加速器核素68Ge的分离纯化工艺研究

Study on Separation and Purification Process of Cyclotron-produced Nuclide 68Ge

  • 摘要: 锗-68(68Ge)是发生器制备正电子核素镓-68(68Ga)的关键前体核素,实现其规模化生产对于68Ga标记药物的临床应用具有重大意义。本研究建立了一种从加速器辐照Ga-Ni合金靶中高效分离纯化68Ge的方法,通过羟肟酸树脂与Sephadex G-25树脂联用的双柱分离纯化方式,获得高核纯度和高化学纯度的68Ge核素产品。采用硫酸-过氧化氢在95 ℃下溶解Ga-Ni合金靶,系统探究了羟肟酸树脂与Sephadex G-25树脂对Ge的吸附行为,并优化了淋洗和解吸条件。在此基础上,利用自主设计的自动化分离装置进一步优化双柱分离纯化工艺,并通过68Ge分离热实验验证该工艺路线。双柱分离纯化实验结果表明,在优选的淋洗条件下,绝大部分Ga、Ni、Co、Zn、Fe和Cu等杂质元素可在羟肟酸树脂分离阶段被去除,而残留的少量杂质元素可在Sephadex G-25树脂分离阶段被进一步纯化。经热实验验证,68Ge平均回收率大于90%,68Ge核纯度大于99.9%,高活度产品中主要杂质元素含量均低于5.5 μg/GBq。本研究建立的双柱分离工艺稳定、高效,可用于68Ge的规模化纯化制备。

     

    Abstract: Germanium-68 (68Ge) is a critical precursor for the 68Ge/68Ga generator, which produces the positron-emitting radionuclide gallium-68 (68Ga). The large-scale production of 68Ge is of great significance for the clinical application of 68Ga-labeled radiopharmaceuticals. A primary production route involves the proton irradiation of solid Ga-Ni alloy target. However, the subsequent target dissolution solution contains not only the desired 68Ge but also high concentrations of stable metal impurities (e.g., Ga, Ni, Co, Fe, Cu, Zn) from the target matrix and co-produced radionuclidic impurities (e.g., 65Zn, 56,57,58Co, 67Ga), necessitating highly efficient and selective separation processes to meet application requirements. This study developed and validated a novel double-column chromatographic separation method that combines hydroxamate resin and Sephadex G-25 resin for the efficient separation and purification of 68Ge from cyclotron-irradiated Ga-Ni alloy target. First, the Ga-Ni alloy target was dissolved using a sulfuric acid-hydrogen peroxide mixture system at 95 ℃. The resulting solution was then processed through the primary hydroxamate resin. Under optimized high-acidity conditions, the resin exhibited exceptional selectivity, strongly adsorbing 68Ge while allowing the bulk of co-existing metal impurities (Ga, Ni, Co, Zn, Fe, Cu) to be washed away. The adsorbed 68Ge was efficiently recovered by elution with a sodium citrate solution. This intermediate product was subsequently transferred to a secondary Sephadex G-25 column for final purification. Under an alkaline sodium citrate system (pH=12.5), residual cationic impurities were effectively removed, and the purified 68Ge was ultimately recovered in a low-concentration hydrochloric acid solution. The entire chemical workflow, from target dissolution through the double-column chromatographic separation to final product collection, was integrated into a self-designed and custom-built automatic separation apparatus, ensuring reproducibility and operational safety. The adsorption characteristics of germanium on hydroxamate resin and Sephadex G-25 resin were systematically investigated, and the washing and desorption conditions were optimized. The optimized process was then validated through the automated separation tests of 68Ge from irradiated Ga-Ni alloy target. The results of the double-column separation experiments show that under optimized elution conditions, the majority of impurities, including Ga, Ni, Co, Zn, Fe, and Cu, could be effectively removed during the hydroxamate resin separation step, while the residual trace impurities were further purified during the Sephadex G-25 purification step. The results of the 68Ge separation validation tests demonstrate that the process can achieve a 68Ge separation recovery rate exceeding 90%, with a radionuclide purity above 99.9%. Crucially, the contents of key elemental impurities in the high-activity product are all below 5.5 μg/GBq. The developed double-column separation process is stable and efficient, making it suitable for the large-scale purification and preparation of 68Ge.

     

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