Chelating Systems for 99mTc/188Re in the Development of Radiolabeled Peptide Pharmaceuticals
- 作者: Bolzati C.1, Carta D.1, Salvarese N.1, Refosco F.1
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- 期: 卷 12, 编号 5 (2012)
- 页面: 428-461
- 栏目: Oncology
- URL: https://kld-journal.fedlab.ru/1871-5206/article/view/694772
- DOI: https://doi.org/10.2174/187152012800617821
- ID: 694772
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Currently, receptor based radiopharmaceuticals have received great attention in molecular imaging and radiotherapy of cancer, and provide a unique tool for target-specific delivery of radionuclides to pathological tissues. In this context, receptor binding peptides represent an attractive class of target vectors for Nuclear Medicine purposes. The rich chemistry of the group 7 elements elaborated in past years, has allowed the development of different procedures for the preparation of radiolabeled peptides in high yield. This, joint to the use of solid-phase peptide synthesis, has opened the possibility to explore new strategies for approaching the design of new class of radiolabeled receptor-targeted peptides, and to create new versatilities in targeting vehicle design e.g. in synthesis of metal-cyclized peptides or of multivalent targeting agents. This review provides an overview on several aspects of the development of new 99mTc/188Re-peptide based target specific radiopharmaceuticals, in particular on the synthetic strategies employed for modifying molecular vectors, and the application of the different metal-cores and/or building block for preparing high specific activity agents.
作者简介
Cristina Bolzati
,
Email: info@benthamscience.net
Davide Carta
,
Email: info@benthamscience.net
Nicola Salvarese
,
Email: info@benthamscience.net
Fiorenzo Refosco
,
Email: info@benthamscience.net
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