Can CQ be completely replaced by alternative initiators in dental adhesives?

被引:69
作者
Ilie, Nicoleta [1 ]
Hickel, Reinhard [1 ]
机构
[1] Univ Munich, Sch Dent, D-80336 Munich, Germany
关键词
adhesives; degree of cure; mechanical properties;
D O I
10.4012/dmj.27.221
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Despite good clinical acceptance, photoinitiating systems based on camphorquinone and amines raise concerns in terms of yellowing, aging, toxicity, or degradation in low pH conditions. This study aimed to prove whether CQ could be successfully replaced by alternative initiators in adhesive systems. Further, the efficiency of a prototype dual-wavelengtb LED (=Light Emitting Diode) curing unit was analyzed. In two commercial adhesive systems, CQ was completely replaced by Lucirin TPO. The commercial adhesives and their experimental counterparts were evaluated after curing for 10 seconds and 20 second with two dual-wavelength LED units and one regular LED unit, by applying the curing unit on the adhesive surface at two distances of 0 mm and 5 mm. Degree of cure and mechanical properties (Vickers hardness and modulus of elasticity) were assessed after 24-hour storage in distilled water at 37 degrees C. Experimental data showed that the CQ-amine system could be completely replaced by Lucirin TPO when dual-wavelength LED unit was used for photo activation.
引用
收藏
页码:221 / 228
页数:8
相关论文
共 19 条
[1]
New aromatic tert-amines for application as photoinitiator components in photocurable dental materials [J].
Ahn, KD ;
Han, DK ;
Lee, SH ;
Lee, CW .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2003, 204 (13) :1628-1635
[2]
Radical polymeric photoinitiators bearing side-chain camphorquinone moieties linked to the main chain through a flexible spacer [J].
Angiolini, L ;
Caretti, D ;
Rossetti, S ;
Salatelli, E ;
Scoponi, M .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2005, 43 (23) :5879-5888
[3]
ASMUSSEN E, 1985, OPER DENT, V10, P61
[4]
*BASF CORP, 2001, LUC TOP TECHN INF
[5]
BURTSCHER P, 2003, J DENT RES
[6]
Cheong C, 2003, OPER DENT, V28, P747
[7]
Camphorquinone-amines photoinitating systems for the initiation of free radical polymerization [J].
Jakubiak, J ;
Allonas, X ;
Fouassier, JP ;
Sionkowska, A ;
Andrzejewska, E ;
Linden, LÅ ;
Rabek, JF .
POLYMER, 2003, 44 (18) :5219-5226
[8]
Color stability of resin matrix restorative materials as a function of the method of light activation [J].
Janda, R ;
Roulet, JF ;
Kaminsky, M ;
Steffin, G ;
Latta, M .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2004, 112 (03) :280-285
[9]
TIME-RESOLVED ELECTRON-SPIN-RESONANCE STUDY ON RADICAL POLYMERIZATION WITH (2,4,6-TRIMETHYLBENZOYL)DIPHENYLPHOSPHINE OXIDE - DIRECT ESTIMATION OF RATE CONSTANTS FOR ADDITION-REACTIONS OF DIPHENYLPHOSPHONYL RADICALS TO VINYL MONOMERS [J].
KAJIWARA, A ;
KONISHI, Y ;
MORISHIMA, Y ;
SCHNABEL, W ;
KUWATA, K ;
KAMACHI, M .
MACROMOLECULES, 1993, 26 (07) :1656-1658
[10]
Reaction mechanism of monoacyl- and bisacylphosphine oxide photoinitiators studied by P-31-, C-13-, and H-1-CIDNP and ESR [J].
Kolczak, U ;
Rist, G ;
Dietliker, K ;
Wirz, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (27) :6477-6489