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聚乙二醇 3350(PEG 3350)作为一种实用载体,可快速配制 PARPi-FL 制剂以供临床使用。

Polyethylene Glycol 3350 (PEG 3350) as a Practical Vehicle for Rapid Reconstitution of PARPi-FL Formulations for Clinical Use.

机构信息

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Department of Otorhinolaryngology and Head and Neck Surgery, Federal University of São Paulo, São Paulo, SP, Brazil.

出版信息

Mol Imaging Biol. 2023 Apr;25(2):294-302. doi: 10.1007/s11307-022-01756-8. Epub 2022 Jul 26.

Abstract

PARPi-FL is a molecularly specific fluorescent agent that targets poly ADP-ribose polymerase 1, a DNA repair enzyme overexpressed in the nuclei of tumor cells. This imaging agent is being investigated in a clinical trial (NCT03085147) for the detection of oral cancer. The PARPi-FL mouthwash formulation currently being used in the phase I/II clinical trial comprises 1,000 nM of PARPi-FL dissolved first in 4.5 ml of polyethylene glycol (PEG) 300 and then in 9.5 ml of water. This formulation requires a 2-step process that can be cumbersome for routine clinical use. To minimize errors and simplify the formulation process, we have developed a new one-step formulation, which requires only the direct addition of water into a vial containing a mixture of the PARPi-FL and PEG 3350, which is also a powder. In a series of analytical and preclinical studies, we demonstrate that the new formulation of PARPi-FL is stable over 365 days, sustains its characteristics, and performs similar to the previous formulation. Moving forward, the new formulation of the PARPi-FL will be used for patients accrued in the phase II clinical trial.

摘要

PARPi-FL 是一种分子特异性荧光试剂,靶向聚 ADP-核糖聚合酶 1(PARP1),一种在肿瘤细胞核中过度表达的 DNA 修复酶。这种成像剂正在一项临床试验(NCT03085147)中进行研究,用于检测口腔癌。目前在 I/II 期临床试验中使用的 PARPi-FL 漱口水配方包含 1000 nM 的 PARPi-FL,首先溶解在 4.5 ml 的聚乙二醇(PEG)300 中,然后溶解在 9.5 ml 的水中。这种配方需要两步过程,对于常规临床使用可能很麻烦。为了最大限度地减少错误并简化配方过程,我们开发了一种新的一步式配方,只需将水直接添加到含有 PARPi-FL 和 PEG 3350 混合物的小瓶中即可,PEG 3350 也是一种粉末。在一系列分析和临床前研究中,我们证明了新配方的 PARPi-FL 在 365 天内稳定,保持其特性,并与以前的配方性能相似。未来,PARPi-FL 的新配方将用于在 II 期临床试验中入组的患者。

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