Fluoropolymer Functionalization of Organ-on-Chip Platform Increases Detection Sensitivity for Cannabinoids.
Ziqiu TongLars EsserPeter GalettisDavid RuddChristopher D EastonAzadeh NilghazBo PengDouer ZhuHelmut ThissenJennifer H MartinNicolas Hans VoelckerPublished in: Biosensors (2023)
Microfluidic technology is applied across various research areas including organ-on-chip (OOC) systems. The main material used for microfluidics is polydimethylsiloxane (PDMS), a silicone elastomer material that is biocompatible, transparent, and easy to use for OOC systems with well-defined microstructures. However, PDMS-based OOC systems can absorb hydrophobic and small molecules, making it difficult and erroneous to make quantitative analytical assessments for such compounds. In this paper, we explore the use of a synthetic fluoropolymer, poly(4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole- co -tetrafluoroethylene) (Teflon™ AF 2400), with excellent "non-stick" properties to functionalize OOC systems. Cannabinoids, including cannabidiol (CBD), are classes of hydrophobic compounds with a great potential for the treatment of anxiety, depression, pain, and cancer. By using CBD as a testing compound, we examined and systematically quantified CBD absorption into PDMS by means of an LC-MS/MS analysis. In comparison to the unmodified PDMS microchannels, an increase of approximately 30× in the CBD signal was detected with the fluoropolymer surface modification after 3 h of static incubation. Under perfusion conditions, we observed an increase of nearly 15× in the CBD signals from the surface-modified microchannels than from the unmodified microchannels. Furthermore, we also demonstrated that fluoropolymer-modified microchannels are compatible for culturing hCMEC/D3 endothelial cells and for CBD perfusion experiments.
Keyphrases
- high throughput
- ionic liquid
- endothelial cells
- circulating tumor cells
- chronic pain
- atrial fibrillation
- sleep quality
- squamous cell carcinoma
- depressive symptoms
- spinal cord
- neuropathic pain
- mass spectrometry
- pain management
- drug release
- magnetic resonance
- squamous cell
- risk assessment
- vascular endothelial growth factor
- quantum dots
- human health
- crystal structure