Expanded Poly(tetrafluoroethylene) Blood Vessel Grafts with Embedded Reactive Oxygen Species (ROS)-Responsive Antithrombogenic Drug for Elimination of Thrombosis.
Dongfang WangYiyang XuLixia WangXiaofeng WangCuihong RenBo ZhangQian LiJames A ThomsonLih-Sheng TurngPublished in: ACS applied materials & interfaces (2020)
Treatment of cardiovascular diseases suffers from the lack of transplantable small-diameter blood vessel (SDBV) grafts that can prohibit/eliminate thrombosis. Although expanded poly(tetrafluoroethylene) (ePTFE) has the potential to be used for SDBV grafts, recurrence of thrombus remains the biggest challenge. In this study, a reactive oxygen species (ROS)-responsive antithrombogenic drug synthesis and a bulk coating process were employed to fabricate functional ePTFE grafts capable of prohibiting/eliminating blood clots. The synthesized drug that would release antiplatelet ethyl salicylate (ESA), in responding to ROS, was dissolved in a polycaprolactone (PCL) solution, followed by a bulk coating of the as-fabricated ePTFE grafts with the PCL/drug solution. Nuclear magnetic resonance (NMR) spectroscopy, Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and atomic force microscopy (AFM) were employed to investigate and confirm the synthesis and presence of the ROS-responsive drug in the ePTFE grafts. The ESA release functions were demonstrated via the drug-release profile and dynamic anticoagulation tests. The biocompatibility of the ROS-responsive ePTFE grafts was demonstrated via lactate dehydrogenase (LDH) cytotoxicity assays, live and dead cell assays, cell morphology, and cell-graft interactions. The ROS-responsive, antithrombogenic ePTFE grafts provide a feasible way for maintaining long-term patency, potentially solving a critical challenge in SDBV applications.
Keyphrases
- reactive oxygen species
- cell death
- dna damage
- magnetic resonance
- atomic force microscopy
- cancer therapy
- single cell
- electron microscopy
- drug release
- cardiovascular disease
- cell therapy
- pulmonary embolism
- adverse drug
- drug delivery
- high throughput
- single molecule
- stem cells
- high resolution
- metabolic syndrome
- risk assessment
- emergency department
- atrial fibrillation
- type diabetes
- coronary artery disease
- climate change
- optical coherence tomography
- optic nerve
- free survival