(Circulation. 1997;96:154-165.)
© 1997 American Heart Association, Inc.
Articles |
From the Thoraxcenter (E.C., E.B., M.J.B.K., J.R.T.C.R., P.W.S.), Departments of Nuclear Medicine (W.H.B., A.R., E.P.K.) and Pharmacy (I.M. van G.), University Hospital Dijkzigt, Rotterdam, Netherlands.
Correspondence to E. Camenzind, MD, Department of Interventional Cardiology, Thoraxcenter Room Bd 376, University Hospital Dijkzigt, Erasmus University Rotterdam, Dr Molewaterplein 40, 3015 GD Rotterdam, Netherlands.
Background Demonstration and quantification of
site-specific intracoronary administration of compounds has
been confined thus far to the experimental animal laboratory. The aim
of this study was to describe a scintigraphic method to demonstrate
site-specific intracoronary drug delivery in humans. The
methods allow on-line visualization and off-line quantification of
site-specifically infused
-emitting compounds.
Methods and Results In 12 patients after balloon
angioplasty, 99mTc-labeled heparin was administered at the
site of dilatation by use of a coil balloon. Both the infusion period
and the washout period after the end of infusion were monitored with a
-camera. A curve of counts per pixel as a function of time was
derived that showed an accumulation phase during infusion followed by a
washout phase after the end of infusion. Both phases were fitted by
regression analysis and showed a linear accumulation pattern
and a biexponential washout pattern. After correction for background
counts, 99mTc decay, and body attenuation, peak heparin
amount and regional bioavailability were calculated. Peak amount was
defined as the initial point of the slow washout component of the
biexponential curve (elimination component), and regional
bioavailability was defined as the area under the curve of accumulation
and washout phase. Half-life and retention time, defined as seven
half-lives, were obtained by use of the elimination component after
correction for 99mTc decay. Mean peak delivered amount was
45±44 IU (236±228 µg), corresponding to an efficiency of delivery
ranging from 1% to 8% of the totally infused dose. Total regionally
bioavailable heparin reached 244±194 IU·h (1.28±1.01 mg·h).
Retention time varied from 12 to 90 hours (mean, 50:33±22:50
hours:minutes).
Conclusions Site-specific intracoronary heparin delivery after angioplasty by means of the coil balloon was demonstrated in humans, and regional pharmacokinetics was quantified by use of a radioisotopic technique.
Key Words: balloon angioplasty radioisotopes scintigraphy heparin
This article has been cited by other articles:
![]() |
E. Camenzind Treatment of In-Stent Restenosis -- Back to the Future? N. Engl. J. Med., November 16, 2006; 355(20): 2149 - 2151. [Full Text] [PDF] |
||||
![]() |
R. F. Bonvini, T. Hendiri, and E. Camenzind Inflammatory response post-myocardial infarction and reperfusion: a new therapeutic target? Eur. Heart J. Suppl., October 1, 2005; 7(suppl_I): I27 - I36. [Abstract] [Full Text] [PDF] |
||||
![]() |
J C Spratt and E Camenzind Plaque stabilisation by systemic and local drug administration Heart, December 1, 2004; 90(12): 1392 - 1394. [Full Text] [PDF] |
||||
![]() |
N. F. Meneveau, B. D. Klugherz, B. Chaquor, M. A. Golden, M. M. Jouille, E. Macarek, P. B. Weisz, and R. L. Wilensky Separate and Combined Effects of Local and Continuous Intravenous Administration of {beta}-Cyclodextrin Tetradecasulfate on Intimal Hyperplasia after Angioplasty in Porcine Coronary Arteries Journal of Cardiovascular Pharmacology and Therapeutics, March 1, 2003; 8(1): 53 - 60. [Abstract] [PDF] |
||||
![]() |
M. J. B. Kutryk, D. P. Foley, M. van den Brand, J. N. Hamburger, W. J. van der Giessen, P. J. deFeyter, N. Bruining, M. Sabate, and P. W. Serruys Local intracoronary administration of antisense oligonucleotide against c-myc for the prevention of in-stent restenosis: Results of the randomized investigation by the thoraxcenter of antisense dna using local delivery and ivus after coronary stenting (ITALICS) trial J. Am. Coll. Cardiol., January 16, 2002; 39(2): 281 - 287. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. M. Sasseen, B. D. Gray, D. Gal, R. Lorinc, D. C. Carpenter, B. D. Klugherz, and R. L. Wilensky Local Delivery of a Hydrophobic Heparin Reduces Neointimal Hyperplasia After Balloon Injury in Rat Carotid but not Pig Coronary Arteries Journal of Cardiovascular Pharmacology and Therapeutics, December 1, 2001; 6(4): 377 - 383. [Abstract] [PDF] |
||||
![]() |
I. Fishbein, M. Chorny, S. Banai, A. Levitzki, H. D. Danenberg, J. Gao, X. Chen, E. Moerman, I. Gati, V. Goldwasser, et al. Formulation and Delivery Mode Affect Disposition and Activity of Tyrphostin-Loaded Nanoparticles in the Rat Carotid Model Arterioscler. Thromb. Vasc. Biol., September 1, 2001; 21(9): 1434 - 1439. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. John, H. A. Rajasinghe, S. Itescu, S. Suratwalla, K. Lietz, A. D. Weinberg, A. Kocher, D. M. Mancini, R. E. Drusin, M. C. Oz, et al. Factors affecting long-term survival (>10 years) after cardiac transplantation in the cyclosporine era J. Am. Coll. Cardiol., January 1, 2001; 37(1): 189 - 194. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Widimsky Intracoronary drug delivery: mechanically too rough, pharmacologically too weak? Eur. Heart J., November 1, 2000; 21(21): 1729 - 1730. [PDF] |
||||
![]() |
N Meneveau, F Schiele, G Grollier, B Farah, J.M Lablanche, K Khalife, J Machecourt, N Danchin, J.E Wolf, M Simpson, et al. Local delivery of nadroparin for the prevention of neointimal hyperplasia following stent implantation: results of the IMPRESS Trial. A multicentre, randomized, clinical, angiographic and intravascular ultrasound study Eur. Heart J., November 1, 2000; 21(21): 1767 - 1775. [Abstract] [PDF] |
||||
![]() |
C. Herdeg, M. Oberhoff, A. Baumbach, A. Blattner, D. I. Axel, S. Schroder, H. Heinle, and K. R. Karsch Local paclitaxel delivery for the prevention of restenosis: biological effects and efficacy in vivo J. Am. Coll. Cardiol., June 1, 2000; 35(7): 1969 - 1976. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. G. Lehmann, J. J. Popma, J. A. Werner, A. J. Lansky, and R. L. Wilensky Vascular remodeling and the local delivery of cytochalasin B after coronary angioplasty in humans J. Am. Coll. Cardiol., March 1, 2000; 35(3): 583 - 591. [Abstract] [Full Text] [PDF] |
||||
![]() |
P.W. Serruys, D.P. Foley, G. Jackson, H. Bonnier, C. Macaya, M. Vrolix, A. Branzi, J. Shepherd, H. Suryapranata, P.J. de Feyter, et al. A randomized placebo-controlled trial of fluvastatin for prevention of restenosis after successful coronary balloon angioplasty: Final results of the fluvastatin angiographic restenosis (FLARE) trial Eur. Heart J., January 1, 1999; 20(1): 58 - 69. [Abstract] [PDF] |
||||
![]() |
R. L. Wilensky, K. Mehdi, K. M. Sowinski, Sang Hong Baek, and K. L. March Increased Intramural Retention After Local Delivery of Molecules with Increased Binding Properties: Implications for Regional Delivery of Pharmacologic Agents Journal of Cardiovascular Pharmacology and Therapeutics, January 1, 1999; 4(2): 103 - 112. [Abstract] [PDF] |
||||
![]() |
B. D. Klugherz, N. Meneveau, W. Chen, F. Wade-Whittaker, G. Papandreou, R. Levy, and R. L. Wilensky Sustained Intramural Retention and Regional Redistribution Following Local Vascular Delivery of Polylactic-Coglycolic Acid and Liposomal Nanoparticulate Formulations Containing Probucol Journal of Cardiovascular Pharmacology and Therapeutics, January 1, 1999; 4(3): 167 - 174. [Abstract] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1997 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |