|
|
||||||||
Departments of Nuclear Medicine and Internal Medicine, University Hospital Nijmegen; Utrecht Institute for Pharmaceutical Sciences, Department of Pharmaceutics, Utrecht University, The Netherlands
Correspondence: For correspondence or reprints contact: Els Th.M. Dams, MD, University Hospital Nijmegen, Department of Nuclear Medicine, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
ABSTRACT
Scintigraphic techniques are routinely used for the evaluation of the extent and severity of inflammatory bowel disease. Currently, the radiopharmaceutical of choice is 99mTc-hexamethyl propyleneamine oxime (HMPAO)-leukocytes. We studied the imaging potential of two recently developed 99mTc-labeled agents, polyethylene glycol (PEG)-coated liposomes and hydrazinonicotinate (HYNIC) IgG, in a rabbit model of acute colitis, and compared them with that of 99mTc-labeled, granulocyte-enriched (>90%), white blood cells. Methods: Acute colitiswas induced in rabbits by retrograde instillation of trinitrobenzene sulfonic acid. After 48 hr, 37 MBq of each radiopharmaceutical was administered intravenously. Gamma camera images were taken at 0, 1, 2, 4, 10 and 24 hr. At 4 and 24 hr postinjection, groups of rabbits were killed, and the uptake of the radiolabel in the dissected tissues was determined. For each af fected 5-cm segment, the colitis index (CI, affected-to-normal-colon-uptake ratio) was calculated and correlated to the macroscopically scored severity of inflammation. Results: All three agents visualized the colitis lesions within 1 hr postinjection. The CI correlated with the severity of the abnormalities. With increasing severity, the CI at 4 hr postinjection for liposomes was 3.89 ± 0.73, 4.41 ± 0.47 and 5.76 ± 0.65; for IgG 1.67 ± 0.08, 3.92 ± 0.44 and 6.14 ± 0.65; and for granulocytes 2.90 ± 0.09,6.15 ± 0.96 and 9.36 ± 3.35. For liposomes, the CI further increased during 24-hr postinjection to 6.56 ± 0.84,8.50 ± 0.53 and 10.61 ± 1.34, respectively. The CI for the other two agents did not change significantly with time. Conclusion: In this rabbit model, 99mTc-labeled granulocytes, IgG and liposomes all rapidly visualized colonie inflammation. Granulocytes and liposomes showed the highest CI. Technetium-99m-labeled PEG-liposomes may be an attractive alternative for labeled leukocytes to image inflammatory bowel disease, because they can be prepared off the shelf and no handling of blood is required.
Key Words: colitis liposomes immunoglobulin granulocytes white blood cells inflammation inflammatory bowel disease imaging technetium-99m
This article has been cited by other articles:
![]() |
J. E.M. van Eerd, W. J.G. Oyen, T. D. Harris, H. J.J.M. Rennen, D. S. Edwards, F. H.M. Corstens, and O. C. Boerman Scintigraphic Imaging of Infectious Foci with an 111In-LTB4 Antagonist Is Based on In Vivo Labeling of Granulocytes J. Nucl. Med., May 1, 2005; 46(5): 786 - 793. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E.M. van Eerd, P. Laverman, W. J.G. Oyen, T. D. Harris, D. S. Edwards, C. E. Ellars, F. H.M. Corstens, and O. C. Boerman Imaging of Experimental Colitis with a Radiolabeled Leukotriene B4 Antagonist J. Nucl. Med., January 1, 2004; 45(1): 89 - 93. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Gratz, H. J.J.M. Rennen, O. C. Boerman, W. J.G. Oyen, P. Mast, T. M. Behr, and F. H.M. Corstens 99mTc-HMPAO-Labeled Autologous Versus Heterologous Leukocytes for Imaging Infection J. Nucl. Med., July 1, 2002; 43(7): 918 - 924. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Gratz, H. J.J.M. Rennen, O. C. Boerman, W. J.G. Oyen, and F. H.M. Corstens Rapid Imaging of Experimental Colitis with 99mTc-Interleukin-8 in Rabbits J. Nucl. Med., June 1, 2001; 42(6): 917 - 923. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Moghimi, A. C. Hunter, and J. C. Murray Long-Circulating and Target-Specific Nanoparticles: Theory to Practice Pharmacol. Rev., June 1, 2001; 53(2): 283 - 318. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Laverman, A. H. Brouwers, E. Th. M. Dams, W. J. G. Oyen, G. Storm, N. van Rooijen, F. H. M. Corstens, and O. C. Boerman Preclinical and Clinical Evidence for Disappearance of Long-Circulating Characteristics of Polyethylene Glycol Liposomes at Low Lipid Dose J. Pharmacol. Exp. Ther., June 1, 2000; 293(3): 996 - 1001. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY | THE JOURNAL OF NUCLEAR MEDICINE |