Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Catherine F. Foulon"'
Autor:
Ming Kuan Chyan, Janna Quinn, Pradip M. Pathare, D. K. Hamlin, Michael R. Zalutsky, D. Scott Wilbur, Timothy J. Wedge, Robert L. Vessella, Reudi Risler, M. Frederick Hawthorne, Catherine F. Foulon, Brian B. Kegley
Publikováno v:
Bioconjugate Chemistry. 15:203-223
An investigation has been conducted to assess the in vivo stability of a series of astatinated benzamides and astatinated nido-carborane compounds in mice. It was hypothesized that the higher bond strength of boron-astatine bonds in the nido-carboran
Publikováno v:
Nuclear Medicine and Biology. 28:769-777
Receptor-mediated internalization of monoclonal antibodies (mAbs), such as those specific for the epidermal growth factor receptor variant III (EGFRvIII), can lead to rapid loss of radioactivity from the target cell. In the current study, the anti-EG
Autor:
Yinhua Yu, Catherine F. Foulon, Fengji Xu, Robert C. Bast, Michael R. Zalutsky, Xiao-Guang Zhao, Susan Slade, Donna J. Affleck
Publikováno v:
Nuclear Medicine and Biology. 26:781-790
Monoclonal antibody (MAb) internalization can have a major effect on tumor retention of radiolabel. Two anti-HER-2/neu MAbs (TA1 and 520C9) were radioiodinated using the iodogen, N-succinimidyl 5-iodo-3-pyridinecarboxylate (SIPC), and tyramine-cellob
Publikováno v:
Bioconjugate Chemistry. 10:867-876
Radioimmunopretargeting is based on the separate injection of a modified mAb and the radionuclide and most frequently exploits the very high avidity of biotin for streptavidin (SA). Currently, we are evaluating the therapeutic potential of directly l
Publikováno v:
Nuclear Medicine and Biology. 26:405-411
Monoclonal antibodies (MAbs) such as the anti-epidermal growth factor variant III (EGFRvIII) MAb L8A4 are rapidly internalized, which can lead to rapid loss of radioactivity from the tumor cell. The aim of this study was to evaluate the potential uti
Publikováno v:
Nuclear Medicine and Biology. 25:81-88
We report herein the preparation and biological evaluation of two radioastatinated biotin conjugates, (3-[211At]astatobenzoyl)norbiotinamide and ((5-[211At]astato-3-pyridinyl)carbonyl)norbiotinamide. Both conjugates were stable in the presence of hum
Publikováno v:
Bioconjugate Chemistry. 8:179-186
A new class of radioiodinated biotin conjugated is described in which the amido bond between biotin and the labeled prosthetic group is reversed. One conjugate, (3-[125I]iodobenzoyl)norbiotinamide (4c, [125I]IBB) was labeled with Na125I in one step f
Publikováno v:
Applied Radiation and Isotopes. 46:1039-1046
The fastest and most reliable preparation of radiolabeled 5-iodo-2′-deoxyuridine ([ 123/125/131 I]IUdR) is accomplished by iododemetallation. We describe a series of improvements to a previously published synthesis of radiolabeled IUdR by demercura
Publikováno v:
Nuclear medicine and biology. 24(2)
Biotinyl-3-[ 211 At]astatoanilide ([ 211 At]AtBA) was prepared in more than 80% yield by destannylation. In vitro , [ 211 At]AtBA exhibited a high affinity for streptavidin, and was stable after incubation in human serum, cerebrospinal fluid and dist
Autor:
Kwan-Hwa Chi, Hsin-Ell Wang, Fu-Du Chen, Yee Chao, Ren-Shyan Liu, Shuan-Lan Chou, Yu-Shan Wang, Sang-Hue Yen
Publikováno v:
Journal of Nuclear Medicine; Feb2001, Vol. 42 Issue 2, p345-351, 7p, 5 Graphs