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Electrochemical separation and purification of yttrium-86

机译:钇86的电化学分离与纯化

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摘要

For quantitative determination of in vivo dosimetry of Y-90-labeled radiotherapeuticals by means of PET, the positron emitting analogue yttrium-86 was produced at a low energy ("medical") cyclotron via the known Sr-86(p, n)Y-86 reaction. Using 200 mg of (SrCO3)-Sr-86 (enrichment 95.6%) and protons of 15.1 MeV energy, average yields of Y-86 of 48 +/- 8 MBq/ muAh were produced. After dissolution of 16 SrCO3 in 3 ml of 0.6 N HNO3, Y-86 was deposited in a simple and highly efficient electrochemical two-step procedure onto a platinum cathode at 450 mA (= 20 mA/cm(2)). The isotope was finally removed from the electrode by 100-300 mul of 0.5-1.0N HCl or 0.3-0.6N HNO3 resulting in an overall recovery of 88 +/- 6% (corrected for decay). Up to 1 GBq of Y-86 with high radionuclidic and radiochemical purity were obtained after a 2.5 h irradiation and a radiochemical separation time of 2 h. An lCP/AES analysis of the separated fraction showed a very small amount of strontium (< 0. 1 ppm). The chemical purity of Y-86, essential for efficient labeling, was successfully demonstrated by means of complex formation with DOTA and a DOTA-conjugated peptide, exhibiting labeling yields higher than 98%. [References: 13]
机译:为了通过PET定量确定Y-90标记的放射治疗剂的体内剂量,通过已知的Sr-86(p,n)Y在低能(“医学”)回旋加速器中产生了发射正电子的类似物钇-86。 -86反应。使用200 mg(SrCO3)-Sr-86(富集95.6%)和质子为15.1 MeV的能量,可以得到48-+ /-8 MBq / muAh的Y-86平均产量。将16 SrCO3溶解在3 ml的0.6 N HNO3中后,Y-86以简单高效的电化学两步程序以450 mA(= 20 mA / cm(2))沉积在铂阴极上。最后用100-300 mul 0.5-1.0N HCl或0.3-0.6N HNO3从电极上除去同位素,从而使总回收率达到88 +/- 6%(已校正衰减)。经过2.5 h的辐射和2 h的放射化学分离时间,获得了高达1 GBq的具有高放射性核素和放射化学纯度的Y-86。分离出的馏分的LCP / AES分析显示出非常少量的锶(<0. 1 ppm)。 Y-86的化学纯度,对于有效标记至关重要,已通过与DOTA和DOTA缀合肽的复合物形成成功证明,其标记收率高于98%。 [参考:13]

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