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肝胆动态显像剂的制备与组成。

The preparation and composition of HIDA.

作者信息

Nicholson R W, Herman K J, Shields R A, Testa H J

出版信息

Eur J Nucl Med. 1980 Aug;5(4):313-7. doi: 10.1007/BF00445617.

Abstract

The compositions of four "brands" of Tc-HIDA-dimethyl HIDA (Sorin Biomedica), diethyl HIDA (Solco), diethyl HIDA (The Radiochemical Centre), and para-butyl HIDA (Sorin Biomedica)--were investigated at varying times after their preparation from "instant kits", by using Sephadex gel column chromatography. Up to three peaks of activity were seen in each chromatogram, representing free reduced technetium, the monocomplex, and the biscomplex of Tc-HIDA respectively. In all cases the free reduced technetium component diminished to reach a plateau at less than 4% of total activity, by 1 h. In both "brands" of diethyl HIDA there was a transformation from the monocomplex to the biscomplex which took about one hour. The rate of this transformation was increased by raising the temperature of incubation, or by agitation during incubation. In the para-butyl HIDA this transformation was again noted, but was incomplete. In the dimethyl HIDA the monocomplex form was not seen. There was no noticeable disintegration of any Tc-HIDA complex up to 6 h. It is suggested that HIDA should be incubated for 1 h after preparation, before use, to achieve a stable composition.

摘要

采用葡聚糖凝胶柱色谱法,对从“即用试剂盒”制备后的不同时间点,四种“品牌”的锝-二甲基HIDA(索林生物医学公司)、二乙基HIDA(索尔科公司)、二乙基HIDA(放射化学中心)和对丁基HIDA(索林生物医学公司)的成分进行了研究。在每个色谱图中可观察到多达三个活性峰,分别代表游离还原锝、锝-二甲基亚氨基二乙酸单络合物和双络合物。在所有情况下,游离还原锝成分在1小时内减少至总活性的4%以下并达到平稳状态。在二乙基HIDA的两个“品牌”中,单络合物向双络合物的转变耗时约1小时。提高孵育温度或在孵育过程中搅拌可加快这种转变的速度。在对丁基HIDA中也观察到了这种转变,但不完全。在二甲基HIDA中未见到单络合物形式。在长达6小时的时间内,未观察到任何锝-二甲基亚氨基二乙酸络合物有明显分解。建议在制备后使用前,将二甲基亚氨基二乙酸孵育1小时,以获得稳定的成分。

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