一种在鲎试剂凝胶凝块试验中克服由于过量阳离子和放射性药物黏性引起的假阳性反应的方法。

Arpit Mitra, Sangita Lad, Sudeep Sahu, Savita Kulkarni
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引用次数: 0

摘要

目的:用细菌内毒素检查法(BET)检测和定量放射性药物(rp)的内毒素,是给药的前提。在用于此目的的两种既定方法(动力学显色试验:KCM和凝胶凝块细菌内毒素试验:GC-BET)中,药典推荐GC-BET来评估由于样品中存在各种成分而在测定过程中显示的干扰。在本研究中,研究了用于肽受体放射性核素治疗(PRRT)的[177Lu]Lu-DOTATATE中阳离子过量的影响,并制定了一种方案来否定所观察到的增强。此外,还标准化了对极粘性[131I]I-Lipiodol进行GC-BET的方案。方法:以LRW为稀释剂,以最大有效稀释度(MVD)对[177Lu]Lu-DOTATATE和[131I]I-Lipiodol进行GC-BET。为了消除在[177Lu]Lu-DOTATATE中观察到的假阳性,加入了不同浓度的氯化钙(CaCl2),并评估了最初观察到的干扰的逆转。为了克服对[131I]I-Lipiodol进行GC-BET的困难,对方案进行了各种修改,如不同转速和时间间隔的轨道涡。在MVD下也对研究的rp进行KCM测定。结果:在MVD, [177Lu]Lu-DOTATATE在GC-BET中呈假阳性。然而,用于标记[177Lu]Lu-DOTATATE的所有单个试剂均未出现任何假阳性。最后,在添加2mM CaCl2(终浓度)的情况下进行检测,可以消除假阳性。此外,由于[131I]I-Lipiodol的粘度,通过在3000 rpm下旋转5分钟的轨道涡流解决了GC-BET的复杂性。结论:我们的研究证明,由于过量M3+离子的存在,GC-BET中[177Lu]Lu-DOTATATE出现假阳性。此外,我们的研究首次展示了通过使用修改的协议和假设增强背后的原因来否定这些假阳性结果的方法。此外,我们的研究首次证明了像[131I]I-Lipiodol这样的粘性RPs的简单旋涡步骤可以解决由于RPs的粘性而在进行GC-BET时遇到的问题。
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A method to prevail false positive responses due to excess cations and viscous nature of Radiopharmaceuticals in Limulus Amebocyte Lysate Gel Clot test.

Objectives: Bacterial endotoxin test (BET) for detection and quantification of endotoxin in radiopharmaceuticals (RPs), used for therapy or diagnosis, is prerequisite to administration in patients. Out of the two established methods used for this purpose (Kinetic Chromogenic Assay: KCM and Gel Clot Bacterial Endotoxin Test: GC-BET), GC-BET is recommended by pharmacopeias to evaluate the interferences exhibited during the assay due to presence of various ingredients in samples. In the present study, the influence of excess of cations in [177Lu]Lu-DOTATATE, used for Peptide Receptor Radionuclide Therapy (PRRT), were studied and a protocol to negate the enhancement observed was developed. Additionally, a protocol for carrying out GC-BET for extremely viscous [131I]I-Lipiodol was standardized.

Methods: GC-BET was performed for [177Lu]Lu-DOTATATE and [131I]I-Lipiodol at maximum valid dilution (MVD), using LRW as a diluent. To negate the false positivity observed in case of [177Lu]Lu-DOTATATE, various concentrations of calcium chloride (CaCl2) were added and evaluated for the reversal of the interference observed initially. To prevail the difficulty in performing GC-BET for [131I]I-Lipiodol various modification in the protocols like orbital vortexing at different rpm and time intervals were performed. KCM assays were also performed for studied RPs at MVD.

Results: It was observed that at MVD, [177Lu]Lu-DOTATATE exhibited false positivity in GC-BET. However, all the individual reagents used in labeling of [177Lu]Lu-DOTATATE did not show any false positivity. Finally, performing the assay with an addition of 2mM CaCl2 (final concentration) nullified the false positivity. Further, intricacy in performing GC-BET for [131I]I-Lipiodol due to its viscosity was resolved by orbital vortexing at 3000 rpm for 5 minutes.

Conclusions: Our study proved that false positivity was observed in GC-BET for [177Lu]Lu-DOTATATE due to the presence excess M3+ ions. Further, our study is the first of its kind which demonstrated methods for negating these false positive results by using modified protocol and hypothesizing the reason behind the enhancement. Additionally, ours is the first study which proved that a simple step of vortexing the viscous RPs like [131I]I-Lipiodol can resolved the problems encountered during performing GC-BET due to viscosity of RPs.

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来源期刊
Asia Oceania Journal of Nuclear Medicine and Biology
Asia Oceania Journal of Nuclear Medicine and Biology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.80
自引率
0.00%
发文量
28
审稿时长
12 weeks
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