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A trial study of leukocyte labeling with stabilized Tc-99m D,L-HMPAO by methylene blue and sodium phosphate buffer

  • C. H. Kao*
  • , W. T. Huang
  • , S. P. Wey
  • , S. P. Changlai
  • , K. K. Liao
  • , C. S. Tsai
  • *Corresponding author for this work
  • Veterans General Hospital-Taichung Taiwan
  • National Tsing Hua University
  • Chung Shan Medical University

Research output: Contribution to journal › Journal Article › peer-review

1 Scopus citations

Abstract

We attempted to label leukocytes with stabilized Tc-99m D,L-HMPAO by methylene blue and sodium phosphate buffer (S-HMPAO). Methods: The results were compared with unstabilized Tc-99m D,L-HMPAO (U-HMPAO). U-HMPAO was obtained by reconstituting a commercial vial of D,L-HMPAO. Stabilization of the kit was performed by the addition of methylene blue. The leukocytes were labeled using a modified published method. The test samples of S-HMPAO and U- HMPAO were prepared immediately, and stood for 0.5, 1, 2, 4, and 6 h, respectively, at room temperature before analysis. Results: In comparison with U-HMPAO: (1) the radiochemical purity of S-HMPAO was higher; (2) the labeling efficiencies of S-HMPAO labeled leukocytes were higher and consistent; (3) the viability of S-HMPAO labeled leukocytes was as high as the viability of U-HMPAO labeled leukocytes at any time; and (4) the percentages of disintegrated from S-HMPAO labeled leukocytes in plasma were lower. Conclusion: S-HMPAO is more stable than U-HMPAO and can provide higher leukocyte labeling efficiency. S-HMPAO, therefore, has the potential to replace U-HMPAO as a leukocyte-labeling agent.

Original languageEnglish
Pages (from-to)513-519
Number of pages7
JournalApplied Radiation and Isotopes
Volume50
Issue number3
DOIs
StatePublished - 03 1999

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