Papers by Keyword: Protein Adsorption

Abstract: This study is to investigate the effect of PAM on protein adsorption and osteoblastic cells adhesion to HA bioceramics. PAM was immobilized on the surface of HA bioceramics for bone scaffold by chelating. The outermost layer of the specimens was analyzed by XPS and FT-IR. The protein adsorption test was performed using the 10% bovine calf serum absorbed on the specimens in vitro. The osteoblastic cells were inoculated and cultured on the scaffolds. SEM, MTT test and ALP activity test evaluated the cell attachment, proliferation and activity on the scaffolds. Characteristic peaks in XPS and FT-IR spectra indicated PAM being immobilized on the surface of the bioceramics. PAGE and 2-D DIGE results indicated that HA absorbed more acidic proteins, while PAM-HA absorbed more basic and neutral proteins.The cell culture test indicated that the cells actively proliferated on the scaffolds. There was no significant difference between the ALP activity of the cells cultured for 1d, 3d, 5d and 7d on PAM-HA and that of the controls. PAM had no obvious effect on the cytocompatibility of HA, and PAM-HA bioceramics could be used as bone scaffold with potential ability to improve osteogenesis.

Abstract: The effect of Mn on the protein adsorption of calcium phosphate coatings is investigated in this work. Mn containing β-tricalcium phosphate (Mn-TCP) is first prepared through a coprecipitation based methods. Then Mn-TCP is dispersed into the fluoridated hydroxyapatite (FHA) precursor sol. Mn-TCP/FHA biphasic coatings are prepared with these sols. After cell culture, it is found the amount of protein adsorbed on the coatings following this rule: Mn-TCP/FHA > β-TCP/FHA > FHA. That is ascribed to two reasons: a) Ca and PO4 releasing can promote the activity of cells; b) Mn releasing promotes protein activation even at quite low concentration.

Abstract: Protein adsorption onto metal oxide surfaces is an essential aspect of the cascade of biological reactions taking place at all interfaces between implanted materials and the biological environment. The types and amounts of adsorbed proteins mediate subsequent adhesion, proliferation and differentiation of cells. Protein adsorption to surfaces of metal oxides and their kinetics are important in the formation and growth of seashells, one of the toughest natural ceramics, in modern bio-analytical devices as well as in bone and teeth implant technology. This paper describes results obtained in a feasibility study of how to use metal-oxide particles to obtain biosensors with a high turnover. The most important features of proteins are outlined describing them as purpose-built "polymers" from amino acids with specific conformations. Some key aspects of Metaloxide (MeO) surfaces in water and the influence of electrostatic and hydrophobic interaction on protein adsorption are reported. Results concerning the interaction between different proteins and MeO surfaces in water are discussed in detail. Examples of purely electrostatic interactions of proteins with MeO surfaces as well as the influence of hydrophobic interaction are elucidated. An outlook of the implications of the new insights on natural and synthetic materials will be given concerning bio-compatibility, bio-mineralization and self assembly of materials.

Abstract: The selective protein adsorption property and the local structure around carbonate ions of nanocrystalline hydroxy-carbonate apatite were examined in this study. Considerable change in the selectivity in the adsorption of BSA and β2-MG was observed due to the incorporation of thecarbonate ions in hydroxyapatite lattice. Since the protein adsorption property seems to be related to the surface charge density of hydroxyapatite due to the carbonation, the chemical states of the incorporated carbonate ions were examined by the 31C CP-MAS NMR spectroscopy. At least four peaks assignable to carbonate ions in A-site(OH-) and B-site(PO4 3-) were observed in 13C CP-MAS NMR spectrum. Thus, we must take into consideration that the surface charge distribution and the decrement of polar groups such as OH- groups due to the distribution of carbonate ions in both Aand B-sites of the hydroxyapatite lattice are particularly favorable for β2-MG adsorption rather than for BSA adsorption.

Abstract: Mesoporous HAp aggregates were composed of needle-like crystals that were aligned to the c-axes direction perpendicular to the flat surface of plate-like aggregates. The pore size distributions of the HAp aggregates increased with increasing heat treatment temperature e.g. 3-20 and 26-52 nm, respectively, before and after heat-treated at 600 °C. The adsorption proteins on the mesoporous HAp aggregates were investigated by liquid chromatography using the HAp aggregates as an adsorbent. Elution molarity ratios of acidic proteins on the mesoporous HAp aggregates before and after heat-treatment at 600 °C increased with increasing molecular weight in the order of ferritin > fibrinogen > catalase > albumin, whereas the elution molarity ratios of basic proteins were considerably lower than those of acidic proteins. These results suggested that penetration of the large size acidic proteins into the pore of the as-prepared mesoporous HAp aggregate was slightly inhibited but were the proteins could easily penetrate into the pore of the heat-treated mesoporous HAp aggregates and then were selectively adsorbed on the mesoporous wall consisting of the a-surface of the HAp aggregate. Conversely, the basic proteins could be adsorbed on the wide outer surface of the plate-like HAp aggregates. Therefore, the elution molarity ratios of basic proteins decreased with decreasing the specific surface area by the heat treatment, independent of the mesoporous structure.

Abstract: Polystyrene (PS), polyethylene (PE), polypropylene (PP), glass and stainless steel were exposed to aqueous solutions of a series amphiphilic polymers at room temperature, including N-isopropylacrylamide (NIPAM)-based polymers, polyvinylpyrrolidone (PVP), polypropylene oxide (PPO)-polyethylene oxide (PEO) block copolymers and PEO. Dynamic contact angle measurements of the material surfaces before and after the treatment indicate that only NIPAM-based polymers can adsorb on both hydrophobic and hydrophilic surfaces. The surface morphologies of the materials before and after polymer adsorption were investigated by profilometry. Protein adsorption on the surfaces pre-adsorbed NIPAM-based polymers was investigated by dual polarisation interferometry (DPI) and profilometry using lysozyme as the model protein. The results obtained indicate that NIPAM-based polymers can significantly improve the biofouling resistance of synthetic surfaces.

Abstract: The structural change of bovine serum albumin (BSA) was analyzed by means of ultraviolet (UV) and circular dichroism (CD) spectroscopy due to in contact with ceramics powders such as Al2O3, SiO2, TiO2, ZrO2, hydroxyapatite and b-tricalcium phosphate. The absorbance of the UV spectra increased for the BSA solution in contact with TiO2, ZrO2 and Al2O3, that is, the BSA solution clouded. This indicated the aggregation of BSA after contact with those ceramics powders. The CD spectroscopy showed that the ordered secondary structure of BSA was diminished on contact with TiO2 and ZrO2. We discussed the protein adsorption property of ceramics on the basis of the magnitude of the interaction forces between proteins and the bioceramics.

Abstract: Hydroxyapatite (HA) coating applied on metallic orthopedic joint implants can improve bone apposition, presumably through selective protein adsorption from blood plasma. However, the detailed interaction mechanism of HA coating with serum proteins remains to be largely elucidated. Protein adsorption behavior of a biomimetic apatite (BAp) coating in bovine calf serum and alpha calf fraction was investigated in this study. Plasma sprayed HA (PSHA) coating was tested in alpha calf fraction. The microstructure and composition of the coatings before and after serum incubation were characterized and the proteins adsorbed during the incubation were extracted from the coatings and analyzed. Microstructural transformation of the BAp coating accompanied by selective serum protein adsorption was observed after incubation in both media. The total protein amount adsorbed by the BAp coating in alpha calf faction was about three times that of the PSHA coating. To test the potential use of BAp coating as a carrier of therapeutic agents, interaction between the BAp coating and transforming growth factor (TGF)-β1 was studied. The growth factor was successfully loaded onto the coating in a sodium acetate buffer. Because of its high affinity to the coating, TGF-β1 could not be easily eluted in a bovine serum albumin containing solution but could be recovered after coating dissolution in acid. The strong protein adsorption property of the BAp coating was found to be due mainly to its unique nanoporous structure. The BAp coating can serve as an ideal carrier of therapeutic agents for aiding in the healing of bone and soft tissues.

Abstract: The aim of this work was the exploration of a potential biocompatible membrane prepared from a modified polyetheretherketone (PEEK-WC). The physico-chemical properties of PEEK-WC were characterised by Differential Scanning Calorimetry and FT-Infrared Spectroscopy. The surface affinity of this membrane to human plasma and proteins such as albumin, fibrinogen and immunoglobulins G was evaluated and compared with that of commercial membranes. The wettability of all investigated membranes was established by water contact angle measurements. PEEK-WC membranes exhibited moderate wettability and low protein adsorption, differently from other commercial membranes such as cellulose acetate membrane. A preferential adsorption of hydrophilic proteins as albumin on the membrane surfaces was observed. Human plasma adsorption on membranes followed the same trend as individual protein solutions.