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Hybrid nanostructured coating for increased resistance of prosthetic devices to staphylococcal colonization.
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PMID:  23281840     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Prosthetic medical device-associated infections are responsible for significant morbidity and mortality rates. Novel improved materials and surfaces exhibiting inappropriate conditions for microbial development are urgently required in the medical environment. This study reveals the benefit of using natural Mentha piperita essential oil, combined with a 5 nm core/shell nanosystem-improved surface exhibiting anti-adherence and antibiofilm properties. This strategy reveals a dual role of the nano-oil system; on one hand, inhibiting bacterial adherence and, on the other hand, exhibiting bactericidal effect, the core/shell nanosystem is acting as a controlled releasing machine for the essential oil. Our results demonstrate that this dual nanobiosystem is very efficient also for inhibiting biofilm formation, being a good candidate for the design of novel material surfaces used for prosthetic devices.
Ion Anghel; Alexandru Mihai Grumezescu
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Type:  Journal Article     Date:  2013-01-02
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Title:  Nanoscale research letters     Volume:  8     ISSN:  1931-7573     ISO Abbreviation:  Nanoscale Res Lett     Publication Date:  2013  
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Created Date:  2013-03-18     Completed Date:  2013-03-19     Revised Date:  2013-04-18    
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Nlm Unique ID:  101279750     Medline TA:  Nanoscale Res Lett     Country:  United States    
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Languages:  eng     Pagination:  6     Citation Subset:  -    
Department of Science and Engineering of Oxidic Materials and Nanomaterials, Faculty of Applied Chemistry and Materials Science, University Politehnica of Bucharest, Polizu Street no 1-7, Bucharest 011061, Romania.
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Journal ID (nlm-ta): Nanoscale Res Lett
Journal ID (iso-abbrev): Nanoscale Res Lett
ISSN: 1931-7573
ISSN: 1556-276X
Publisher: Springer
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Copyright ©2013 Anghel and Grumezescu; licensee Springer.
Received Day: 19 Month: 10 Year: 2012
Accepted Day: 16 Month: 12 Year: 2012
collection publication date: Year: 2013
Electronic publication date: Day: 2 Month: 1 Year: 2013
Volume: 8 Issue: 1
First Page: 6 Last Page: 6
PubMed Id: 23281840
ID: 3599461
Publisher Id: 1556-276X-8-6
DOI: 10.1186/1556-276X-8-6

Hybrid nanostructured coating for increased resistance of prosthetic devices to staphylococcal colonization
Ion Anghel12 Email:
Alexandru Mihai Grumezescu3 Email:
1ENT, “Carol Davila” University of Medicine and Pharmacy, Traian Vuia no.6, Bucharest 020956, Romania
2Doctor Anghel Medical Center, Theodor Sperantia Street, Bucharest, 30932, Romania
3Department of Science and Engineering of Oxidic Materials and Nanomaterials, Faculty of Applied Chemistry and Materials Science, University Politehnica of Bucharest, Polizu Street no 1-7, Bucharest 011061, Romania


Staphylococcus aureus was recognized as a major pathogen soon after its discovery in the late nineteenth century. This organism causes a broad range of conditions, ranging from asymptomatic colonization to severe invasive infections which can progress to complicated septicemia, osteomyelitis, septic arthritis, or endocarditis [1,2]. S. aureus is a major cause of nosocomial infections and is responsible for significant morbidity, mortality, and an extended hospital stay [3,4]. This Gram-positive bacterium possesses specific surface proteins such as fibronectin-binding proteins, collagen-binding proteins, and fibrinogen-binding proteins, which have been implicated as mediators in specific bacterial binding to the extracellular matrix and subsequent biofilm development [1,5-7].

The increased use of prosthetic devices during the past decades has been accompanied by a constantly increased number of prosthetic device infections [8]. S. aureus is a widespread bacterium, being found on the skin and mucosa of healthy persons; therefore, prosthesis-associated infections incriminating this pathogen are frequently encountered [9]. Prosthesis-associated infections could be the results of microbial colonization by three routes: (a) direct inoculation at the time of implantation, (b) hematogenous spreading during bacteremia, or (c) direct contiguous spreading from an adjacent infectious focus [10].

One of the most severe complications is a biofilm-associated infection of a prosthetic device due to the fact that biofilm bacteria are different from planktonic cells, being usually more resistant. The biofilm cells are resistant to all kinds of antimicrobial substances: antibiotics, antiseptics, disinfectants; this kind of resistance, consecutive to biofilm formation, is phenotypic, behavioral, and more recently, called tolerance [43,44].

Among the promising approaches to combat biofilm infections is the generation of surface modification of devices to reduce microbial attachment and biofilm development as well as incorporation of antimicrobial agents to prevent colonization. Essential oils (EOs) and their components are gaining increasing interest in the food, cosmetic, and pharmaceutical industries because of their relatively safe status, their wide acceptance by consumers, and their exploitation for potential multi-purpose functional use [11].

Plants of the genus Mentha produce a class of natural products known as mono-terpenes (C10), characterized by p-menthone skeleton. Members of this genus are the only sources for the production of one of the most economically important essential oil, menthol, throughout the world [12]. Mentha piperita, commonly called peppermint, is a well-known herbal remedy used for a variety of symptoms and diseases, recognized for its carminative, stimulating, antispasmodic, antiseptic, antibacterial, and antifungal activities [4,13,14]. However, their use for clinical purposes is limited by the high volatility of the major compounds.

Due to their high biocompatibility [15] and superparamagnetic behavior, magnetite nanoparticles (Fe3O4) have attracted attention to their potential applications especially in biomedical fields [16,17], such as magnetic resonance imaging [18-20], hyperthermia [21], biomedical separation and purification [22], bone cancer treatment [21], inhibition of biofilm development [23,24], stabilization of volatile organic compounds [25], antitumoral treatment without application of any alternating magnetic field [26], drug delivery or targeting [27-33], modular microfluidic system for magnetic-responsive controlled drug release, and cell culture [34].This paper reports a new nano-modified prosthetic device surface with anti-pathogenic properties based on magnetite nanoparticles and M. piperita essential oil.


All chemicals were used as received. FeCl3 (99.99%), FeSO4·7H2O (99.00%), NH3(28% NH3 in H2O, ≥99.99% trace metal basis), lauric acid (C12) (98.00%), CHCl3 (anhydrous, ≥99%, contains 0.5% to 1.0% ethanol as stabilizer),and CH3OH (anhydrous, 99.8%) were purchased from Sigma-Aldrich. Prosthetic device represented by catheter sections were obtained from ENT (Otolarincology), Department of Coltea Hospital, Bucharest, Romania.

Fabrication of nano-modified prosthetic device

For the fabrication of the nano-modified prosthetic device, we used a recently published method [35] in order to design a new anti-pathogenic surface coated with nanofluid by combining the unique properties of magnetite nanoparticles to prevent biofilm development and the antimicrobial activity of M. piperita essential oil.

M. piperita plant material was purchased from a local supplier and subjected to essential oil extraction. A Neo Clevenger-type apparatus was used to perform microwave-assisted extractions. Chemical composition was settled by GC-MS analysis according to our recently published paper [36].

Magnetite (Fe3O4) is usually prepared by precipitation method [37-39]. The core/shell nanostructure used in this paper was prepared and characterized using a method we previously described [40]. Briefly, sodium laurate (C12) was added under stirring to a basic aqueous solution of NH3, and then FeSO4/FeCl3 (1:2 molar ratio) was dropped under continuous stirring up to pH = 8, leading to the formation of a black precipitate. The product was repeatedly washed with methanol and separated with a strong NdFeB permanent magnet. The obtained powder was identified as magnetite by XRD. Dimension of the core/shell structure not exceeding 5 nm and their spherical shape were confirmed by TEM analysis. The FT-IR analysis identified the organic coating agent, i.e., lauric acid on the surface of the magnetite nanoparticles. In order to fabricate a modified surface of prosthetic device, core/shell/EO nanofluid was used to create a coated shell. The layer of core/shell/EO nanofluid on the prosthetic device was achieved by submerging the catheter pieces in 5 mL of nanofluid (represented by solubilized core/shell/EO in CHCl3 (0.33% w/v) aligned in a magnetic field of 100 kgf applied for 1 s.

The catheter pieces were allowed to dry at room temperature. The rapid drying was facilitated by the convenient volatility of chloroform [41]. The coated prosthetic devices were then sterilized by ultraviolet irradiation for 15 min. Figure 1 presents a schematic representation of biofilm development on the surface of the prosthetic device coated/uncoated with anti-pathogenic nanofluid.

TG analysis

The thermogravimetric (TG) analysis of theFe3O4@C12 and Fe3O4@C12@EO was followed with a Netzsch TG 449C STA Jupiter instrument (Netzsch, Selb, Germany). Samples were screened with 200 mesh prior to analysis, placed in an alumina crucible, and heated at 10 K·min−1 from room temperature to 800°C, under the flow of 20 mL min−1of dried synthetic air (80% N2 and 20% O2).

Biofilm development on nano-modified prosthetic device surface

The adherence of S. aureus ATCC 25923 was investigated in six multiwell plates using a static model for monospecific biofilm developing. Catheter pieces of 1 cm with and without coated shell were distributed in plastic wells (one per well) and immersed in the liquid culture medium represented by nutrient broth. The plastic wells were inoculated with 300 μL of 0.5 McFarland microbial suspensions and incubated for 24 h at 37°C. After incubation the culture medium was removed, and the prosthetic device samples were washed three times in phosphate buffered saline (PBS) in order to remove the nonadherent strains and moved into sterile wells. Then, fresh broth was added, the incubation being continued for 72 h. Viable cell counts (VCCs) have been achieved for both working variants (coated and uncoated prosthetic devices) after 24, 48, and 72 h of incubation, respectively, in order to establish the dynamics of the biofilm development and of the inhibitory effect exhibited by the proposed coating system. The adhered cells have been removed from the catheter sections by vortexing and brief sonication, and serial tenfold dilutions ranging from 10−4 to 10−12 of the obtained inocula have been spotted on Muller-Hinton agar, incubated for 24 h at 37°C, and assessed for VCCs [23,42]. All tests were performed in triplicate.

Characterization of biofilm development on the surface of nano-modified prosthetic device

After 24, 48, and 72 h of incubation, the samples prepared as described above were removed from the plastic wells, washed three times with PBS, fixed with cold methanol, and dried before microscopic examination. The biofilm development on the surface of coated and uncoated prosthetic devices was visualized using a Hitachi S2600N scanning electron microscope (SEM; Tokyo, Japan) at 25 keV, in primary electron fascicles, on samples covered with a thin silver layer.

Results and discussion

The increasing occurrence of multiresistant pathogenic bacterial strains has gradually rendered traditional antimicrobial treatment ineffective. The prognosis is worsened by the formation of bacterial biofilms on the biomaterials used in medicine, even if the planktonic cells are susceptible to some antibiotics. Public reports stated that 60% to 85% of all microbial infections involve biofilms developed on natural intact or damaged tissues or artificial devices [43]. These infections are characterized by slow onset, middle-intensity symptoms, chronic evolution, and high tolerance to antibiotics and other antimicrobials [44].

The efficiency of essential oils, polyphenolic extracts obtained from foregoing plants, and their synergic effects as alternative strategies for the treatment of severe infections caused by highly resistant bacteria was tested on the following species: methicillin-resistant S. aureus, extended-spectrum beta-lactamases producing Escherichia coli, and multiresistant Pseudomonas aeruginosa[8]. Previous studies have demonstrated that the mint essential oil (Mentha sp.) exhibited synergistic inhibitory effects with low pH and sodium chloride against Listeria and inhibited some organisms such as S. aureus, E. coli, Candida albicans, Acinetobacter baumanii, Enterococcus faecalis, Klebsiella pneumoniae, Salmonella enterica subsp. enterica serotype Typhimurium, and Serratia marcescens[45]. The analyzed M. piperita EO proved to be rich in β-pinene, limonene, menthone, isomenthol, and menthol. These results are in concordance with reported literature [46,47]. We have suggested before the efficiency of nanosystem-vectored essential oil strategy [23]. The Fe3O4/C12 nanoparticles seem not to be cytotoxic on the HEp2 cell line, which is a great advantage for the in vivo use of these nanostructure systems for biomedical applications with minor risks of the occurrence of side effects [48].

TG analysis is plotted in Figure 2. The mass loss of EO is up to approximately 170°C, while the mass loss of C12 is between 170°C and 375°C. To avoid errors due to overlapping the two regions of weight loss, EO content was estimated as the difference between weight loss for the region at approximately 375°C for both materials, and it is approximately 17.3%.

The dynamics of viable cells embedded in the biofilm developed on the catheter device samples showed a significant decrease of the biofilm viable cells, as compared with the uncoated surface (Figure 3). The number of biofilm-embedded cells at 24, 48, and 72 h was almost the same in the case of the coated surface. By comparison, in the case of the uncoated device surface, an ascendant trend of the VVCs was observed for the three analyzed time points. These results suggest that the antibiofilm effect of the obtained coating is remanent, probably due to the gradual release of the essential oil compounds from the coating.

SEM images support the quantitative data, revealing the presence of a well-developed biofilm on the uncoated catheter, as compared with the functionalized one (Figure 4).Taken together, these results are demonstrating that the proposed solution for obtaining a nano-modified prosthetic device is providing an additional barrier to S. aureus colonization, an aspect which is very important for the readjustment of the treatment and prevention of infections associated with prosthetic devices.


In this study, we report the fabrication of a 5 nm core/shell nanostructure combined with M. piperita essential oil to obtain a unique surface coating with improved resistance to bacterial adherence and further development of staphylococcal biofilm. The obtained results proved that the proposed strategy is manifesting a dual benefit due to its anti-adherence and microbicidal properties. The microbicidal effect could be explained by the stabilization, decrease of volatility, and controlled release of the essential oil from the core/shell nanostructure. The results reveal a great applicability for the biomedical field, opening new directions for the design of anti-pathogenic film-coated-surface-based core/shell nanostructure and natural products.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

IA conceived of the study, provided the microbial strain, and drafted the manuscript together with AMG. AMG performed the fabrication of the nano-modified prosthetic devices, obtained the essential oil, and performed the biological analyses. Both authors read and approved the final manuscript.


This paper is supported by the PN-II-PT-PCCA-2011-3.2-0284: ‘Novel nanostructured prosthetic tubular devices with antibacterial and antibiofilm properties induced by physico-chemical and morphological changes’ funded by the National University Research Council in Romania. We thank G. Voicu for the kind assistance with the SEM and TG, and M. C. Chifiriuc for helping with the biological analyses and useful discussions.

Zhou H,Xiong ZY,Li HP,Zheng YL,Jiang YQ,An immunogenicity study of a newly fusion protein Cna-FnBP vaccinated against Staphylococcus aureus infections in a mice modelVaccineYear: 2006244830483710.1016/j.vaccine.2006.03.02016616974
Polgreen PM,Herwaldt LA,Staphylococcus aureus colonization and nosocomial infections: implications for preventionCurr Infect Dis ReportYear: 2004643544110.1007/s11908-004-0062-x
Van Werkum JW,Ten Berg JM,Thijs Plokker HW,Kelder JC,Suttorp MJ,Rensing BJWM,Tersmette M,Staphylococcus aureus infection complicating percutaneous coronary interventionsInt J CardiolYear: 200812820120610.1016/j.ijcard.2007.05.03717673313
Banu O,Bleotu C,Chifiriuc MC,Savu B,Stanciu G,Antal C,Alexandrescu M,Lazǎr V,Virulence factors of Staphylococcus aureus and Pseudomonas aeruginosa strains involved in the etiology of cardiovascular infectionsBiointerface Res App ChemYear: 201117277
Kuusela P,Fibronectin binds to Staphylococcus aureusNatureYear: 197827671872010.1038/276718a0732875
Boden MK,Flock J-I,Fibrinogen-binding protein/clumping factor from Staphylococcus aureusInfect ImmunYear: 198957235823632744851
Speziale P,Raucci G,Visai L,Switalski LM,Timpl R,Hook M,Binding of collagen to Staphylococcus aureusCowan I J BacteriolYear: 19861677781
Holban AM,Lazăr V,Inter-kingdom cross-talk: the example of prokaryotes - eukaryotes communicationBiointerface Res Appl ChemYear: 2011195110
Fowler VG,Fey PD,Reller LB,Chamis AL,Corey GR,Rupp ME,The intercellular adhesion locus ica is present in clinical isolates of Staphylococcus aureus from bacteremic patients with infected and uninfected prosthetic jointsMed Microbiol ImmunolYear: 200118912713110.1007/s430-001-8018-511388609
Zimmerli W,Prosthetic joint infection: diagnosis and treatmentCurr Infect Dis ReportYear: 2000237737910.1007/s11908-000-0059-z
Rodrigues L,Duarte A,Figueiredo AC,Brito L,Teixeira G,Moldao M,Monteiro A,Chemical composition and antibacterial activity of the essential oils from the medicinal plant Mentha cervina L. grown in PortugalMed Chem ResYear: 2012213485349010.1007/s00044-011-9858-z
Chakraborty A,Chattopadhyay S,Stimulation of menthol production in Mentha piperita cell cultureIn Vitro Cell Dev Biol-PlantYear: 20084451852410.1007/s11627-008-9145-y
Flamini G,Cioni PL,Puleio R,Morelli I,Panizzi L,Antimicrobial activity of the essential oil of Calamintha nepeta and its constituent pulegone against bacteria and fungiPhytother ResYear: 19991334935110.1002/(SICI)1099-1573(199906)13:4<349::AID-PTR446>3.0.CO;2-Z10404547
Gulluce M,Sahin F,Sokmen M,Ozer H,Daferera D,Sokmen A,Polissiou M,Adiguzel A,Ozkan H,Antimicrobial and antioxidant properties of the essential oils and methanol extract from Mentha longifolia L. ssp. longifoliaFood ChemYear: 20071031449145610.1016/j.foodchem.2006.10.061
Medeiros SF,Santos AM,Fessi H,Elaissari A,Stimuli-responsive magnetic particles for biomedical applicationsInt J PharmYear: 201140313910.1016/j.ijpharm.2010.10.01120951779
Tao K,Song S,Ding J,Dou H,Sun K,Carbonyl groups anchoring for the water dispersibility of magnetite nanoparticlesColloid Polym SciYear: 201128936136910.1007/s00396-011-2380-5
Grumezescu AM,Saviuc C,Holban A,Hristu R,Stanciu G,Chifiriuc C,Mihaiescu D,Balaure B,Lazar V,Magnetic chitosan for drug targeting and in vitro drug delivery responseBiointerface Res Appl ChemYear: 20111160
Pankhurst QA,Thanh NKT,Jones SK,Dobson J,Progress in applications of magnetic nanoparticles in biomedicineJ Phys D: Appl PhysYear: 20094222400110.1088/0022-3727/42/22/224001
Mantle MD,Quantitative magnetic resonance micro-imaging methods for pharmaceutical researchInt J PharmYear: 201141717310.1016/j.ijpharm.2010.11.03521115106
Schweiger C,Pietzonka C,Heverhagen J,Kissel T,Novel magnetic iron oxide nanoparticles coated with poly(ethylene imine)-g-poly(ethylene glycol) for potential biomedical application: synthesis, stability, cytotoxicity and MR imagingInt J PharmYear: 201140813013710.1016/j.ijpharm.2010.12.04621315813
Andronescu E,Ficai M,Voicu G,Manzu D,Ficai A,Synthesis and characterization of collagen/hydroxyapatite – magnetite composite material for bone cancer treatmentJ Mat Sci-Mat MedYear: 2010212237224210.1007/s10856-010-4076-7
Ficai D,Ficai A,Alexie M,Maganu M,Guran C,Andronescu E,Amino-functionalized Fe3O4/SiO2/APTMS nanoparticles with core-shell structure as potential materials for heavy metals removalRev Chim (Bucharest)Year: 201162622625
Grumezescu AM,Saviuc C,Chifiriuc MC,Hristu R,Mihaiescu DE,Balaure P,Stanciu G,Lazar V,Inhibitory activity of Fe3O4/oleic acid/usnic acid—core/shell/extra-shell nanofluid on S. aureus biofilm developmentIEEE T NanoBioSciYear: 201110269274
Anghel I,Grumezescu AM,Andronescu E,Anghel AG,Ficai A,Saviuc C,Grumezescu V,Vasile BS,Chifiriuc MC,Magnetite nanoparticles for functionalized textile dressing to prevent fungal biofilms developmentNanoscale Res LettYear: 2012750110.1186/1556-276X-7-50122950367
Chifiriuc MC,Grumezescu V,Grumezescu AM,Saviuc CM,Lazar V,Andronescu E,Hybrid magnetite nanoparticles/Rosmarinus officinalis essential oil nanobiosystem with antibiofilm activityNanoscale Res LettYear: 2012720910.1186/1556-276X-7-20922490675
Grumezescu AM,Andronescu E,Ficai A,Yang CH,Huang KS,Vasile BS,Voicu G,Mihaiescu DE,Bleotu C,Magnetic nanofluid with antitumoral propertiesLett Appl NanoBioSciYear: 201215660
Grumezescu AM,Andronescu E,Ficai A,Bleotu C,Mihaiescu DE,Chifiriuc MC,Synthesis, characterization and in vitro assessment of the magnetic chitosan-carboxymethylcellulose biocomposite interactions with the prokaryotic and eukaryotic cellsInt J PharmYear: 201243677177710.1016/j.ijpharm.2012.07.06322884836
Andronescu E,Grumezescu AM,Ficai A,Gheorghe I,Chifiriuc M,Mihaiescu DE,Lazar V,In vitro efficacy of antibiotic magnetic dextran microspheres complexes against Staphylococcus aureus and Pseudomonas aeruginosa strainsBiointerface Res Appl ChemYear: 20122332338
Wang H,Wang S,Liao Z,Zhao P,Su W,Niu R,Chang J,Folate-targeting magnetic core–shell nanocarriers for selective drug release and imagingInt J PharmYear: 2011430343
Grumezescu AM,Mihaiescu DE,Tamaş D,Hybrid materials for drug delivery of rifampicin: evaluation of release profileBiointerface Res Appl ChemYear: 20111229235
Grumezescu AM,Andronescu E,Ficai A,Saviuc C,Mihaiescu D,Chifiriuc MC,Deae-cellulose/Fe(3)O(4)/cephalosporins hybrid materials for targeted drug deliveryRom J MatYear: 201141383387
Mihaiescu DE,Horja M,Gheorghe I,Ficai A,Grumezescu AM,Bleotu C,Chifiriuc MC,Water soluble magnetite nanoparticles for antimicrobial drugs deliveryLett Appl NanoBioSciYear: 201214549
Yang CH,Huang KS,Wang CY,Hsu YY,Chang FR,Lin YS,Microfluidic-assisted synthesis of hemispherical and discoidal chitosan microparticles at an oil/water interfaceElectrophoresisYear: 201233213173318010.1002/elps.20120021122949174
Lin Y-S,Huang K-S,Yang C-H,Wang C-Y,Yang Y-S,Hsu H-C,Liao Y-J,Tsai C-W,Microfluidic synthesis of microfibers for magnetic-responsive controlled drug release and cell culturePLoS OneYear: 201273e3318410.1371/journal.pone.003318422470443
Anghel I,Limban C,Grumezescu AM,Anghel AG,Bleotu C,Chifiriuc MC,In vitro evaluation of anti-pathogenic surface coating nanofluid, obtained by combining Fe3O4/C12nanostructures and 2-((4-ethylphenoxy)methyl)-N-(substituted-phenylcarbamothioyl)-benzamidesNanoscale Res LettYear: 2012751310.1186/1556-276X-7-51322992217
Grumezescu AM,Chifiriuc CM,Marinaş I,Saviuc C,Mihaiescu D,Lazǎr V,Ocimum basilicum and Mentha piperita essential oils influence the antimicrobial susceptibility of Staphylococcus aureus strainsLett Appl NanoBioSciYear: 201211417
Ficai D,Ficai A,Vasile BS,Ficai M,Oprea O,Guran C,Andronescu C,Synthesis of rod-like magnetite by using low magnetic fieldDigest J Nanomat BiostructYear: 20116943951
Manzu D,Ficai A,Voicu G,Vasile BS,Guran C,Andronescu E,Polysulfone based membranes with desired pores characteristicsMat PlastYear: 2010472427
Mihaiescu DE,Grumezescu AM,Mogosanu DE,Traistaru V,Balaure PC,Buteica A,Hybrid organic/inorganic nanomaterial for controlled cephalosporins releaseBiointerface Res Appl ChemYear: 201114147
Grumezescu AM,Andronescu E,Ficai A,Mihaiescu DE,Vasile BS,Bleotu C,Synthesis, characterization and biological evaluation of a magnetite/lauric acid core/shell nanosystemLett Appl NanoBioSciYear: 201213135
Saviuc C,Grumezescu AM,Chifiriuc MC,Bleotu C,Stanciu G,Hristu R,Mihaiescu D,Lazar V,In vitro methods for the study of microbial biofilmsBiointerface Res Appl ChemYear: 201113240
Saviuc C,Grumezescu AM,Bleotu C,Holban A,Chifiriuc C,Balaure P,Lazar V,Phenotipical studies for raw and nanosystem embedded Eugenia carryophyllata buds essential oil effect on Pseudomonas aeruginosa and Staphylococcus aureus strainsBiointerface Res Appl ChemYear: 20111111118
Lazar V,Chifiriuc C,Medical significance and new therapeutical strategies for biofilm associated infectionsRom Arch Microb ImmunolYear: 201069125138
Donlan RM,Costerton JW,Biofilms: survival mechanisms of clinically relevant microorganismsClinical Microbiol RevYear: 20021516719310.1128/CMR.15.2.167-193.200211932229
Kalemba D,Matla M,Smętek A,Antimicrobial activities of essential oilsDietary Phytochem MicrobYear: 20122012157183
Lis-Balchin M,Deans SG,Hart S,A study of the variability of commercial peppermint oils using antimicrobial and pharmacological parametersMed Sci ResYear: 199725151152
Maffei M,Sacco T,Chemical and morphometrical comparison between two peppermint notomorphsPlanta MedYear: 19875321421610.1055/s-2006-96267517268996
Limban C,Grumezescu AM,Saviuc C,Voicu G,Predan G,Sakizlian R,Chifiriuc MC,Optimized anti-pathogenic agents based on core/shell nanostructures and 2-((4-ethylphenoxy)ethyl)-N-(substituted phenyl carbamothioyl)-benzamidesInt J Mol SciYear: 201213125841259710.3390/ijms13101258423202915


[Figure ID: F1]
Figure 1 

Biofilm development on the surface of the prosthetic device coated/uncoated with anti-pathogenic nanofluid. (a)staphylococcal biofilm development on the surface of the prosthetic device, (b) nano-modified surface of the prosthetic device, (c) inhibition of staphylococcal biofilm development on the nano-modified surface of the prosthetic device.

[Figure ID: F2]
Figure 2 

TGA diagram of Fe3O4@C12 and Fe3O4@C12@EO.

[Figure ID: F3]
Figure 3 

Viable cell counts recovered from S. aureus biofilms developed on the (nano-modified) catheter pieces. Samples were plated after 24h, 48h and 72h of incubation.

[Figure ID: F4]
Figure 4 

SEM micrographs of in vitro staphylococcal biofilm development on the surface of prosthetic devices. (1) Unmodified prosthetic device sections, (2) nano-coated prosthetic device sections, (a) surface of the prosthetic device, and (b) transversal section of the prosthetic device.

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