Controlled delivery of antimicrobial gallium ions from phosphate-based glasses

Acta Biomaterialia

Volumn 5, Issue 4, 2009, Pages 1198-1210

  Valappil, S P ^a   Ready, D ^b   Abou Neel, E A ^a   Pickup, D M ^c   O'Dell, L A ^d   Chrzanowski, W ^a   Pratten, J ^a   Newport, R J ^c   Smith, M E ^d   Wilson, M ^a   Knowles, J C ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^c UNIVERSITY OF KENT   (United Kingdom)

^d UNIVERSITY OF WARWICK   (United Kingdom)

Author keywords

Antimicrobial; Biofilm; Drug delivery; Glass; Microbiology

Indexed keywords

BACTERIA; BIOFILMS; CALCIUM; CONTROLLED DRUG DELIVERY; DEGRADATION; GALLIUM COMPOUNDS; IONS; TARGETED DRUG DELIVERY;

ANTI-BACTERIAL ACTIVITY; CALCIUM CONTENT; CALCIUM ION CONCENTRATION; CONTROLLED-DELIVERY; DEGRADATION RATE; ION RELEASE; NEW THERAPEUTIC AGENT; P.AERUGINOSA; PHOSPHATE BASED GLASS; PSEUDOMONAS AERUGINOSA;

GLASS;

CALCIUM ION; GALLIUM; GLASS; PHOSPHATE;

ANTIBIOTIC SENSITIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; BACTERIAL VIABILITY; BIOFILM; COLONY FORMING UNIT; CONFOCAL MICROSCOPY; CONTROLLED DRUG RELEASE; CONTROLLED STUDY; DEGRADATION; DRUG DELIVERY SYSTEM; DRUG SOLUBILITY; GROWTH INHIBITION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; PSEUDOMONAS INFECTION;

PSEUDOMONAS AERUGINOSA;

EID: 64249106651     PISSN: 17427061     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.actbio.2008.09.019     Document Type: Article

References (39)

1. Costerton J.W., Stewart P.S., and Greenberg E.P. Bacterial biofilms: a common cause of persistent infections. Science 284 (1999) 1318-1322
2. Drenkard E., and Ausubel F.M. Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation. Nature 416 (2002) 740-743
3. Donlan R.M., and Costerton J.W. Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev 15 (2002) 167-193
4. Shirtliff M.E., Mader J.T., and Camper A.K. Molecular interactions in biofilms. Chem Biol 9 (2002) 859-871
5. Sauer K., Camper A.K., Ehrlich G.D., Costerton J.W., and Davies D.G. Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J Bacteriol 184 (2002) 1140-1154
6. Ceri H.M., Olson E., Stremick C., Read R.R., Morck D., and Buret A. The Calgary biofilm device: new technology for rapid determination of antibiotic susceptibilities of bacterial biofilms. J Clin Microbiol 37 (1999) 1771-1776
7. Oie S., Huang Y., Kamiya A., Konishi H., and Nakazawa T. Efficacy of disinfectants against biofilm cells of methicillin-resistant Staphylococcus aureus. Microbios 85 (1996) 223-230
8. Shiau A.L., and Wu C.L. The inhibitory effect of Staphylococcus epidermidis slime on the phagocytosis of murine peritoneal macrophages is interferon-independent. Microbiol Immunol 42 (1998) 33-40
9. Kaneko Y., Thoendel M., Olakanmi O., Britigan B.E., and Singh P.K. The transition metal gallium disrupts Pseudomonas aeruginosa iron metabolism and has antimicrobial and antibiofilm activity. J Clin Invest 117 (2007) 877-888
10. Olakanmi O., Britigan B.E., and Schlesinger L.S. Gallium disrupts iron metabolism of mycobacteria residing within human macrophages. Infect Immun 68 (2000) 5619-5627
11. Yan G.H., Wang G.J., and Li Y.C. Effects of alpha-dimethylamino cyclohexoxyl dimethyl gallium on ultrastructure of erythrocytic stage of Plasmodium berghei and P. yoelii. Acta Pharmacol Sin 12 (1991) 530-533
12. Harrington J.R., Martens R.J., Cohen N.D., and Bernstein L.R. Antimicrobial activity of gallium against virulent Rhodococcus equi in vitro and in vivo. J Vet Pharmacol Ther 29 (2006) 121-127
13. Valappil S.P., et al. Antimicrobial gallium-doped phosphate-based glasses. Adv Funct Mater 18 (2007) 732-741
14. Valappil S.P., et al. Effect of silver content on the structure and antibacterial activity of silver-doped phosphate-based glasses. Antimicrob Agents Chemother 51 (2007) 4453-4461
15. Cartmell S.H., Doherty P.J., Rhodes N.P., Hunt J.A., Healy D.M., and Gilchrist T. Haemocompatiblity of controlled release glass. J Mater Sci Mater Med 9 (1998) 1-7
16. Gilchrist T., Healy D.M., and Drake C. Controlled silver-releasing polymers and their potential for urinary tract infection control. Biomaterials 12 (1991) 76-78
17. Bellantone M., Coleman N.J., and Hench L.L. Bacteriostatic action of a novel four-component bioactive glass. J Biomed Mater Res 51 (2000) 484-490
18. Norrby S.R., Nord C.E., and Finch R. Lack of development of new antimicrobial drugs: a potential serious threat to public health. Lancet Infect Dis 5 (2005) 115-119
19. Mulligan A.M., Wilson M., and Knowles J.C. Effect of increasing silver content in phosphate-based glasses on biofilms of Streptococcus sanguis. J Biomed Mater Res A 67 (2003) 401-412
20. Abou Neel E.A., O'Dell L., Smith M.E., and Knowles J.C. Processing, characterisation, and biocompatibility of zinc modified metaphosphate based glasses for biomedical applications. J Mater Sci Mater Med 19 (2008) 1669-1679
21. Abou Neel E.A., and Knowles J.C. Physical and biocompatibility studies of novel titanium dioxide doped phosphate-based glasses for bone tissue engineering applications. J Mater Sci Mater Med 19 (2008) 377-386
22. Massiot D., et al. Modelling one- and two-dimensional solid state NMR spectra. Magn Reson Chem 40 (2002) 70-76
23. 27Al NMR of ceramics and glasses. Masters Thesis. University of Warwick; 2004.
24. 4 (x = 0.0, 0.20, 0.50, 0.80 and 1.00). J Solid State Chem 176 (2003) 37-46
25. Walton R.I., and O'Hare D. An X-ray absorption fine structure study of amorphous precursors of a gallium silicate zeolite. J Phys Chem Solids 62 (2001) 1469-1479
26. Bunker B.C., Arnold G.W., and Wilder J.A. Phosphate glass dissolution in aqueous solutions. J Non-Cryst Solids 64 (1984) 291-316
27. Watanabe M., Sato S., and Saito H. The mechanism of the hydrolysis of condensed phosphates. IV. The hydrolysis of pyro-, tripoly-, trimeta-, and tetrametaphosphates in aqueous organic solvents. Bull Chem Soc Jpn 49 (1976) 2474-2478
28. Narasimhan J., Antholine W.E., and Chitambar C.R. Effect of gallium on the tyrosyl radical of the iron-dependent M2 subunit of ribonucleotide reductase. Biochem Pharmacol 44 (1992) 2403-2408
29. Hassett D.J., Woodruff W.A., Wozniak D.J., Vasil M.L., Cohen M.S., and Ohman D.E. Cloning and characterization of the Pseudomonas aeruginosa sodA and sodB genes encoding manganese- and iron-cofactored superoxide dismutase: demonstration of increased manganese superoxide dismutase activity in alginate-producing bacteria. J Bacteriol 175 (1993) 7658-7665
30. Kirkpatrick R.J., and Brow R.K. Nuclear magnetic resonance investigation of the structures of phosphate and phosphate-containing glasses-a review. Solid State Nucl Magn Reson 5 (1995) 9-21
31. MacKenzie K.J.D., and Smith M.E. Multinuclear solid state NMR of inorganic materials (2002), Pergamon p. 654
32. 5 by MAS and solution NMR and vibrational spectroscopy: II. Structure of the phosphate network. Spectrochim Act Part A 56 (2000) 435-446
33. 31P MAS chemical shifts of metaphosphate glasses. J Am Ceram Soc 74 (1991) 1287-1290
34. Smith M.E., and van Eck E.R.H. Recent advances in experimental solid state NMR methodology for half-integer spin quadrupolar nuclei. Prog Nucl Magn Reson Spectrosc 34 (1999) 159-201
35. Kohn S.C., Smith M.E., Dirken P.J., van Eck E.R.H., Kentgens A.P.M., and Dupree R. Sodium environments in dry and hydrous albite glasses: improved Na-23 solid state NMR data and their implications for water dissolution mechanisms. Geochim Cosmochim Acta 62 (1998) 79-87
36. Nishi K., Shimizu K., Takamatsu M., Yoshida H., Satsuma A., Tanaka T., et al. Deconvolution analysis of Ga K-edge XANES for quantification of gallium coordinations in oxide environments. J Phys Chem B 102 (1998) 10190-10195
37. Fletcher D.A., McMeeking R.F., and Parkin D. The United Kingdom chemical database service. J Chem Inf Comput Sci 36 (1996) 746-749
38. 3 glasses. J Non-Cryst Solids 333 (2004) 307-315
39. 2O glass system. Biomaterials 25 (2004) 491-499