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U.S. Department of Energy
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Localization of low density lipoproteins in vivo: Final technical report, September 28, 1987--September 27, 1988

Technical Report ·
OSTI ID:6785105
We have found that low density lipoprotein derivatized with I-123- tyramine cellobiose (I-123-TyC-LDL) behaves like native LDL when used for biodistribution studies in animals and in humans, and that I-123-TyC-LDL appears more promising than Tc-99m-labeled LDL for nuclear imaging of the coronary circulation. Unfortunately, isolation of LDL for direct derivatization with I-123-TyC is both time-consuming and affords a low but real probability of contamination. Methods for radiolabelling LDL indirectly or without prior purification would circumvent this problem. Moreover, modifications that could increase the specific activity of I-123-labelled LDL are desirable. For this project we proposed to establish a novel, rapid method for indirect radioiodination of LDL particles to be used in experimental and clinical nuclear imaging studies. We have found that small, model beta-strand peptides (MBPs) very selectively bind to LDL and that MBPs can be labelled with I-123-TyC. We have analyzed the in vivo behavior of two different types of semisynthetic I-123-TyC-LDL particles/endash/generated by adsorption of radiolabelled MBPs to native LDL/endash/in rabbits. With either preparation, clearance of radiolabelled MBPs from the circulation was more rapid than that of native LDL. 6 refs., 6 figs.
Research Organization:
Chicago Univ., IL (USA)
DOE Contract Number:
FG02-87ER60614
OSTI ID:
6785105
Report Number(s):
DOE/ER/60614-1; ON: DE89005749
Country of Publication:
United States
Language:
English