Literature DB >> 17574990

A new tool for molecular imaging: the microvolumetric beta blood counter.

Laurence Convert1, Guillaume Morin-Brassard, Jules Cadorette, Mélanie Archambault, M'hamed Bentourkia, Roger Lecomte.   

Abstract

UNLABELLED: Radiotracer kinetic modeling in small animals with PET allows absolute quantification of physiologic and biochemical processes in vivo. It requires blood and tissue tracer concentrations as a function of time. Manual sampling, the reference method for blood tracer concentration measurements, requires fairly large amounts of blood besides being technically difficult and time-consuming. An automated microvolumetric beta blood counter (microBC) was designed to circumvent these limitations by measuring the blood activity in real time with PET scanning.
METHODS: The microBC uses direct beta-particle detection to reduce its footprint and is entirely remote controlled for sampling protocol selection and real-time monitoring of measured parameters. Sensitivity has been determined for the most popular PET radioisotopes ((18)F, (13)N, (11)C, (64)Cu). Dispersion within the sampling catheter has been modeled to enable automatic correction. Blood curves obtained with the microBC were compared with manual samples and PET-derived data. The microBC was used to estimate the myocardial blood flow (MBF) of mice injected with (13)N-ammonia and to compare the myocardial metabolic rate of glucose (MMRG) of rats injected with (18)F-FDG for arterial and venous cannulation sites.
RESULTS: The sensitivity limit ranges from 3 to 104 Bq/microL, depending on the isotope and the catheter used, and was found to be adequate for most small-animal studies. Automatic dispersion correction appears to be a good approximation of dispersion-free reference curves. Blood curves sampled with the microBC are well correlated with curves obtained from manual samples and PET images. With correction for dispersion, the MBF of anesthetized mice at rest was found to be 4.84 +/- 0.5 mL/g/min, which is comparable to values found in the literature for rats. MMRG values derived from the venous blood tracer concentration are underestimated by 60% as compared with those derived from arterial blood.
CONCLUSION: The microBC is a compact automated counter allowing real-time measurement of blood radioactivity for pharmacokinetic studies in animals as small as mice. Reliable and reproducible, the device makes it possible to increase the throughput of pharmacokinetic studies with reduced blood sample handling and staff exposure, contributing to speed up new drug development and evaluation.

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Year:  2007        PMID: 17574990     DOI: 10.2967/jnumed.107.042606

Source DB:  PubMed          Journal:  J Nucl Med        ISSN: 0161-5505            Impact factor:   10.057


  10 in total

Review 1.  Determination of the Input Function at the Entry of the Tissue of Interest and Its Impact on PET Kinetic Modeling Parameters.

Authors:  M'hamed Bentourkia
Journal:  Mol Imaging Biol       Date:  2015-12       Impact factor: 3.488

2.  Development of a high-sensitivity BGO well counter for small animal PET studies.

Authors:  Seiichi Yamamoto; Hiroshi Watabe; Yasukazu Kanai; Tadashi Watabe; Masao Imaizumi; Eku Shimosegawa; Jun Hatazawa
Journal:  Radiol Phys Technol       Date:  2011-10-11

3.  [¹¹C]acetate and PET/CT assessment of muscle activation in rat studies.

Authors:  Sara Trombella; David García; Didier J Colin; Stéphane Germain; Yann Seimbille; Osman Ratib
Journal:  Int J Comput Assist Radiol Surg       Date:  2015-07-26       Impact factor: 2.924

4.  Optimization of a Model Corrected Blood Input Function from Dynamic FDG-PET Images of Small Animal Heart In Vivo.

Authors:  Min Zhong; Bijoy K Kundu
Journal:  IEEE Trans Nucl Sci       Date:  2013-10       Impact factor: 1.679

5.  Use of a beta microprobe system to measure arterial input function in PET via an arteriovenous shunt in rats.

Authors:  Geoff Warnock; Mohamed-Ali Bahri; David Goblet; Fabrice Giacomelli; Christian Lemaire; Joel Aerts; Alain Seret; Xavier Langlois; Andre Luxen; Alain Plenevaux
Journal:  EJNMMI Res       Date:  2011-08-10       Impact factor: 3.138

6.  P-glycoprotein at the blood-brain barrier: kinetic modeling of 11C-desmethylloperamide in mice using a 18F-FDG μPET scan to determine the input function.

Authors:  Lieselotte Moerman; Dieter De Naeyer; Paul Boon; Filip De Vos
Journal:  EJNMMI Res       Date:  2011-07-29       Impact factor: 3.138

7.  Kinetic Modeling and Graphical Analysis of 18F-Fluoromethylcholine (FCho), 18F-Fluoroethyltyrosine (FET) and 18F-Fluorodeoxyglucose (FDG) PET for the Fiscrimination between High-Grade Glioma and Radiation Necrosis in Rats.

Authors:  Julie Bolcaen; Kelly Lybaert; Lieselotte Moerman; Benedicte Descamps; Karel Deblaere; Tom Boterberg; Jean-Pierre Kalala; Caroline Van den Broecke; Filip De Vos; Christian Vanhove; Ingeborg Goethals
Journal:  PLoS One       Date:  2016-08-25       Impact factor: 3.240

8.  FDG kinetic modeling in small rodent brain PET: optimization of data acquisition and analysis.

Authors:  Malte F Alf; Marianne I Martić-Kehl; Roger Schibli; Stefanie D Krämer
Journal:  EJNMMI Res       Date:  2013-08-06       Impact factor: 3.138

9.  Development and performance test of an online blood sampling system for determination of the arterial input function in rats.

Authors:  Friedrich Roehrbacher; Jens P Bankstahl; Marion Bankstahl; Thomas Wanek; Johann Stanek; Michael Sauberer; Julia Muellauer; Thales Schroettner; Oliver Langer; Claudia Kuntner
Journal:  EJNMMI Phys       Date:  2015-01-14

10.  Comparison between kinetic modelling and graphical analysis for the quantification of [18F]fluoromethylcholine uptake in mice.

Authors:  Dominique Slaets; Filip De Vos
Journal:  EJNMMI Res       Date:  2013-09-14       Impact factor: 3.138

  10 in total

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