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99mTc-MAG3的放射性药代动力学、肾清除率及剂量学

Radiopharmacokinetics, renal clearance and dosimetry of 99mTc-MAG3.

作者信息

Arteaga de Murphy C, Molina-Trinidad E, Meléndez-Alafort L, Ferro-Flores G, Reyes-Herrera L, Sepúlveda-Méndez J, Sandoval-Guzmán B, Hoyo-Vadillo C

机构信息

Departamento de Medicina Nuclear y Clínica de Tiroides, Instituto Nacional de Nutrición (INNSZ), México, D.F.

出版信息

Arch Med Res. 1999 Jan-Feb;30(1):49-54. doi: 10.1016/s0188-0128(98)00004-9.

Abstract

BACKGROUND

Technetium-99m-mercaptoacetyltriglycine (99mTc-MAG3) is a radiopharmaceutical for tubular function and can be prepared with 99m-technetium and the ligand Bz-MAG3 (Instituto Nacional de Investigaciones Nucleares, Mexico City). No radiopharmacokinetic parameters have been found for the healthy adult Mexican population with 99mTc-MAG3, prepared with the nationally produced or imported Bz-MAG3 kit.

METHODS

The radiopharmacokinetic parameters and the clearance of 99mTc-MAG3 in seven healthy Mexican volunteers were determined by the single- and multi-sample methods. Computer programs were used for the calculations.

RESULTS

Using several plasma samples from 0-43 min and the BIEXP program, it was shown that 99mTc-MAG3 follows a two-compartment model of distribution, with an apparent volume in the central compartment Vdcc = 3.8 + 0.7 l, a volume of distribution at steady state Vdss = 6.7 + 1.0 l, T1/2 alpha = 0.07 + 0.02 h-1, T1/2 beta = 0.49 + 0.15 h-1, mean residence time MRT = 0.60 + 0.17 h and clearance = 208 + 57 (ml/min)/1.73 m2. In comparison, the clearance value with a single sample drawn 43 min post-injection and calculated with Tauxe's formula was 193 +/- 59 (ml/min)/m2.

CONCLUSIONS

The 15 ml difference between the two methods is neither statistically different (p = 0.11) nor important for routine clinical studies. The single-sample method is recommended because it is reliable and can be done at the same time that the dynamic renal scan is acquired. Estimated absorbed radiation dose was calculated for several organs.

摘要

背景

锝-99m-巯基乙酰三甘氨酸(99mTc-MAG3)是一种用于评估肾小管功能的放射性药物,可由99m锝和配体Bz-MAG3制备(墨西哥城国家核研究所)。对于使用国产或进口Bz-MAG3试剂盒制备的99mTc-MAG3,尚未发现健康成年墨西哥人群的放射性药代动力学参数。

方法

通过单样本和多样本方法测定了7名健康墨西哥志愿者体内99mTc-MAG3的放射性药代动力学参数和清除率。使用计算机程序进行计算。

结果

利用0至43分钟内的多个血浆样本和BIEXP程序,结果显示99mTc-MAG3遵循二室分布模型,中央室的表观容积Vdcc = 3.8 + 0.7升,稳态分布容积Vdss = 6.7 + 1.0升,α半衰期T1/2α = 0.07 + 0.02小时-1,β半衰期T1/2β = 0.49 + 0.15小时-1,平均驻留时间MRT = 0.60 + 0.17小时,清除率 = 208 + 57(毫升/分钟)/1.73平方米。相比之下,注射后43分钟采集单个样本并用陶克斯公式计算的清除率值为193 +/- 59(毫升/分钟)/平方米。

结论

两种方法之间15毫升的差异在统计学上无显著差异(p = 0.11),对常规临床研究也无重要影响。推荐单样本方法,因为它可靠且可在进行动态肾扫描的同时完成。计算了多个器官的估计吸收辐射剂量。

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