This is a competing continuation application whose overall goal is to ensure that resin-based materials which are placed onto teeth as part of dental care can continue to be used safely. Resin based materials which polymerize in the mouth are now used by dentists in many ways to help prevent tooth decay and for tooth repair and replacement. Bonding technologies, which are all based on this class of materials, are used for fissure sealing to help prevent decay, for bonding orthodontic brackets to teeth, and as part of many different types of tooth repair to improve appearance and function. It is very likely that new and modified materials of the same general type will continue to be developed and that the use of this type of material in dentistry will continue to increase in the coming years. The materials are very helpful to patients and have remarkably few negative side effects. However, severe allergic dermatitis in some dentists and other dental workers is linked to the use of the materials, and the incidence of such allergy appears to be increasing. Fortunately, allergic responses are less common in patients, but we do not know why this is so or whether it will continue to be so. Some patients experience pain in the dental pulp after resins are used in deep fillings, for reasons that may be related to direct chemical damage caused by released chemicals, by allergy to them, or to both. It has previously been shown in laboratory studies that two chemicals are released from these materials during the first days after they are placed on teeth.
The first aim will be to confirm this release in experimental animals (guinea pigs), and study what happens to the chemicals in the body (their uptake, distribution, time of storage, breakdown and excretion).
The second aim will be to study mechanisms of allergic responses to these chemicals at the cellular and molecular level using guinea pigs and mice.
The third aim will be to determine whether there are differences between the risk of allergy with skin contact (as can occur in dental workers) relative to contact with the inside of the mouth and through tooth structure to the tooth pulp (as can occur in patients) in the same animals.
The fourth aim will be to study allergic responses at the cellular and molecular level using blood and other tissues donated by volunteer dentists and other dental workers, to ensure that the experimental studies of the phenomenon using animal models and animal tissues in culture are valid. The studies described will help to prevent and treat adverse effects of this class of dental materials.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE010331-07
Application #
6379744
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Program Officer
Kousvelari, Eleni
Project Start
1993-09-01
Project End
2003-04-30
Budget Start
2001-05-01
Budget End
2002-04-30
Support Year
7
Fiscal Year
2001
Total Cost
$193,651
Indirect Cost
Name
University of California Los Angeles
Department
Dentistry
Type
Schools of Dentistry
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Paranjpe, A; Sung, E C; Cacalano, N A et al. (2008) N-acetyl cysteine protects pulp cells from resin toxins in vivo. J Dent Res 87:537-41
Paranjpe, Avina; Cacalano, Nicholas A; Hume, Wyatt R et al. (2007) N-acetylcysteine protects dental pulp stromal cells from HEMA-induced apoptosis by inducing differentiation of the cells. Free Radic Biol Med 43:1394-408
Paranjpe, A; Bordador, L C F; Wang, M-Y et al. (2005) Resin monomer 2-hydroxyethyl methacrylate (HEMA) is a potent inducer of apoptotic cell death in human and mouse cells. J Dent Res 84:172-7
Reichl, F X; Durner, J; Hickel, R et al. (2001) Distribution and excretion of TEGDMA in guinea pigs and mice. J Dent Res 80:1412-5
Hamid, A; Okamoto, A; Iwaku, M et al. (1998) Component release from light-activated glass ionomer and compomer cements. J Oral Rehabil 25:94-9
Hamid, A; Hume, W R (1997) The effect of dentine thickness on diffusion of resin monomers in vitro. J Oral Rehabil 24:20-5
Hamid, A; Hume, W R (1997) A study of component release from resin pit and fissure sealants in vitro. Dent Mater 13:98-102
Hamid, A; Hume, W R (1997) Diffusion of resin monomers through human carious dentin in vitro. Endod Dent Traumatol 13:1-5
Hamid, A; Sutton, W; Hume, W R (1996) Variation in phosphoric acid concentration and treatment time and HEMA diffusion through dentin. Am J Dent 9:211-4
Gerzina, T M; Hume, W R (1996) Diffusion of monomers from bonding resin-resin composite combinations through dentine in vitro. J Dent 24:125-8

Showing the most recent 10 out of 11 publications