisphenol‐A from water. The extracted target analytes were separated and quantified by high‐performance liquid chromatography using a fluorescence