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68Ga-PET : a powerful generator-based alternative to cyclotron-based PET radiopharmaceuticals

机译:68Ga-PET:基于发生器的强大替代基于回旋加速器的PET放射性药物

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摘要

PET (positron emission tomography) is a powerful diagnostic and imaging technique which requires short-lived positron emitting isotopes. The most commonly used are accelerator-produced 11C and 18F. An alternative is the use of metallic positron emitters. Among them 68Ga deserves special attention because of its availability from long-lived 68Ge/68Ga generator systems which render 68Ga radiopharmacy independent of an onsite cyclotron. The coordination chemistry of Ga3+ is dominated by its hard acid character. A variety of mono- and bifunctional chelators have been developed which allow the formation of stable 68 Ga3+ complexes and convenient coupling to biomolecules. 68Ga coupling to small biomolecules is potentially an alternative to 18F- and 11C-based radiopharmacy. In particular, peptides targeting G-protein coupled receptors overexpressed on human tumour cells have shown preclinically and clinically high and specific tumour uptake. Kit-formulated precursors along with the generator may be provided, similar to the 99Mo/99mTc-based radiopharmacy, still the mainstay of nuclear medicine.
机译:PET(正电子发射断层扫描)是一种功能强大的诊断和成像技术,需要短寿命的正电子发射同位素。最常用的是加速器生产的11C和18F。一种替代方法是使用金属正电子发射器。其中68Ga值得特别关注,因为它具有使用寿命长的68Ge / 68Ga发生器系统,该系统使68Ga放射性药物独立于现场回旋加速器。 Ga3 +的配位化学主要由其硬酸特性决定。已经开发了多种单官能和双官能螯合剂,其允许形成稳定的68 Ga3 +复合物并方便地与生物分子偶联。 68Ga与小生物分子的偶联可能是基于18F和11C的放射性药物的替代方法。特别地,在人肿瘤细胞上过表达的靶向G蛋白偶联受体的肽已显示出临床前和临床上高和特异性的肿瘤摄取。与基于99Mo / 99mTc的放射性药物(仍是核医学的主体)类似,可以提供试剂盒形式的前体以及发生器。

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