| Microfluidic Radiometal Labeling Systems for Biomolecules | |
| Reichert, D E ; Kenis, P J. A. | |
| 关键词: radiometals; microfluidics; biomolecules; | |
| DOI : 10.2172/1032377 RP-ID : DOE/ER/64682-1 PID : OSTI ID: 1032377 |
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| 学科分类:放射科、核医学、医学影像 | |
| 美国|英语 | |
| 来源: SciTech Connect | |
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【 摘 要 】
In a typical labeling procedure with radiometals, such as Cu-64 and Ga-68; a very large (~ 100-fold) excess of the non-radioactive reactant (precursor) is used to promote rapid and efficient incorporation of the radioisotope into the PET imaging agent. In order to achieve high specific activities, careful control of reaction conditions and extensive chromatographic purifications are required in order to separate the labeled compounds from the cold precursors. Here we propose a microfluidic approach to overcome these problems, and achieve high specific activities in a more convenient, semi-automated fashion and faster time frame. Microfluidic reactors, consisting of a network of micron-sized channels (typical dimensions in the range 10 - 300??m), filters, separation columns, electrodes and reaction loops/chambers etched onto a solid substrate, are now emerging as an extremely useful technology for the intensification and miniaturization of chemical processes. The ability to manipulate, process and analyze reagent concentrations and reaction interfaces in both space and time within the channel network of a microreactor provides the fine level of reaction control that is desirable in PET radiochemistry practice. These factors can bring radiometal labeling, specifically the preparation of radio-labeled biomolecules such as antibodies, much closer to their theoretical maximum specific activities.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201704210000069LZ | 636KB |
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