Sykes T R, Woo T K, Baum R P, Qi P, Noujaim A A
Biomira Research Inc., Alberta, Canada.
J Nucl Med. 1995 Oct;36(10):1913-22.
Direct radiolabeling methods currently rely on the addition of exogenous chemical reagents to create the necessary binding sites for 99mTc binding to monoclonal antibodies (MAbs). This work describes the use of ultraviolet (UV) light to facilitate photoactivation of MAbs for 99mTc radiolabeling.
The parameters of exposure wavelength and solution composition were investigated to provide a basis for further development. Based on these results, various murine MAbs and a chimeric MAb were photoactivated using a 300-nm (nominal) wavelength, eight-lamp (3.9 W each) photochemical reactor providing exposure for defined time periods. The MAb preparations were stored frozen and subsequently labeled by the addition of pertechnetate. For MAb-170, the photoactivated preparation was compared to a stannous ion reduced preparation by radiochemical (radiolabeling yield, serum stability cysteine challenge), biochemical (SDS-PAGE, IEF, SE-HPLC) and immunochemical (immunoreactivity) assays and biodistribution studies in mice.
Photoactivation produced high radiolabeling yields for all the MAbs studied and MAb-170 produced comparable in vitro quality control profiles and in vivo biodistribution data.
The use of this relatively simple, short and easily controlled photoactivation process for MAbs facilitates facile radiolabeling with 99mTc and provides an alternative to the direct chemical radiolabeling procedures.
目前直接放射性标记方法依赖于添加外源性化学试剂来创建99mTc与单克隆抗体(MAb)结合所需的结合位点。本研究描述了利用紫外线(UV)光促进单克隆抗体的光活化以进行99mTc放射性标记。
研究了曝光波长和溶液组成参数,为进一步开发提供依据。基于这些结果,使用300nm(标称)波长、八灯(每盏3.9W)光化学反应器对各种鼠单克隆抗体和一种嵌合单克隆抗体进行光活化,曝光特定时间段。单克隆抗体制剂冷冻保存,随后通过添加高锝酸盐进行标记。对于单克隆抗体-170,通过放射化学(放射性标记产率、血清稳定性半胱氨酸激发)、生化(SDS-PAGE、IEF、SE-HPLC)和免疫化学(免疫反应性)分析以及小鼠体内生物分布研究,将光活化制剂与亚锡离子还原制剂进行比较。
光活化对所有研究的单克隆抗体都产生了高放射性标记产率,单克隆抗体-170产生了可比的体外质量控制概况和体内生物分布数据。
对单克隆抗体使用这种相对简单、时间短且易于控制的光活化过程便于用99mTc进行放射性标记,并为直接化学放射性标记程序提供了一种替代方法。