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锝-99m 巯基乙酰三甘氨酸试剂盒配方:正常志愿者和肾衰竭患者的初步结果。

Technetium-99m MAG3 kit formulation: preliminary results in normal volunteers and patients with renal failure.

作者信息

Taylor A, Eshima D, Christian P E, Wooten W W, Hansen L, McElvany K

机构信息

Department of Radiology, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

J Nucl Med. 1988 May;29(5):616-22.

PMID:2967353
Abstract

Previous studies have shown that [99mTc]mercaptoacetyltriglycine (MAG3) purified by high performance liquid chromatography (HPLC) is a very promising new renal imaging agent which has characteristics very similar to [131I]orthoiodohippurate. An easily prepared kit formulation has been developed and evaluated in ten normal volunteers and three patients on hemodialysis. The average radiochemical purity was 96.6%. There were no adverse reactions. In the volunteers, the relative uptake +/- 1 s.d. was 49.1% +/- 2.6% for the right kidney and 50.9% +/- 2.6% or the left kidney. Urine activity was 71.4% +/- 6.4% of the injected dose at 30 min and 94.4% +/- 2.2% at 180 min. The 60-min plasma clearance was 340.0 +/- 79.0 ml/min and the volume of distribution was 5.15 +/- 1.1I. Approximately 0.5% of the injected dose was present in the gallbladder at 30-60 min postinjection. Gut activity was not present 30-60 min postinjection but reached 1% of the injected dose by 3 hr. In the hemodialysis patients, approximately 1% of the injected dose was present in the gallbladder and 0.5% in the gut at 30-60 min; gut activity increased to approximately 5% at 3 hr. In summary, results using the kit formulation compare favorably to previously published data using the HPLC purified material. Based on these preliminary results, the kit formulation is expected to have widespread clinical utility.

摘要

先前的研究表明,通过高效液相色谱法(HPLC)纯化的[99mTc]巯基乙酰三甘氨酸(MAG3)是一种非常有前景的新型肾脏显像剂,其特性与[131I]邻碘马尿酸非常相似。现已开发出一种易于制备的试剂盒配方,并在10名正常志愿者和3名血液透析患者中进行了评估。平均放射化学纯度为96.6%。未出现不良反应。在志愿者中,右肾的相对摄取量±1标准差为49.1%±2.6%,左肾为50.9%±2.6%。30分钟时尿液放射性活度为注射剂量的71.4%±6.4%,180分钟时为94.4%±2.2%。60分钟时的血浆清除率为340.0±79.0 ml/min,分布容积为5.15±1.1I。注射后30 - 60分钟,约0.5%的注射剂量存在于胆囊中。注射后30 - 60分钟肠道内无放射性,但到3小时时达到注射剂量的1%。在血液透析患者中,注射后30 - 60分钟,约1%的注射剂量存在于胆囊中,0.5%存在于肠道中;3小时时肠道放射性增加至约5%。总之,使用试剂盒配方的结果与先前发表的使用HPLC纯化材料的数据相比具有优势。基于这些初步结果,该试剂盒配方有望具有广泛的临床应用价值。

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