FeuersteinO., PersmanN., WeissE. I.2004. Phototoxic effect of visible light on Porphyromonas gingivalis and Fusobacterium nucleatum: An in vitro study. Photochem. Photobiol., 80:412–415.
2.
FeuersteinO., GinsburgI., DayanE., VelerD., WeissE. I.2005. Mechanism of visible light phototoxicity on Porphyromonas gingivalis and Fusobacterium nucleatum. Photochem. Photobiol., 81:1186–1189.
3.
HenryC. A., JudyM., DyerB., WagnerM., MatthewsJ. L.1995. Sensitivity of Porphyromonas and Prevotella species in liquid media to argon laser. Photochem. Photobiol., 61:410–413.
4.
PapageorgiouP., KatsambasA., ChuA.2000. Phototherapy with blue (415 nm) and red (660 nm) light in the treatment of acne vulgaris. Br. J. Dermatol., 142:973–978.
5.
KawadaA., AraganeY., KameyamaH., SangenY., TezukaT.2002. Acne phototherapy with a high-intensity, enhanced, narrow-band, blue light source: An open study and in vitro investigation. J. Dermatol. Sci., 30:129–135.
6.
MacleanM., MacGregorS. J., AndersonJ. G., WoolseyG.2008. High-intensity narrow-spectrum light inactivation and wavelength sensitivity of Staphylococcus aureus. FEMS Microbiol. Lett., 285:227–232.
7.
MurdochL. E., MacleanM., MacGregorS. J., AndersonJ. G.2010. Inactivation of Campylobacter jejuni by exposure to high-intensity 405-nm visible light. Foodborne Pathog. Dis., 7:1211–1216.
8.
GanzR. A., ViveirosJ., AhmadA., AhmadiA., KhalilA., TolkoffM. J., NishiokaN. S., HamblinM. R.2005. Helicobacter pylori in patients can be killed by visible light. Lasers Surg. Med., 36:260–265.
9.
HamblinM. R., ViveirosJ., YangC., AhmadiA., GanzR. A., TolkoffM. J.2005. Helicobacter pylori accumulates photoactive porphyrins and is killed by visible light. Antimicrob. Agents Chemother., 49:2822–2827.
10.
LipovskyA., NitzanY., FriedmannH., LubartR.2009. Sensitivity of Staphylococcus aureus strains to broadband visible light. Photochem. Photobiol., 85:255–260.
11.
LipovskyA., NitzanY., GedankenA., LubartR.2010. Visible light-induced killing of bacteria as a function of wavelength: implication for wound healing. Lasers Surg. Med., 42:467–472.
12.
AshkenaziH., NitzanY., GalD.2003. Photodynamic effects of antioxidant substituted porphyrin photosensitizers on gram-positive and -negative bacteria. Photochem. Photobiol., 77:186–191.
13.
NitzanY., Balzam–SudakevitzA., AshkenaziH.1998. Eradication of Acinetobacter baumannii by photosensitized agents in vitro. J. Photochem. Photobiol. B Biol., 42:211–218.
14.
NitzanY., WexlerH. M., FinegoldS. M.1994. Inactivation of anaerobic-bacteria by various photosensitized porphyrins or by hemin. Curr. Microbiol., 29:125–131.
AlivisatosA. P.1996. Semiconductor clusters, nanocrystals, and quantum dots. Science, 271:933–937.
17.
CuiY., WeiQ., ParkH., LieberC. M.2001. Nanowire nanosensors for highly sensitive and selective detection of biological and chemical species. Science, 293:1289–1292.
18.
FubiniB.1997. Surface reactivity in the pathogenic response to particulates. Environ. Health Perspect., 105,Suppl. 5:1013–1020.
19.
ApplerotG., LipovskyA., DrorR., PerkasN., NitzanY., LubartR., GedankenA.2009. Enhanced antibacterial activity of nanocrystalline ZnO due to increased ROS-mediated cell injury. Adv. Funct. Mater., 19:842–852.
20.
LipovskyA., TzitrinovichZ., FriedmannH., ApplerotG., GedankenA., and LubartR.2009. EPR study of visible light-induced ROS generation by nanoparticles of ZnO. J. Phys. Chem. C. Nanomater. Interfaces, 113:15997–16001.
21.
HirakawaT., YawataK., NosakaY.2007. Photocatalytic reactivity for O2- and OH radical formation in anatase and rutile TiO2 suspension as the effect of H2O2 addition. Appl. Catal. A. Gen., 325:105–111.
22.
LipovskyA., GedankenA., NitzanY., LubartR.2011. Enhanced inactivation of bacteria by metal-oxide nanoparticles combined with visible light irradiation. Lasers Surg. Med., 43:236–240.
23.
OphusE. M., RodeL., GylsethB., NicholsonD. G., SaeedK.1979. Analysis of titanium pigments in human-lung tissue. Scand. J. Work Environ. Health, 5:290–296.
24.
LindenschmidtR. C., DriscollK. E., PerkinsM. A., HigginsJ. M., MaurerJ. K., BelfioreK. A.1990. The comparison of a fibrogenic and 2 nonfibrogenic dusts by bronchoalveolar lavage. Toxicol. Appl. Pharmacol., 102:268–281.
25.
JengH. A., SwansonJ.2006. Toxicity of metal oxide nanoparticles in mammalian cells. J. Environ. Sci. Health A. Tox. Hazard. Subst. Environ. Eng., 41:2699–2711.
26.
SchrandA. M., RahmanM. F., HussainS. M., SchlagerJ. J., SmithD. A., SyedA. F.2010. Metal-based nanoparticles and their toxicity assessment. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol., 2:544–568.
27.
LipovskyA., NitzanY., GedankenA., LubartR.2010. Visible light-induced killing of bacteria as a function of wavelength: implication for wound healing. Lasers Surg. Med., 42:467–472.
28.
PolV. G., WildermuthG., FelscheJ., GedankenA., Calderon–MorenoJ.2005. Sonochemical deposition of Au nanoparticles on titania and the significant decrease in the melting point of gold. J Nanosci Nanotechnol, 5:975–979.
29.
PolV. G., MotieiM., GedankenA., Calderon–MorenoJ., MastaiY.2003. Sonochemical deposition of air-stable iron nanoparticles on monodispersed carbon spherules. Chem. Mater., 15:1378–1384.
30.
PerelshteinI., ApplerotG., PerkasN., Wehrschetz–SiglE., HasmannA., GuebitzG. M., GedankenA.2009. Antibacterial properties of an in situ generated and simultaneously deposited nanocrystalline zno on fabrics. ACS Appl. Mater. Interfaces, 1:363–366.
