𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cytotoxicity of urethane dimethacrylate composites before and after aging and leaching

✍ Scribed by Mohsen, N. M. ;Craig, R. G. ;Hanks, C. T.


Book ID
101256974
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
309 KB
Volume
39
Category
Article
ISSN
0021-9304

No coin nor oath required. For personal study only.

✦ Synopsis


The in vitro cytotoxicity of urethane dimethacrylate composites cured at different times by visible light and after different aging times and extraction treatments was evaluated using succinic dehydrogenase activity in the mitochondria of a fibroblastic cell line to reflect cell viability. In addition, extractable chemicals associated with cell response were identified. The composite samples were tested untreated, polished, or extracted with water or 75% ethanolwater. Balb/c 3T3 fibroblasts were used as the cell culture system while MTT-formazan production was used as the toxicity parameter. Cell viability was calculated as a percentage of Teflon controls. Identification of the chemicals was measured by extracting the composites with 75% ethanolwater, separating the extract by HPLC, and identifying the fractions with mass spectroscopy. In general, cell viability increased continuously with curing time for differently treated samples at high aging times (288 h) while it decreased when the composites were not aged (0 h). In addition, for 75% ethanol or water-extracted composites, cell viability increased within the first 24 h of aging and reached a plateau after 72 h. Lowest cytotoxicity occurred when the samples were extracted with the 75% ethanol solution. The highest cytotoxic effects were found when the samples were untreated. Slightly reduced cytotoxic effects were seen with polished composites. The results suggest that curing the light-activated composites for a minimum of 150 s and postcuring for 24 h is required to attain comparable biocompatibility with the Teflon control. Removing the oxygeninhibited layer from these composites decreased the cytotoxicity by 33% while extracting the composites with 75% ethanol-water decreased it by 77%. Chemicals released from the surface accounted for approximately 40% of cellular response while about 60% of the response was due to chemical components released from the bulk. The primary leachable component from the composites was UDMA monomer. Small quantities of 1,6 hexane diol methacrylate, camphoroquinone, and 2,4,6-tritertiarybutyl phenol also were found.


πŸ“œ SIMILAR VOLUMES


Cytotoxicity of a BIS-GMA dental composi
✍ Anne Rathbun, M. ;Craig, Robert G. ;Hanks, Carl T. ;Filisko, Frank E. πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 823 KB

## Abstract Cell culture techniques were used to determine the source of cytotoxic agents in a commercial BIS‐GMA composite. The material was polymerized according to the manufacturerβ€²s directions and leachable components were removed by room temperature extraction in ethanol, chloroform, or toluen

Application of flow cytometry to determi
✍ Nassiri, M. Reza ;Hanks, Carl T. ;Cameron, Mark J. ;Strawn, Susan E. ;Craig, Rob πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 570 KB

The effects of an oligomer, urethane dimethacrylate (UDMA), on two human cell lines were studied using flow cytometry (FCM). Untreated and treated cultures of propidium iodine-stained KB (epidermal oral carcinoma cells) and human foreskin fibroblast (HFF) cells were analyzed for cellular DNA content