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1.
J Nanosci Nanotechnol ; 10(4): 2583-9, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20355467

RESUMEN

As biomedical materials, titanium and titanium alloys (Ti-6Al-4V) are superior to many materials in terms of mechanical properties and biocompatibility. However, they are still not sufficient for prolonged clinical use because the biocompatibility of these materials must be improved. In this study, the prevention of the attachment of test microorganism on the Ti alloy surfaces by thiol (-SH) and hydroxyl (-OH) functional group containing monomer in plasma based electron beam generator was reported in order to prepare anti-fouling surfaces. The precursor, 11-mercaptoundecanoic acid is used as plasma source to create nano-film with 30-60 nm approximately. The surface chemistry and topology of uncoated and coated samples are characterized by Fourier Transform Infrared Spectroscopy (FTIR) and Atomic Force Microscopy (AFM). Static contact angle measurements are performed to state the change of surface hydrophilicity. All coated samples are tested in-vitro environment with Staphylococcus epidermidis that is chosen as the test bacteria strain in view of its significance for the pathogenesis of medical-device-related infections. This test is repeated after certain period of times and samples are waited in dynamic fluid media in order to investigate the stability of nano-coating. Plasma polymerized 11-mercaptoundecanoic acid film (PP MUA) with 42 +/- 4 nm is found alternative, stabile and simple method to create bacterial anti-fouling surfaces. The static contact angle of the coated surface is 34 +/- 80 whereas the uncoated surface is 57 +/- 50. For the coated surface, the presence of C-OH and C==O groups in infrared spectra defining the PP MUA is achieved by the plasma polymerization. The attachment of the model microorganism on the biomaterial surface prepared by PP MUA is reduced 85.3% if compared to unmodified control surface.


Asunto(s)
Aleaciones/química , Materiales Biocompatibles Revestidos/química , Cristalización/métodos , Nanoestructuras/química , Staphylococcus epidermidis/fisiología , Compuestos de Sulfhidrilo/química , Titanio/química , Adhesión Bacteriana/fisiología , Sustancias Macromoleculares/química , Ensayo de Materiales , Conformación Molecular , Nanoestructuras/ultraestructura , Nanotecnología/métodos , Tamaño de la Partícula , Propiedades de Superficie
2.
Biosens Bioelectron ; 17(9): 727-34, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12191920

RESUMEN

The aim of this study is to develop an immunoaffinity sensor based on piezoelectric crystals for human serum albumin (HSA) detection in aqueous media. Quartz crystals were treated with ethylene diamine (EDA) plasma in a glow-discharge apparatus in order to substitute amino groups on their surfaces. Then anti-HSA antibodies were immobilized via these amino groups by using glutaraldehyde (GA) as cross-linker. Immobilization of the antibody on the quartz crystal was examined for different pH, antibody concentration and treatment time. The optimum conditions for anti-HSA immobilization were evaluated by the measurements of the activity of the surface against HSA. The optimum values of pH, antibody concentration and treatment time were found 6.2, 0.15 mg/ml and 2 h, respectively. For detection of HSA into the solution, two methods were used. In the first (dip and dry) method, the frequency shifts were measured in air after the 1 h interaction of the anti-HSA immobilized crystals with HSA solution. In the other (direct) method, the frequency shifts were followed continuously for 60 min. while the probe was immersed in the HSA solution. An increase for the frequency shifts was observed with increasing of HSA concentration of 16-128 microg/ml. Both the immobilization and antibody-interaction conditions were found important on the extend of these specific interaction. The relations between the HSA concentrations and frequency shifts were exponential in both methods.


Asunto(s)
Complejo Antígeno-Anticuerpo/análisis , Técnicas Biosensibles/instrumentación , Inmunoensayo/instrumentación , Cuarzo/química , Albúmina Sérica/análisis , Adsorción , Anticuerpos/química , Anticuerpos/inmunología , Especificidad de Anticuerpos , Técnicas Biosensibles/métodos , Cristalización , Electroquímica , Diseño de Equipo , Etilenodiaminas/química , Glutaral/química , Calor , Humanos , Concentración de Iones de Hidrógeno , Inmunoensayo/métodos , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Albúmina Sérica/inmunología
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