The effect of vehicle on the tissue distribution profiles of radioiodinated cholesterol esters in the rat

Several groups have examined the possible use of radioiodinated cholesterol esters to achieve selective uptake of radioactivity in the adrenal cortex and have obtained variable results. This study indicates that the tissue distribution profile varies not only with the type of ester, but also with the vehicle employed for administration. Radioiodinated 19-iodocholesteryl (125-IC), iodocholesteryl palmitate (125-ICP)and iodocholesteryl oleate (125-ICO) were dissolved in either tween vehicle (saline containing 1.6% tween 80 and 10% ethanol) or myristate vehicle (isopropyl myristate-ethanol, 1:5 v/v) and administered i.v. to rats. Irrespective of the agent, considerably more radioactivity appeared in the target organs when the tween vehicle was employed. When the myristate vehicle was used, higher levels of radioactivity appeared in the lung. This finding suggests precipitation of the agents from the myristate vehicle occurred upon administration. In the tween vehicle, 125-ICO showed almost three times greater predilection for adrenal cortex than 125-ICP with levels of activity approaching those seen for 125-IC. Adrenal activity and adrenal to non-target ratios were sufficient for visualization of the adrenals at 5 days after injection of 125-ICO in the tween vehicle. Lipid extraction and TLC analysis of tissue radioactivity revealed that radioactivity in the adrenal and ovary was predominantly in an esterified form. Further analysis of the esters present after injection of 125-ICP showed these to be a mixture of mono and polyunsaturated esters. The site of hydrolysis and subsequent reesterification is an interesting biochemical aspect that remains to be elucidated.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/24488/1/0000764.pd

The measurement of testosterone and oestradiol-17[beta] using iodinated tracers and incorporating an affinity chromatography extraction procedure

The development of sensitive radioimmunoassays (RIA) for testosterone and oestradiol-17[beta], utilising 125I-radioligands, is described. Use of an homologous bridge at the same site of attachment, for both the radioligand and the steroid-carrier protein conjugate employed in raising antibodies, normally results in a loss of assay sensitivity and precision. This was overcome in the oestradiol assay by utilising an heterologous configuration at the site of attachment (11[alpha] vs 11[beta]). In contrast, for testosterone, even though an homologous bridge and site of attachment was used for the radioligand and the steroid-carrier protein conjugate, a very sensitive assay with extremely high antibody titres (dilution of 1:2 x 106) was achieved. This finding was repeated with a different antiserum suggesting that the "bridge binding" phenomenon may be related to the position of attachment to the steroid molecule. In addition, an antibody-Sepharose 4B affinity chromatography extraction procedure has been developed for both oestradiol and testosterone. This approach allows the measurement of very low concentrations of steroids from large volumes of a variety of biological fluids. As antibody-linked Sepharose 4B uses high concentrations of antibody, steroids of similar structure are extracted from biological fluids. However, the cross-reactivity of these related steroids are very low in the RIA's, ensuring good specificity.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/25490/1/0000031.pd