Abstract
High-performance liquid chromatography (hplc) has been used to separate and quantificate the dimethyl ester (DME) derivatives of the four biliverdin isomers of the IX series: biliverdin-IXα, -IXβ, -IXγ, and -IXδ. Samples of 0.5 to 10.0 nmol of biliverdin DME were detected quantitatively upon elution by monitoring the absorbance at 375 nm. A technique was developed in which p-bromoacetanilide (Dupont's recommended test compound for their Zorbax column) is used as a marker for biliverdin-IXα DME. To facilitate quantification of biliverdin-IXβ DME, its extinction coefficient was determined. This method has been used to study biliverdin isomers in various biological species. High-resolution NMR (360 MHz) was used to further characterize the isomers. © 1980.
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CITATION STYLE
Rasmussen, R. D., Yokoyama, W. H., Blumenthal, S. G., Bergstrom, D. E., & Ruebner, B. H. (1980). High-performance liquid chromatographic separation and quantification of the four biliverdin dimethyl ester isomers of the IX series. Analytical Biochemistry, 101(1), 66–74. https://doi.org/10.1016/0003-2697(80)90041-X
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