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Real-time Analyses of Retinol Transport by the Membrane Receptor of Plasma Retinol Binding Protein
Published on: January 28, 2013
Synthesis of 13C2-Retinyl Acetate and Dose Preparation for Retinol Isotope Dilution Tests
Sherry A Tanumihardjo1, Jesse Sheftel1, Khushi Tanna1
1Department of Nutritional Sciences, University of Wisconsin-Madison.
Abstract:
The retinol isotope dilution (RID) test is the most sensitive method to assess vitamin A status by estimating total liver reserves, considered the reference standard. For gas chromatography-combustion-isotope ratio mass spectrometry detection, 13C is added to the retinol moiety. The synthetic procedure for 13C-retinyl acetate begins with the naturally occurring β-ionone. Briefly, C18-tetraene ketone is synthesized from β-ionone and purified. If a 13C4-retinyl acetate is desired, the carbanion of 13C2-labeled triethylphosphonoacetate can be used to add two 13C's to the β-ionone moiety before adding acetone's three carbons to synthesize the C18-tetraene ketone. If a 13C3-retinyl acetate is desired, the three carbons of the acetone could be labeled with 13C. For the most commonly used 13C2-retinyl acetate for future analysis by gas-chromatography-combustion isotope ratio mass spectrometry, a modified Wittig-Horner procedure is used, and unlabeled C18 tetraene ketone is reacted with the carbanion of 13C2-labeled triethylphosphonoacetate to add two-13C's to the 14 and 15 positions of the retinol molecule. The resulting ethyl ester is reduced to the alcohol and esterified to 13C2-retinyl acetate with acetic anhydride. The all-trans isomer is purified on 8%-water-deactivated alumina using relatively innocuous, highly volatile, solvents-hexanes and diethyl ether-which are removed by rotary evaporation and sonification of oil doses. The product is characterized by ultraviolet-visible (UV-Vis) spectroscopy, thin layer chromatography (TLC), and high-pressure liquid chromatography (HPLC) against analytical standards. The concentrated dose is stored dissolved in soybean oil at -80 °C. Final doses are diluted in soybean oil (~200 µL/dose) and quantified by UV-Vis spectroscopy against the vehicle soybean oil. Doses are measured for delivery to humans with a positive displacement pipette or tuberculin syringes for the RID test. Using appropriate assumptions, total body stores are calculated, and total liver reserves are estimated.
