2017
DOI: 10.1039/c6lc01569g
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Automatic concentration and reformulation of PET tracers via microfluidic membrane distillation

Abstract: Short-lived radiolabeled tracers for positron emission tomography (PET) must be rapidly synthesized, purified, and formulated into injectable solution just prior to imaging. Current radiosynthesizers are generally designed for clinical use, and the HPLC purification and SPE formulation processes often result in a final volume that is too large for preclinical and emerging in vitro applications. Conventional technologies and techniques for reducing this volume tend to be slow, resulting in radioactive decay of … Show more

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Cited by 12 publications
(5 citation statements)
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“…Similarly, an effective evaporation technique concentrated the solution, leading to a rapid concentration of samples containing short-lived radiolabeled tracers. 83 Another option for an evaporative membrane entails the adoption of a dense material, such as PDMS. Microfluidic devices composed of dense material have gas-permeable walls, which permit evaporation through them (i.e., pervaporation).…”
Section: Evaporation Pervaporation and Condensation Of Solutionsmentioning
confidence: 99%
“…Similarly, an effective evaporation technique concentrated the solution, leading to a rapid concentration of samples containing short-lived radiolabeled tracers. 83 Another option for an evaporative membrane entails the adoption of a dense material, such as PDMS. Microfluidic devices composed of dense material have gas-permeable walls, which permit evaporation through them (i.e., pervaporation).…”
Section: Evaporation Pervaporation and Condensation Of Solutionsmentioning
confidence: 99%
“…A final concentration of the product solution could be performed by solid-phase [223] and also by on-chip solid phase extraction [224]. A novel method reported the use of sweeping gas membrane distillation, in order to rapidly perform the concentration and formulation process in a fully automated microfluidic system [225].…”
Section: Microfluidic Technologymentioning
confidence: 99%
“…Ideally, it does not rely on cleaning procedures and aligns with the state-of-the art approach of single-use disposables. To date, efforts in this direction have focused on development of microfluidic approaches for radiopharmaceutical manufacturing (Amaraesekera et al 2013; Audrain 2007; Awasthi et al 2014; Bejot et al 2010; Bouvet et al 2011; Bouvet et al 2012; Bouvet and Wuest 2013; Chen et al 2014; Collier et al 2010, 2017; De Leonardis et al 2010, 2011; Gaja et al 2012; Gillies et al 2006; Lu and Pike 2007; Lu and Pike 2010; Elizarov 2009; Elizarov et al 2010; Fortt and Gee 2013; Kealey et al 2011; Keng et al 2012b; Keng and van Dam 2015; Lee et al 2005; Liow et al 2005; Liu et al 2011; Liu et al 2013; Lu et al 2004, 2009, 2010; Matesic et al 2017; Miller 2009; Miller et al 2010, 2011; Pascali et al 2010, 2011, 2013; Pascali and Salvadori 2016; Rensch et al 2012, 2013; Selivanova et al 2012; Simms et al 2012; Steel et al 2007; Ungersboeck et al 2011, 2012a, 2012b; Voccia et al 2009; Wang et al 2010; Wang et al 2019; Wester et al 2009; Wheeler et al 2010; Yokell et al 2012; Zeng et al 2013), as well as purification/reformulation (Chao et al 2017) and quality control (QC) testing (Ha et al 2017; Taggart et al 2016; Ly et al 2018). While the benefits of microreactors for radiopharmaceutical synthesis have been well documented in this multitude of literature precedent, and they have been used to prepare radiopharmaceuticals for clinical use (Lebedev et al 2013; Liang et al 2014a, 2014b; Rensch et al 2014), there are continuing challenges that have prevented them from commercialization and really transitioning into widespread use to date (Chiu et al 2017).…”
Section: Introductionmentioning
confidence: 99%