PMID- 26418753 OWN - NLM STAT- MEDLINE DCOM- 20161010 LR - 20161230 IS - 1552-4965 (Electronic) IS - 1549-3296 (Linking) VI - 104 IP - 2 DP - 2016 Feb TI - Biocompatibility of common polyimides with human endothelial cells for a cardiovascular microsensor. PG - 406-12 LID - 10.1002/jbm.a.35578 [doi] AB - The cardiovasculature is an emerging niche for polyimide microdevices, yet the biocompatibility of polyimides with human endothelial cells has not been reported in the literature. In this study, we have evaluated an experimental polyimide-based pressure sensor for biological safety to determine its suitability for intravascular operation by using an in vitro model of human endothelium, following ISO 10993-5 protocols for extract tests and direct contact tests. First, SV-HCEC cells were incubated with extracts derived from common microfabrication polyimides utilized in the transducer (PMDA-ODA, BPDA-PPD, and a proprietary thermoplastic adhesive), and then labeled with selective probes to evaluate the effect of the polyimides on mitochondria and cell viability. Flow cytometry analysis showed that incubation of SV-HCECs with polyimide extracts resulted in no significant change in mitochondrial membrane potential (detected by JC-1) or apoptotic (annexin V) and necrotic (propidium iodide) cell death, when compared to incubation with extracts of high-density polyethylene (HDPE) and untreated cells used as negative controls. Second, primary human endothelial cells were incubated in direct contact with the completed sensor and then labeled with selective probes for live-dead analysis (calcein-AM, ethidium homodimer-1). Endothelial cells showed no loss of viability when compared to negative controls. Combined, the studies show no significant change in early markers of stress or more strict markers of viability in endothelial cells treated with the polyimides tested. We conclude that these common microfabrication polyimides and the derived sensor are not cytotoxic to human endothelial cells, the primary cell type that cardiovascular sensors will contact in vivo. CI - (c) 2015 Wiley Periodicals, Inc. FAU - Starr, Peter AU - Starr P AD - University of Texas Health Science Center, San Antonio, Texas, 78229. AD - University of Texas, San Antonio, Texas, 78249. FAU - Agrawal, C Mauli AU - Agrawal CM AD - University of Texas, San Antonio, Texas, 78249. FAU - Bailey, Steven AU - Bailey S AD - University of Texas Health Science Center, San Antonio, Texas, 78229. AD - University of Texas, San Antonio, Texas, 78249. LA - eng PT - Journal Article DEP - 20151015 PL - United States TA - J Biomed Mater Res A JT - Journal of biomedical materials research. Part A JID - 101234237 RN - 0 (Resins, Synthetic) RN - 39355-34-5 (polyimide resin) RN - 9002-88-4 (Polyethylene) SB - IM MH - Apoptosis/*drug effects MH - Endothelial Cells/*metabolism/pathology MH - Humans MH - Materials Testing/*methods MH - Mitochondrial Membranes/*drug effects MH - Polyethylene/chemistry MH - Resins, Synthetic/*chemistry OTO - NOTNLM OT - biocompatibility OT - cardiovascular OT - microfabrication OT - polyimides OT - sensor EDAT- 2015/09/30 06:00 MHDA- 2016/10/11 06:00 CRDT- 2015/09/30 06:00 PHST- 2015/06/01 00:00 [received] PHST- 2015/08/18 00:00 [revised] PHST- 2015/09/24 00:00 [accepted] PHST- 2015/09/30 06:00 [entrez] PHST- 2015/09/30 06:00 [pubmed] PHST- 2016/10/11 06:00 [medline] AID - 10.1002/jbm.a.35578 [doi] PST - ppublish SO - J Biomed Mater Res A. 2016 Feb;104(2):406-12. doi: 10.1002/jbm.a.35578. Epub 2015 Oct 15.