Impedimetric and Plasmonic Sensing of Collagen I Using a Half-Antibody-Supported, Au-Modified, Self-Assembled Monolayer System

From MDPI via Jisc Publications RouterHistory: accepted 2021-07-05, pub-electronic 2021-07-08Publication status: PublishedThis research presents an electrochemical immunosensor for collagen I detection using a self-assembled monolayer (SAM) of gold nanoparticles (AuNPs) and covalently immobilized half-reduced monoclonal antibody as a receptor; this allowed for the validation of the collagen I concentration through two different independent methods: electrochemically by Electrochemical Impedance Spectroscopy (EIS), and optically by Surface Plasmon Resonance (SPR). The high unique advantage of the proposed sensor is based on the performance of the stable covalent immobilization of the AuNPs and enzymatically reduced half-IgG collagen I antibodies, which ensured their appropriate orientation onto the sensor’s surface, good stability, and sensitivity properties. The detection of collagen type I was performed in a concentration range from 1 to 5 pg/mL. Moreover, SPR was utilized to confirm the immobilization of the monoclonal half-antibodies and sensing of collagen I versus time. Furthermore, EIS experiments revealed a limit of detection (LOD) of 0.38 pg/mL. The selectivity of the performed immunosensor was confirmed by negligible responses for BSA. The performed approach of the immunosensor is a novel, innovative attempt that enables the detection of collagen I with very high sensitivity in the range of pg/mL, which is significantly lower than the commonly used enzyme-linked immunosorbent assay (ELISA)

The Dependence of the Properties of Recycled PET Electrospun Mats on the Origin of the Material Used for Their Fabrication

Plastic materials are one of the significant components of construction materials omnipresent in all areas of the industry and everyday life. One of these plastics is polyethylene terephthalate (PET). Due to its processing properties, with a simultaneous low production cost, PET has been used in many industrial applications, including the production of various types of bottles. Moreover, the high consumption of PET bottles causes the accumulation of large amounts of their waste and necessitates finding an effective way to recycle them. Electrospinning is a well-known non-complicated method for the fabrication of nonwovens from polymers and composites, which can be utilized in many fields due to their outstanding properties. In addition, it might be a promising technique for the recycling of plastic materials. Therefore, in this study, the electrospinning approach for the recycling of two types of PET bottle wastes—bottles made of virgin PET and bottles made of recycled PET (PET bottles) has been utilized, and a comparison of the properties of the obtained materials have been performed. The fibers with diameters of 1.62 ± 0.22, 1.64 ± 0.18, and 1.89 ± 0.19 have been produced from solutions made of virgin PET granulate, PET bottles, and PET bottles made of recycled bottles, respectively. Obtained fibers underwent morphological observation using a scanning electron microscope. Physico-chemical properties using FTIR, gel chromatography, and differential scanning calorimetry have been evaluated, and mechanical properties of obtained mats have been investigated. Cytotoxicity tests using the L929 mouse fibroblast cell line revealed no cytotoxicity for all tested materials

Evaluation of the Shape Memory Effect of Random and Aligned Electrospun Polyurethane Mats with Different Fibers Diameter

Fibrous shape memory scaffolds composed of thermoplastic polyurethane based on a mixture of polycaprolactone diols were fabricated. The effect of the fiber diameter and arrangement– random (rPU) or aligned (aPU), on crystallinity, mechanical properties, and shape memory was analyzed. The diameters of the fibers were controlled by changing the concentration of polyurethane (PU) solutions in the range of 5% to 16% and fibers alignment by utilization of different collectors. The chemical structure was confirmed by Fourier Transformed Infrared spectroscopy (FTIR), crystallinity was evaluated based on differential scanning calorimetry (DSC,) and mechanical properties were measured by the tensile test. Additionally, shape memory programming was performed using a dynamic mechanical analyzer (DMA), and shape recovery was evaluated in the air and in the water environment. DSC results showed that the electrospinning process did not change the crystallinity or melting temperature of synthesized thermoplastic polyurethanes. The melting temperature of the crystalline switching segments was around 26–27 °C, and the crystalline phase of hard segments was around 130 °C. Shape memory properties were analyzed in the contest of the fiber diameter and alignment of the fibers, while changes in the fibers’ diameters from 360 nm to 1760 nm did not result in significant changes in shape recovery coefficient (Rr) especially evaluated in the air. The longitudinal fiber alignment enhanced mechanical and shape recovery to up to 96% for aPU, with the highest fiber diameter when evaluated in water

Detection of Circulating Tumor Cells Using Membrane-Based SERS Platform: A New Diagnostic Approach for ‘Liquid Biopsy’

The detection and monitoring of circulating tumor cells (CTCs) in blood is an important strategy for early cancer evidence, analysis, monitoring of therapeutic response, and optimization of cancer therapy treatments. In this work, tailor-made membranes (MBSP) for surface-enhanced Raman spectroscopy (SERS)-based analysis, which permitted the separation and enrichment of CTCs from blood samples, were developed. A thin layer of SERS-active metals deposited on polymer mat enhanced the Raman signals of CTCs and provided further insight into CTCs molecular and biochemical composition. The SERS spectra of all studied cells—prostate cancer (PC3), cervical carcinoma (HeLa), and leucocytes as an example of healthy (normal) cell—revealed significant differences in both the band positions and/or their relative intensities. The multivariate statistical technique based on principal component analysis (PCA) was applied to identify the most significant differences (marker bands) in SERS data among the analyzed cells and to perform quantitative analysis of SERS data. Based on a developed PCA algorithm, the studied cell types were classified with an accuracy of 95% in 2D PCA to 98% in 3D PCA. These results clearly indicate the diagnostic efficiency for the discrimination between cancer and normal cells. In our approach, we exploited the one-step technology that exceeds most of the multi-stage CTCs analysis methods used and enables simultaneous filtration, enrichment, and identification of the tumor cells from blood specimens

Morphology and Chemical Purity of Water Suspension of Graphene Oxide FLAKES Aged for 14 Months in Ambient Conditions. A Preliminary Study

Graphene and its derivatives have attracted scientists’ interest due to their exceptional properties, making them alluring candidates for multiple applications. However, still little is known about the properties of as-obtained graphene derivatives during long-term storage. The aim of this study was to check whether or not 14 months of storage time impacts graphene oxide flakes’ suspension purity. Complementary micro and nanoscale characterization techniques (SEM, AFM, EDS, FTIR, Raman spectroscopy, and elemental combustion analysis) were implemented for a detailed description of the topography and chemical properties of graphene oxide flakes. The final step was pH evaluation of as-obtained and aged samples. Our findings show that purified flakes sustained their purity over 14 months of storage

High-resolution microscopy assisted mechanical modeling of ultrafine electrospun network

This paper demonstrates a novel hi-resolution microscopy-assisted computational approach to mechanical modeling of ultrafine electrospun networks (ESN). Morphological data extracted from X-ray microtomography (μCT) of ESN made of poly(lactic-co-glycolic acid) (PLGA), supplemented by data acquired from the nanoscale flexural test of a single fiber, was used to create a volumetric finite element (FE) model of the investigated ESN. The results of the carried-out FE simulation have been successfully validated against the results of the quasi-static tensile test. The accuracy and the reliability of the μCT-based ESN geometry have been proved by the comparison with the scanning electron microscopy (SEM) data and by the numerical analysis of fluid flow across the rendered ESN structure. The designed methodology enables the analysis of potential factors affecting the mechanical properties of electrospun structures made of aliphatic polyesters, like the depth of fiber fusion, the ESN geometric inaccuracies, and the fiber diameter distribution. Moreover, in the study, the novel experimental setup enabling for single fiber AFM flexural test was proposed, assuming deposition of fibers directly on polystyrene (PS) substrate containing crater-like wells. Additionally, the presented study contains the numerical analysis of the effect of the substrate stiffness on the results of the three-point bending test of a single fiber

Processing of (Co)Poly(2-oxazoline)s by Electrospinning and Extrusion from Melt and the Postprocessing Properties of the (Co)Polymers

Poly(2-oxazoline) (POx) matrices in the form of non-woven fibrous mats and three-dimensional moulds were obtained by electrospinning and fused deposition modelling (FDM), respectively. To obtain these materials, poly(2-isopropyl-2-oxazoline) (PiPrOx) and gradient copolymers of 2-isopropyl- with 2-n-propyl-2-oxazoline (P(iPrOx-nPrOx)), with relatively low molar masses and low dispersity values, were processed. The conditions for the electrospinning of POx were optimised for both water and the organic solvent. Also, the FDM conditions for the fabrication of POx multi-layer moulds of cylindrical or cubical shape were optimised. The properties of the POx after electrospinning and extrusion from melt were determined. The molar mass of all (co)poly(2-oxazoline)s did not change after electrospinning. Also, FDM did not influence the molar masses of the (co)polymers; however, the long processing of the material caused degradation and an increase in molar mass dispersity. The thermal properties changed significantly after processing of POx what was monitored by increase in enthalpy of exo- and endothermic peaks in differential scanning calorimetry (DSC) curve. The influence of the processing conditions on the structure and properties of the final material were evaluated having in a mind their potential application as scaffolds

Biological and Corrosion Evaluation of In Situ Alloyed NiTi Fabricated through Laser Powder Bed Fusion (LPBF)

In this work, NiTi alloy parts were fabricated using laser powder bed fusion (LBPF) from pre-alloyed NiTi powder and in situ alloyed pure Ni and Ti powders. Comparative research on the corrosive and biological properties of both studied materials was performed. Electrochemical corrosion tests were carried out in phosphate buffered saline at 37 °C, and the degradation rate of the materials was described based on Ni ion release measurements. Cytotoxicity, bacterial growth, and adhesion to the surface of the fabricated coupons were evaluated using L929 cells and spherical Escherichia coli (E. coli) bacteria, respectively. The in situ alloyed NiTi parts exhibit slightly lower corrosion resistance in phosphate buffered saline solution than pre-alloyed NiTi. Moreover, the passive layer formed on in situ alloyed NiTi is weaker than the one formed on the NiTi fabricated from pre-alloyed NiTi powder. Furthermore, in situ alloyed NiTi and NiTi made from pre-alloyed powders have comparable cytotoxicity and biological properties. Overall, the research has shown that nitinol sintered using in situ alloyed pure Ni and Ti is potentially useful for biomedical applications