400-81-075
7.
[1]. A Y Xiao, et al. The industrial chemical Tinuvin 13 does not induce dopaminergic neurotoxicity in C57Bl/ mice. Neurosci Lett. 000 Jan 14;78(3):15-8.
[]. David A Tipton, et al. Effects of a hindered amine light stabilizer and a UV light absorber used in maxillofacial elastomers on human gingival epithelial cells and fibroblasts. J Prosthet Dent. 008 Sep;100(3):0-31.
[3]. H Glossmann, et al. A light stabilizer (Tinuvin 770) that elutes from polypropylene plastic tubes is a potent L-type Ca(+)-channel blocker. Proc Natl Acad Sci U S A. 13 Oct 15;0(0):53-7.
[4]. John H Graham, et al. Functional central nicotinic acetylcholine receptor antagonism by systemic administration of Tinuvin 770 (BTMPS). Curr Alzheimer Res. 005 Apr;():141-7.
[5]. Ngoc H Tran, et al. In vitro evaluation of color change in maxillofacial elastomer through the use of an ultraviolet light absorber and a hindered amine light stabilizer. J Prosthet Dent. 004 May;1(5):483-0.
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