DOI QR코드

DOI QR Code

18FDG Synthesis and Supply: a Journey from Existing Centralized to Future Decentralized Models

  • uz Zaman, Maseeh (Section of Nuclear Medicine, Department of Radiology, Aga Khan University Hospital) ;
  • Fatima, Nosheen (Department of Nuclear Cardiology, Visiting Faculty, Karachi Institute of Heart Disease) ;
  • Sajjad, Zafar (Section of Nuclear Medicine, Department of Radiology, Aga Khan University Hospital) ;
  • Zaman, Unaiza (Students MBBS, Dow Medical College, Dow University of Health Sciences) ;
  • Tahseen, Rabia (Students MBBS, Dow Medical College, Dow University of Health Sciences) ;
  • Zaman, Areeba (Students MBBS, Dow Medical College, Dow University of Health Sciences)
  • Published : 2015.01.06

Abstract

Positron emission tomography (PET) as the functional component of current hybrid imaging (like PET/CT or PET/MRI) seems to dominate the horizon of medical imaging in coming decades. $^{18}$Flourodeoxyglucose ($^{18}FDG$) is the most commonly used probe in oncology and also in cardiology and neurology around the globe. However, the major capital cost and exorbitant running expenditure of low to medium energy cyclotrons (about 20 MeV) and radiochemistry units are the seminal reasons of low number of cyclotrons but mushroom growth pattern of PET scanners. This fact and longer half-life of $^{18}F$ (110 minutes) have paved the path of a centralized model in which $^{18}FDG$ is produced by commercial PET radiopharmacies and the finished product (multi-dose vial with tungsten shielding) is dispensed to customers having only PET scanners. This indeed reduced the cost but has limitations of dependence upon timely arrival of daily shipments as delay caused by any reason results in cancellation or rescheduling of the PET procedures. In recent years, industry and academia have taken a step forward by producing low energy, table top cyclotrons with compact and automated radiochemistry units (Lab-on-Chip). This decentralized strategy enables the users to produce on-demand doses of PET probe themselves at reasonably low cost using an automated and user-friendly technology. This technological development would indeed provide a real impetus to the availability of complete set up of PET based molecular imaging at an affordable cost to the developing countries.

Keywords

References

  1. Alavi A, Lakhani P, Mavi A, Kung JW, Zhuang H (2004). PET: A revolution in medical imaging. Radiol Clin N Am, 42, 983-1001. https://doi.org/10.1016/j.rcl.2004.08.012
  2. ABT Molecular Imaging, Inc., Louisville, Tennessee, USA, http://advancedbiomarker.com/
  3. Avril N (2004). GLUT1 Expression in tissue and 18F-FDG Uptake. J Nucl Med, 45, 930-32.
  4. Brown RS, Goodman TM, Zasadny KR, Greenson JK, Wahl RL (2002). Expression of hexokinase II and Glut-1 in untreated human breast cancer. Nuclear Med Biol, 29, 443-53. https://doi.org/10.1016/S0969-8051(02)00288-3
  5. Casella V, Ido T, Wolf AP, et al (1980). Anhydrous F-18 labeled elemental fluorine for radiopharmaceutical preparation. J Nucl Med, 21, 750-57.
  6. Chung JH, Cho KJ, Lee SS, et al (2004). Overexpression of Glut1 in lymphoid follicles correlates with false-positive 18F-FDG PET results in lung cancer staging. J Nucl Med, 45, 999-1003.
  7. Delbeke D, Coleman RE, Guiberteau MJ, et al (2006). Procedure guideline for tumor imaging with 18F-FDG PET/CT 1.0. J Nucl Med, 47, 885-95.
  8. Directory of cyclotrons used for radionuclide production in member states, 2006 Update. IAEA Tech. Rep. IAEADCRP/2006 (Vienna, 2006).
  9. Fowler JS, Ido T (2002). Initial and subsequent approach for the synthesis of 18FDG. Semin Nucl Med, 32, 6-12. https://doi.org/10.1053/snuc.2002.29270
  10. Fukuchi K, Ohta H, Matsumura K, Ishida Y (2007). Benign variations and incidental abnormalities of myocardial FDG uptake in the fasting state as encountered during routine oncology positron emission tomography studies. Br J Radiol, 80, 3-11. https://doi.org/10.1259/bjr/92105597
  11. Gallagher BM, Fowler JS, Gutterson NI, et al (1978). Metabolic trapping as a principle of radiopharmaceutical design: some factors responsible for the biodistribution of [18F] 2-deoxy-2-fl uoro-D-glucose. J Nucl Med, 19, 1154-61.
  12. Gambhir SS, Czernin J, Schwimmer J, et al (2001). A tabulated summary of the FDG PET literature. J Nucl Med, 42, 1-93.
  13. Ghotbi N, Iwanaga M, Ohtsuru A, Ogawa Y, Yamashita S (2007). Cancer screening with whole body PET/CT for healthy asymptomatic people in Japan: Re-evaluation of its test validity and radiation exposure. Asian Pac J Cancer Prev, 93, 93-7.
  14. "Google Scholar "Abass Alavi". Retrieved 2013-06-11.
  15. Guidance on facility design and production of-publications. www-pub.iaea.org/MTCD/Publications/PDF/Pub1515_web.pdf.
  16. Hamacher K, Coenen HH, Stocklin G (1986). Efficient stereospecific synthesis of NCA 2-[18F]-fluoro-2-deoxy-D-glucose using aminopolyether supported nucleophilic substitution. J Nucl Med, 27, 235-38.
  17. Ido T, Wan CN, Casella V, et al (1978). Labeled 2-deoxy-Dglucose analogs: 18F-labeled 2-deoxy-2-fluoro-D-glucose, 2-deoxy-2-fluoro-D-mannose and 14C-2-deoxy-2-fluoro-Dglucose". J Labeled Compounds Radiopharm, 24, 174-83
  18. Lawrence EO, Edlefson NE (1930). On the production of high speed protons. Science, LXXII, 376-7.
  19. Liu NB, Zhu L, Li MH, et al (2013). Diagnostic value of 18FDG PET/CT in comparison to bone scintigraphy, CT and 8FDG PET for detection of bone metastases. Asian Pac J Cancer Prev, 14, 3647-52. https://doi.org/10.7314/APJCP.2013.14.6.3647
  20. Mochizuki T, Tsukamoto E, Kuge Y, et al (2001). FDG uptake and glucose transporter subtype expressions in experimental tumor and inflammation models. J Nucl Med, 42, 1551-5.
  21. Radiopharmaceuticals UECo. Fludeoxyglucose F18 (Systemic). USP-DI: Drug Information for the health care professional. Vol I. greenwood village, Colorado: Thomson MICROMEDEX; 2003:electronic monograph.
  22. Schlyer DJ (2004). PET tracers and radiochemistry. Ann Acad Med Singapore, 33, 146-54.
  23. Schmor P (2011). Review of cyclotrons for the production of radioactive isotopes for medical and industrial applications. Reviews Accelerator Science Technology, 4, 103-16. https://doi.org/10.1142/S1793626811000574
  24. Tateishi U, Yamaguchi U, Seki K, Terauchi T, Arai Y, Hasegawa T (2006). Glut-1 expression and enhanced glucose metabolism are associated with tumour grade in bone and soft tissue sarcomas: a prospective evaluation by 18F-fluorodeoxyglucose positron emission tomography. Eurp Jourl Nucl Med Mol Img, 33, 683-91. https://doi.org/10.1007/s00259-005-0044-8

Cited by

  1. “Click Chip” Conjugation of Bifunctional Chelators to Biomolecules vol.28, pp.4, 2017, https://doi.org/10.1021/acs.bioconjchem.6b00703
  2. Design considerations for a pulse line ion accelerator (PLIA)-based PET isotope generator vol.45, pp.8, 2018, https://doi.org/10.1002/mp.13050