|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Molecular Imaging |
1 From Schering, Research Laboratories, Müllerstrasse 178, D-13342 Berlin, Germany. Received March 19, 2003; revision requested May 27; final revision received September 2; accepted September 29. Address correspondence to P.H. (e-mail: peter.hauff@schering.de).
PURPOSE: To evaluate the feasibility of using intravenously administered L-selectin ligand-specific polymer-stabilized air-filled microparticles (MPs) for active targeting of peripheral lymph nodes under normal conditions in animal models.
MATERIALS AND METHODS: L-selectin ligand-specific MPs and two control substances (immunoglobulin Misotype MPs and native MPs) were each administered in three conscious mice as a single intravenous bolus injection (1.4 x 107 MPs/kg). All mice were sacrificed 30 minutes after administration. Lymph nodes (cervical, inguinal, axillary, popliteal, mesenteric), spleen (positive control), and kidney (blood pool control) were removed and examined for MP-related stimulated acoustic emission (SAE) signals by using harmonic color Doppler ultrasonography (US) in a tank containing degassed water. A second experiment was performed in six anesthetized beagle dogs by using the same MP formulation. Each of the MP formulations was administered in two anesthetized dogs as a single intravenous bolus injection (1 x 107 MPs/kg). The popliteal lymph nodes, spleen (positive control), and kidney (blood pool control) were examined in vivo with US for MP-related SAE signals 30 minutes after administration. Fisher exact test for the one-side alternative was used for mouse data analysis.
RESULTS: The lymph nodes of all mice (P = .05) and the popliteal lymph nodes of both dogs treated with L-selectin ligand-specific MPs showed clear MP-related SAE signals, whereas the lymph nodes of all mice and the popliteal lymph nodes of four dogs that received the control substances did not show any SAE signals.
CONCLUSION: Use of an intravenously administered L-selectin ligand-specific US contrast agent is feasible for active lymph node targeting in mice and dogs.
© RSNA, 2004
Index terms: Animals Contrast media, experimental studies Lymphatic system, US, 998.12983, 998.12988 Molecular analysis Ultrasound (US), experimental studies
This article has been cited by other articles:
![]() |
M. Palmowski, J. Huppert, G. Ladewig, P. Hauff, M. Reinhardt, M. M. Mueller, E. C. Woenne, J. W. Jenne, M. Maurer, G. W. Kauffmann, et al. Molecular profiling of angiogenesis with targeted ultrasound imaging: early assessment of antiangiogenic therapy effects Mol. Cancer Ther., January 1, 2008; 7(1): 101 - 109. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-N. Qian, B. Berghuis, G. Tsarfaty, M. Bruch, E. J. Kort, J. Ditlev, I. Tsarfaty, E. Hudson, D. G. Jackson, D. Petillo, et al. Preparing the "Soil": The Primary Tumor Induces Vasculature Reorganization in the Sentinel Lymph Node before the Arrival of Metastatic Cancer Cells Cancer Res., November 1, 2006; 66(21): 10365 - 10376. [Abstract] [Full Text] [PDF] |
||||
![]() |
V R Stewart and P S Sidhu New directions in ultrasound: microbubble contrast. Br. J. Radiol., March 1, 2006; 79(939): 188 - 194. [Full Text] [PDF] |
||||
![]() |
P. Hauff, S. Seemann, R. Reszka, M. Schultze-Mosgau, M. Reinhardt, T. Buzasi, T. Plath, S. Rosewicz, and M. Schirner Evaluation of Gas-filled Microparticles and Sonoporation as Gene Delivery System: Feasibility Study in Rodent Tumor Models Radiology, August 1, 2005; 236(2): 572 - 578. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Blomley Can Microbubbles Be Targeted to Lymph Nodes? Radiology, June 1, 2004; 231(3): 611 - 612. [Full Text] [PDF] |
||||