Probing the influence of strontium doping and annealing temperature on the structure and biocompatibility of hydroxyapatite nanorods.

Among numerous biologically important metal cations, strontium (Sr2+) has received much attention in bone tissue regeneration because of its osteoinductive properties combined with its ability to inhibit osteoclast activity. In this study, strontium-doped hydroxyapatite (Sr-HAp) nanorods with varying molar ratios of Ca : Sr (10 : 0, 9 : 1, 5 : 5, 3 : 7 and 0 : 10) were synthesized using the chemical precipitation technique. The synthesized Sr-HAp nanostructures were characterized using powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy, energy dispersive X-ray spectroscopy, and Raman and Fourier transform infrared (FTIR) spectroscopies to understand their structural and morphological features, and composition. XRD results revealed the formation of HAp nanostructures, whose unit cell volume increased as a function of the dopant level. The reaction process investigation showed the formation of hydroxyapatite (HAp), strontium apatite (SAp) and various Sr-HAp phases. FESEM micrographs displayed the morphological transformation of Sr-HAp from nanorods to nanosheets upon increasing the dopant level. In the FTIR spectra, the bands of the PO43- group shifted towards a lower wavenumber upon increasing the dopant concentration in Sr-HAp that signifies the structural distortion due to the presence of a large amount of strontium ions. The peaks of PO43- and OH- vibrations in the Raman spectra were further analysed to corroborate the structural distortion of Sr-HAp. Selected area electron diffraction patterns obtained using TEM reveal the reduced crystallinity of Sr-HAp due to Sr-doping, which is in line with the XRD results. Finally, the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay showed that the synthesized Sr-HAp has no toxic effect on the survival and growth of mesenchymal stem cells. In summary, the synthesized novel Sr-HAp nanorods exhibit great promise for bone tissue engineering applications.

A study on electroactive PVDF/mica nanosheet composites with an enhanced γ-phase for capacitive and piezoelectric force sensing.

Herein, a multifunctional poly(vinylidene fluoride) (PVDF)/mica nanosheet composite (PMNC) thin film was developed for preparing a capacitive and piezoelectric force sensor. A high electroactive γ-phase content (89%) of PVDF was achieved through a facile rapid cooling process of PMNC films. The crystallinity of PVDF decreased upon the addition of mica nanosheets, while the dielectric constant increased significantly (∼300%). The capacitance-based PMNC pressure sensor was found to be sensitive to the applied pressure. On the other hand, piezoelectric voltages of 18 V (single layer) and 32 V (multi-layer) were generated for PMNCs loaded with 1% mica nanosheets. Furthermore, a PMNC based nanogenerator generated a power density of 8.8 µW cm-2 and showed excellent durability (>60 000 cycles). High flexibility, lightweight and skin-friendly PMNCs could be a potential material in applications such as energy harvesting, energy storage, actuators, and self-powered and smart wearable electronic devices.

Highly sensitive and wearable NO2gas sensor based on PVDF nanofabric containing embedded polyaniline/g-C3N4nanosheet composites.

In this study, a highly flexible and wearable nitrogen dioxide (NO2) gas sensor was fabricated based on electrospun poly(vinylidene fluoride) (PVDF)/polyaniline (PANi)/graphitic-carbon nitride (g-C3N4) blend nanocomposite (EBNC). g-C3N4/PANi nanocomposite (GPC) was synthesized byin situpolymerization technique prior to its incorporation into PVDF nanofibers, which ensured uniformity of dispersion. For the comparison study, PVDF/GPC nanocomposite film was fabricated using doctor blade technique. EBNC sensor exhibited high sensitivity, selectivity, reproducibility along with quick response and complete recovery. Electrospinning and GPC synergistically improved the performance of the EBNC based gas sensor. The superior gas sensing ability along with its low cost and the use of scalable electrospinning technique could make this system a promising one for the detection of gaseous NO2.

Cationic surfactant assisted enhancement of dielectric and piezoelectric properties of PVDF nanofibers for energy harvesting application.

Poly(vinylidene fluoride) (PVDF) is among the most versatile polymers due to its wide range of properties, including dielectric, piezoelectric and ferroelectric properties. However, more frequently than not a range of processing routes and/or additives have been used to enhance such properties. In this study, PVDF nanofibers were electrospun from PVDF solution that contained tetra-n-butyl ammonium chloride (TBAC) at different loadings (1, 2, 3, and 5 wt%). The effect of TBAC on the morphology, crystallinity, and polymorphism of PVDF was studied using various characterization techniques. Addition of TBAC significantly improved the electroactive ß-phase of PVDF. The highest ß-phase content of 89% was attained at a TBAC loading of 3 wt%. Consequently, the dielectric and piezoelectric properties of the PVDF nanofibers improved significantly. A nanogenerator fabricated using 3 wt% TBAC/PVDF nanofibers exhibited the maximum voltage output of 17.2 V (under 5 N force) and the maximum power density of ∼1.4 µW cm-2 (under 3 N force). Improved dielectric and piezoelectric properties of PVDF upon the addition of a small amount of TBAC could be useful for researchers in upbringing the material for flexible electronic devices.

Development of a new flexible nanogenerator from electrospun nanofabric based on PVDF/talc nanosheet composites.

Herein, a flexible piezoelectric nanogenerator composed of electrospun talc/PVDF [poly(vinylidene fluoride)] nanocomposite fabrics has been developed. These nanocomposite fabrics demonstrated enhanced mechanical and piezoelectric properties compared with pristine PVDF nanofabrics. In particular, nanocomposite fabrics with 0.50 wt% talc yielded 89.6% of polar ß-phase in the PVDF matrix, thereby augmenting its piezoelectric response. X-ray diffraction, Fourier transform infrared spectroscopy, and differential scanning calorimetry conclusively affirmed the promotion of polar ß-phase in the talc/PVDF nanocomposite fabrics. The 0.50 wt% talc/PVDF nanocomposite fabric based nanogenerator produced an open-circuit voltage and power density of 9.1 V and 1.12 µW cm-2, respectively, under repetitive finger tapping mode (under a load of 3.8 N). Furthermore, the nanogenerator was also subjected to frequency modulated-shaker mode, wherein an output voltage of 8.9 V was produced. Improved flexibility, mechanical robustness, and enhanced piezoelectric responsiveness of this nanogenerator could possibly pave the way for its use in portable self-powered devices.

Polymorph nickel titanate nanofibers as bifunctional electrocatalysts towards hydrogen and oxygen evolution reactions.

Producing pure H2 and O2 to sustain the renewable energy sources with minimal environmental damage is a key objective of photo/electrochemical water-splitting research. Metallic Ni-based electrocatalysts are expensive and eco-hazardous. This has rendered the replacement or reduction of Ni content in Ni-based electrocatalysts a decisive criterion in the development of bifunctional electrocatalytic materials. In the current study, spinel/ilmenite composite nickel titanate (NTO) nanofibers were synthesised using sol-gel assisted electrospinning followed by pyrolysis at different soaking temperatures (viz., 773, 973, and 1173 K). The presence of a defective spinel NTO phase (SNTO) distributed uniformly along the nanofibers was confirmed by X-ray photoelectron and Raman spectroscopy. The electron micrographs revealed the morphological change of NTO nanofibers from a mosaic to bamboo structure with an increase in pyrolysis soaking temperature. The electrocatalytic activity of NTO nanofibers obtained at different pyrolysis soaking temperatures for alkaline water-splitting was studied. The highly defective SNTO manifests properties similar to metallic Ni and favours H2 evolution through the hydrogen evolution reaction (HER) by adsorbing more H+ ions on active sites. In contrast, the ilmenite NTO favours O2 discharge. These results are explained based on the morphology of the NTO nanofibers. The mosaic structure which has higher porosity and greater SNTO content shows excellent HER performance. In contrast, the large bamboo structured NTO nanofibers which have lesser porosity and SNTO content cage the bigger (OH)ads ions at their catalytic sites to facilitate OER performance.

Synergism of fictitious forces on nickel cobaltite nanofibers: electrospinning forces revisited.

Randomly oriented nanofibers of nickel cobaltite (NCO) were fabricated using sol-gel electrospinning followed by calcination. The precursor fibers were collected on rotating disc (RDI) and rotating drum (RDR) collectors. Variable fictitious forces produce continuous deflection at each fiber landing position on the RDI collector, which subjects the nanofibers to non-bundling. On the other hand, in the case of the RDR collector, the fictitious forces act just at the surface, and these forces merely cause slip of the fibers along the rotational axis of the RDR. This slip along with the retained Columbic charges on the surface of the fibers produces fiber bundling, which affects the morphological and structural properties of the NCO nanofibers obtained by calcining the precursor fibers. The use of the RDI collector in sol-gel electrospinning is a simple and optimal method of fabricating precursor nanofibers, which yields non-agglomerated and impurity-free inorganic nanofibers.

Heteroplasmy due to coexistence of mtCOI haplotypes from different lineages of the Thrips tabaci cryptic species group.

Heteroplasmy is the existence of multiple mitochondrial DNA haplotypes within the cell. Although the number of reports of heteroplasmy is increasing for arthropods, the occurrence, number of variants, and origins are not well studied. In this research, the occurrence of heteroplasmy was investigated in Thrips tabaci, a putative species complex whose lineages can be distinguished by their mitochondrial DNA haplotypes. The results from this study showed that heteroplasmy was due to the occurrence of mitochondrial cytochrome oxydase I (mtCOI) haplotypes from two different T. tabaci lineages. An assay using flow cytometry and quantitative real-time PCR was then used to quantify the per cell copy number of the two mtCOI haplotypes present in individuals exhibiting heteroplasmy from nine geographically distant populations in India. All of the T. tabaci individuals in this study were found to exhibit heteroplasmy, and in every individual the per cell copy number of mtCOI from lineage 3 comprised 75-98% of the haplotypes detected and was variable among individuals tested. There was no evidence to suggest that the presense of lineage-specific haplotypes was due to nuclear introgression; however, further studies are needed to investigate nuclear introgression and paternal leakage during rare interbreeding between individuals from lineages 2 and 3.

On-Demand Guided Bone Regeneration with Microbial Protection of Ornamented SPU Scaffold with Bismuth-Doped Single Crystalline Hydroxyapatite: Augmentation and Cartilage Formation.

Guided bone regeneration (GBR) scaffolds are futile in many clinical applications due to infection problems. In this work, we fabricated GBR with an anti-infective scaffold by ornamenting 2D single crystalline bismuth-doped nanohydroxyapatite (Bi-nHA) rods onto segmented polyurethane (SPU). Bi-nHA with high aspect ratio was prepared without any templates. Subsequently, it was introduced into an unprecedented synthesized SPU matrix based on dual soft segments (PCL-b-PDMS) of poly(ε-caprolactone) (PCL) and poly(dimethylsiloxane) (PDMS), by an in situ technique followed by electrospinning to fabricate scaffolds. For comparison, undoped pristine nHA rods were also ornamented into it. The enzymatic ring-opening polymerization technique was adapted to synthesize soft segments of PCL-b-PDMS copolymers of SPU. Structure elucidation of the synthesized polymers is done by nuclear magnetic resonance spectroscopy. Sparingly, Bi-nHA ornamented scaffolds exhibit tremendous improvement (155%) in the mechanical properties with excellent antimicrobial activity against various human pathogens. After confirmation of high osteoconductivity, improved biodegradation, and excellent biocompatibility against osteoblast cells (in vitro), the scaffolds were implanted in rabbits by subcutaneous and intraosseous (tibial) sites. Various histological sections reveal the signatures of early cartilage formation, endochondral ossification, and rapid bone healing at 4 weeks of the critical defects filled with ornamented scaffold compared to SPU scaffold. This implies osteogenic potential and ability to provide an adequate biomimetic microenvironment for mineralization for GBR of the scaffolds. Organ toxicity studies further confirm that no tissue architecture abnormalities were observed in hepatic, cardiac, and renal tissue sections. This finding manifests the feasibility of fabricating a mechanically adequate nanofibrous SPU scaffold by a biomimetic strategy and the advantages of Bi-nHA ornamentation in promoting osteoblast phenotype progression with microbial protection (on-demand) for GBR applications.

Structure-property relationship of sol-gel electrospun ZnO nanofibers developed for ammonia gas sensing.

Zinc oxide (ZnO) based nanomaterials have been used in various gas sensors due to the wide band gap (3.37eV), large exciton binding energy and high mobility of charge carriers of ZnO. In this work, nanocrystalline ZnO nanofiber mats were synthesized through combined sol-gel electrospinning techniques followed by calcination, in which poly(styrene-co-acrylonitrile) and zinc acetate were used as the binder and precursor, respectively. Average diameter of the ZnO nanofibers decreased from 400 to 60nm, while their grain size and crystallinity were enhanced by increasing the calcination temperature. Morphology and structure of the ZnO nanofiber mats were characterized by high resolution transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. ZnO nanofiber mats were found to be superhydrophilic (contact angle was close to 0°) by contact angle measurements. The sensitivity of these ZnO nanofibers in detecting gaseous ammonia was tested using an indigenous set up. Due to their high surface area and superhydrophility, these ZnO nanofiber mats were highly sensitive in sensing gaseous ammonia and the sensitivity of these mats increased as a function of their calcination temperatures.

The cowpea trypsin inhibitor promoter drives expression in response to cellular maturation in Arabidopsis thaliana.

The bowman-birk type trypsin inhibitors accumulate in high concentration in legume and cereal seeds, especially during seed maturation and are considered to be involved in insect tolerance. The 5' flanking sequences of the trypsin inhibitor was isolated from cowpea genomic DNA using anchor PCR. Analysis of sequences showed presence of seed specific RY elements and also other elements associated with seed development such as abscisic acid responsive elements (ABA responsive elements; ABRE) and dehydration responsive elements (DRE). Spatial and temporal control of the promoter driven expression pattern was analyzed using gus as reporter. Expression was found to occur both in embryo and endosperm; starting from torpedo stage of embryogenesis and continuing till the stage of final maturation i.e. bent cotyledon stage. Additional expression analyses showed that the promoter actually drives expression in tissues like leaves, roots, stipules, etc., but followed a specific pattern. Comparative analysis of expression in seeds and other organs indicated that the promoter driven expression is in response to cellular maturation.