Bovine Serum Albumin Adhesion Research Articles

Engineered composite dressing with exudate management capabilities for the process of entire wound healing

A timely antibacterial dressing that can adapt to dynamic wound environments poses a significant challenge in burn research and management. Herein, a four-layered composite dressing is reported. At its core, it features a modified micropore arrayed Janus membrane with a super-hydrophobic polyurethane layer on one side and a super-hydrophilic hydrogel on the other. This unique design enables the dressing to maintain stable and durable self-pumping capabilities, effectively transferring wound exudate to the upper foam layer. The self-pumping rate exceeds that of traditional foam dressings, being approximately 1.39 times more efficient in absorbing excess wound exudate. The composite dressing demonstrates an impressive water donation capacity when tested on 45% gelatin-simulated skin, achieving a water donation rate of (59.20 ± 2.66)%. Furthermore, the water vapor permeability of the composite dressing outperforms hydrocolloids by approximately 3.66 times. Additionally, the composite dressing, when loaded with super-hydrophilic nanometer zinc oxide, exhibits a potent antibacterial effect. The dressing's surface reduces cellular, platelet, fibrinogen, and bovine serum albumin adhesion, reducing the risk of tissue adhesion. During a 20-day trial covering deep II-degree burn wounds, the dressing demonstrated excellent biocompatibility. It effectively compresses the inflammatory phase, promotes vascularization, and significantly accelerates the regeneration of skin accessory organs. This innovative dressing exhibits great potential for use throughout the entire wound-healing process in future burn treatments.

Adsorption characteristics of bovine serum albumin on the surface of 316L stainless steel coated with diethoxydimethylsilane/chitosan composite films

In this study, diethoxydimethylsilane (DEDMS) was blended with chitosan (CS) to fabricate DEDMS/CS composite films, which were deposited on the surface of 316L stainless steel to assess their anticoagulant properties. A neat CS film exhibits a high concentration of bovine serum albumin (BSA) protein adhesion of 458.3 ± 6.2 μg/L in a bicinchoninic acid protein assay because the carbonyl and amide functional groups on the CS surface easily form hydrogen bonds with the carboxylic acid functional groups of the BSA protein. The DEDMS/CS composite films exhibited lower BSA adhesion concentration than neat CS films because some of the carbonyl and amide functional groups on the surface of CS were replaced by the –Si-O-Si and –Si-(CH3)2 functional groups. Increasing the DEDMS content in the DEDMS/CS composite films led to a higher concentration of –Si-O-Si and –Si-(CH3)2 functional groups on the surface and lower BSA adhesion concentration. Blending excess amounts of DEDMS caused an undesirable rougher surface morphology because of the hydrolysis and self-condensation reactions of DEDMS; this deteriorated the anticoagulant properties of the composite films. The study confirmed that a DEDMS/CS composite film with an appropriate DEDMS/CS content ratio of 8/92 mL/mL possesses hydrophobic characteristics and the lowest BSA protein adhesion of 155.5 ± 1.0 μg/L and has potential for biomedical coating applications.

Bioinspired Polycation Functionalization of the Polyurethane Surface for Enhanced Lubrication, Antibacterial Property, and Anticoagulation

Endowing the implanted biomaterial with a wide range of functions, such as lubrication and antibacterial and anticoagulation properties, is essential for their safe clinical use. In the present study, based on the superlubrication mechanism of articular cartilage, a branched polyelectrolyte polymer (PEI-PMPC) was successfully synthesized based on tert-butyl hydroperoxide-initiated grafting polymerization and then applied to the biocompatible polyurethane (PU) surface. Specifically, the PU sheet was pretreated by polydopamine (PDA), and the PEI-PMPC polymer was grafted onto the PDA-modified PU surface by Schiff base reaction to generate a solid PDA/PEI-PMPC coating. The unmodified and modified surfaces were characterized by Fourier transform infrared spectroscopy, water contact angle, X-ray photoelectron spectroscopy, and surface zeta potential. To compare the lubrication, antibacterial behavior, and hemocompatibility, the relevant properties of the modified surfaces were evaluated by the tribological test, plate count method, surface morphology, hemolysis rate, activated partial thromboplastin time, and thrombin time. The experimental results demonstrated that the adhesion of bovine serum albumin, Escherichia coli, Staphylococcus aureus, platelets, and red blood cells was significantly decreased on the PEI-PMPC-modified PU surface compared with that of the unmodified PU surface. The multi-functional properties of the coating were attributed to the hydration layer formed by zwitterionic phosphorylcholine groups, and additionally, the cationic PEI served to kill the bacteria adhering to the surface. In summary, the bioinspired coating proposed in this study could potentially be used as a promising surface functionalization strategy for biomedical implants.

Mitigation of protein fouling by magnesium ions and the related mechanisms in ultrafiltration process

Although protein is an important membrane foulant in the water body that may be significantly affected by the coexisting common cation magnesium (Mg2+), the effect of Mg2+ on protein fouling is rarely reported. In this context, this study selected bovine serum albumin (BSA) as the model foulant, and investigated its fouling characteristics at different Mg2+ concentrations (0–100 mM). Filtration tests showed that the protein fouling can be significantly mitigated by adding Mg2+, and the specific filtration resistance (SFR) of pure BSA (3.56 × 1014 m kg−1) was at least 5 times that of BSA-Mg2+ solutions (0.5–100 mM). In addition, an optimal Mg2+ concentration exists, which can achieve the lowest BSA SFR. A series of characterizations indicated that the main contributors to the differences in BSA SFR were the changes in BSA adhesion capacity and the thickness and structure of the foulant layer. Basically, the above results were attributed to the hydration repulsion effect of Mg2+, which prevented tight adhesion of foulants to the membrane. Moreover, the lowest BSR SFR at 1 mM Mg2+ was achieved not only by the hydration repulsion effect but also by the particle size compression due to the conformational change of BSA molecules. This combined effect led to the lowest foulant retention on the membrane surface and delivered to the lowest SFR. This study conducts a thorough inspection into the specific effect of Mg2+ on protein fouling and provides a fresh insight into protein fouling control in the UF process.

Fabrication of patterned polymer brushes using programmable modulated light-excited controllable radical polymerization

In the present work, programmable light pattern produced by digital micro-mirror device (DMD) spatial light modulator was employed to initiate the atom transfer radial polymerization (ATRP) for fabricating the patterned polymer brushes on the silicon substrate surface. Results from a series of characterization methods such as optical microscopy, 3D optical surface profiler, and X-ray photoelectron spectroscopy proved the poly (ethylene glycol) methyl acrylate (PEGMA) brushes with complex structures were successfully generated. The thickness of PEGMA brushes could be regulated by adjusting the DMD light modulation parameter including pattern size, gray value and exposure time. The contact angle measurements showed the PEGMA brushes could improve the hydrophilicity property of substrate surface. The antifouling property of the patterned surfaces with different shapes were tested, and the results indicated that the PEGMA brushes could effectively resist the adhesion of bovine serum albumin (BSA) protein, leading to the selective arrangement of protein. The reported method for generating the polymer brush patterns shows great potential for the manipulation of surface property in facilitating a range amount of applications from anti-biofouling coating, interface lubrication to biomimetic and smart surfaces.

Hydrophilic and Positively Charged Polyvinylidene Fluoride Membranes for Water Treatment with Excellent Anti-Oil and Anti-Biocontamination Properties.

Membrane fouling limits the rapid development of membrane separations. In this study, a blend membrane containing polycationic liquid (P(BVImBr1-co-PEGMA1)) is presented that can improve the antifouling performance of polyvinylidene fluoride (PVDF) membranes. By mixing the polycationic liquid into PVDF, an improved membrane-surface hydrophilicity and enlarged membrane porosity were detected. The water contact angle decreased from 82° to 67°, the porosity enlarged from 7.22% to 89.74%, and the pure water flux improved from 0 to 631.68 L m−2 h−1. The blend membrane surfaces were found to be always positively charged at pH 3~10. By applying the membranes to the filtration of oil/water emulsion and bovine serum albumin (BSA) solution, they showed a very high rejection rate to pollutants in wastewater (99.4% to oil droplets and 85.6% to BSA). The positive membrane surface charge and the increased membrane hydrophilicity resulted in excellent antifouling performance, with the flux recovery rates of the dynamic filtration tests reaching 97.3% and 95.5%, respectively. Moreover, the blend membranes demonstrated very low BSA adhesion and could even kill S. aureus, showing excellent antifouling properties.

Fabrication of surface microstructure for the ultrafiltration membrane based on “active–passive” synergistic antifouling and its antifouling mechanism of protein

In this work, four types of ultrafiltration membranes with different antifouling capacities were prepared by the introduction of maleic anhydride (MA), polyethylene glycol (PEG), polyethyleneimine (PEI), and PEG-g-PEI via “surface deposition–grafting” technique. The microstructure of the membrane surface was characterized and antifouling capacity was determined by investigating the influence of functional hydrophilic groups on the antifouling capacity and the formation process of the fouling layer. It was found that the membrane grafted with PEG-g-PEI had better anti-protein-fouling capacity than that of other membranes. The flux recovery rate stayed at 98.26% despite the higher positive charge of its surface. The irreversible resistance was as low as 0.54% and could effectively delay the formation of irreversible fouling. Also, the adhesion of bovine serum albumin (BSA) on the membrane surface was reduced to only 28.59 nN. The “active–passive” synergistic mechanism of antifouling increased the dispersion and flocculation capacities of the grafted functional polymer chains. The repulsion effect of the hydration layer was also enhanced. The effectiveness of this proposed mechanism was demonstrated based on research on the antifouling ability, the characterization of the hydration layer microstructure, and the adhesion of BSA on the membrane surface. This work provides a reference for fabricating a membrane with advanced antifouling capacity and has a deeper understanding on the antifouling mechanism.

Direct measurements of interaction forces of bovine serum albumin and lysozyme with stainless steel by atomic force microscopy

The adsorption of proteins on metal surfaces is important in various fields of engineering and science. Thus, it is necessary to understand the very complex phenomena of interactions between proteins and metal surfaces. In this study, we directly measured the interactions between proteins and stainless steel (SS) surfaces, the most common metal in engineering, by atomic force microscopy (AFM). Bovine serum albumin (BSA) and lysozyme (LSZ) were chemically attached to the tip of an AFM probe, and the interaction forces between the probe tip and the SS substrate were measured. The approaching forces between the proteins and metal surfaces were dominated by electrostatic double-layer and steric repulsion. However, the dependence of adhesion force on pH was not totally consistent with the approaching forces for both proteins. The adhesion of BSA to the SS surface was strongest in mildly acidic solutions, whereas that of LSZ was almost independent of pH. This result indicates that local interactions between the functional groups of proteins and SS, particularly the interactions between carboxyl and hydroxyl groups, are significant. The dependence of the adhesion forces on the contact time reveals that the mechanical properties (hardness) of proteins also have a significant effect on their adhesion on surfaces.

Adhesion force evolution of protein on the surfaces with varied hydration extent: Quantitative determination via atomic force microscopy

The adhesion force evolution of protein on surfaces with continuously varied hydrophobicity/hydration layer has not been completely clarified yet, limiting the further development of environmental applications such as membrane anti-biofouling and selective adsorption of the functional surfaces. Herein, chemical force spectroscopy using atomic force microscopy (AFM) was utilized to quantify the evolution of the adhesion forces of protein on hydration surfaces in water, where bovine serum albumin (BSA) was immobilized on an AFM tip as the representative protein. The stiffness, roughness and charge properties of the substrate surfaces were kept constant and the hydrophobicity was the only variant to monitor the role of hydrated water layers in protein adhesion. The adhesion force increased non-monotonically as a function of hydrophobicity of substrate surfaces, which was related to the concentration of humic acid, and independent of pH values and ionic strength. The non-monotonic variation occurred in the range of contact angle at 60−80° due to the mutual restriction between solid–liquid interface energy and solid–solid interface energy. Hydrophobic attraction was the dominant force that drove adhesion of BSA to these model substrate surfaces, but the passivation of hydration layers at the interface could weaken the hydrophobic attraction. In contrast to the measurements in water, the adhesion forces decreased as a function of surface hydrophobicity when measured in air, because capillary forces from condensation water dominated adhesion forces. The passivation of hydration layers of protein was revealed by quantitatively determining the evolution of adhesion forces on the hydration surfaces of varying hydrophobicity, which was ignored by traditional adhesion theory.

Fabrication and performance evaluation of polymeric membrane using blood compatible hydroxyapatite for artificial kidney application.

In the current study, a phase inversion scheme was employed to fabricate hydroxyapatite (HA)/polysulfone (PSF)-based asymmetric membranes using a film applicator with water as a solvent and nonsolvent exchanging medium. Fourier Transform Infrared (FTIR) and X-ray diffraction (XRD) spectroscopic studies were conducted to confirm the bonding chemistry and purity of filler. The inherent thick nature of PSF generated sponge-like shape while the instantaneous demixing process produced finger-like pore networks in HA/PSF-based asymmetric membranes as exhibited by scanning electron microscope (SEM) micrographs. The FTIR spectra confirmed noncovalent weak attractions toward the polymer surface. The leaching ratio was evaluated to observe the dispersion behavior of HA filler in membrane composition. Hydrophilicity, pore profile, pure water permeation (PWP) flux, and molecular weight cutoff (MWCO) values of all formulated membranes were also calculated. Antifouling results revealed that HA modified PSF membranes exhibited 43% less adhesion of bovine serum albumin (BSA) together with >86% recovery of flux. Membrane composition showed 74% total resistance, out of which 60% was reversible resistance. Biocompatibility evaluation revealed that the modified membranes exhibited prothrombin time (PT), and thrombin time (TT) comparable with typical blood plasma, whereas proliferation of living cells over membrane surface proved its nontoxic behavior toward biomedical application. The urea and creatinine showed effective adsorption aptitude toward HA loaded PSF membranes.

Influence of Hydrogen Bond and Sodium Alginate on Bovine Serum Albumin Adhesion on ZnSe Surface

Serum albumin is the most abundant protein in mammalian plasma and is often used as a model to understand the adhesion behavior of proteins on surfaces. Attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) is used to non-destructively and dynamically detect the chemical change information between the protein and the surface during the adhesion process, which is especially suitable for in-situ measurement of samples in water. Therefore, the adhesion of bovine serum albumin (BSA) on the surface in H2O and D2O is investigated by ATR-FTIR technology, which effectively avoids the interference of the characteristic peak of deformation vibration of liquid H2O (1645 cm−1) on the amide I band of BSA. Sodium alginate, a polysaccharide widely present in the ocean, is introduced into the BSA solution to explore the changes in the adhesion process of proteins on the surface of ZnSe, and polarized ATR-FTIR spectra are also collected to study the adhesion orientation of BSA. Sodium alginate presents a negative effect on the adhesion of BSA on the surface and there is no specific orientation of BSA on the surface.

Grafting embedded poly(ionic liquid) brushes on biomimetic sharklet resin surface for anti-biofouling applications

In this work, we combined 3D printing technology and subsurface-initiated ring opening metathesis polymerization (ROMP) to construct a multi-scale brush-based antifouling surface. A biomimetic sharklet structured substrate embedded with ROMP initiator was prepared by 3D printing with commercial acrylic resin. Then, the embedded poly(ionic liquid) brushes were grafted onto the as-prepared biomimetic sharklet via subsurface-initiated ROMP of a novel ionic liquid monomer containing benzotriazole and imidazole groups ([BNIm][Br]). A series of characterization including infrared spectroscopy, X-ray photoelectron spectroscopy and atomic force microscope proved the successful grafting of poly([BNIm][Br]) brushes on the as-prepared surface. X-ray photoelectron spectroscopy etching and friction tests demonstrated that poly([BNIm][Br]) can be grafted not only on the surface but on the subsurface of the as-prepared surface, and the as-prepared poly(ionic liquid) brush-based surfaces showed satisfactory wear resistance compared to traditional surface initiated ROMP. Subsequently, we evaluated the anti-biofouling properties of poly([BNIm][Br]) brushes. The results indicated that poly(ionic liquid) brushes can obviously resist adhesion of bovine serum albumin and have good anti-bacterial activity against both E. coli and S. aureus. The as-prepared poly(ionic liquid) brush-based biomimetic surface also exhibited considerable antifouling performance for microalgae (Porphyridium and Dunaliella) due to the synergistic effect of the surface composition and microstructure.

Surface properties of chitosan/montmorillonite films for biomedical applications

In this study, we firstly investigated the surface and protein adsorption properties of montmorillonite (MMT)/chitosan (CS) composite films with various MMT/CS weight ratios for metallic implants coating applications. Bicinchoninic acid (BCA) protein assay results show that the neat CS film exhibits a high concentration of bovine serum albumin (BSA) protein adhesion because the abundant carbonyl and amide functional groups on the surface of the CS film easily form hydrogen bonds with the copious carboxylic acid groups on the surface of the BSA protein. The MMT/CS composite films with MMT/CS = 3, 5, 8, and 10 possess a much lower BSA adhesion concentration than that of the neat CS film, as some of the carbonyl and amide functional groups on the surface of the composite films are replaced by the –Si–O–Si and –Al–O–Al groups. Among these MMT/CS composite films, the film with MMT/CS = 5 exhibits the lowest BSA adsorption concentration because it possesses a higher MMT content than those with MMT/CS = 1 and 3 and a smoother and non-porous surface than those with MMT/CS = 8 and 10. According to our results, MMT/CS composite films with appropriate MMT/CS weight ratios exhibit better surface and protein adsorption properties than neat CS for biomedical applications.

Grafting Robust Thick Zwitterionic Polymer Brushes via Subsurface-Initiated Ring-Opening Metathesis Polymerization for Antimicrobial and Anti-Biofouling.

In the present work, high-thickness zwitterionic polymer brushes based on imidazolium salts were successfully grafted via a novel subsurface-initiated ring-opening metathesis polymerization (subsurface-initiated ROMP) from polydimethylsiloxane (PDMS), and their antifouling performance was evaluated in detail. First, an initiator-embedded PDMS was prepared via copolymerization of PDMS prepolymer and ROMP initiator, and then zwitterionic polymer brushes were grafted via subsurface-initiated ROMP from surface to subsurface of the PDMS due to the implanted ROMP initiator. Results from a series of characterization methods such as infrared spectroscopy, X-ray photoelectron spectroscopy, contact angle, and atomic force microscopy proved the zwitterionic polymer brushes' successful grafting. The grafting thickness of zwitterionic polymer brushes via subsurface-initiated ROMP can reach the micron scale, and the as-prepared zwitterionic polymer based surfaces showed good lubricating properties compared to traditional surface-initiated ROMP, which hints that polymer brushes can be grafted not only on the surface but also on the subsurface of PDMS. The protein adhesion test and biofouling assay of zwitterionic polymer brushes were tested in the laboratory, and the results indicated that the zwitterionic polymer-functionalized PDMS can effectively resist the adhesion of bovine serum albumin and algae (Porphyridium and Dunaliella) and has good anti-bacterial activity against both Escherichia coli and Staphylococcus aureus.

Antifouling zwitterionic pSBMA‐MSN particles for biomedical applications

Mesoporous silica nanoparticles (MSNs) are one of the most promising nanocarriers in biomedicine. Nonetheless, surface modification has been pointed out as a condition necessary for drug delivery applications, where stability and biocompatibility are extremely important for the vehicle performance. Likewise, zwitterionic polymers are outstanding candidates in biological fields, where poly(sulfobetaine methacrylate) (pSBMA) has been widely studied. These polymers, known as antifouling materials, are able to render a surface capacity to avoid protein adhesion. In this work, a core‐shell nanocarrier was created, where pSBMA was covalently grafted by atom transfer radical polymerization (ATRP) onto a previously functionalized MSN surface. Brush morphologies with different chain lengths ( , between 6500 and 32 300) and graft densities (σpSBMA, between 0.15 and 0.51 molecules of pSBMA per nm2 of MSN) were obtained. Protein adhesion resistance was evaluated with two proteins: fibronectin (FN) and bovine serum albumin (BSA). The best nanocarrier synthesized allowed a reduction of 96% of FN and 76% of BSA adhesion (compared with an adsorption of 100% assigned to the native material). Since the influence of the brush morphology is seldom studied or reported, this work aims to comprehend how the configuration of the polymer brushes affected their antifouling capacity, in order to use this pSBMA‐MSN product for biomedical applications, notably as a possible drug delivery nanocarrier. Future work will analyze the solution behavior of the zwitterionic brushes to evaluate variations of temperature and pH values as possible mechanisms of delivery.

Effect of protein on PVDF ultrafiltration membrane fouling behavior under different pH conditions: interface adhesion force and XDLVO theory analysis

To further determine the fouling behavior of bovine serum albumin (BSA) on different hydrophilic PVDF ultrafiltration (UF) membranes over a range of pH values, self-made atomic force microscopy (AFM) colloidal probes were used to detect the adhesion forces of membrane–BSA and BSA–BSA, respectively. Results showed that the membrane–BSA adhesion interaction was stronger than the BSA–BSA adhesion interaction, and the adhesion force between BSA–BSA-fouled PVDF/PVA membranes was similar to that between BSA–BSA-fouled PVDF/PVP membranes, which indicated that the fouling was mainly caused by the adhesion interaction between membrane and BSA. At the same pH condition, the PVDF/PVA membrane–BSA adhesion force was smaller than that of PVDF/ PVP membrane–BSA, which illustrated that the more hydrophilic the membrane was, the better antifouling ability it had. The extended Derjaguin–Landau–Verwey–Overbeek (XDLVO) theory predicts that the polar or Lewis acid–base (AB) interaction played a dominant role in the interfacial free energy of membrane–BSA and BSA–BSA that can be affected by pH. For the same membrane, the pH values of a BSA solution can have a significant impact on the process of membrane fouling by changing the AB component of free energy.

Biological behaviour of thin films consisting of Au nanoparticles dispersed in a TiO2 dielectric matrix

In this work it was studied the possible use of thin films, composed of Au nanoparticles (NPs) embedded in a TiO2 matrix, in biological applications, by evaluating their interaction with a well-known protein, Bovine Serum Albumin (BSA), as well as with microbial cells (Candida albicans). The films were produced by one-step reactive DC magnetron sputtering followed by heat-treatment. The samples revealed a composition of 8.3 at.% of Au and a stoichiometric TiO2 matrix. The annealing promoted grain size increase of the Au NPs from 3 nm (at 300 °C) to 7 nm (at 500 °C) and a progressive crystallization of the TiO2 matrix to anatase. A broad localized surface plasmon resonance (LSPR) absorption band (λ = 580–720 nm) was clearly observed in the sample annealed at 500 °C, being less intense at 300 °C. The biological tests indicated that the BSA adhesion is dependent on surface nanostructure morphology, which in turn depends on the annealing temperature that changed the roughness and wettability of the films. The Au:TiO2 thin films also induced a significant change of the microbial cell membrane integrity, and ultimately the cell viability, which in turn affected the adhesion on its surface. The microstructural changes (structure, grain size and surface morphology) of the Au:TiO2 films promoted by heat-treatment shaped the amount of BSA adhered and affected cell viability.

Enhanced protein adsorption and patterning on nanostructured latex-coated paper

Specific interactions of extracellular matrix proteins with cells and their adhesion to the substrate are important for cell growth. A nanopatterned latex-coated paper substrate previously shown to be an excellent substrate for cell adhesion and 2D growth was studied for directed immobilization of proteins. The nanostructured latex surface was formed by short-wavelength IR irradiation of a two-component latex coating consisting of a hydrophilic film-forming styrene butadiene acrylonitrile copolymer and hydrophobic polystyrene particles. The hydrophobic regions of the IR-treated latex coating showed strong adhesion of bovine serum albumin (cell repelling protein), fibronectin (cell adhesive protein) and streptavidin. Opposite to the IR-treated surface, fibronectin and streptavidin had a poor affinity toward the untreated pristine latex coating. Detailed characterization of the physicochemical surface properties of the latex-coated substrates revealed that the observed differences in protein affinity were mainly due to the presence or absence of the protein repelling polar and charged surface groups. The protein adsorption was assisted by hydrophobic (dehydration) interactions.

Carboxybetaine Methacrylate-Modified Nylon Surface for Circulating Tumor Cell Capture

Conventional in vitro circulating tumor cell (CTC) detection methods are always limited by blood sample volume because of the requirement of a large amount of blood. The aim of this study was to overcome the limitation by designing and making an in vivo CTC capture device. In this study, we designed and prepared a kind of proper material to serve the purpose of intervention. A method employing 3-aminopropyltriethoxysilane (γ-APS) as the coupling reagent to graft carboxybetaine methacrylate (CBMA) and to immobilize an anti-epithelial cell adhesion molecular (EpCAM) antibody on Nylon was developed. The results of X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy proved the successful graft of γ-APS and CBMA to Nylon. Furthermore, the predicted improvement in the biocompatibilities of our modified Nylon was confirmed by water contact angle measurement, bovine serum albumin adhesion, platelet adhesion, plasma recalcification time determination, and cytotoxicity tests. The tumor cells adhesion experiment revealed that Nylon with the antibody immobilized on it had an affinity for EpCAM positive tumor cells higher than that of pristine Nylon. Additionally, the capture ability of the CTCs was demonstrated in a nude mouse tumor model using the interventional device made of the modified Nylon wire. The positive results suggest that CBMA-grafted and anti-EpCAM antibody-immobilized Nylon is a promising new material for in vivo CTC capture devices.

Study of BSA protein adsorption/release on hydroxyapatite nanoparticles

Three different spherical, rod and fibrous morphologies of hydroxyapatite (HA) nanoparticles have been prepared through control over the processing parameters like temperature, pH and Ca:P ratio. Protein adsorption/release with respect to HA nanoparticle morphologies are investigated using model protein bovine serum albumin (BSA). BSA adsorption on HA nanoparticles follows Langmuir adsorption isotherm. Thermal analysis and FT-IR spectrum confirms the BSA adhesion and retention of their secondary structure. High surface area with high Ca:P ratio nanorod adsorbs relatively more amount (28mg BSA/gm of nanorod HA) of BSA within 48h in comparison with counterpart fibroid and spherical morphologies. Slow and steady BSA release (75wt% of adsorbed BSA in 96h) from nanorod HA is found as futuristic drug delivery media.