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| 3. |
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| 4. |
- Lilja, Mirjam, 1981-, et al.
(författare)
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Drug loading and release of Tobramycin from Hydroxyapatite coated fixation pins
- 2013
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Ingår i: Journal of materials science. Materials in medicine. - : Springer Science and Business Media LLC. - 0957-4530 .- 1573-4838. ; 24:9, s. 2265-2274
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Tidskriftsartikel (refereegranskat)abstract
- This paper evaluates the loading and release properties of Tobramycin incorporated by adsorptive loading from a solution into plasma sprayed and biomimetically coated Hydroxyapatite (HA) fixation pins. The aim of this study is to contribute towards designing a functional implant surface offering local release of the antibiotic agent to prevent post-surgical infections. Cathodic arc deposition is used to coat stainless steel fixation pins with a bioactive, anatase phase dominated, TiO2 coating onto which a HA layer is grown biomimetically. The loading and release properties are evaluated by studying the subsequent release of Tobramycin using high performance liquid chromatography and correlated to the differences in HA coating microstructure and the physical conditions under loading. The results from these studies show that a dual loading strategy consisting of a solution temperature of 90 °C and a pressure of 6 bar during a loading time of 5 min release a sufficient amount of Tobramycin to guarantee the inhibition of Staphylococcus aureus up to 2 days for plasma sprayed HA coatings and for 8 days for biomimetic coatings. The present study emphasizes the advantages of the nanoporous structure of biomimetically deposited HA over the more dense structure of plasma sprayed HA coatings in terms of antibiotic incorporation and subsequent sustained release and provides a valuable outline for the design of implant surfaces aiming for a fast-loading and controlled, local drug administration.
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| 5. |
- Lilja, Mirjam, et al.
(författare)
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Effect of deposition parameters on the photocatalytic activity and bioactivity of TiO(2) thin films deposited by vacuum arc on Ti-6Al-4V substrates
- 2012
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Ingår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials. - : Wiley. - 1552-4973 .- 1552-4981. ; 100B:4, s. 1078-1085
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Tidskriftsartikel (refereegranskat)abstract
- This article evaluates the influence of the main parameters in a cathodic arc deposition process on the microstructure of titanium dioxide thin coatings and correlates these to the photocatalytic activity (PCA) and in vitro bioactivity of the coatings. Bioactivity of all as deposited coatings was confirmed by the growth of uniform layers of hydroxyapatite (HA) after 7 days in phosphate buffered saline at 37°C. Comparison of the HA growth after 24 h indicated enhanced HA formation on coatings with small titanium dioxide grains of rutile and anatase phase. The results from the PCA studies showed that coatings containing a mixed microstructure of both anatase and rutile phases, with small grain sizes in the range of 26-30 nm and with a coating thickness of about 250 nm, exhibited enhanced activity as compared with other microstructures and higher coating thickness. The results of this study should be valuable for the development of new bioactive implant coatings with photocatalytically induced on-demand antibacterial properties.
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| 6. |
- Lilja, Mirjam, 1981-, et al.
(författare)
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Impact of Biomechanical Forces on Antibiotics Release Kinetics from Hydroxyapatite Coated Surgical Fixation Pins
- 2013
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Ingår i: Journal of Biomaterials and Nanobiotechnology. - : Scientific Research Publishing, Inc.. - 2158-7027 .- 2158-7043. ; 4:4, s. 343-350
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Tidskriftsartikel (refereegranskat)abstract
- This work investigates the impact of biomechanical wear and abrasion on the antibiotic release profiles of hydroxyapa-tite (HA) coated fixation pins during their insertion into synthetic bone. Stainless steel fixation pins are coated with crystalline TiO2 by cathodic arc evaporation forming the bioactive layer for biomimetic deposition of Tobramycin con-taining HA. Tobramycin is either introduced by co-precipitation during HA formation or by adsorption-loading after HA deposition. The samples containing antibiotics are inserted into bone mimicking polyethylene foam after which the drug release is monitored using high performance liquid chromatography. This analysis shows that HA coating wear and delamination significantly decrease the amount of drug released during initial burst, but only marginally influence the sustained release period. Spalled coating fragments are found to remain within the synthetic bone material structure. The presence of HA within this structure supports the assumption that the local release of Tobramycin is not only ex-pected to eliminate bacteria growth directly at the pin interface but as well at some distance from the implant. Further-more, no negative effect of gamma sterilization could be observed on the drug release profile. Overall, the observed results demonstrate the feasibility of a multifunctional implant coating that is simultaneously able to locally deliver clinically relevant doses of antibiotics and an HA coating capable of promoting osteoconduction. This is a potentially promising step toward orthopaedic devices that combine good fixation with the ability to treat and prevent post-surgical infections.
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| 7. |
- Lilja, Mirjam, 1981-, et al.
(författare)
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Influence of microstructure and chemical composition of sputter deposited TiO2 thin films on in vitro bioactivity
- 2011
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Ingår i: Journal of materials science. Materials in medicine. - : Springer. - 0957-4530 .- 1573-4838. ; 22:12, s. 2727-2734
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Tidskriftsartikel (refereegranskat)abstract
- Functionalisation of biomedical implants viasurface modifications for tailored tissue response is agrowing field of research. Crystalline TiO2 has been provento be a bone bioactive, non-resorbable material. In contactwith body fluids a hydroxyapaptite (HA) layer forms on itssurface facilitating the bone contact. Thus, the path ofimproving biomedical implants via deposition of crystallineTiO2 on the surface is interesting to follow. In thisstudy we have evaluated the influence of microstructureand chemical composition of sputter deposited titaniumoxide thin films on the in vitro bioactivity. We find thatboth substrate bias, topography and the flow ratio of thegases used during sputtering affect the HA layer formed onthe films after immersion in simulated body fluid at 37C.A random distribution of anatase and rutile crystals, formedat negative substrate bias and low Ar to O2 gas flow ratios,are shown to favor the growth of flat HA crystal structureswhereas higher flow ratios and positive substrate biasinduced growth of more spherical HA structures. Thesefindings should provide valuable information when optimizingthe bioactivity of titanium oxide coatings as well asfor tailoring process parameters for sputtered-based productionof bioactive titanium oxide implant surfaces.
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| 8. |
- Lilja, Mirjam, 1981-, et al.
(författare)
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Photocatalytic and antimicrobial properties of surgical implant coatings of titanium dioxide deposited though cathodic arc evaporation
- 2012
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Ingår i: Biotechnology letters. - : Springer Science and Business Media LLC. - 0141-5492 .- 1573-6776. ; 41:6, s. 740-746
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Tidskriftsartikel (refereegranskat)abstract
- Nanostructured crystalline titaniumdioxide coatings deposited by cathodic arc evaporated on titanium grade five medical implant substrates were demonstrated to exhibit UV-induced photocatalytic activity that can be utilized to provide bactericidal effects against Staphylococcus epidermidis. The photocatalytic activity of the coatings was confirmedvia degradation of Rhodamine B under UV illumination.A 90 %reduction of viable bacteria was achieved in a clinically suitable time of only 2 min with a UVdose of 2.4 J delivered at 365 nm. These results areencouraging for the development of antimicrobialsurfaces in orthopedics and dentistry in order to prevent or treat post-surgical infections.
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| 9. |
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| 10. |
- Lilja, Mirjam, 1981-, et al.
(författare)
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Photocatalytic and bioactive TiO2 thin films deposited by vacuum arc
- 2012
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Ingår i: European Cells & Materials. - Aberystwyth : University of Wales. - 1473-2262. ; 23:Suppl. 5, s. 48-
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Tidskriftsartikel (refereegranskat)abstract
- Improving biomedical implants via deposition of functionalised surface coatings is a growing field of research. With respect to implant surfaces, infections present a major problem, and result mostly from the contamination of the surface by bacteria during surgery. UV irradiation induced photocatalysis on crystalline TiO2 implant surfaces may present a promising way to decontaminate surfaces while at the same time providing a bioactive surface for enhanced tissue integration.
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| 11. |
- Sörensen, Jan Henrik, et al.
(författare)
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Biomechanical and Antibacterial Properties of Tobramycin Loaded Hydroxyapatite Coated Fixation Pins
- 2014
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Ingår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials. - : Wiley. - 1552-4973 .- 1552-4981. ; 102:7, s. 1381-1392
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Tidskriftsartikel (refereegranskat)abstract
- The present study investigates the use of nanoporous, biomimetic hydroxyapatite (HA) coatings deposited on TiO2 coated fixation pins as functional implant surfaces for the local release of Tobramycin in order to prevent bacterial colonization. The impact of HA-coating thickness, coating morphology and biomechanical forces during insertion into synthetic bone on the drug loading and release properties are analyzed. The coatings are shown to exhibit bactericidal effects against Staphylococcus aureus in agar medium for a duration of 6 days after loading by adsorption with Tobramycin for only 5 min at elevated temperature and pressure. Furthermore, high performance liquid chromatography analysis shows a drug release in phosphate buffered saline for 8 days with antibiotic concentration remaining above the minimal inhibitory concentration for S. aureus during the entire release period. Biomechanical insertion tests into synthetic bone and conventional scratch testing demonstrate adhesive strength at the HA/TiO2 interface. Biocompatibility is verified by cell viability tests. Outgrowth endothelial cells, as well as primary osteoblasts, are viable and firmly attached to both HA and TiO2 surfaces. The results presented are encouraging and support the concept of functional HA coatings as local drug delivery vehicles for biomedical applications to treat as well as to prevent post-surgical infections.
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| 12. |
- Sörensen, Jan H, et al.
(författare)
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Co-precipitation of Tobramycin into Biomimetically Coated Orthopedic Fixation Pins Employing Submicron-Thin Seed Layers of Hydroxyapatite
- 2014
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Ingår i: Current Drug Delivery. - : Bentham Science Publishers Ltd.. - 1567-2018 .- 1875-5704. ; 11:4, s. 501-510
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Tidskriftsartikel (refereegranskat)abstract
- Implant migration, loosening and cut-out as well as nosocomial infections are current problems during surgery. New innovative strategies to overcome these issues are emphasized in today's research. The currentwork presents a novel strategy involving co-precipitation ofTobramycin with biomimetic hydroxyapatite (HA) formation to produce implant coatings that may ensure controlled local drug delivery to prevent early bacterial colonization of the implant. A sub-micron thin HA layer served as seed layer for the co-precipitation process and allowed for incorporation of Tobramycin in the coating from a stock solution of antibiotic concentrations as high as 20 mg/ml. Concentrations from 0.5 to 20 mg/ml Tobramycin and process temperatures of 37 °C and 60 °C were tested to assess the optimal parameters resulting in a thin Tobramycin delivering HA coating on discs and orthopedic fixation pins. The coating morphology and thickness as well as drugrelease profile were evaluated via scanning electron microscopy and high performanceliquid chromatography. The coatings were found to deliver pharmaceutically relevant amounts of Tobramycinover a period as of12 days. To the best of our knowledge, this is the longest release period ever observed for a fast-loaded biomimetic implant coating. The presented approach may form thefoundation for development of combination device/antibiotic delivery vehicles tailored to meet well-defined clinical needs combatting infections and ensuring fast implant in-growth.
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| 13. |
- Welch, Ken, et al.
(författare)
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Bioactive and photocatalytically active surgical implant surfaces
- 2012
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Ingår i: Euro Bio-inspired Materials, International School and Conference on Biological Materials Science, 20-23 March.
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Konferensbidrag (refereegranskat)abstract
- Improving biomedical implants via deposition of functionalised surface coatings is a growing field of research. An enhanced bone-bonding capability by induction of hydroxyapatite (HA) formation on the implant surface is a critical characteristic of a bioactive implant coating. In the field of implants, infections present a major problem, and result mostly from the contamination of the implant surface by bacteria during surgery. There is a need for antibacterial surface treatments, which can prevent the bacterial colonization and biofilm formation without compromising the biocompatibility of the implant itself.Crystalline TiO2 is not only a bioactive, non-resorbable material, it also exhibits excellent superhydrophilic and photocatalytic properties when irradiated with UV light. Thus, UV irradiation induced photocatalysis on crystalline TiO2 implant surfaces may present an effective method for decontaminating implant surfaces.In our study we have evaluated the influence of the main deposition parameters in the cathodic evaporation process on the microstructure of TiO2 thin films and correlated these to the photocatalytic activity (PCA) and in vitro bioactivity of the coatings.Bioactivity of all as deposited coatings was confirmed by the growth of uniform layers of HA after 7 days in phosphate buffered saline at 37 °C. Comparison of the HA growth after 24 hours indicated enhanced HA formation on coatings with small titanium dioxide grains of the rutile and the anatase phase. The results from the PCA studies showed that coatings containing a mixed microstructure of both anatase and rutile phases, with small grain sizes in the range of 26-30 nm and with a coating thickness of about 250 nm, exhibited enhanced activity as compared to other microstructures and higher coating thickness. The results of this study should be valuable for the development of new bioactive implant coatings with photocatalytically induced on-demand antibacterial properties.
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| 14. |
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| 15. |
- Akhtar, Sultan, et al.
(författare)
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Real-Space Transmission Electron Microscopy Investigations of Attachment of Functionalized Magnetic Nanoparticles to DNA-Coils Acting as a Biosensor
- 2010
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 114:41, s. 13255-13262
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Tidskriftsartikel (refereegranskat)abstract
- The present work provides the first real-space analysis of nanobead-DNA coil interactions. Immobilization of oligonucleotide-functionalized magnetic nanobeads in rolling circle amplified DNA-coils was studied by complex magnetization measurements and transmission electron microscopy (TEM), and a statistical analysis of the number of beads hybridized to the DNA-coils was performed. The average number of beads per DNAcoil using the results from both methods was found to be around 6 and slightly above 2 for samples with 40 and 130 nm beads, respectively. The TEM analysis supported an earlier hypothesis that 40 nm beads are preferably immobilized in the interior of DNA-coils whereas 130 nm beads, to a larger extent, are immobilized closer to the exterior of the coils. The methodology demonstrated in the present work should open up new possibilities for characterization of interactions of a large variety of functionalized nanoparticles with macromolecules, useful for gaining more fundamental understanding of such interactions as well as for optimizing a number of biosensor applications.
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| 16. |
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| 17. |
- Akhtar, Sultan, et al.
(författare)
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Visualization of functionalization of nano-particles and graphene in the TEM
- 2010
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Ingår i: Advanced Materials Workshop 2010.
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Konferensbidrag (refereegranskat)abstract
- Recently, the activity on functionalized nano-objects has strongly increased. Yet, there are, to our knowledge no techniques available that visualize the attachment of molecules to nano-entities such as nanoparticles and graphene. In this work, we show a methodology to analyse the attachment of molecules to nanoparticles and graphene. The difficulty of such transmission electron microscopy (TEM) characterization consists in the high beam sensitivity of these nanoobjects. We employed a high resolution- as well as diffraction contrast-imaging methods to characterize graphene. First, we have developed a method to measure the thickness of free-standing graphene-like layers. The refinement of these imaging techniques enabled the imaging of functionalized C60 (fullerene) on top of a few-layer graphene flake by TEM. We also developed a methodology to visualize the attachment of functionalized gold and magnetic nanoparticles (different sizes) to nonstained and unlabeled single strand DNA-coils. This technique can be used to understand the interaction of a large variety of functionalized nanoparticles with their solution environment and/or macromolecular structures for their large applications.
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| 18. |
- Atluri, Rambabu, 1981-
(författare)
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Novel Syntheses, Structures and Functions of Mesoporous Silica Materials
- 2010
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The field of mesoporous silica has been studied for about 20 years but it is still an area attracting a lot of attention. The use of novel templating molecules and several issues related to the synthesis and fine structural details are still poorly understood. These aspects are of special relevance to the theme of this thesis, which includes novel work on three fronts; the synthesis, characterization and applications of mesoporous materials. The work described in this thesis aims to contribute to the mesoporous field by developing novel methods of mesoporous silica synthesis without relying on surfactant micelles as the templating agent but focusing instead on the stacking arrangement of aromatic molecules such as folic acid. The novel route presented here leads to 2D hexagonal structures with p6mm symmetry possessing high mesoporosity and large surface areas. The versatility of this route at various synthesis temperatures and using hydrothermal treatments has also been investigated. A novel strategy is also proposed for the synthesis of mesocaged materials with Pm3n symmetry structures. The mechanism relies on the penetration of the neutral propylamino moiety of a co-structure directing agent into the hydrophobic core of the surfactant micelles. Beside these novel pathways, the effect of hydrothermal treatment (HT) at 100 oC on the 3D cubic Ia3d structure (AMS-6) over a long period of time was also examined, and the results show a phase transformation from a 3D cubic Ia3d to a 2D hexagonal p6mm structure and a return to the 3D cubic Ia3d structure at a later stage in the synthesis. This unexpected result is discussed. In this work, the detailed structural characterization of mesoporous materials using electron microscopy techniques is an important task. In particular, to extend previous knowledge, the fine structural details of mesocaged materials possessing Pm3n symmetry prepared with various amphiphilic surfactants under acidic and alkaline conditions has been investigated using electron crystallography and sorption studies. The results show subtle fine structural differences with materials prepared under alkaline conditions exhibiting the largest mesocage sizes. The cage and window sizes are primarily determined by the charge density of the surfactant and the thickness of the hydration layer surrounding the surfactant micelles. The relationship between the mesoporous structure and its function has been investigated by evaluating the rate of release of amphiphilic molecules, used as model molecules, from the internal pore structures of mesoporous materials with different pore geometries. In a similar study, the rate of proton diffusion from a liquid surrounding the mesoporous nanoparticles into the pore system of AMS-n was also assessed. The results show that the diffusion coefficients for the proton absorption process are higher than those for the release of the surfactant template molecules, with more complex 3D mesocaged particles showing the highest diffusion coefficients in both cases. Finally, the quantity of CO2 adsorption was measured by modifying the internal surfaces of mesocaged material with n-propylamino groups. Results show that the cage-connecting window sizes limit the surface coverage of n-propylamino groups by pore blocking and affect the volume of CO2 adsorption. In addition, at the molecular level, CO2 adsorption shows physisorption or chemisorption depending on the localized distribution of n-propylamino groups, as studied by in-situ infrared spectroscopy.
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| 19. |
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| 20. |
- Blom, Tobias
(författare)
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Fabrication and Applications of a Focused Ion Beam Based Nanocontact Platform for Electrical Characterization of Molecules and Particles
- 2010
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The development of new materials with novel properties plays an important role in improving our lives and welfare. Research in Nanotechnology can provide e.g. cheaper and smarter materials in applications such as energy storage and sensors. In order for this development to proceed, we need to be able to characterize the material properties at the nano-, and even the atomic scale. The ultimate goal is to be able to tailor them according to our needs. One of the great challenges concerning the characterization of nano-sized objects is how to achieve the physical contact to them. This thesis is focused on the contacting of nanoobjects with the aim of electrically characterizing them and subsequently understanding their electrical properties. The analyzed nanoobjects are carbon nanosheets, nanotetrapods, nanoparticles and molecular systems. Two contacting strategies were employed in this thesis. The first strategy involved the development of a focused ion beam (FIB) based nanocontact platform. The platform consists of gold nanoelectrodes, having nanogaps of 10-30 nm, on top of an insulating substrate. Gold nanoparticles, double-stranded DNA and cadmium telluride nanotetrapods have been trapped in the gaps by using dielectrophoresis. In certain studies, the gold electrodes have also been coated with conducting or non-conducting molecules, prior to the trapping of gold nanoparticles, in order to form molecular junctions. These junctions were subsequently electrically characterized to evaluate the conduction properties of these molecular systems. For the purpose of better controlling the attachment of molecules to the nanoelectrodes, a novel route to synthesize alkanedithiol coated gold nanoparticles was developed. The second contacting strategy was based on the versatility of the FIB instrument as a platform for in-situ manipulation and electrical characterization of non-functionalized and functionalized carbon nanosheets, where it was found that the functionalized samples had an increased conductivity by more than one order of magnitude. Both contacting strategies proved to be valuable for building knowledge around contacting and electrical characterization of nanoobjects
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| 21. |
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| 22. |
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| 23. |
- Cai, Yanling, et al.
(författare)
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Bacteria viability assessment after photocatalytic treatment
- 2014
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Ingår i: 3 Biotech. - : Springer. - 2190-5738 .- 2190-572X. ; 4:2, s. 149-157
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Tidskriftsartikel (refereegranskat)abstract
- The aim of the present work was to evaluate several methods for analyzing the viability of bacteria after antibacterial photocatalytic treatment. Colony-forming unit (CFU) counting, metabolic activity assays based on resazurin and phenol red and the Live/Dead® BacLight™ bacterial viability assay (Live/Dead staining) were employed to assess photocatalytically treated Staphylococcus epidermidis and Streptococcus mutans. The results showed conformity between CFU counting and the metabolic activity assays, while Live/Dead staining showed a significantly higher viability post-treatment. This indicates that the Live/Dead staining test may not be suitable for assessing bacterial viability after photocatalytic treatment and that, in general, care should be taken when selecting a method for determining the viability of bacteria subjected to photocatalysis. The present findings are expected to become valuable for the development and evaluation of photocatalytically based disinfection applications
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| 24. |
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| 25. |
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| 26. |
- Cai, Yanling, et al.
(författare)
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Disinfection Kinetics and Contribution ofReactive Oxygen Species When EliminatingBacteria with TiO2 Induced Photocatalysis
- 2014
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Ingår i: Journal of Biomaterials and Nanobiotechnology. - : Scientific Research Publishing, Inc.. - 2158-7027 .- 2158-7043. ; 5:3, s. 200-209
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Tidskriftsartikel (refereegranskat)abstract
- Titania (TiO2) induced photocatalysis has been widely investigated and applied as a disinfectionstrategy in many industrial and clinical applications. Reactive oxygen species (ROS), including hydroxylradicals (•OH), superoxide radicals ( •−2 O ) and hydrogen peroxide (H2O2), generated in thephotocatalytic reaction process are considered to be the active components prompting the bactericidaleffect. In the present work, the kinetics of photocatalytic inactivation of Staphylococcus epidermidisand specific contributions of •OH, •−2 O and H2O2 to the bactericidal process were studiedusing two disinfection settings sutilizing photocatalytic resin-TiO2 nanocomposite surfacesand suspended TiO2 nanoparticles, respectively. In antibacterial tests against S. epidermidis with alayer of bacterial suspension on the resin-TiO2 surfaces, H2O2 was found to be the most efficientROS component contributing to the antibacterial effect. Disinfection kinetics showed a two-stepbehavior with an initial region having a lower disinfection rate followed by a higher rate regionafter 10 min of UV irradiation. By contrast, in antibacterial tests with suspended bacteria andphotocatalytic TiO2 nanoparticles, •OH and H2O2 showed equal significance in the bacterial inactivationhaving a typical Chick-Watson disinfection kinetics behavior with a steady disinfection rate.The results contribute to the understanding of the bactericidal mechanism and kinetics of photocatalyticdisinfection that are essential for designing specific antibacterial applications of photocatalyticmaterials.
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| 27. |
- Cai, Yanling, et al.
(författare)
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Photocatalysis induces bioactivity of an organic polymer based material
- 2014
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 4:101, s. 57715-57723
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Tidskriftsartikel (refereegranskat)abstract
- Several materials, like bioglasses, sintered hydroxyapatite and Ti metals and alloys, have the ability to bond to living bone in vivo, which is a desirable property of biomaterials called bioactivity. In this work, we present a novel strategy to develop bioactivity on the non-bioactive surface of a resin-TiO2 nanocomposite through photocatalysis. The results show that UV irradiation (365 nm, 10 mW cm(-2)) for 8 to 16 h on the resin-TiO2 nanocomposite immersed in water induces bioactivity as indicated by hydroxyapatite growth following immersion of the samples in Dulbecco's phosphate buffered saline for 7 days at 37 degrees C. While a nonirradiated resin-TiO2 surface did not show any hydroxyapatite deposition, a surface after 16 h of UV irradiation was fully covered by hydroxyapatite. In vitro cell adhesion of osteoblast-like MG63 cells confirmed the biocompatibility and bioactivity of the resin-TiO2 surfaces with a hydroxyapatite deposition layer, while the non-irradiated resin-TiO2 surface showed no cell adhesion. Resin-TiO2 nanocomposites, with or without UV irradiation, proved to be nontoxic to two human cell lines, human dermal fibroblasts (hDF) and MG63 cells. It was also shown that an increased dose of UV irradiation decreased bacterial adhesion, which is an additional benefit of the UV treatment and a favourable property for biomedical applications. The combined benefits of biocompatibility, bioactivity, decreased bacterial adhesion and the highly efficient disinfection property of TiO2 photocatalysis under UV light make this resin-TiO2 material an interesting candidate for implant and biomedical device applications.
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| 28. |
- Cai, Yanling, et al.
(författare)
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Photocatalytic Antibacterial Effects Are Maintained on Resin-Based TiO2 Nanocomposites after Cessation of UV Irradiation
- 2013
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Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:10, s. e75929-
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Tidskriftsartikel (refereegranskat)abstract
- Photocatalysis induced by TiO2 and UV light constitutes a decontamination and antibacterial strategy utilized in many applications including self-cleaning environmental surfaces, water and air treatment. The present work reveals that antibacterial effects induced by photocatalysis can be maintained even after the cessation of UV irradiation. We show that resin-based composites containing 20% TiO2 nanoparticles continue to provide a pronounced antibacterial effect against the pathogens Escherichia coli, Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus mutans and Enterococcus faecalis for up to two hours post UV. For biomaterials or implant coatings, where direct UV illumination is not feasible, a prolonged antibacterial effect after the cessation of the illumination would offer new unexplored treatment possibilities.
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| 29. |
- Cai, Yanling, et al.
(författare)
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Photocatalytic inactivation of biofilms on bioactive dental adhesives
- 2014
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Ingår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials. - : Wiley. - 1552-4973 .- 1552-4981. ; 102:1, s. 62-67
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Tidskriftsartikel (refereegranskat)abstract
- Biofilms are the most prevalent mode of microbial life in nature and are 10-1000 times more resistant to antibiotics than planktonic bacteria. Persistent biofilm growth associated at the margin of a dental restoration often leads to secondary caries, which remains a challenge in restorative dentistry. In this work, we present the first in vitro evaluation of on-demand photocatalytic inactivation of biofilm on a novel dental adhesive containing TiO2 nanoparticles. Streptococcus mutans biofilm was cultured on this photocatalytic surface for 16 h before photocatalytic treatment with ultraviolet-A (UV-A) light. UV-A doses ranging from 3 to 43 J/cm(2) were applied to the surface and the resulting viability of biofilms was evaluated with a metabolic activity assay incorporating phenol red that provided a quantitative measure of the reduction in viability due to the photocatalytic treatments. We show that an UV-A irradiation dose of 8.4 J/cm(2) leads to one order of magnitude reduction in the number of biofilm bacteria on the surface of the dental adhesives while as much as 5-6 orders of magnitude reduction in the corresponding number can be achieved with a dose of 43 J/cm(2). This material maintains its functional properties as an adhesive in restorative dentistry while offering the possibility of a novel dental procedure in the treatment or prevention of bacterial infections via on-demand UV-A irradiation. Similar materials could be developed for the treatment of additional indications such as peri-implantits.
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| 30. |
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| 31. |
- Cai, Yanling
(författare)
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Titanium Dioxide Photocatalysis in Biomaterials Applications
- 2013
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Despite extensive preventative efforts, the problem of controlling infections associated with biomedical materials persists. Bacteria tend to colonize on biocompatible materials and form biofilms; thus, novel biomaterials with antibacterial properties are of great interest. In this thesis, titanium dioxide (TiO2)-associated photocatalysis under ultraviolet (UV) irradiation was investigated as a strategy for developing bioactivity and antibacterial properties on biomaterials. Although much of the work was specifically directed towards dental materials, the results presented are applicable to a wide range of biomaterial applications.Most of the experimental work in the thesis was based on a resin-TiO2 nanocomposite that was prepared by adding 20 wt% TiO2 nanoparticles to a resin-based polymer material. Tests showed that the addition of the nanoparticles endowed the adhesive material with photocatalytic activity without affecting the functional bonding strength. Subsequent studies indicated a number of additional beneficial properties associated with the nanocomposite that appear promising for biomaterial applications. For example, irradiation with UV light induced bioactivity on the otherwise non-bioactive nanocomposite; this was indicated by hydroxyapatite formation on the surface following soaking in Dulbecco’s phosphate-buffered saline. Under UV irradiation, the resin-TiO2 nanocomposite provided effective antibacterial action against both planktonic and biofilm bacteria. UV irradiation of the nanocomposite also provided a prolonged antibacterial effect that continued after removal of the UV light source. UV treatment also reduced bacterial adhesion to the resin-TiO2 surface.The mechanisms involved in the antibacterial effects of TiO2 photocatalysis were studied by investigating the specific contributions of the photocatalytic reaction products (the reactive oxygen species) and their disinfection kinetics. Methods of improving the viability analysis of bacteria subjected to photocatalysis were also developed.
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| 32. |
- Carlsson, Daniel O., et al.
(författare)
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A Comparative Study of the Effects of Rinsing and Aging of Polypyrrole/Nanocellulose Composites on Their Electrochemical Properties
- 2013
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 117:14, s. 3900-3910
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Tidskriftsartikel (refereegranskat)abstract
- The effects of polymerization conditions, rinsing, and storage on composites composed of polypyrrole (PPy) and Cladophora nanocellulose in terms of purity, chemical composition, conductivity, and electroactivity were investigated using conductivity measurements, cyclic voltammetry, FTIR-ATR, XPS, and ICP-AES. A clear correlation between rinsing volume and PPy degradation was found using water- or NaCl-rinsing solutions as evidenced by conductivity and electroactivity losses. It was further found, through FTIR-ATR as well as XPS-measurements, that this degradation was caused by incorporation of hydroxyl groups in the PPy-layer. The extent of degradation correlated with a shift in the FTIR-ATR peak around 1300 cm(-1), showing that FTIR-ATR may be used as a quick diagnostic tool to evaluate the extent of degradation. By the use of acidic rinsing solution, this degradation effect was eliminated and resulted in superior samples in terms of both conductivity and electroactivity and also in a more efficient removal of reactants. Upon ambient storage, over a period of 200 days, a gradual decrease in conductivity was found for initially highly conductive samples. The electroactivity, on the other hand, was relatively unaffected by storage, showing that conductivity measurements alone are ineffective to determine the degree of polymer degradation if the water content is not controlled. Also, FTIR-ATR measurements indicated that the oxidation state did not change to any large extent upon storage and that only minor degradation of PPy occurred. The results presented herein thus offer valuable guidelines on how to develop simple and reliable postsynthesis treatments of conducting polymer paper composites with performance fulfilling requirements on stability, electroactivity, and purity in applications such as environmentally friendly energy storage devices and biomedical applications.
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| 33. |
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| 34. |
- Carlsson, Daniel O., et al.
(författare)
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Cooxidant-free TEMPO-mediated oxidation of highly crystalline nanocellulose in water
- 2014
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Ingår i: RSC Advances. - 2046-2069. ; 4:94, s. 52289-52298
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Tidskriftsartikel (refereegranskat)abstract
- Selective oxidation of C6 hydroxyls to carboxyls through 2,2,6,6,-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation, where the oxidizing species (TEMPO+) is generated by cooxidants, such as NaBrO, NaClO or NaClO2, has become a popular way to modify the surfaces of nanocellulose fibrils in aqueous solutions. Employing highly crystalline nanocellulose from Cladophora sp. algae we demonstrate that the same degree of oxidation (D.O.) can be achieved within approximately the same time by replacing the cooxidants with electrogeneration of TEMPO+ in a bulk electrolysis setup. The D.O. is controlled by the oxidation time and the maximum D.O. achieved (D.O. 9.8%, 0.60 mmol g-1 of carboxylic acids and 0 mmol g-1 aldehydes) corresponds to complete oxidation of the surface-confined C6. This shows that TEMPO+ is not sterically hindered from completely oxidizing the fibril surface of Cladophora nanocellulose, in contrast to earlier hypotheses that were based on results with wood-derived nanocellulose. The oxidation does not significantly affect the morphology, the specific surface area (>115 m2 g-1) or the pore characteristics of the water-insoluble fibrous particles that were obtained after drying, but depolymerization corresponding to [similar]20% was observed. For extensive oxidation times, the product recovery of water-insoluble fibrils decreased significantly while significant amounts of charge passed through the system. This could indicate that the oxidation proceeds beyond the fibril surface, in contrast to the current view that TEMPO-mediated oxidation is confined only to the surface.
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| 35. |
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| 36. |
- Carlsson, Daniel O., et al.
(författare)
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Electroactive nanofibrillated cellulose aerogel composites with tunable structural and electrochemical properties
- 2012
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Ingår i: Journal of Materials Chemistry. - : Royal Society of Chemistry (RSC). - 0959-9428 .- 1364-5501. ; 22:36, s. 19014-19024
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Tidskriftsartikel (refereegranskat)abstract
- This work presents conductive aerogel composites of nanofibrillated cellulose (NFC) and polypyrrole (PPy) with tunable structural and electrochemical properties. The conductive composites are prepared by chemically polymerizing pyrrole onto TEMPO-oxidized cellulose nanofibers dispersed in water and the various nanostructures are obtained employing different drying methods. Supercritical CO2 drying is shown to generate high porosity aerogel composites with the largest surface area (246 m(2) g(-1)) reported so far for a conducting polymer-paper based material, whereas composites produced by ambient drying attain high density structures with mechanical properties significantly surpassing earlier reported values for cellulose-conducting polymer composites when normalized with respect to the content of reinforcing cellulose (Young's modulus = 0.51 GPa, tensile strength = 10.93 MPa and strain to failure = 2.5%). Electrochemical measurements clearly show that differences in the porosity give rise to dramatic changes in the voltammetric and chronoamperometric behavior of the composites. This indicates that mass transport rate limitations also should be considered, in addition to the presence of a distribution of PPy redox potentials, as an explanation for the shapes of the voltammetric peaks. A specific charge capacity of similar to 220 C g(-1) is obtained for all composites in voltammetric experiments performed at a scan rate of 1 mV s(-1) and this capacity is retained also at scan rates up to 50 mV s(-1) for the high porosity composites. The composites should be applicable as electrodes in structural batteries and as membranes in ion exchange applications requiring exchange membranes of high mechanical integrity or high porosity.
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| 37. |
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| 38. |
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| 39. |
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| 40. |
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| 41. |
- Carlsson, Daniel O
(författare)
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Structural and Electrochemical Properties of Functionalized Nanocellulose Materials and Their Biocompatibility
- 2014
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Nanocellulose has received considerable interest during the last decade because it is renewable and biodegradable, and has excellent mechanical properties, nanoscale dimensions and wide functionalization possibilities. It is considered to be a unique and versatile platform on which new functional materials can be based.This thesis focuses on nanocellulose from wood (NFC) and from Cladophora algae (CNC), functionalized with surface charges or coated with the conducting polymer polypyrrole (PPy), aiming to study the influence of synthesis processes on structural and electrochemical properties of such materials and assess their biocompatibility.The most important results of the work demonstrated that 1) CNC was oxidized to the same extent using electrochemical TEMPO-mediated oxidation as with conventional TEMPO processes, which may facilitate easier reuse of the reaction medium; 2) NFC and CNC films with or without surface charges were non-cytotoxic as assessed by indirect in vitro testing. Anionic TEMPO-CNC films promoted fibroblast adhesion and proliferation in direct in vitro cytocompatibility testing, possibly due to its aligned fibril structure; 3) Rinsing of PPy-coated nanocellulose fibrils, which after drying into free-standing porous composites are applicable for energy storage and electrochemically controlled ion extraction, significantly degraded the PPy coating, unless acidic rinsing was employed. Only minor degradation was observed during long-term ambient storage; 4) Variations in the drying method as well as type and amount of nanocellulose offered ways of tailoring the porosities of nanocellulose/PPy composites between 30% and 98%, with increments of ~10%. Supercritical CO2-drying generated composites with the largest specific surface area yet reported for nanocellulose/conducting polymer composites (246 m2/g). The electrochemical oxidation rate was found to be controlled by the composite porosity; 5) In blood compatibility assessments for potential hemodialysis applications, heparinization of CNC/PPy composites was required to obtain thrombogenic properties comparable to commercial hemodialysis membranes. The pro-inflammatory characteristics of non-heparinized and heparinized composites were, to some extent, superior to commercial membranes. The heparin coating did not affect the solute extraction capacity of the composite.The presented results are deemed to be useful for tuning the properties of systems based on the studied materials in e.g. energy storage, ion exchange and biomaterial applications.
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| 42. |
- Carlsson, Daniel O., et al.
(författare)
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Tailoring porosities and electrochemical properties of composites composed of microfibrillated cellulose and polypyrrole
- 2014
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 4:17, s. 8489-8497
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Tidskriftsartikel (refereegranskat)abstract
- Composites of polypyrrole and nanocellulose (PPy/nanocellulose) have a high potential as electrodes in energy-storage devices and as membranes for electrochemically controlled ion-exchange systems. In the present work, it is demonstrated that such composites with 42-72% porosity can be produced by using microfibrillated cellulose (MFC) prepared through enzymatic pretreatment or carboxymethylation, or by using different amounts of MFC in the composite synthesis. Together with previous work, this shows that the porosity of PPy/nanocellulose composites can be tailored from 30 to 98% with increments of similar to 10%. Employing the full porosity range of the composites, it is demonstrated that the electrochemical oxidation rate of the materials depends on their porosity due to limitations in the counter ion diffusion process. By tailoring the porosities of PPy/nanocellulose composites, the electrochemical properties can consequently be controlled. The latter provides new possibilities for the manufacturing of electrochemically controlled ion-extraction and energy storage devices with optimized volumetric energy and power densities.
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| 43. |
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| 44. |
- Dalslet, Bjarke Thomas, et al.
(författare)
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Bead magnetorelaxometry with an on-chip magnetoresistive sensor
- 2011
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Ingår i: Lab on a Chip. - : Royal Society of Chemistry (RSC). - 1473-0197 .- 1473-0189. ; 11:2, s. 296-302
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Tidskriftsartikel (refereegranskat)abstract
- Magnetorelaxometry measurements on suspensions of magnetic beads are demonstrated using a planar Hall effect sensor chip embedded in a microfluidic system. The alternating magnetic field used for magnetizing the beads is provided by the sensor bias current and the complex magnetic susceptibility spectra are recorded as the 2nd harmonic of the sensor response. The complex magnetic susceptibility signal appears when a magnetic bead suspension is injected, it scales with the bead concentration, and it follows the Cole-Cole expression for Brownian relaxation. The complex magnetic susceptibility signal resembles that from conventional magnetorelaxometry done on the same samples apart from an offset in Brownian relaxation frequency. The time dependence of the signal can be rationalized as originating from sedimented beads.
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| 45. |
- de la Torre, Teresa Zardan Gomez, et al.
(författare)
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Molecular diagnostics using magnetic nanobeads
- 2010
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Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6596.
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Konferensbidrag (refereegranskat)abstract
- In this paper, we investigate the volume-amplified magnetic nanobead detection assay with respect to bead size, bead concentration and bead oligonucleotide surface coverage in order to improve the understanding of the underlying microscopic mechanisms. It has been shown that: (i) the immobilization efficiency of the beads depends on the surface coverage of oligonucleotides, (ii) by using lower amounts of probe-tagged beads, detection sensitivity can be improved and (iii) using small enough beads enables both turn-off and turn-on detection. Finally, biplex detection was demonstrated.
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| 46. |
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| 47. |
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| 48. |
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| 49. |
- Engström, Anna, et al.
(författare)
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Detection of Rifampicin Resistance in Mycobacterium tuberculosis by Padlock Probes and Magnetic Nanobead- Based Readout
- 2013
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Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:4, s. e62015-
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Tidskriftsartikel (refereegranskat)abstract
- Control of the global epidemic tuberculosis is severely hampered by the emergence of drug-resistant Mycobacterium tuberculosis strains. Molecular methods offer a more rapid means of characterizing resistant strains than phenotypic drug susceptibility testing. We have developed a molecular method for detection of rifampicin-resistant M. tuberculosis based on padlock probes and magnetic nanobeads. Padlockprobes were designed to target the most common mutations associated with rifampicinresistance in M. tuberculosis, i.e. at codons 516, 526 and 531 in the gene rpoB. Fordetection of the wild type sequence at all three codons simultaneously, a padlock probe and two gap-fill oligonucleotides were used in a novel assay configuration, requiring three ligation events for circularization. The assay also includes a probe for identificationof the M. tuberculosis complex. Circularized probes were amplified by rolling circle amplification. Amplification products were coupled to oligonucleotide-conjugatedmagnetic nanobeads and detected by measuring the frequency-dependent magneticresponse of the beads using a portable AC susceptometer.
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| 50. |
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