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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Coupling a gamma-ray detector with asymmetrical flow field flow fractionation (AF4): Application to a drug-delivery system for alpha-therapy
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Coupling a gamma-ray detector with asymmetrical flow field flow fractionation (AF4): Application to a drug-delivery system for alpha-therapy

机译:耦合具有不对称流场流量分馏(AF4)的伽马射线检测器:应用于α-治疗的药物输送系统

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Alpha-particle-emitting radionuclides have been the subject of considerable investigation as cancer therapeutics, since they have the advantages of high potency and specificity. Among alpha-emitting radionuclides that are medically relevant and currently available, the lead-212/bismuth-212 radionuclide pair could constitute an in vivo generator. Considering its short half-life (T-1/2 = 60.6 min), Bi-212 can only be delivered using labelled carrier molecules that would rapidly accumulate in the target tumor. To expand the range of applications, an interesting method is to use its longer half-life parent Pb-212 (T-1/2 = 10.6h) that decays to Bi-212. The challenge consists in keeping Bi-212 bound to the vector after the Pb-212 decay. Preclinical and clinical studies have shown that a variety of vectors may be used to target alpha-emitting radionuclides to cancer cells. Nanoparticles, notably liposomes, allow combined targeting options, achieving high specific activities, easier combination of imaging and therapy and development of multimodality therapeutic agents (e.g., radionuclide therapy plus chemotherapy). The aim of this work consists in assessing the in vitro stability of Pb-212/Bi-212 encapsulation in the liposomes. Indeed, the release of the radionuclide from the carrier molecules might causes toxicity to normal tissues. To reach this goal, Asymmetrical Flow Field-Flow Fractionation (AF4) coupled with a Multi-Angle Light Scattering detector (MALS) was used and coupling with a gamma (gamma) ray detector was developed. AF4-MALS-gamma was shown to be a powerful tool for monitoring the liposome size together with the incorporation of the high energy alpha emitter. This was successfully extended to assess the stability of Bi-212-radiolabelled liposomes in serum showing that more than 85% of Pb-212/Bi-212 is retained after 24 h of incubation at 37 degrees C. (C) 2018 Elsevier B.V. All rights reserved.
机译:α-颗粒发光的放射性核素是作为癌症治疗的大量调查的主题,因为它们具有高效力和特异性的优点。在具有医学相关和目前可用的α发射放射性核素中,引线-212 / Bis5-212放射性核素对可以构成体内发生器。考虑到其短半衰期(T-1/2 = 60.6分钟),Bi-212只能使用标记的载体分子递送,所述载体分子将迅速积聚在靶肿瘤中。为了扩展应用范围,有趣的方法是使用其衰减到Bi-212的较长半衰期的父PB-212(T-1/2 = 10.6h)。挑战在于在PB-212衰减之后保持与向量的BI-212保持束缚。临床前和临床研究表明,各种载体可用于将α-发射的放射性核素靶向癌细胞。纳米粒子,特别是脂质体,允许组合靶向选项,实现高特异性活动,更容易成像和治疗和多层治疗剂的开发(例如,放射性核素治疗加上化疗)。这项工作的目的在于评估脂质体中PB-212 / BI-212包封的体外稳定性。实际上,来自载体分子的放射性核素的释放可能导致正常组织的毒性。为了达到该目标,使用与多角度光散射检测器(MAL)耦合的不对称流场 - 流分馏(AF4)并开发与伽马(伽马)射线检测器耦合。 AF4-MALS-GAMMA被证明是一种强大的工具,用于将脂质体大小与掺入高能α发射器一起监测。成功扩展以评估血清中Bi-212-放射性标记脂质体的稳定性,显示出在37℃的34℃的孵育24小时后,超过85%的Pb-212 / Bi-212保留。(c)2018 Elsevier BV所有权利保留。

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