Silicone polymers containing the light-activated antimicrobial agent methylene blue with or without gold nanoparticles were evaluated for their ability to reduce the microbial load on surfaces in a clinical environment. When irradiated with white light, polymers containing nanogold were more effective in this respect than those containing only methylene blue

Ismail, S

Parkin, I

Perni, S

Pratten, J

Wilson, M

arXiv

We report on two XMM-Newton observations of the bright narrow-line Seyfert 1 galaxy Ark 564 taken 1 yr apart (2000 June and 2001 June). The 0.6-10 keV continuum is well described by a soft blackbody component (kT~ 140-150 eV) plus a steep power law (?~ 2.50-2.55). No significant spectral changes are observed between the two observations, although the X-ray flux in the second observation is ~40-50 per cent lower. In both observations, we detect a significant absorption edge at a rest-frame energy of ~0.73 keV, corresponding to O VII. The presence of the absorption feature is confirmed by a simultaneous Chandra grating observation in 2000 June, although the best-fitting edge threshold is at a slightly lower energy in the Chandra data, possibly because of a different parametrization of the underlying X-ray continuum. We find tentative evidence for a broad iron emission line in the 2000 June observation. The results from an analysis of the power spectral density (PSD) function are also presented. The present XMM-Newton data support the idea that the PSD shows two breaks, although the location of the high-frequency break requires further constraints

VIGNALI, CRISTIAN

Brandt W. N.

Boller T.h.

Fabian A. C.

Vaughan S.

Archivio istituzionale della ricerca - Alma Mater Studiorum Università di Bologna

Arakelian 564: An XMM-Newton view

Vignali, Cristian

Brandt, W. N.

Boller, Th.

Fabian, A. C.

Vaughan, Simon

Max Planck Society eDoc Server

Arakelian 564: an XMM-Newton view

UCL Discovery

Efficacy of a Novel Light-Activated Antimicrobial Coating for Disinfecting Hospital SurfacesAuthor(s): Salim Ismail, BSc; Stefano Perni, PhD; Jonathan Pratten, PhD; Ivan Parkin, PhD;Michael Wilson, DScReviewed work(s):Source: Infection Control and Hospital Epidemiology, Vol. 32, No. 11 (November 2011), pp.1130-1132Published by: The University of Chicago Press on behalf of The Society for Healthcare Epidemiology ofAmericaStable URL: http://www.jstor.org/stable/10.1086/662377 .Accessed: 19/09/2012 06:48Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at .http://www.jstor.org/page/info/about/policies/terms.jsp .JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range ofcontent in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new formsof scholarship. For more information about JSTOR, please contact support@jstor.org. .The University of Chicago Press and The Society for Healthcare Epidemiology of America are collaboratingwith JSTOR to digitize, preserve and extend access to Infection Control and Hospital Epidemiology.http://www.jstor.org infection control and hospital epidemiology november 2011, vol. 32, no. 11c o n c i s e c o m m u n i c a t i o nEfficacy of a Novel Light-ActivatedAntimicrobial Coating for DisinfectingHospital SurfacesSalim Ismail, BSc;1 Stefano Perni, PhD;1Jonathan Pratten, PhD;1 Ivan Parkin, PhD;2Michael Wilson, DSc1Silicone polymers containing the light-activated antimicrobial agentmethylene blue with or without gold nanoparticles were evaluatedfor their ability to reduce the microbial load on surfaces in a clinicalenvironment. When irradiated with white light, polymers containingnanogold were more effective in this respect than those containingonly methylene blue.Infect Control Hosp Epidemiol 2011;32(11):1130-1132Nosocomial infections pose a significant threat to hospitalpatients, staff, and visitors. Clinical environments often har-bor pathogens that may then be transmitted to healthcareworkers and patients. The use of light-activated antimicrobialagents (photosensitizers) embedded in polymers is a novelapproach that may be used for decontaminating surfaces.1Recently, the incorporation of gold (Au) nanoparticles intothese polymers has been shown to improve their antimicro-bial effectiveness in vitro.2 Here, we show that silicone poly-mers containing the photosensitizer methylene blue (MB) andAu nanoparticles can be used to reduce environmental con-tamination in a dental clinic and that high numbers of meth-icillin-resistant Staphylococcus aureus (MRSA) can be killedunder similar lighting conditions.methodsSilicone polymers. Silicone polymers were prepared as de-scribed elsewhere.2Light source. The light source used was a General Electric28-W Starcoat BIAX 2D T5 compact fluorescent lamp (GELighting). This was suspended between clamp stands atop ashelving unit 35 cm above the base of the stands.3 Ambientclinical lights were kept on during each experiment. For lab-oratory experiments, the light source was fixed in a refrig-erated incubator at 22C. Light intensity during experimentswas measured using a digital luxmeter.Clinical testing. Clinical testing was conducted as de-scribed elsewhere.3Laboratory testing. MRSA strain eMRSA-164 was used todetermine the ability of the polymers to kill a clinically rel-evant organism. eMRSA-16 was cultured in brain-heart in-fusion broth for 16 hours at 37C. This was diluted to givea suspension containing approximately 108 colony-formingunits (CFUs)/mL. Triplicate samples of each coating (control,MB, and MB  Au) were placed in a humidity chamber, andeach was inoculated with 250 mL of the bacterial suspension.The chamber was placed in the incubator for 6 or 24 hours.The light intensity was similar to that used in the clinic ex-periments. To assess the effect of each coating in the dark, aduplicate humid chamber was covered with aluminum foiland placed in the incubator for 24 hours. Survivors wereenumerated by viable counting as described elsewhere.3Statistical analyses. The effect of coating treatment (con-trol, MB, and MB  Au) on the viable count of microbeswas evaluated using repeated-measures (2-way) analysis ofvariance. For all analyses, differences were considered statis-tically significant when P was less than .05.resultsThe mean light intensity at the surface of the coatings in theclinic was 2,305 lux. The overall mean counts ( standarderror of the mean [SEM]) of microbes on the settle platesafter 48 hours were CFUs/cm2 (anaerobic cul-3.49 0.35tivation) and CFUs/cm2 (aerobic cultivation).5.04 0.28Control silicone coatings showed a higher microbial load,with overall mean counts ( SEM) of CFUs/8.23 2.42cm2 (anaerobic cultivation) and CFUs/cm2 (aer-13.80 1.95obic cultivation). For anaerobically cultivated microbes, sil-icone coatings containing MB and those containing MB Au showed 51.3% and 71.2% mean reductions in the recoveryof viable microbes, respectively, compared with control coat-ings (Figure 1). The number of aerobically cultivated mi-crobes was reduced by 32.7% and 54.8%, respectively, oncoatings containing MB and those containing MB  Au. ForMB  Au coatings, these reductions were significant for bothaerobic ( ) and anaerobic ( ) microbes. ThePp .001 Pp .014reduction observed on coatings containing only MB was atan intermediary level that was not significantly different fromthe reduction observed on control coatings or on those con-taining MB  Au, for both aerobically ( andPp .063 Pp, respectively) and anaerobically ( and.348 Pp .546 Pp, respectively) cultivated microbes..358The overall mean light intensities ( SEM) for the 6- and24-hour irradiation experiments with MRSA wereand , respectively. When ir-2,368.8 22.41 2,102.4 16.59radiated for 24 hours, silicone coatings containing MB andthose containing MB  Au achieved substantial reductionsof 99.33% and 99.99%, respectively, compared with controlcoatings (Figure 2A). This level of killing was highly signif-icant for both coating types ( ). There was no signif-P ! .001icant difference in the level of killing observed between coat-ings containing MB and those containing MB  Au over 24hours ( ). When control, MB, and MB  Au poly-Pp .381mers were kept in the dark, increases of 133%, 204%, and215%, respectively, in the viable count were found. When theirradiation time was reduced to 6 hours (Figure 2B), coatingscontaining MB and those containing MB  Au reduced theviable count by 56.51% and 92.30%, respectively, comparedefficacy of light-activated antimicrobial coatings 1131figure 2. Survival of methicillin-resistant Staphylococcus aureus(MRSA) suspensions on the surface of silicone elastomers exposedto 28-W fluorescent light. A, Bars represent the mean number ofMRSA ( standard error of the mean [SEM]) recovered after a 24-hour incubation (22C), expressed as a percentage of the initialMRSA inoculum at time zero. Results are from 3 independent ex-periments performed in triplicate. An asterisk ( ) indicates that the∗reduction in the recovery of viable bacteria is significantly different( ) from that for the control coating. B, Bars represent theP ! .05mean number of MRSA ( SEM) recovered after a 6-hour incu-bation (22C), expressed as a percentage of the initial MRSA in-oculum at time zero. Results are from 5 independent experimentsperformed in triplicate. An asterisk ( ) indicates that the reduction∗in the recovery of viable bacteria is significantly different ( )P ! .05from that for the control coating, and a caret (^) indicates that theenhancement in the reduction of viable MRSA is significantly dif-ferent ( ) from that for the MB coating.P ! .05figure 1. Recovery of viable microbes from the surface of siliconeelastomer samples placed in a dental clinic for 48 hours and exposedto light from a 28-W fluorescent lamp. Bars represent the meannumber of colony-forming units (CFUs;  standard error of themean) per silicone coating for aerobically and anaerobically culti-vated microbes. Results are from 20 independent experiments per-formed in duplicate. An asterisk ( ) indicates that the reduction in∗the recovery of viable microbes is significantly different ( )P ! .05from that for the control coating. MB, methylene blue; Au, gold.with control coatings. This reduction was highly significantfor both coating types ( for MB and forPp .006 P ! .001MB  Au). MB  Au polymers showed a further reductionof 82.29% of viable microbes detected on coatings containingMB and a significant enhancement ( ) in the reduc-Pp .003tion of total viable MRSA by 35.79% compared with MBcoatings.discussionThe results of this study show that silicone polymers con-taining MB and 2-nm gold nanoparticles are able to reducethe microbial load in a clinical environment when irradiatedwith white light at an intensity similar to that encounteredadjacent to a patient during treatment as well as in certainother areas of hospitals. Regulations specify minimum lightintensities of 1,000 lux for accident and emergency depart-ments, 10,000 lux for pathology laboratories, and up to100,000 lux for operating theaters.5 Polymers containing onlyMB were less effective than those that also contained goldnanoparticles, as the latter achieved statistically significantreductions of 71% and 55% for anaerobically and aerobicallycultivable microbes, respectively. It was of interest to deter-mine the ability of the polymers to kill very high numbersof a clinically important bacterium, MRSA, under lightingconditions similar to those used in clinical testing. Whenexposed to white light of more than 2,000 lux, silicone poly-mers containing MB and those containing MB  Au inoc-ulated with 108 CFUs of MRSA were able to achieve reduc-tions of more than 99% in the viable count over 24 hours.This confirms the potential for these types of polymers tobe useful antimicrobial coatings. Although there was nodifference in the MRSA-killing ability of MB polymers and1132 infection control and hospital epidemiology november 2011, vol. 32, no. 11MB  Au polymers over 24 hours, over a 6-hour periodthe MB  Au polymers were more effective than MB poly-mers at reducing MRSA numbers.When tested in a dental clinic, the coatings appeared tobe less effective at reducing microbial numbers than they wereunder laboratory conditions. However, the clinical setting isa diverse environment with multiple factors that contributeto microbial flux at any given time. The amount and type ofclinical activity taking place, the level of air flow, and theprevailing ambient temperature all contribute to the extentof the microbial load. In such an environment, there willlikely be continual arrival of new microbes on surfaces. Giventhat there is likely to be a lag between the arrival of a microbeon a surface and light-activated killing, it is possible thatmicrobes settling on coating surfaces immediately before re-moval from the clinic were not killed because of insufficienttime to enable lethal photosensitization. Additionally, somemicrobial species are more difficult to kill than others—forexample, gram-positive bacteria are more susceptible thangram-negative bacteria.6 Similarly, the liquid matrix in whichmicrobes in clinical environments are suspended (saliva, se-rum) has an effect on microbial survival and on the effec-tiveness of lethal photosensitization.7 Therefore, it is unlikelythat antimicrobial-coated surfaces would be completely freeof microbes at any given time.In this study, we have demonstrated the ability of MB-embedded silicone polymers to reduce the microbial load ina clinic. We have also shown that the incorporation of 2-nmgold nanoparticles into these polymers enhances the reduc-tion in microbial load. This is the first report, to our knowl-edge, of the effectiveness of such nanogold-containing poly-mers under fluorescent lighting in a clinical environment.acknowledgmentsWe thank Elizabeth Watts for allowing us the use of a dental clinic at theEastman Dental Hospital and Dr. Aviva Petrie for assistance with statisticalanalyses. I.P. thanks the Wolfson/Royal Society for a merit award.Financial support. This work was funded by a grant from the HigherEducation Funding Council for England.Potential conflicts of interest. M.W.’s research group has received fundingfor research on light-activated antimicrobial agents from Ondine Biomedical,Vancouver, Canada; he also holds stock options in this company, whichlicenses from his employer (University College London) patents relating tothe use of light-activated antimicrobial agents. All other authors report noconflicts of interest relevant to this article.Affiliations: 1. Division of Microbial Diseases, UCL Eastman Dental In-stitute, University College London, London, United Kingdom; 2. Depart-ment of Chemistry, University College London, London, United Kingdom.Address correspondence to Michael Wilson, DSc, Division of MicrobialDiseases, UCL Eastman Dental Institute, University College London, 256Gray’s Inn Road, London WC1X 8LD, United Kingdom (mike.wilson@ucl.ac.uk).Received April 12, 2011; accepted June 30, 2011; electronically publishedSeptember 20, 2011. 2011 by The Society for Healthcare Epidemiology of America. All rightsreserved. 0899-823X/2011/3211-0014$15.00. DOI: 10.1086/662377references1. Decraene V, Pratten J, Wilson M. Cellulose acetate containingtoluidine blue and rose bengal is an effective antimicrobial coatingwhen exposed to white light. Appl Environ Microbiol 2006;72:4436–4439.2. Perni S, Piccirillo C, Pratten J, et al. The antimicrobial propertiesof light-activated polymers containing methylene blue and goldnanoparticles. Biomaterials 2009;30:89–93.3. Decraene V, Pratten J, Wilson M. An assessment of the activityof a novel light-activated antimicrobial coating in a clinical en-vironment. Infect Control Hosp Epidemiol 2008;29:1181–1184.4. Murchan S, Aucken H, O’Neill GL, et al. Emergence, spread, andcharacterization of phage variants of epidemic methicillin-resis-tant Staphylococcus aureus 16 in England and Wales. J Clin Mi-crobiol 2004;42:5154–5160.5. Chartered Institute of Building Service Engineers. CIBSE LightingGuide LG2: Hospitals and Healthcare Buildings. 1989.6. Usacheva MN, Teichert MC, Biel MA. Comparison of the meth-ylene blue and toluidine blue photobactericidal efficacy againstgram-positive and gram-negative microorganisms. Lasers SurgMed 2001;29:165–173.7. Decraene V, Pratten J, Wilson M. Novel light-activated antimi-crobial coatings are effective against surface-deposited Staphy-lococcus aureus. Curr Microbiol 2008;57:269–273.

Efficacy of a novel light-activated antimicrobial coating for disinfecting hospital surfaces.

We report on two XMM-Newton observations of the bright narrow-line Seyfert 1 galaxy Ark 564 taken one year apart (2000 June and 2001 June). The 0.6-10 keV continuum is well described by a soft blackbody component (kTau approximately equal 140-150 eV) plus a steep power law (Tau approximately equal to 2.50-2.55). No significant spectral changes are observed between the two observations, although the X-ray flux in the second observation is approximately equal to 40-50 per cent lower. In both observations we detect a significant absorption edge at a rest-frame energy of approximately equal to 0.73 keV, corresponding to O VII. The presence of the absorption feature is confirmed by a simultaneous Chandra grating observation in 2000 June, although the best-fitting edge threshold is at a slightly lower energy in the Chandra data, possibly because of a different parameterization of the underlying X-ray continuum. We find tentative evidence for a broad iron emission line in the 2000 June observation. The results from an analysis of the power spectral density (PSD) function are also presented. The present XMM-Newton data support the idea that the PSD shown two breads, although the location of the high-frequency break requires further constraints

Efficacy of a novel light-activated antimicrobial coating for disinfecting hospital surfaces.

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