Multifunctional Substrates Research Articles

Application and Development of Hydrogel in Soilless Culture

AbstractSoilless culture refers to the method of cultivating plants without soil as a growing medium, and the use of hydrogel in soilless culture overcomes many technical difficulties, but there are many applications that just stay at the experimental level, with fewer applications in fields. Although many new functionalized hydrogels may help to overcome the shortcomings of traditional media and give them more functionality, little research on hydrogels over the past decades has been reflected in soilless culture techniques. This paper details the concept and development of soilless culture, as well as several applications of hydrogels in soilless culture, including the use of hydrogels as soilless culture substrates and the application of hydrogel membranes. The important roles of different types of hydrogels in soilless culture, such as antimicrobial properties, salt tolerance and high water absorption, are highlighted, and these excellent properties largely overcome a series of drawbacks of traditional cultivation methods. The application of hydrogels in pest control is also discussed. Hydrogel applications to soilless culture have better prospects for the creation of more promising multifunctional composite hydrogel membranes and hydrogel substrates capable of supporting plants throughout their growth cycle.

Spinous Au@Ag Bimetallic Nanowires: Synthesis and In Situ Monitoring SERS of Plasmonic Catalysis.

In situ monitoring of reactant transformations at metal catalyst surfaces and/or interfaces, combined with the identification of intermediate species and products, is vital for elucidating catalytic processes and behaviors. We developed innovative spinous Au@Ag nanowires (NWs) with a bimetallic structure and dense alloy protrusions, demonstrating both catalytic activity and surface-enhanced Raman spectroscopy (SERS) capabilities, thereby facilitating in situ SERS tracking of reactions. The spinous Au@Ag NWs exhibit sharp spikes on their surface, providing a large number of catalytically active sites. They demonstrate outstanding sensitivity, signal reproducibility, and homogeneity when detecting representative dye molecules like crystal violet. Furthermore, the spinous Au@Ag NWs exhibit outstanding catalytic performance, enhancing the separation and movement of photogenerated electron-hole pairs. This research offers important insights for the design of multifunctional SERS substrates and paves the way for new opportunities in the in situ monitoring of catalytic processes.

Highly flexible and transparent colorless polyimide substrate sandwiched between plasma polymerized fluorocarbon and InGaTiO for high performance flexible perovskite solar cells

ABSTRACT We integrated transparent antireflective coatings and transparent electrodes onto flexible colorless polyimide (CPI) substrates to fabricate high-performance flexible perovskite solar cells. Multifunctional PPFC/CPI/IGTO substrates were fabricated by sputtering the optimal plasma-polymerized fluorocarbon (PPFC) antireflective coating and InGaTiO (IGTO) electrode films on both sides of the CPI substrate. By applying PPFC with a low refractive index (1.38) as an antireflective coating, the transparency of the PPFC/CPI/IGTO substrate increased by an additional 1.2%. In addition, owing to the amorphous characteristics of the PPFC and IGTO layers, the PPFC/CPI/IGTO substrate showed constant sheet resistance and transmittance change even after 10,000 cycles during the bending tests. The flexible perovskite solar cells, fabricated on the PPFC/CPI/IGTO substrate, exhibited an increase in current density of 1.48 mA/cm2 after the deposition of the PPFC antireflective coating. These results confirmed that the PPFC/CPI/IGTO substrate was durable against high-temperature treatment, flexible, and exhibited excellent electrical characteristics. This enhanced the efficiency and durability of the flexible perovskite solar cells. Moreover, the hydrophobic PPFC layer allowed the self-cleaning of inflexible perovskite solar cells. Given these attributes, the PPFC/CPI/IGTO structure has been recognized as a good choice for multifunctional substrates of flexible perovskite solar cells, presenting the potential for enhancing performance.

Innovative Synthesis of Adhesive-Assisted and Recyclable Fe3O4@PD-Ag Photomagnetic Nanocomposites as SERS probes for Ultrasensitive Thiram Detection on Fruit Peels

Surface-enhanced Raman spectroscopy (SERS) with enormous advantages has emerged as a powerful tool for both highly sensitive structural detection of analytes and various imaging applications. A notable advancement in the realm of multifunctional SERS substrates is the integration of magnetic nanoparticles endowed with magnetic manipulation capabilities and noble metal nanoparticles exhibiting plasmonic resonance properties. This synergistic combination offers substantial practical benefits for trace analysis across diverse fields. In this paper, a new paradigm of Fe3O4@PEI-DTC-Ag (Fe3O4@PD-Ag) photomagnetic nanocomposites based on magnetic Fe3O4 nanoparticles (NPs), the noble metal silver quantum dots (Ag QDs) and the adhesive layer polyethyleneimine dithiocarbamate (PEI-DTC) for convenient recycling and ultrasensitive SERS detection was developed by engineering hydrothermal and seed-growth methods. The SERS performance of the Fe3O4@PD-Ag substrates with varying amounts of Ag was evaluated by detecting 4-aminothiophenol (4-ATP). Among the tested samples, Fe3O4@PD-Ag-4 with a silver solution volume of 200 ml exhibited the optimal performance, showcasing an enhancement factor (EF) of 4.418 × 105. Moreover, the relative standard deviations (RSDs) were calculated to be less than 11.5 %, demonstrating the SERS substrates exhibit good uniformity and spectral reproducibility. Of note, the SERS substrate has demonstrated successful trace detection of thiram molecules, achieving a limit of detection (LOD) of up to 10-9 M. The intensity of SERS signals shows a linear correlation with the logarithm of thiram concentration, ranging from 10-4 to 10-9 M, thus providing compelling evidence for quantitative detection. Importantly, the Fe3O4@PD-Ag-4 SERS substrate also showcases outstanding performance for detecting thiram in real food, underscoring its significant potential for application in food safety monitoring.

Viral gene detection based on multifunctional microspheres and AgNPs coated substrate interface area SERS scheme

Surface-enhanced Raman spectroscopy (SERS) has emerged as an effective method for detecting viral genes in aqueous solutions. However, SERS has a low efficiency and poor reproducibility in multi-component aqueous solutions. Thus, developing a SERS scheme with stable hotspots generation, significant enhancement effects, and efficient viral gene enrichment remains a challenge. This study sought to proposes an enhanced hotspot generation scheme combining multifunctional microspheres and SERS substrates, which can achieve stable enhancement in the interface area. Multifunctional microspheres can be used to selectively enrich target biomolecules in aqueous solutions. Furthermore, simulation results show that these microspheres can synergistically form a stable enhancement area with SERS substrates. Finally, this scheme was used for immunocapture and Raman detection of hemagglutinin 7 (H7) and neuraminidase 9 (N9) specific gene in an aqueous solution containing multiple types of influenza viral genes. The relationship between the characteristic peaks and concentrations was analysed using two-dimensional correlation analysis. Spectral data analysis revealed an exceedingly high linear correlation between the selected characteristic peak intensity and concentrations. The calculation results show that the SERS enhancement factor of the proposed scheme for the H7 and N9 specific gene are 9.23×107 and 1.59×108, respectively. Notably, the detection limit of this scheme was 1 pM. Therefore, this scheme holds the promise to realize the detection of viral genes in heterogeneous, complex, and dynamic aqueous biological samples.

SERS Materials with Small‐Molecule Sensitivity for Biological Diagnosis

AbstractSmall molecule metabolites depict a biological system‘s status and help monitor disease conditions. Surface‐enhanced Raman scattering (SERS) holds considerable promise as an instant and non‐destructive detection tool for biological diagnosis. With single‐molecular sensitivity, molecular fingerprint and water compatible, SERS provides valuable information about chemical structures and analyte compositions, especially desirable in biological diagnosis. Design and fabrication of effective, stable SERS substrates can be one of the major research priorities to provide small‐molecule tracing with high sensitivity, selectivity, and reproducibility. Significant efforts have been directed towards creating high‐performance and multifunctional SERS substrates spanning from coinage metals to semiconductor materials. However, most SERS substrates are suffering from unsatisfied sensitivity for tracing small molecules such as volatile organic compounds (VOCs) and other biomarkers. This review summarized recent advances in SERS‐active substrates and their sensing for small biomarker molecules, especially VOCs in diagnosis.

Highly Efficient and Reliable Organic Light–Emitting Diodes Enabled by a Multifunctional Hazy Substrate for Extreme Environments

AbstractAs transparent, flexible, and wearable organic electronics degrade under normal outdoor environmental conditions (e.g., water vapor, oxygen, and UV light) and extreme environments, including washing or rain, a customized encapsulation technology is required to improve device reliability. Herein, a simple process is presented for fabricating multifunctional hazy substrates (MFHSs) with excellent gas diffusion barrier (GDB), flexibility, UV reflectance, light scattering, and waterproof properties. First, a spiky polyethylene terephthalate (PET) surface is produced with 76.0% optical haze through ion‐beam treatment followed by the formation of a hydrophobic layer to achieve a waterproof effect (contact angle: 153.3°). Then, a multifunctional multibarrier film is fabricated based on a nano‐laminated distributed Bragg reflector and functional polymer on the functional PET substrate to serve as a GDB and UV filter. This multibarrier film has excellent mechanical and chemical stabilities, in addition to having a water vapor transmission rate of 10−6 g m−2 day−1 and UV transmittance of <3%. The so‐fabricated MFHS not only increases the device efficiency by 73% but also enables a highly flexible and environmentally stable organic light–emitting diode. The surface treatment and encapsulation technologies developed in this study are expected to increase the lifetime of organic devices and facilitate high outdoor usability.

Transient Dual‐Response Iontronic Strain Sensor Based on Gelatin and Cellulose Nanocrystals Eutectogel Nanocomposites

AbstractThe emergence of wearable strain sensors in soft electronics has the potential to revolutionize healthcare and robotics. However, current sensors are based on petroleum‐based conductive composites that have a limited strain range. Ionic conductors such as hydrogels offer expanded strain range but have poor long‐term stability and restricted temperature operating window. Deep eutectic solvents (DESs) are promising nonaqueous electrolytes alternatives with green credentials. By combining DES electrolytes with biopolymers, transient ionic conductors are developed with high stretchability, and excellent chemical and thermal stability. Herein, cellulose nanocrystals (CNC) are incorporated, bearing ─OSO3H or ─COOH groups, to gelatin‐based eutectogels to produce nanocomposites with enhanced properties and additional functionalities. The eutectogel nanocomposite containing 1.0 wt.% COOH‐CNC demonstrate enhanced stretchability (375%) and ionic conductivity (3.0 mS cm−1) compared to the pristine gelatin‐based eutectogel (300% strain and 2.0 mS cm−1, respectively). Moreover, the spontaneous assembly of CNC within the eutectogel results in birefringence, which changes when stretching the nanocomposites. Thus, CNC incorporation provides the gelatin‐based eutectogel with a dual‐response capabilities when stretched, expanding their applications to new areas such as transient multi‐responsive strain sensors for wearable electronics, and multifunctional substrates for soft robotics, without compromising overall performance or sustainability.

Extending the range of metal ions SERS detection using hybrid plasmonic/ZIF-8 particles

Nanosensors based on surface-enhanced Raman spectroscopy (SERS) have emerged as a class of promising optical tools for the ultrasensitive quantification of metal ions of environmental and biological interest. A central bottleneck in this field is the availability of suitable surface receptors able to convert the selective binding with these vibrationless analytes into measurable SERS signals. In this work, we tackle this issue by employing a hybrid substrate comprising a highly SERS-active plasmonic core and a ZIF-8 metal-organic framework (MOF) shell. The ZIF-8 shell firmly captures aromatic receptors close to the plasmonic structure regardless of their intrinsic affinity for the metallic surface and without altering their ability to coordinate metal ions. Furthermore, it imparts molecular sieving abilities enabling the direct use of the SERS sensing platform in complex media such as biological fluids. This was demonstrated by using different classes of chromogenic reagents (bathocuproine, a 2,6':2′,2″-terpyridine derivative, and Arsenazo III) which were exploited for the SERS detection of both transition and alkaline earth metal ions (i.e., divalent copper, cobalt and calcium ions). Notably, we successfully applied this approach for the detection of Cu(II) in untreated urine samples for Wilson's disease diagnosis. Overall, we believe this class of multifunctional hybrid substrates will serve as a valuable material for expanding the applicability of SERS spectroscopy in real-life environmental and biomedical metal ions analysis.

Facile In-Situ photocatalytic reduction of AuNPs on multilayer Core-Shell Fe3O4@SiO2@PDA magnetic nanostructures and their SERS application

Surface-enhanced Raman scattering (SERS) is a promising analytical technique for the rapid, sensitive, and repeatable detection in various SERS application fields. Herein, a new type of potential magnetically recyclable SERS substrate was designed and rapidly synthesized via a facile three-step template method. First, the magnetic ferroferric oxide (Fe3O4) cores were prepared by a convenient solvothermal approach, and coated with a thin layer of silica by a sol–gel process in order to improve their stability in complicated environments. Next, the negatively charged polydopamine (PDA)/K6[SiW11VIVO40]·7H2O (PDA/SiW11V) outer shell was assembled upon the magnetic Fe3O4@SiO2 core–shell nanoparticles via a layer-by-layer sequential adsorption process using the stickiness of PDA. The SiW11V multilayer shell can be used as the subsequent photocatalytic reduction precursors for the in-situ loading of high-density gold nanoparticles (AuNPs), without any other organic additives. The AuNPs decorated multilayer core–shell Fe3O4@SiO2@PDA magnetic nanostructures were employed as a potential magnetically recyclable SERS substrate, and showed excellent SERS performance. Using crystal violet (CV) as a model target, the as-fabricated AuNPs modified multilayer core–shell Fe3O4@SiO2@PDA magnetic nanostructures SERS substrates exhibited significant enhancement, and pushed the detection limit down to 10-12 M. Aside from the ultrahigh sensitivity, these SERS substrates also possess an excellent reproducibility (relative standard deviation (RSD) ∼ 8.3%), long-term stability (75 days), and unique chemical stability capability in different organic solvents and different environments with pH ≤ 10. Furthermore, a real-life application is also performed by the detection of melamine in spiked milk solution using the as-prepared magnetic nanostructures SERS-active substrates (limit of detection (LOD), 10-8 M). These results highlight that the rational design and controllable synthesis of multifunctional magnetic SERS substrates is a promising strategy in many different application fields such as biosensing, photoelectrocatalysis, and medical diagnosis.

Gradual evolution of hydrogen-bonding patterns with the carbamoylcyanonitrosomethanide anion in a series of aliphatic diammonium salts.

Developing the structures of organic materials that rely on the hydrogen bonding of multifunctional substrates is often complicated due to a competition between various possible motifs. In this context, the illustrative case of the carbamoylcyanonitrosomethanide anion, [ONC(CN)-C(O)NH2]-, suggests sufficient control over the crystal lattice with a set of supramolecular synthons, which are specific to all the present nitroso, carbamoyl and cyano groups. The structures of the carbamoylcyanonitrosomethanide salts of ethane-1,2-diammonium, C2H10N22+·2C3H2N3O2-, (1), piperazine-1,4-diium, C4H12N22+·2C3H2N3O2-, (2), butane-1,4-diammonium, C4H14N22+·2C3H2N3O2-, (3), and hexane-1,6-diammonium, C6H18N22+·2C3H2N3O2-, (4), reveal two- and three-dimensional hydrogen-bonded frameworks governed by a set of site-selective interactions. The strongest N-H...O hydrogen bonds [N...O= 2.6842 (17)-2.8718 (17) Å, mean 2.776 (2) Å] are associated with the polarized ammonium N-H donors and nitroso O-atom acceptors, which sustain invariant motifs in the form of nitroso/ammonium dimers. Subtle structural changes within this series of compounds concern the rupture of some weaker interactions, i.e. mutual hydrogen bonds of the carbamoyl groups in (1)-(3) [N...O= 2.910 (2)-2.9909 (18) Å; mean 2.950 (2) Å] and carbamoyl/nitrile hydrogen bonds in (1), (2) and (4) [N...N= 2.936 (2)-3.003 (3) Å, mean 2.977 (2) Å], providing a gradual evolution of the hydrogen-bonding pattern. A hierarchy of the synthons involving three different groups could be applicable to supramolecular synthesis with polyfunctional methanide species, suggesting also a degree of control over layered and interpenetrated hydrogen-bonded networks.

Design principles of theuse of alkynes in radical cascades.

One of the simplest organic functional groups, the alkyne, offers a broad canvas for the design of cascade transformations in which up to three new bonds can be added to each of the two sterically unencumbered, energy-rich carbon atoms. However, kinetic protection provided by strong π-orbital overlap makes the design of new alkyne transformations a stereoelectronic puzzle, especially on multifunctional substrates. This Review describes the electronic properties contributing to the unique utility of alkynes in radical cascades. We describe how to control the selectivity of alkyne activation by various methods, from dynamic covalent chemistry with kinetic self-sorting to disappearing directing groups. Additionally, we demonstrate how the selection of reactive intermediates directly influences the propagation and termination of the cascade. Diverging from a common departure point, a carefully planned reaction route can allow access to a variety of products.

Two-dimensional glass/p-ATP/Ag NPs as multifunctional SERS substrates for label-free quantification of uric acid in sweat

Abnormal uric acid (UA) content in body fluids can fully reflect the status of metabolism and immunity in the body. We have developed a simple, efficient and label-free surface enhanced Raman scattering (SERS) method for UA detection. Briefly, p-aminothiophenol (p-ATP) was used as the internal standard molecule and linking molecule to prepare a glass/p-ATP/Ag NPs SERS substrate. The Raman characteristic peak of p-ATP at 1076 cm−1 can be used as an internal standard molecule to correct the signal fluctuation of UA detection. The results show that the SERS method owns a linear response with a ranging from 5 × 10-6 to 10-3 M of UA characteristic peak of both 693 cm−1 and 493 cm−1 with a determination coefficient (R2) of 0.9878 and 0.9649, respectively. Additionally, the SERS sensor has been further used for the analysis of UA in sweat and good recoveries were obtained for the sensing of sweat. We believe that the developed SERS substrate has potential for applications in healthcare monitoring.

Selective hydrogenation via precise hydrogen bond interactions on catalytic scaffolds

The active site environment in enzymes has been known to affect catalyst performance through weak interactions with a substrate, but precise synthetic control of enzyme inspired heterogeneous catalysts remains challenging. Here, we synthesize hyper-crosslinked porous polymer (HCPs) with solely -OH or -CH3 groups on the polymer scaffold to tune the environment of active sites. Reaction rate measurements, spectroscopic techniques, along with DFT calculations show that HCP-OH catalysts enhance the hydrogenation rate of H-acceptor substrates containing carbonyl groups whereas hydrophobic HCP- CH3 ones promote non-H bond substrate activation. The functional groups go beyond enhancing substrate adsorption to partially activate the C = O bond and tune the catalytic sites. They also expose selectivity control in the hydrogenation of multifunctional substrates through preferential substrate functional group adsorption. The proposed synthetic strategy opens a new class of porous polymers for selective catalysis.

Innovative ceramic-matrix composite substrates with tunable electrical conductivity for high-power applications

ABSTRACT A wide band gap semiconductor power module can operate at higher voltages as compared with its traditional silicon counterpart. However, its insulating system undergoes stronger electric fields at the triple point between the ceramic substrate, the metallic tracks and the encapsulating polymer, which can dramatically reduce its lifespan. Here we report an original concept based on the local modification of the substrate properties to mitigate such electrical stress. Numerical simulations revealed its potential to reduce this constraint by up to 50%. This concept was realized by developing, through a practical approach, a novel substrate made of an AlN-based ceramic (material A) integrating a nanocomposite volume endowed with controlled properties and geometry. This approach implies first the spark plasma sintering of the AlN powder with additives (Y2O3, CaF2) to endow the material A with a very low electrical conductivity (σ) and high thermal conductivity (k). Graphene nanoplatelets (GNP) were incorporated within this material to fabricate a nanocomposite with a controlled σ anisotropy that otherwise reached a striking ratio of 106 at 20°C for 1.25 vol% GNP. Our approach secondly aimed at developing an effective process allowing to integrate this nanocomposite into the material A with a very high degree of reproducibility. It finally consisted in establishing the electrical contacts on the achieved substrate and encapsulating it for breakdown testing. The novel substrate enabled a mitigation of the electrical constraint by diminishing its intensity and shifting it from the triple point to a less constrained area. It already brought an improvement in breakdown voltage (VB) by 15% as compared to the traditional substrate, and revealed the potential for achieving higher VB as well. This work lays the foundation for the development of novel multifunctional ceramic-matrix composite substrates sought for power electronics as well as for other potential applications.

Superelastic and multifunctional fibroin aerogels from multiscale silk micro-nanofibrils exfoliated via deep eutectic solvent

Superelastic silk fibroin (SF)-based aerogels can be used as multifunctional substrates, exhibiting a promising prospect in air filtration, thermal insulation, and biomedical materials. However, fabrication of the superelastic pure SF aerogels without adding synthetic polymers remains challenging. Here, the SF micro-nano fibrils (SMNFs) that preserved mesostructures are extracted from SF fibers as building blocks of aerogels by a controllable deep eutectic solvent liquid exfoliation technique. SMNFs can assemble into multiscale fibril networks during the freeze-inducing process, resulting in all-natural SMNF aerogels (SMNFAs) with hierarchical cellular architectures after lyophilization. Benefiting from these structural features, the SMNFAs demonstrate desirable properties including ultra-low density (as low as 4.71 mg/cm3) and superelasticity (over 85 % stress retention after 100 compression cycles at 60 % strain). Furthermore, the potential applications of superelastic SMNFAs in air purification and thermal insulation are investigated to exhibit their functionality, mechanical elasticity, and structural stability. This work provides a reliable approach for the fabrication of highly elastic SF aerogels and endows application prospects in air purification and thermal insulation opportunities.

Recyclable SERS monitoring of food quality based on the shrubby morphology of titania oxide-triggered electromagnetic “hotspots”

Constructing of plasmonic substrate with the capability of detecting nutritional food quality will soon be emerged as the frontier research directions with broad prospects in surface-enhanced Raman scattering (SERS) technology ascribed to an improvement of living standards. Herein, a novel TiO2 framework with a shrubby morphology was successfully constructed on carbon cloth (CC) matrix to trigger significantly enhanced electromagnetic “hotspots” after dense Ag network with numerous sharp corners and edges was formed by a photo-induced reduction. Particularly, the structure-dependent optical performance was investigated for these as-prepared CC/TiO2/Ag hybrid substrates, screening out an optimal one with an enhancement factor of 6.38 × 107. Regarding a prominent photocatalytic efficiency ascribed to the high electron-hole separation efficiency assisted by the CC matrix and Ag decoration, a recyclable SERS-based monitoring of quercetin (QR) was achieved in teas, demonstrating recovery values distributed from 88.9 % to 106.4 %. The strategy proposed here opened a new way to create high-density “hotspots” for multifunctional SERS substrates, which might play a crucial role in food quality monitoring applications.

Ag Nanoparticles Decorated ZnO Nanorods as Multifunctional SERS Substrates for Ultrasensitive Detection and Catalytic Degradation of Rhodamine B.

Industrial wastewater containing large amounts of organic pollutants is a severe threat to the environment and human health. Thus, the rapid detection and removal of these pollutants from wastewater are essential to protect public health and the ecological environment. In this study, a multifunctional and reusable surface-enhanced Raman scattering (SERS) substrate by growing Ag nanoparticles (NPs) on ZnO nanorods (NRs) was produced for detecting and degrading Rhodamine B (RhB) dye. The ZnO/Ag substrate exhibited excellent sensitivity, and the limit of detection (LOD) for RhB was as low as 10−11 M. Furthermore, the SERS substrate could efficiently degrade RhB, with a degradation efficiency of nearly 100% within 150 min. Moreover, it retained good SERS activity after multiple repeated uses. The interaction between Ag NPs, ZnO, and RhB was further investigated, and the mechanism of SERS and photocatalysis was proposed. The as-prepared ZnO/Ag composite structure could be highly applicable as a multifunctional SERS substrate for the rapid detection and photocatalytic degradation of trace amounts of organic pollutants in water.

Development of Multifunctional Commercial Pure Titanium-Polyethylene Glycol Drug-Eluting Substrates with Enhanced Optical and Antithrombotic Properties.

Development of multifunctional advanced stent implants (metal/polymer composite)-drug-eluting stents with superior material and optical properties is still a challenge. In this research work, multifunctional metal-polymer composite drug-eluting substrates (DES) for stent application were developed by using commercially pure titanium (cpTi) and polyethylene glycol (PEG). Surface modifications on titanium substrates were carried out by sodium hydroxide under various concentrations; 5M (6 and 24 h) and 10M (6 and 24 h). It induces a nanoporous structure which facilitates the larger area for encapsulation of the drug, Aspirin (ASA) via intermolecular forces followed by polymer coating of PEG (MW-20,000) by physical adsorption process, which is structured as layer-by-layer gathering. The developed cpTi-PEG DES were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), optical energy bandgap, static contact angle measurement, antithrombotic and drug release studies. The development of sodium titanate oxide prompted surface nano-features revealed by SEM and XRD. Moreover, FTIR confirms the presence of ASA and PEG functional groups over the cpTi surface. Drug release studies fitted with Ritger-Peppas kinetic model (≤ 60%), which indicates the super case II transport mechanisms (n > 1). Further UV-visible absorbance spectrum was quantified by the Tauc plot, which shows the broadening of the energy bandgap (Eg). In addition, the shrink in blood clots was more around the Tib2/ASA/PEG.Please confirm the inserted city name in affiliations [1,2] are correct and amend if necessary.Yes, city name "Rourkela" is correct. Developed cpTi-PEG DES has improved optical properties and prevent thrombus formation which suggesting it a potential substrate to overcome prime clinical challenges.

Conductive Supramolecular Polymer Nanocomposites with Tunable Properties to Manipulate Cell Growth and Functions.

Synthetic bioactive nanocomposites show great promise in biomedicine for use in tissue growth, wound healing and the potential for bioengineered skin substitutes. Hydrogen-bonded supramolecular polymers (3A-PCL) can be combined with graphite crystals to form graphite/3A-PCL composites with tunable physical properties. When used as a bioactive substrate for cell culture, graphite/3A-PCL composites have an extremely low cytotoxic activity on normal cells and a high structural stability in a medium with red blood cells. A series of in vitro studies demonstrated that the resulting composite substrates can efficiently interact with cell surfaces to promote the adhesion, migration, and proliferation of adherent cells, as well as rapid wound healing ability at the damaged cellular surface. Importantly, placing these substrates under an indirect current electric field at only 0.1 V leads to a marked acceleration in cell growth, a significant increase in total cell numbers, and a remarkable alteration in cell morphology. These results reveal a newly created system with great potential to provide an efficient route for the development of multifunctional bioactive substrates with unique electro-responsiveness to manipulate cell growth and functions.