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On-demand radiosynthesis of N -succinimidyl-4-[ 18 F]fluorobenzoate ([ 18 F]SFB) on an electrowetting-on-dielectric microfluidic chip for 18 F-labeling of protein.

Authors :
Kim HK
Javed MR
Chen S
Zettlitz KA
Collins J
Wu AM
Kim CCJ
Michael van Dam R
Keng PY
Source :
RSC advances [RSC Adv] 2019 Oct 09; Vol. 9 (55), pp. 32175-32183. Date of Electronic Publication: 2019 Oct 09 (Print Publication: 2019).
Publication Year :
2019

Abstract

An all-electronic, droplet-based batch microfluidic device, operated using the electrowetting on dielectric (EWOD) mechanism was developed for on-demand synthesis of N -succinimidyl-4-[ <superscript>18</superscript> F]fluorobenzoate ([ <superscript>18</superscript> F]SFB), the most commonly used <superscript>18</superscript> F-prosthetic group for biomolecule labeling. In order to facilitate the development of peptides, and proteins as new diagnostic and therapeutic agents, we have diversified the compact EWOD microfluidic platform to perform the three-step radiosynthesis of [ <superscript>18</superscript> F]SFB starting from the no carrier added [ <superscript>18</superscript> F]fluoride ion. In this report, we established an optimal microliter droplet reaction condition to obtain reliable yields and synthesized [ <superscript>18</superscript> F]SFB with sufficient radioactivity for subsequent conjugation to the anti-PSCA cys-diabody (A2cDb) and for small animal imaging. The three-step, one-pot radiosynthesis of [ <superscript>18</superscript> F]SFB radiochemistry was adapted to a batch microfluidic platform with a reaction droplet sandwiched between two parallel plates of an EWOD chip, and optimized. Specifically, the ratio of precursor to base, droplet volume, reagent concentration, reaction time, and evaporation time were found be to be critical parameters. [ <superscript>18</superscript> F]SFB was successfully synthesized on the EWOD chip in 39 ± 7% ( n = 4) radiochemical yield in a total synthesis time of ∼120 min ([ <superscript>18</superscript> F]fluoride activation, [ <superscript>18</superscript> F]fluorination, hydrolysis, and coupling reaction, HPLC purification, drying and reformulation). The reformulation and stabilization step for [ <superscript>18</superscript> F]SFB was important to obtain a high protein labeling efficiency of 33.1 ± 12.5% ( n = 3). A small-animal immunoPET pilot study demonstrated that the [ <superscript>18</superscript> F]SFB-PSCA diabody conjugate showed specific uptake in the PSCA-positive human prostate cancer xenograft. The successful development of a compact footprint of the EWOD radiosynthesizer has the potential to empower biologists to produce PET probes of interest themselves in a standard laboratory.<br />Competing Interests: Drs van Dam and Keng are consultants to Sofie Biosciences. The Regents of the University of California have licensed technology to Sofie Biosciences that was invented by Drs van Dam, and Keng, and have taken equity in Sofie Biosciences as part of the licensing transaction.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2046-2069
Volume :
9
Issue :
55
Database :
MEDLINE
Journal :
RSC advances
Publication Type :
Academic Journal
Accession number :
35530758
Full Text :
https://doi.org/10.1039/c9ra06158d