Synthesis of antibacterial TiO2/PLGA composite biofilms

Nanomedicine: Nanotechnology, Biology, and Medicine

Volumn 10, Issue 5, 2014, Pages e1097-e1107

  Wu, Jau Yi ^a   Li, Ching Wen ^a   Tsai, Ching Hsiu ^a   Chou, Chih Wei ^b   Chen, Dar Ren ^c   Wang, Gou Jen ^a  

^a NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

^b CHINA MEDICAL UNIVERSITY   (Taiwan)

^c CHANGHUA CHRISTIAN HOSPITAL   (Taiwan)

Author keywords

Antibacterial material; Artificial dressing; Titanium dioxide

Indexed keywords

BIOCOMPATIBILITY; BIOFILMS; CELL CULTURE; ENDOTHELIAL CELLS; ESCHERICHIA COLI; OXIDES; SOL-GEL PROCESS; SOL-GELS;

ANTI-BACTERIAL ACTIVITY; ANTIBACTERIAL MATERIALS; ANTIBACTERIAL PROPERTIES; COMPOSITE BIOMATERIALS; CONCENTRATION RATIO; DISINFECTION EFFICIENCY; POLY LACTIC-CO-GLYCOLIC ACID; STAPHYLOCOCCUS AUREUS;

TITANIUM DIOXIDE;

ANTIINFECTIVE AGENT; POLYGLACTIN; TITANIUM DIOXIDE; TITANIUM DIOXIDE NANOPARTICLE; LACTIC ACID; POLYGLYCOLIC ACID; POLYLACTIC ACID-POLYGLYCOLIC ACID COPOLYMER; TITANIUM;

ABSORPTION; ANIMAL CELL; ANIMAL MODEL; ANTIBACTERIAL ACTIVITY; ARTICLE; BIOCOMPATIBILITY; BIOFILM; CAROTID ARTERY; CATTLE; CELL STRUCTURE; CELL SURVIVAL; COMPOSITE MATERIAL; CONTACT ANGLE; CONTROLLED STUDY; CRYSTAL STRUCTURE; CYTOTOXICITY; DISINFECTION; ENDOTHELIUM CELL; ESCHERICHIA COLI; FIBROBLAST; FLUORESCENCE; HUMAN; HUMAN CELL; IMPLANTATION; IRRADIATION; KERATINOCYTE; MACROPHAGE; MOISTURE; NONHUMAN; POWDER; RAT; SCANNING ELECTRON MICROSCOPY; STAPHYLOCOCCUS AUREUS; SUBCUTANEOUS TISSUE; SURVIVAL RATE; SYNTHESIS; TENSILE STRENGTH; WOUND HEALING; X RAY DIFFRACTION; CHEMISTRY; DRUG EFFECTS;

BOVINAE; ESCHERICHIA COLI; RATTUS; STAPHYLOCOCCUS AUREUS;

ANTI-BACTERIAL AGENTS; BIOFILMS; LACTIC ACID; POLYGLYCOLIC ACID; TITANIUM;

EID: 84903520117     PISSN: 15499634     EISSN: 15499642     Source Type: Journal    
DOI: 10.1016/j.nano.2014.01.002     Document Type: Article

References (50)

1. Stadelmann W.K., Digenis A.G., Tobin G.R. Physiology and healing dynamics of chronic cutaneous wounds. Am J Surg 1998, 176:26S-38S.
2. McGrath J.A., Eady R.A.J., Pope F.M. Anatomy and organization of human skin. Rook's Textbook of Dermatology 2004, 4190. Blackwell Publishing. 7th ed. T. Burns, S. Breathnach, N. Cox, C. Griffiths (Eds.).
3. Pivarcsi A., Nagy I., Kemeny L. Innate immunity in the skin: how keratinocytes fight against pathogens. Curr Immunol Rev 2005, 1(1):29-42.
4. Tang L., Wu J.J., Ma Q., Cui T., Andreopoulos F.M., Gil J., Valdes J., Davis S.C., Li J. Human lactoferrin stimulates skin keratinocyte function and wound re-epithelialization. Br J Dermatol 2010, 163(1):38-47.
5. Midwood K.S., Williams L.V., Schwarzbauer J.E. Tissue repair and the dynamics of the extracellular matrix. Int J Biochem Cell Biol 2004, 36(6):1031-1037.
6. Duncan M.R., Berman B. Stimulation of collagen and glycosaminoglycan production in cultured human adult dermal fibroblasts by recombinant human interleukin 6. J Investig Dermatol 1991, 97:689-692.
7. Nissen N.N., Polverini P.J., Koch A.E., Volin M.V., Gamelli R.L., DiPietro L.A. Vascular endothelial growth factor mediates angiogenic activity during the proliferative phase of wound healing. Am J Pathol 1998, 152(6):1445-1452.
8. Jayakumar R., Prabaharan M., Kumar P.T.S., Nair S.V., Tamura H. Biomaterials based on chitin and chitosan in wound dressing applications. Biotechnol Adv 2011, 29(3):322-337.
9. Ishihara M., Nakanishi K., Ono K., Sato M., Kikuchi M., Saito Y., Yura H., Matsui T., Hattori H., Uenoyama M., Kurita A. Photocrosslinkable chitosan as a dressing for wound occlusion and accelerator in healing process. Biomaterials 2002, 23(3):833-840.
10. Kumar P.T.S., Abhilash S., Manzoor K., Nair S.V., Tamura H., Jayakumar R. Preparation and characterization of novel β-chitin/nanosilver composite scaffolds for wound dressing applications. Carbohydr Polym 2010, 80(3):761-767.
11. MacNeil S. Progress and opportunities for tissue-engineered skin. Nature 2007, 445:874-880.
12. Arora S., Jain J., Rajwade J.M., Paknikar K.M. Interactions of silver nanoparticles with primary mouse fibroblasts and liver cells. Toxicol Appl Pharmacol 2009, 236(3):310-318.
13. 2O nanoparticles against drug-resistant bacteria and leishmania parasites. Future Microbiol 2011, 6:933-940.
14. 2 on Enterobacter cloacae - comparative study with other Gram (-) bacteria. Journal of Photochemistry and Photobiology A-Chemistry 2003, 157:81-85.
15. 2 and microorganism, nature, and intensity of UV irradiation. Applied Catalysis B-Environmental 2007, 76:257-263.
16. Seil J.T., Webster T.J. Reduced Staphylococcus aureus proliferation and biofilm formation on zinc oxide nanoparticle PVC composite surfaces. Acta Biomater 2011, 7:2579-2584.
17. Huang Z., Zheng X., Yan D., Yin G., Liao X., Kang Y., Yao Y., Huang D., Hao B. Toxicological effect of ZnO nanoparticles based on bacteria. Langmuir 2008, 24:4140-4144.
18. Mitoraj D., Janczyk A., Strus M., Kisch H., Stochel G., Heczko P.B., Macyk W. Visible light inactivation of bacteria and fungi by modified titanium dioxide. Photochem Photobiol Sci 2007, 6:642-648.
19. Paszek E., Czyz J., Woznicka O., Jakubiak D., Wojnarowicz J., Lojkowski W., Stepien E. Zinc oxide nanoparticles impair the integrity of human umbilical vein endothelial cell monolayer in vitro. J Biomed Nanotechnol 2012, 8:957-967.
20. 2 composite nano thin film for antimicrobial application. Nanotechnology 2011, 22:115603.
21. 2 concentration. Applied Catalysis B-Environmental 2003, 44:263-284.
22. ISO 22196:2007 Plastics - measurement of antibacterial activity on plastics surfaces. International Organization for Standardization 2007.
23. Li D., Kaner R.B. Shape and aggregation control of nanoparticles: not shaken, not stirred. J Am Chem Soc 2006, 128:968-975.
24. Chwalibog A., Sawosz E., Hotowy A., Szeliga J., Mitura S., Mitura K., Grodzik M., Orlowski P., Sokolowska A. Visualization of interaction between inorganic nanoparticles and bacteria or fungi. Int J Nanomedicine 2010, 5:1085-1094.
25. 2 against E. coli, P. aeruginosa and S. aureus. J Optoelectronics Biomed Mater 2012, 4:9-17.
26. Varghese S., Kuriakose S., Jose S. Antimicrobial activity of carbon nanoparticles isolated from natural sources against pathogenic Gram-negative and Gram-positive bacteria. J Nanosci 2013, 457865, 5 pages.
27. 2O nanoparticles toxicity against Gram-positive and Gram-negative bacteria. J Gen Appl Microbiol 2013, 59:83-88.
28. 2 particle mixture with oxidizer against Staphylococcus aureus. Jpn J Infect Dis 2009, 62:378-380.
29. Xue C., Wu J., Lan F., Liu W., Yang X., Zeng F., Xu H. Nano titanium dioxide induces the generation of ROS and potential damage in HaCaT cells under UVA irradiation. J Nanosci Nanotechnol 2010, 10(12):8500-8507.
30. Iavicol I., Leso V., Fontana L., Bergamaschi A. Toxicological effects of titanium dioxide nanoparticles: a review of in vitro mammalian studies. Eur Rev Med Pharmacol Sci 2011, 15(5):481-508.
31. Chien K.B., Shah R.N. Novel soy protein scaffolds for tissue regeneration: material characterization and interaction with human mesenchymal stem cells. Acta Biomater 2012, 8(2):694-703.
32. Waser-Althaus J., Salamon A., Waser M., Padeste C., Kreutzer M., Pieles U., Müller B., Peters K. Differentiation of human mesenchymal stem cells on plasma-treated polyetheretherketone. J Mater Sci Mater Med 2014, 25(2):515-525.
33. Wang G.J., Lin Y.C., Hsu S.H. The fabrication of PLGA microvessel scaffolds with nano-patterned inner walls. Biomed Microdevices 2010, 12(5):841-848.
34. Cai K., Frant M., Bossert J., Hildebrand G., Liefeith K., Jandt K.D. Surface functionalized titanium thin films: zeta-potential, protein adsorption and cell proliferation. Colloids Surf B: Biointerfaces 2006, 50(1):1-8.
35. Altankov G., Richau K., Groth Th. The role of surface zeta potential and substratum chemistry for regulation of dermal fibroblasts interaction. Mater Werkst 2003, 34(12):1120-1128.
36. 2 coating promotes human mesenchymal stem cell proliferation without the loss of their capacity for chondrogenic differentiation. Biofabrication 2013, 5(2):025009.
37. 2 nanoparticles, a common component of sunscreens and cosmetics, on human keratinocytes. Cell Death Dis. 2013, 4:e549.
38. Arora S., Rajwade J.M., Paknikar K.M. Nanotoxicology and in vitro studies: the need of the hour. Toxicol Appl Pharmacol 2012, 258(2):151-165.
39. Davda J., Labhasetwar V. Characterization of nanoparticle uptake by endothelial cells. Int J Pharm 2002, 233:51-59.
40. Marano F., Hussain S., Rodrgues-Lima F., Baeza-Squiban A., Boland S. Nanoparticles: molecular targets and cell signalling. Arch Toxicol 2011, 85:733-741.
41. Buyukhatipoglu K., Clyne A.M. Superparamagnetic iron oxide nanoparticles change endothelial cell morphology and mechanics via reactive oxygen species formation. J Biomed Mater Res A 2011, 96:186-195.
42. 2 nanoparticles. Toxicology 2008, 254:82-90.
43. Cao Y., Zhang B., Croll T., Rolfe B.E., Campbell J.H., Campbell G.R., Martin D., Cooper-White J.J. Engineering tissue tubes using novel multilayered scaffolds in the rat peritoneal cavity. Biomed Mater Res A 2008, 87A:719-727.
44. Gretzer C., Emanuelsson L., Liljensten E., Thomsen P. The inflammatory cell influx and cytokines changes during transition from acute inflammation to fibrous repair around implanted materials. Biomaterials Science-Polymer Edition 2006, 17:669-687.
45. Hu W.J., Eaton J.W., Tang L.P. Molecular basis of biomaterial-mediated foreign body reactions. Blood 2001, 98:1231-1238.
46. Kao W.J., Hubbell J.A., Anderson J.M. Protein-mediated macrophage adhesion and activation on biomaterials: a model for modulating cell behavior. Mater Sci Mater Med 1999, 10:601-605.
47. Kang B.C., Kang K.S., Lee Y.S. Biocompatibility and long-term toxicity of InnoPol((R)) implant, a biodegradable polymer scaffold. Exp Anim 2005, 54:37-52.
48. Chang H., Ho C.C., Yang C.S., Chang W.H., Tsai M.H., Tsai H.T., Lin P. Involvement of MyD88 in zinc oxide nanoparticle-induced lung inflammation. Exp Toxicol Pathol 2013, 65(6):887-896.
49. Ho C.C., Chang H., Tsai H.T., Tsai M.H., Yang C.S., Ling Y.C., Lin P. Quantum dot 705, a cadmium-based nanoparticle, induces persistent inflammation and granuloma formation in the mouse lung. Nanotoxicology 2013, 7(1):105-115.
50. Ambalavanan N., Stanishevsky A., Bulger A., Halloran B., Steele C., Vohra Y., Matalon S. Titanium oxide nanoparticle instillation induces inflammation and inhibits lung development in mice. Physiol-Lung Cell Mol Physiol 2013, 304:L152-L161.