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Radiolabelling of glucose-Tyr3-octreotate with 125I and analysis of its metabolism in rats: Comparison with radiolabelled DOTA-Tyr3-octreotate

Publication ,  Journal Article
Petrik, M; Laznickova, A; Laznicek, M; Zalutsky, MR
Published in: Anticancer Research
November 1, 2007

Background: Somatostatin analogues labelled with radiometals or radiohalogens are useful for the imaging and treatment of somatostatin receptor-containing tumours. In this study, the procedures for the radioiodination of glucose-Tyr3-octreotate (gluc-Tyr 3-tate) and radiolabelling of DOTA-Tyr3-octreotate (DOTA-Tyr3-tate) with 111In, 177Lu and 125I were compared and their metabolism in rats was analyzed. The usefulness of high performance liquid chromatography (HPLC) analysis and instant thin-layer chromatography on silica gel (ITLC-SG) for both radiochemical purity determination and analysis of metabolism in urine was investigated. Materials and Methods: For labelling with radiometals, the formation of a complex with the 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) functionality of the peptide was employed. Radioiodination was performed by the chloramime-T method. The radiochemical purity of radiolabelled peptides and the analyses of rat urine were determined by HPLC and/or ITLC-SG methods. Male Wistar rats were used in the elimination studies. Results: DOTA-Tyr3-tate was simply radiolabelled with radiometals with high yield and high radiochemical purity. Stopping of the reaction was a critical step for radioiodination, therefore labelling of gluc-Tyr3-tate and DOTA-Tyr3-tate with 125I was not so simple and the reaction product had to be purified by preparative HPLC analysis. Whereas 111In-DOTA-Tyr3-tate and 177Lu-DOTA-Tyr3-tate were eliminated in rat urine in a practically unchanged form, a significant proportion of metabolites was observed with radioiodinated peptides, particularly at longer time intervals. Conclusion: Labelling of DOTA-Tyr3-tate with radiometals is simple and the radiochemical purity of prepared compounds is very high, while iodination of the peptides demands purification of the product by preparative HPLC. The analysis of rat urine showed that excretion of radioiodinated peptides included a significant proportion of metabolites.

Duke Scholars

Published In

Anticancer Research

ISSN

0250-7005

Publication Date

November 1, 2007

Volume

27

Issue

6 B

Start / End Page

3941 / 3946

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
 

Citation

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Petrik, M., Laznickova, A., Laznicek, M., & Zalutsky, M. R. (2007). Radiolabelling of glucose-Tyr3-octreotate with 125I and analysis of its metabolism in rats: Comparison with radiolabelled DOTA-Tyr3-octreotate. Anticancer Research, 27(6 B), 3941–3946.
Petrik, M., A. Laznickova, M. Laznicek, and M. R. Zalutsky. “Radiolabelling of glucose-Tyr3-octreotate with 125I and analysis of its metabolism in rats: Comparison with radiolabelled DOTA-Tyr3-octreotate.” Anticancer Research 27, no. 6 B (November 1, 2007): 3941–46.
Petrik M, Laznickova A, Laznicek M, Zalutsky MR. Radiolabelling of glucose-Tyr3-octreotate with 125I and analysis of its metabolism in rats: Comparison with radiolabelled DOTA-Tyr3-octreotate. Anticancer Research. 2007 Nov 1;27(6 B):3941–6.
Petrik M, Laznickova A, Laznicek M, Zalutsky MR. Radiolabelling of glucose-Tyr3-octreotate with 125I and analysis of its metabolism in rats: Comparison with radiolabelled DOTA-Tyr3-octreotate. Anticancer Research. 2007 Nov 1;27(6 B):3941–3946.

Published In

Anticancer Research

ISSN

0250-7005

Publication Date

November 1, 2007

Volume

27

Issue

6 B

Start / End Page

3941 / 3946

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis