Simulated Biological Solution Research Articles

Influence of household smoking habits on inhalation bioaccessibility of trace elements and light rare earth elements in Canadian house dust

In this study, total concentration and inhalation bioaccessibility (dissolution in simulated biological solution) of trace elements (TE) and rare earth elements (REE) were assessed in PM10 from Canadian house dust samples with smoking (n = 25) and non-smoking (n = 25) status. Compared to the natural background concentrations in Canadian soils, median Zn, Pb, Cd and Cu concentrations in PM10 were 10–23 fold higher, while median La, Ce and Pr concentrations were 1.6–2.4 fold higher. Mann-Whitney tests (α = 0.05) indicated no difference between the median TE concentrations based on the smoking status of the household; however, median REE concentrations were significantly higher in the PM10 of smoking households. Additionally, Cd and Ni were positively correlated (Spearman r, p < 0.05) to La, Ce and Nd in smoking households, suggesting that tobacco combustion may have contributed REE in the PM10 of these households. Median inhalation-ingestion bioaccessibility assay outcomes of arsenic (As) and lead (Pb) was higher in the non-smoking households when compared to smoking households (Mann Whitney test, α = 0.05), suggesting that tobacco combustion products may be associated with less soluble species of As and Pb. Although REE bioaccessibility was negligible in simulated lung epithelial fluid regardless of the smoking status of the household, bioaccessibility in the lung-gastric phase was 23.6–27.6% in the smoking household and 34.7–36.7% in the non-smoking households, indicating a significantly lower REE dissolution in PM10 of smoking households. In contrast, between 17 and 21.9% bioaccessibility of REE was observed when artificial lysosomal fluid was used, where the outcome was not significantly affected by the smoking status. This study indicates that despite a higher median REE concentration in the PM10 of smoking households, inhalation bioaccessibility may be significantly influenced by the mineralogy.

The Electrochemical and Mechanical Behavior of Bulk and Porous Superelastic Ti‒Zr-Based Alloys for Biomedical Applications.

Titanium alloys are well recognized as appropriate materials for biomedical implants. These devices are designed to operate in quite aggressive human body media, so it is important to study the corrosion and electrochemical behavior of the novel materials alongside the underlying chemical and structural features. In the present study, the prospective Ti‒Zr-based superelastic alloys (Ti-18Zr-14Nb, Ti-18Zr-15Nb, Ti-18Zr-13Nb-1Ta, atom %) were analyzed in terms of their phase composition, functional mechanical properties, the composition and structure of surface oxide films, and the corresponding corrosion and electrochemical behavior in Hanks’ simulated biological solution. The electrochemical parameters of the Ti-18Zr-14Nb material in bulk and foam states were also compared. The results show a significant difference in the functional performance of the studied materials, with different composition and structure states. In particular, the positive effect of the thermomechanical treatment regime, leading to the formation of a favorable microstructure on the corrosion resistance, has been revealed. In general, the Ti-18Zr-15Nb alloy exhibits the optimum combination of functional characteristics in Hanks’ solution, while the Ti-18Zr-13Nb-1Ta alloy shows the highest resistance to the corrosion environment. The Ti-18Zr-14Nb-based foam material exhibits slightly lower passivation kinetics as compared to its bulk equivalent.

Alginate/chitosan multilayer films coated on IL-4-loaded TiO2 nanotubes for modulation of macrophage phenotype

Macrophage phenotype conversion is crucial for improving post-traumatic angiogenesis and tissue repair. Biomaterials with the ability of skewing macrophage phenotype have attracted widespread attention in the field of tissue engineering. The aim of this study was to transform macrophage phenotype by a three-step process; anodizing, drug loading and coating with polyelectrolyte multilayer (PEM) films. Interleukin (IL)-4, an anti-inflammatory cytokine, was loaded into titania nanotubes (TNTs) on the titanium surface. Subsequently, sodium alginate (ALG) and chitosan (CS) were alternately assembled onto IL-4-loaded TNTs and cross-linked with genipin/calcium chloride, finally forming cross-linked PEM films. The IL-4 release profile and cellular immune response of the modified surface was investigated. In the simulated biological solution, only 20% of IL-4 were detected in the first 3 days, with a sustained release of approximately 5 ng over 10 days. The results of gene expression and protein secretion in macrophages indicated that IL-4-loaded PEM films significantly attenuated the inflammatory activity of macrophages at the later stage through down-regulating the mRNA and protein levels of inflammatory markers. In summary, IL-4 was controlled released from the cross-linked PEM films deposited on the nanotubes, leading to the temporal conversion of macrophage phenotype.

Alginate/chitosan multilayer films coated on IL-4-loaded TiO2 nanotubes for modulation of macrophage phenotype.

Macrophage phenotype conversion is crucial for improving post-traumatic angiogenesis and tissue repair. Biomaterials with the ability of skewing macrophage phenotype have attracted widespread attention in the field of tissue engineering. The aim of this study was to transform macrophage phenotype by a three-step process; anodizing, drug loading and coating with polyelectrolyte multilayer (PEM) films. Interleukin (IL)-4, an anti-inflammatory cytokine, was loaded into titania nanotubes (TNTs) on the titanium surface. Subsequently, sodium alginate (ALG) and chitosan (CS) were alternately assembled onto IL-4-loaded TNTs and cross-linked with genipin/calcium chloride, finally forming cross-linked PEM films. The IL-4 release profile and cellular immune response of the modified surface was investigated. In the simulated biological solution, only 20% of IL-4 were detected in the first 3 days, with a sustained release of approximately 5 ng over 10 days. The results of gene expression and protein secretion in macrophages indicated that IL-4-loaded PEM films significantly attenuated the inflammatory activity of macrophages at the later stage through down-regulating the mRNA and protein levels of inflammatory markers. In summary, IL-4 was controlled released from the cross-linked PEM films deposited on the nanotubes, leading to the temporal conversion of macrophage phenotype.

Characterization of tantalum and tantalum nitride films on Ti6Al4V substrate prepared by filtered cathodic vacuum arc deposition for biomedical applications

This paper explores tantalum and tantalum nitride thin films produced by filtered cathodic vacuum arc deposition method as bio-stable surface treatment for Ti6Al4V titanium alloy. Effect of nitrogen to argon gas ratio on microstructure of the deposited film has been investigated. Corrosion behaviour of the films in simulated biological fluid solution was evaluated by electrochemical impedance spectroscopy. It was found that both the Ta and TaN films enhanced corrosion resistance of the Ti6Al4V substrate with the best protective characteristics achieved by the TaN film deposited at 0.25 N2/Ar gas ratio. The protective characteristic was attributed to the formation of tantalum oxide and oxynitride compound at the surface, as verified by X-ray photoelectron spectroscopy. Increasing N2/Ar gas ratio increased susceptibility to localized corrosion. The corrosion resistance decreased as the thickness of the film increased to 1 μm.

Corrosion behavior of stainless steel weldments in physiological solutions

In this study corrosion behavior of TIG welded 316L stainless steel plates in simulated biological solutions is investigated. The mechanical testing results showed slight decrease in ductility after welding and the fracture surface represented mixed cleavage and inclusions containing dimple structure. The heat affected and weld zone (WZ) demonstrated higher corrosion potential and relatively large pitting tendency than base metal (BM) in both Hank’s and Ringer’s solution. The formation of delta (δ) ferrite in the heat affected and WZ decreased the corrosion resistance as confirmed from potentiodynamic Tafel scans. The decrease in pitting resistance and lower protection tendency of the WZ compared to BM and heat affected zone was also quantified from the cyclic polarization trends.

Cholesterol-imprinted macroporous monoliths: Preparation and characterization.

The development of sorbents for selective binding of cholesterol, which is a risk factor for cardiovascular disease, has a great importance for analytical science and medicine. In this work, two series of macroporous cholesterol-imprinted monolithic sorbents differing in the composition of functional monomers (methacrylic acid, butyl methacrylate, 2-hydroxyethyl methacrylate and ethylene dimethacrylate), amount of a template (4, 6 and 8mol%) used for molecular imprinting, as well as mean pore size were synthesized by in situ free-radical process in stainless steel housing of 50mm×4.6mm i.d. All prepared materials were characterized regarding to their hydrodynamic permeability and porous properties, as well as examined by BET and SEM methods. Imprinting factors, apparent dynamic dissociation constants, the maximum binding capacity, the number of theoretical plates and the height equivalent to a theoretical palate of MIP monoliths at different mobile phase flow rates were determined. The separation of a mixture of structural analogues, namely, cholesterol and prednisolone, was demonstrated. Additionally, the possibility of using the developed monoliths for cholesterol solid-phase extraction from simulated biological solution was shown.

Self-healing characteristic of praseodymium conversion coating on AZNd Mg alloy studied by scanning electrochemical microscopy

Application of rare earth conversion coatings as a surface treatment for magnesium has been the subject of several studies revealing the potential to act as an effective passivating layer. Herein a mechanistic study is presented on the formation of a rare earth conversion layer based on Pr(NO3)3 on AZ80X magnesium alloy in simulated biological (buffered) solution. Scanning electrochemical microscopy (SECM) was used to investigate the insulating properties and degradation behaviour of the Pr conversion layer. The self-healing properties of the conversion layer in the presence of Pr3+ were also studied using SECM. Results revealed the self-healing characteristic of the Pr conversion film in the presence of active, Pr3+, species. The Pr conversion layer provided passivation in the short term by producing an electrochemically inert and insulating layer. SECM results in potentiometric mode elucidated the role of near surface pH in the formation of the conversion coating.

Electrochemical evaluation of AZ 31 magnesium alloy in two simulated biological solutions

PurposeThis paper aims to investigate the corrosion behavior of AZ31 alloy as a prospective biomedical implant in two different simulated biological solutions and various immersion times.Design/methodology/approachResults of electrochemical experiments indicated that corrosion resistance of specimens immersed for 24 h was superior, suggesting that the surface layer is capable of protecting alloy.FindingsScanning electron micrographs revealed that this layer abounds with cracks, exhibiting optimum quality in 24 h immersion time, after which it begins to develop corrosion pits. Energy dispersive spectroscopy analysis suggested that the layer is mainly composed of magnesium hydroxide with precipitates of P and Ca containing species present on its surface, which is an indication of biocompatibility.Originality/valueFinally, corrosion performance of Mg alloy was found to be slightly better in Lac-simulated biological solution (SBF) solution, which is more representative of actual physiological environment as compared to conventional SBF solutions.

Influence of temperature, pH and simulated biological solutions on swelling and structural properties of biomineralized (CaCO3) PVP-CMC hydrogel.

Biomaterials having stimuli response are interesting in the biomedical field. This paper reports about swelling response and internal structural of biomineralized (CaCO3) polyvinylpyrrolidone (PVP) carboxymethylcellulose (CMC) hydrogel having various thicknesses (0.1–0.4 mm). Samples were tested in aqueous solution using temperature ranges from 10 to 40 °C; pH varies from 4 to 9, time 60 min. In addition, an experiment was conducted in the presence of simulated biological solutions (SBS): glucose (GS), physiological fluid (PS) and urea (US) at temperature 37 °C and pH 7.5 for 180 min. It is noticed that the maximum swelling ratio reached in 30–40 °C at pH 7 in aqueous solution. Among biological fluids, the swelling ratio shows: US > PS > GS at temperature 37 °C, pH 7.5, time 150 min. The equilibrium swelling ratio of the test sample in SBS and their non-reformative apparent structure confirm that biomineralized (CaCO3) PVP–CMC hydrogel can be acclaimed for medical application like bone tissue engineering.Graphical

Biocorrosion properties of antibacterial Ti-10Cu sintered alloy in several simulated biological solutions.

Ti-10Cu sintered alloy has shown strong antibacterial properties against S. aureus and E. coli and good cell biocompatibility, which displays potential application in dental application. The corrosion behaviors of the alloy in five different simulated biological solutions have been investigated by electrochemical technology, surface observation, roughness measurement and immersion test. Five different simulated solutions were chosen to simulate oral condition, oral condition with F(-) ion, human body fluids with different pH values and blood system. It has been shown that Ti-10Cu alloy exhibits high corrosion rate in Saliva pH 3.5 solution and Saliva pH 6.8 + 0.2F solution but low corrosion rate in Hank's, Tyrode's and Saliva pH 6.8 solutions. The corrosion rate of Ti-10Cu alloy was in a order of Hank's, Tyrode's, Saliva pH 6.8, Saliva-pH 3.5 and Saliva pH 6.8 + 0.2F from slow to fast. All results indicated acid and F(-) containing conditions prompt the corrosion reaction of Ti-Cu alloy. It was suggested that the Cu ion release in the biological environments, especially in the acid and F(-) containing condition would lead to high antibacterial properties without any cell toxicity, displaying wide potential application of this alloy.

Electrochemical characterization of oxidized nanostructured superelastic Ti-Nb-Zr alloy for medical implants

Metastable Ti-Nb-based shape memory and superelastic alloys are known to be strong candidates for bone implant applications. The issues of the materials’ biochemical and biomechanical compatibility and its characterization are reviewed. Thermomechanical treatment is conventionally applied to these alloys in order to obtain supreme functional properties; the processing scheme comprises cold rolling and post-deformation air annealing. The structure and electrochemical characteristics of annealing-induced oxide films were studied by scanning electron microscopy, open circuit potential measurement and voltammetry. It is shown that the samples after the annealing treatment exhibit higher steady-state potential value and lower anodic dissolution current density in simulated biological solution, compared with the samples with mechanically removed oxide films. At the same time, the samples with thermal oxide films exhibited lower rate of passive layer recovery than those subjected to mechanical renewal of the oxidized surface. This fact underlies the recommendation to remove the annealing-induced oxide film from the implants operating under friction conditions.

Effect of Surface Modification on the Corrosion Resistance of Zr-2.5Nb as Material for Permanent Implants

Zirconium is a potential material for permanent implants. In particular, surface modification induced by anodisation has proved to be effective to improve corrosion resistance while keeping good osseointegration. The combination of zirconium with niobium is supposed to develop a structure that presents a high corrosion resistance and continues having the mechanical resistance necessary for implants. The aim of the present work is to determine the viability of using anodised Zr-2.5Nb as implant material, and compare it with pure Zr. Electrochemical tests performed in the anodizing solution and in a simulated biological solution revealed that by anodising the materials a higher corrosion resistance is obtained. The improvement on the corrosion resistance is particularly noticeable in the case of the pure metal after a short period immersed in the simulated biological solution. But, after a long period of immersion, the alloy shows better performance.

Studying Rare Earth Surface Treatment for Magnesium Using Scanning Electrochemical Microscopy

Rapid dissolution of magnesium alloys in biological solutions limits its successful application as a biodegradable implant where a controlled dissolution/corrosion of magnesium along with healing of tissue is required. Treatment of magnesium surface with rare earth conversion layers has been subject of several studies 1–4 revealing its potential as a passivating layer. Given the biocompatibility properties of such surface treatments, two type of rare earth conversion layers based on Ce(NO3)3 and Pr(NO3)3 have been studied in this present work as surface treatment for AZ80X in simulated biological (buffered) solution. Conversion layers were formed by acid etching the Mg samples in 15mM HCl followed by immersion in 0.05 M Pr(NO3)3 or Ce(NO3)3solutions. Morphology and elemental composition of the conversion layers were characterized by SEM-EDXS.Scanning electrochemical microscope (SECM) was used to investigate protective properties and degradation behaviour of Ce and Pr conversion layers on a local scale. Surface generation/tip collection (SG/TC) mode was used to study the hydrogen evolution rate and localization while AC mode was used to resolve the resistive/capacitive behaviour of conversion layer. Figure 1 represents the schematic SG/TC mode for probing the local hydrogen evolution. Self-healing properties of the conversion layer in presence of Ce3+ and Pr3+was also studied using SECM. Electrochemical impedance spectroscopy (EIS) was used to look at the changes in charge transfer and diffusion phenomena due to the formation of conversion layer and its degradation in the long term. Preliminary results have shown that Ce and Pr conversion layers improve corrosion resistance in the short term by producing an electrochemically stable surface. In the long term, however, conversion layer shows instability in simulated biological fluid and tends to degrade locally exposing the magnesium substrate to corrosive media.1. A. Rudd, C. Breslin, and F. Mansfeld, Corrosion Science, 42, 275-288 (2000).2. M. F. Montemor, a. M. Simões, and M. J. Carmezim, Applied Surface Science, 253, 6922-6931 (2007).3. K. Brunelli, M. Dabalà, I. Calliari, and M. Magrini, Corrosion Science, 47, 989-1000 (2005).4. M. Dabalà, K. Brunelli, E. Napolitani, and M. Magrini, Surface and Coatings Technology, 172, 227-232 (2003).Figure 1 Schematic representation of SG/TC mode SECM for probing hydrogen evolution

Enhancement of Biocompatibility of Metal Implants by Nanoscale TiN/NbN Multilayer Coatings

Titanium nitride (TiN)/niobium nitride (NbN) nanostructured multilayer coatings were prepared by DC reactive magnetron sputtering method using the combination of a titanium and niobium target and an Ar-N2 mixture discharge gas on to 316L stainless steel substrates. The coatings showed a polycrystalline structure with (111) for TiN and (101) for NbN preferential growth. Raman spectroscopy measurements on the multilayer films exhibited the characteristic peaks at 212, 303, 458 and 578 cm-1. A higher hardness of 38 GPa was observed for TiN/NbN coatings. Electrochemical polarization tests were performed in simulated biological fluid solutions at 37 degreesC in order to determine and compare the corrosion behavior of the coated and uncoated 316L SS substrates. The TiN/NbN multilayer coatings could improve the corrosion resistance of 316L SS substrate. The bacterial culture experiments were performed and the bacteria treated samples were examined by epi fluorescence microscope measurements.

High Density Polyethylene Containing Antibacterial Silver Nanoparticles for Medical Applications

AbstractHigh density polyethylene (HDPE) and composites with silver nanoparticles were processed via extrusion and injection moulding. The materials thus produced were tested against Gram‐positive Staphylococcus aureus and Gram‐negative Escherichia coli. The release of silver ions Ag+ from composites was measured by means of ICP‐MS method. Surface parameters such as wettability and roughness were determined because of their effect on the most important processes at biomaterial interface. Scanning electron microscopy was used to investigate the microstructure. Durability tests of polymer and composite materials were carried out in a simulated biological solution by monitoring the pH and electrical conductivity, mass changes as well as the longitudinal ultrasonic wave measurements. Antibacterial tests prove that nanosilver modified materials have bactericidal activity against tested bacteria. Biological durability studies reveal stable behavior of incubated materials. Spectrometric analysis shows that the amount of silver release depends on the immersion time and the amount of nanopowder introduced into the polymer matrix.

Swelling Properties of Chemically Crosslinked Poly(acrylamide-co-maleic acid) Hydrogels

ABSTRACT Chemically crosslinked poly(acrylamide-co-maleic acid) [poly(AAm-co-MA)] hydrogels were prepared by simultaneous free radical copolymerization of acrylamide (AAm) with maleic acid (MA) in presence of di or tri functional crosslinking agents using ammonium persulfate-N,N,N′,N′-tetramethylethylenediamine (APS-TMEDA) redox-initiating system. The poly(AAm-co-MA) hydrogels formation was confirmed by IR studies. The influence of crosslinkers such as N,N′-methylene-bis-acrylamide (MBA) and 2,4,6-triallyloxy-1,3,5-triazine (TATA) on swelling/de-swelling characteristics were studied in detail for poly(AAm-co-MA) hydrogels containing different amounts of maleic acid. The present investigation also deals with the influence of concentration of crosslinker and initiator on the swelling behavior of poly(AAM-co-MA) hydrogels. The effect of various salts on swelling capacity was studied. In addition, the effect of simulated biological fluids and pH solutions on the swelling of hydrogels was also studied in detail.

Influence of Simulated Biological Solutions on the Corrosion Behavior of an Mg Alloy

not Available.

Interfacial reactions of glasses for biomedical application by scanning transmission electron microscopy and microanalysis

Short-term physico-chemical reactions at the interface between bioactive glass particles and biological fluids are studied for three glasses with different bioactive properties; these glasses are in the SiO 2–Na 2O–CaO–P 2O 5–K 2O–Al 2O 3–MgO system. Our aim is to show the difference between the mechanisms of their surface reactions. The relation between the composition and the bioactive properties of these glasses is also discussed. The elemental analysis is performed at the submicrometer scale by scanning transmission electron microscopy associated with energy-dispersive X-ray spectroscopy and electron energy loss spectroscopy. After different immersion times (ranging from 0 to 96 h) of bioactive glass particles in a simulated biological solution, results show the formation of different surface layers at the glass periphery in the case of two bioactive glasses (A9 and BVA). For the third glass (BVH) we do not observe any surface layer formation or any modification of the glass composition. For the two other glasses (A9 and BVA), we observe the presence of different layers: an already observed (Si, O, Al) rich layer at the periphery, a previously demonstrated thin (Si, O) layer formed on top of the (Si, O, Al) layer and a (Ca, P) layer. We determine the different steps of the mechanisms of the surface reactions, which appear to be similar in these glasses, and compare the physico-chemical reactions and kinetics using the different immersion times. The A9 glass permits the observation of all important steps of the surface reactions which lead to bioactivity. This study shows the important relationship between composition and bioactivity which can determine the medical applicability of the glass.

X‐ray microanalysis in STEM of short‐term physicochemical reactions at bioactive glass particle/biological fluid interface. Determination of O/Si atomic ratios

AbstractShort‐term physicochemical reactions at the interface between bioactive glass particles and biological fluids are studied and we focus our attention on the measurements of O/Si atomic ratio. The studied bioactive glass is in the SiO2Na2OCaOP2O5K2OAl2O3MgO system. The elemental analysis is performed at the submicrometre scale by scanning transmission electron microscopy associated with energy‐dispersive x‐ray spectroscopy (EDXS) and electron energy‐loss spectroscopy (EELS). We previously developed an EDXS quantification method based on the ratio method and taking into account local absorption corrections. In this way, we use EELS data to determine, by an iterative process, the local mass thickness, which is an essential parameter for correcting absorption in EDXS spectra. After different immersion times of bioactive glass particles in a simulated biological solution, results show the formation of different surface layers at the bioactive glass periphery. Before 1 day of immersion, we observe the presence of an already shown (Si,O,Al)‐rich layer at the periphery. In this paper, we demonstrate that a thin ‘electron dense’ (Si,O)‐layer is formed on top of the (Si,O,Al)‐layer. In this (Si,O)‐layer, depleted in aluminium, we point out an increase of oxygen weight concentration that can be interpreted by the presence of Si(OH)4 groups, which permit the formation of a (Ca,P)‐layer. Aluminium plays a role in the glass solubility and may inhibit apatite nucleation. After the beginning of the (Ca,P)‐layer formation, the size of the ‘electron dense’ (Si,O)‐layer decreases and tends to disappear. After 2 days of immersion, the (Ca,P)‐layer grows in thickness and leads to apatite precipitation. Copyright © 2004 John Wiley &amp; Sons, Ltd.