journal article·2025-12-22Open access

Understanding the Compatibility of Fluoride-Based Radiopharmaceutical Reaction Solutions and PDMS

Mark Mc Veigh, Charles Frech, Mai Lin, Robert Ta, H. Charles Manning, Leon M. Bellan

Abstract

High Resolution Image Download MS PowerPoint Slide Microfluidic devices offer unique and exciting benefits when applied to radiopharmaceutical manufacturing, and these platforms are now starting to be integrated into commercial products. The field has strayed away from the use of polydimethylsiloxane (PDMS), the most common microfluidic device material, due to its suspected incompatibility with 18 F, the most commonly used radionuclide. However, existing literature provides conflicting conclusions as to the existence and extent of this incompatibility. In this study, we use several analytical instruments to uncover the underlying interaction between fluoride and PDMS. SEM imaging and profilometry confirm the reactive relationship between the two materials and suggest that this interaction only occurs when the reaction solution is fully evaporated and crystallized salts are in contact with PDMS. Furthermore, GC-MS identifies fluoride-containing volatile species that can account for loss of fluoride in previous studies and additionally reveals an incompatibility between PDMS and K 2 CO 3 (a commonly used component of radiofluorination reaction solutions). These results confirm the need for microfluidic radiofluorination devices to avoid the use of PDMS in most contexts but may allow for inexpensive design and testing of liquid state operations (such as concentration, purification, and mixing) using the material.
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Research context

OpenAlex topics: Microfluidic and Capillary Electrophoresis Applications · Innovative Microfluidic and Catalytic Techniques Innovation · Fluorine in Organic Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Interdisciplinary Materials Science

Vanderbilt University

Department of Biomedical Engineering

Cyclotron Radiochemistry Facility

The University of Texas MD Anderson Cancer Center

RADIATE R&D Platform

Department of Nuclear Medicine

Department of Mechanical Engineering

Funding

Vanderbilt University · U.S. Department of Health and Human Services · Cancer Prevention and Research Institute of Texas

References (22)

Show source-provided references
1. 10.2967/jnumed.109.06594610.2967/jnumed.109.065946 ↗
2. 10.1139/cjc-2012-033110.1139/cjc-2012-0331 ↗
3. 10.1109/JMEMS.2017.276412110.1109/JMEMS.2017.2764121 ↗
4. 10.1039/C8LC00167G10.1039/C8LC00167G ↗
5. 10.1007/s11307-020-01515-710.1007/s11307-020-01515-7 ↗
6. 10.1038/s41392-024-02041-610.1038/s41392-024-02041-6 ↗
7. 10.1039/D3LC00779K10.1039/D3LC00779K ↗
8. Tseng W.-Y. · 2010 · 2 · 472
9. 10.1002/macp.20150022510.1002/macp.201500225 ↗
10. 10.1016/j.mee.2019.11115710.1016/j.mee.2019.111157 ↗
11. 10.1116/1.146089610.1116/1.1460896 ↗
12. 10.1063/1.496471710.1063/1.4964717 ↗
13. 10.1016/j.snb.2017.07.06310.1016/j.snb.2017.07.063 ↗
14. 10.1007/s10404-019-2276-010.1007/s10404-019-2276-0 ↗
15. Frank C. · J. Nucl. Med. · 2018 · 59 · 67110.2967/jnumed.117.197426 ↗
16. 10.1186/s41181-019-0077-010.1186/s41181-019-0077-0 ↗
17. 10.1016/j.cej.2022.13498310.1016/j.cej.2022.134983 ↗
18. 10.1126/science.89.2304.17610.1126/science.89.2304.176 ↗
19. 10.1186/s41181-021-00143-y10.1186/s41181-021-00143-y ↗
20. 10.1038/s41598-020-72171-810.1038/s41598-020-72171-8 ↗
21. 10.1002/ejic.20210027510.1002/ejic.202100275 ↗
22. 10.1021/acs.langmuir.8b0158010.1021/acs.langmuir.8b01580 ↗