Polymer Solutions Research Articles

Statistical modeling and optimization of process parameters for additive manufacturing of styrene–ethylene–butylene–styrene block copolymer parts using solvent cast 3D printing technique

AbstractAdditive manufacturing of thermoplastic elastomers is challenging using fused deposition modeling due to their high melt viscosity, low column strength, and poor fusion among layers. Solvent‐cast 3D printing (SC‐3DP) is an efficient alternative to successfully 3D print such materials. However, selection of suitable 3D printing parameters is crucial to realize parts with optimum physicomechanical properties. In this work, statistical modeling and SC‐3DP parameter optimization for styrene–ethylene–butylene–styrene (SEBS) block copolymer were performed. The effect of 3D printing process parameters on shrinkage, relative density, and tensile strength was analyzed using response surface methodology. Experiments were planned as per central composite design and analysis of variance was performed to evaluate the significant parameters. SEBS content in the polymer solution significantly affected the shrinkage of SC‐3DP samples. Moreover, relative density and tensile strength were significantly affected by print speed and layer height. A significant interaction between print speed and layer height was also noticed for tensile strength and relative density of printed samples. Multi‐objective optimization using genetic algorithm was also performed to minimize shrinkage and maximize relative density and tensile strength. Finally, a case study was conducted comparing the physicomechanical properties of SC‐3DP samples printed at optimized process parameters and compression molded samples.Highlights Statistical models were developed using response surface methodology. Genetic algorithm based multi‐objective optimization was performed. Optimum solvent‐cast 3D printing (SC‐3DP) process parameters were determined.

Competitive effects of anion mobility and viscous forces on the interactions of hyaluronic acid and alginic acid with hofmeister salts

The specific ion effect takes into account the hydration, mobility, and kosmotropic/chaotropic effects. However, another important aspect to consider is the solution viscosity, which influences ion mobility. A limited number of publications have considered the impact of specific ion effects on polyelectrolytes. However, none of the studies have considered the viscous effect of polyelectrolytes. This study aims to investigate the impact of kosmotropic and chaotropic anions on negatively charged alginic acid and hyaluronic acid using dynamic light scattering, rheology, and molecular dynamic simulations. Different concentration regimes and the change in the chain conformations in these regimes, along with the viscosity scaling and impact of the salts on the polyelectrolytes, have been discussed. An interesting finding regarding the solution viscosity was reported. The solution viscosity leads to the reversal of the diffusivity and viscosity trend of the polymer with kosmotropes and chaotropes. A threshold is also identified above which viscous forces dominate. Specific ion effects dominate below the threshold. It was concluded that the specific ion effect shows a competitive nature with the viscous forces in the case of a high-viscosity polyelectrolyte solution, which becomes an important aspect to consider for unveiling such interactions. Prior knowledge of the conformations of polymers can be used for designing drug delivery/nutrient delivery systems and for understanding phase separation behavior. Considering the viscosity of polymer solution becomes an important factor which, in turn, impacts the anion's mobility and ultimately influences the polymer conformations.

Diffusion Coefficients of Coated Plasmonic Nanoparticles in Viscous Environment.

The Stokes-Einstein relationship (SER) is not valid anymore in polymeric solutions for nanoparticles. It is thus important to characterize theirdiffusion properties to get a finer understanding of their behavior and to better tune their attributes for biomedical applications. The diffusion of gold and silver nanoparticles with citrate, hyaluronic acid, methyl-polyethylene glycol, and antibody-polyethylene glycol coatings is studied in hyaluronic-based viscous solutions. The diffusion coefficient D is estimated from the Brownian motion thanks to a cost-effective side-illumination device. It is determined that the nanoparticles (hydrodynamic radius rh: 30-135nm) diffuse up to 4-5 times faster than expected using the SER with a macroscopic viscosity from 1 to 30 mPa·s. It is shown that the adapted Huggins equation is a good model to describe the diffusion behavior of nanoparticles using an effective viscosity ηeff given by where where E is the polymer correlation length, Rh the polymer hydrodynamic radius and ηs the solvent viscosity. The values of k and a are given and allow to obtain D with an error of 10-20%. The impact of chemical interactions on the model parameter values are also highlighted, especially due to electrostatic interactions between the polymer and the nanoparticles.

Self‐Assembly of UiO‐66 on Conjugated Polyelectrolytes: Toward Enhanced Photophysical Properties

AbstractIn this study, the synthesis and characterization of the fluorescent metal–organic framework (MOF)‐polymer composites is reported based on zirconium‐based MOFs (UiO‐66 and UiO‐66(OH)₂) and a conjugated polyelectrolyte, poly(phenylene ethynylene) carboxylate (PPE‐CO₂‐108). The defect‐rich nature of these Zr‐MOFs facilitates strong interactions between the polyelectrolyte's carboxylic acid moieties and the open metal sites on the Zr clusters within the MOF nanoparticles. The composites are prepared by a simple impregnation approach, where MOF nanocrystals suspended in HEPES buffer are added to the polymeric solution under sonication for 10 min. The obtained MOF composites (i.e., UiO‐66‐CPE and UiO‐66 (OH)2‐CPE) are characterized using powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer‐Emmett‐Teller (BET) surface area, zeta potential measurements, and UV–vis spectroscopy. The characterization confirmed the homogeneous distribution of the MOF nanocrystals on the polymer as seen in the SEM images, and the interaction with PPE‐CO₂‐108 is confirmed by the decrease in the surface areas from 1050 to 590 m2 g−1 for UiO‐66‐CPE and from 500 to 137 m2 g−1, for UiO‐66(OH)2‐CPE. Fluorescence microscopy revealed strong fluorescence in the microparticles, confirming robust polymer‐MOF interaction. The composites also exhibit improved photostability of the conjugated polyelectrolyte, suggesting their potential for applications in biomedical imaging and other areas requiring stable and bright fluorescent systems.

Development and characterization of orodispersible films containing amlodipine besylate and rosuvastatin calcium based on electrospun fibers

Amlodipine besylate (AML) and rosuvastatin calcium (ROS) are commonly used in the treatment of cardiovascular diseases such as hypertension, dyslipidemia, and coroner artery disease. Orodispersible films (ODFs) have received considerable attention in pharmaceutical development studies as they significantly improve patient compliance. The aim of this study was to develop an ODF formulation containing AML and ROS simultaneously as an electrospun fiber fixed dose preparation. Polymer solutions were evaluated for surface tension, viscosity, and conductivity properties. Preformulation studies were conducted to optimize the electrospinning process. Two different formulations, designated ODF-1 and ODF-2 were the focus of this study. Fiber characterization studies, such as scanning electron microscopy (SEM), Fourier transform-infrared spectroscopy (FT-IR), mechanical properties were performed to assess these two formulations. Furthermore, ODF characterizations, such as disintegration and wetting time, homogeneity of contents, and in vitro dissolution studies were carried out. All formulations exhibited suitable mechanical properties, facilitating easy storage and handling. ODF characterizations revealed rapid disintegration and wetting times for all formulations with over 90 % dissolution in 5 min for both AML and ROS. The overall evaluation of all experiments suggests that ODF-1 may more desirable mechanical properties and a more stable dissolution profile compared to ODF-2. Furthermore, individual ODFs loaded with AML or ROS (AML-ODF-1 and ROS-ODF-1) were prepared by ODF-1 preparation method and then characterized to compare the results with fixed dose ODF results. In conclusion, a promising formulation strategy has been developed to obtain an electrospun fiber ODF formulation containing AML and ROS that is reproducible and suitable for industrial production.

The importance of initial extension rate on elasto-capillary thinning of dilute polymer solutions

This work focuses on inferring the molecular state of the polymer chain required to induce stress relaxation and the accurate measure of the polymer’s longest relaxation time in uniaxial stretching of dilute polymer solutions. This work is facilitated by the discovery that constant velocity applied at early times leads to initial constant extension rate before reaching the Rayleigh–Plateau instability. Such constant rate experiments are used to correlate initial stretching kinematics with the thinning dynamics in the final thinning regime. We show that there is a minimum initial strain-rate required to induce rate independent elastic effects, and measure the longest relaxation time of the material. Below the minimum extension rate, insufficient stretching of the chain is observed before capillary instability, such that the polymer stress is comparable to the capillary stress at long times and stress relaxation is not achieved. Above the minimum strain-rate, the chain reaches a critical stretch before instability, such that during the unstable filament thinning the polymer stress is significantly larger than the capillary stress and rate-independent stress relaxation is observed. Using a single relaxation mode FENE model, we show that the minimum strain rate leads to a required initial stretch of the chain before reaching the Rayleigh–Plateau limit. These results indicate that the chain conformation before entering the Rayleigh Instability Regime, and the stretching induced during the instability, determines the elastic behavior of the filament. Lastly, this work introduces a characteristic dimensionless group, called the stretchability factor, that can be used to quantitatively compare different materials based on the overall material deformation/kinematic behavior, not just the relaxation time. Overall, these results demonstrate a useful methodology to study the stretching of dilute solutions using a constant velocity stretching scheme.

Electrospun poly(ε-caprolactone)/poly(glycerol sebacate) aligned fibers fabricated with benign solvents for tendon tissue engineering.

The electrospinning technique is a commonly employed approach to fabricate fibers intended for various tissue engineering applications. The aim of this study is to develop a novel strategy for tendon repair through the use of aligned poly(ε-caprolactone) (PCL) and poly(glycerol sebacate) (PGS) fibers fabricated in benign solvents, and further explore the potential application of PGS in tendon tissue engineering (TTE). The fibers were characterized for their morphological and physicochemical properties; amniotic epithelial stem cells (AECs) were used to assess the fibers teno-inductive and immunomodulatory potential due to their ability to teno-differentiate undergoing first a stepwise epithelial to mesenchymal transition, and due to their documented therapeutic role in tendon regeneration. The addition of PGS to PCL improved the spinnability of the polymer solution, as well as the uniformity and directionality of the so-obtained fibers. The mechanical properties were in the range of most TTE applications, specifically in the case of PCL/PGS 4:1 and 2:1 ratios. Compared to PCL alone, the same ratios also allowed a better AECs infiltration and growth over 7 days of culture, and triggered the activation of tendon-related genes (SCX, COL1, TNMD) and the expression of tenomodulin (TNMD) at the protein level. Concerning the immunomodulatory properties, both PCL and PCL/PGS fibers negatively affected the immunomodulatory profile of AECs, up-regulating both anti-inflammatory (IL-10) and pro-inflammatory (IL-12) cytokines over 7 days of culture. Overall, PCL/PGS 2:1 fibers fabricated with benign solvents proved to be the most suitable composition for TTE application based on their topographical cues, mechanical properties, biocompatibility, and teno-inductive properties.

Numerical investigation of the effects of variable fluid properties on cilia-driven flow of tangent hyperbolic fluid in a channel with heat and mass transfer: A new approach to microfluidic pumps

Heat, mass transfer, and non-Newtonian fluid flow processes have gained significant interest in various industrial applications due to their substantial significance in the fields of technology, engineering, and science. The aforementioned processes hold significance in the context of polymer solutions, porous industrial materials, ceramic processing, oil recovery, and fluid beds. This study aims to investigate the impact of temperature-dependent viscosity and thermal conductivity on the cilia-driven flow of tangent hyperbolic fluid with mass and heat transfer. The objectives include analyzing how these variable properties affect the velocity, temperature, and concentration profiles within the fluid flow, thereby providing insights into potential applications in bioenergy systems and enhancing the understanding of non-Newtonian fluid dynamics. Viscous dissipation has been taken into consideration. Firstly, governing nonlinear coupled equations are solved in a fixed frame, and then the results are tracked in the wave frame. MATHEMATICA's NDSolve command is utilized to graphically discuss the findings for several different flow parameters. Analytically stated, solving a problem with such a coupled and nonlinear system is tough. The effect of new parameters is discussed on velocity and temperature profile and graphically shown. It has been observed that the thermal conductivity is improved at moderately low temperatures, whereas the opposite pattern is seen at comparatively high temperatures. On the other hand, the temperature distribution demonstrates a behaviour consistent with lowering as the number of heat Bolus increases. The findings that were provided offer beneficial insight into bioenergy systems and serve as a helpful benchmark for both experimental and extra-progressive computational Multiphysics models.

Scaling Laws in Polysaccharide Rheology: Comparative Analysis of Water and Ionic Liquid Systems.

This study investigates the rheological behavior of two plant-based polysaccharides, with different degrees of hydrophilicity, agar (highly hydrophilic) and guar gum (hydrophilic), in water and 1-ethyl-3-methylimidazolium acetate (EMImAc). The rheological response of these polymers is highly dependent on the solvent's ability to disrupt intermolecular associations. In water, agar forms hydrogels, while guar gum behaves as a viscoelastic liquid with slow modes. The plateau modulus (GN0) scales with polymer concentration (c) as GN0 ∼ c3, consistent with other natural polymers. In EMImAc, both polysaccharides form viscoelastic liquids, exhibiting GN0 ∼ c2.3, as expected for semiflexible polymer solutions. However, the terminal relaxation time, τD, and the specific viscosity, ηsp, scale as τD ∼ c5.3 and ηsp ∼ c7.6, indicative of intermolecular chain-chain associations. Despite the solvent or polysaccharide, the fractional viscosity overshoot and the shear strain at the maximum stress show a terminal Weissenberg number dependence similar to other synthetic polymers.

Ion-mediated condensation controls the mechanics of mitotic chromosomes

During mitosis in eukaryotic cells, mechanical forces generated by the mitotic spindle pull the sister chromatids into the nascent daughter cells. How do mitotic chromosomes achieve the necessary mechanical stiffness and stability to maintain their integrity under these forces? Here we use optical tweezers to show that ions involved in physiological chromosome condensation are crucial for chromosomal stability, stiffness and viscous dissipation. We combine these experiments with high-salt histone depletion and theory to show that chromosomal elasticity originates from the chromatin fibre behaving as a flexible polymer, whereas energy dissipation can be explained by modelling chromatin loops as an entangled polymer solution. Taken together, we show how collective properties of mitotic chromosomes, a biomaterial of incredible complexity, emerge from molecular properties, and how they are controlled by the physico-chemical environment.

Influence of Polymer Concentration on the Viscous and (Linear and Non-Linear) Viscoelastic Properties of Hydrolyzed Polyacrylamide Systems in Bulk Shear Field and Porous Media.

Enhanced oil recovery (EOR) methods are generally employed in depleted reservoirs to increase the recovery factor beyond that of water flooding. Polymer flooding is one of the major EOR methods. EOR polymer solutions (especially the synthetic ones characterized by flexible chains) that flow through porous media are not only subjected to shearing forces but also extensional deformation, and therefore, they exhibit not only Newtonian and shear thinning behavior but also shear thickening behavior at a certain porous media shear rate/velocity. Shear rheometry has been widely used to characterize the rheological properties of EOR polymer systems. This paper aims to investigate the effect of the polymers' concentrations, ranging from 25 ppm to 2500 ppm, on the viscous, linear, and non-linear viscoelastic properties of hydrolyzed polyacrylamide (HPAM) in shear field and porous media. The results observed indicate that viscous properties such as Newtonian viscosity increase monotonically with the increase in concentration in both fields. However, linear viscoelastic properties, such as shear characteristic time, were absent for concentrations not critical in both shear rheometry and porous media. Beyond the critical association concentration (CAC), the modified shear thinning index decreases in terms of concentration in both fields, signifying their intensified thinning. At those concentrations higher than CAC, the viscoelastic onset rate remains constant in both fields. In both fields, the shear thickening index, a strict non-linear viscoelastic property, initially increases with concentration and then decreases with concentration, signifying that the polymer chains do not stretch significantly at higher concentrations. Also, another general observation is that the rheological properties of the polymer solutions in both porous media and shear rheometry only follow a similar trend if the concentration is higher than the CAC. At concentrations less than the CAC, the shear and porous media onset rates follow different trends, possibly due to the higher inertial effect in the rheometer.

Preparation of nanoporous poly (L-lactic acid) microspheres with controllable morphology via thermally-induced phase separation

This article describes a facile method to prepare nanoporous poly (l-lactic acid) microspheres via a thermally-induced phase separation method with controllable diameters. It was found that the morphology and diameter of PLLA microspheres were easily controlled by adjusting solvent ratio, quenching temperature, and PLLA concentrations. The results revealed that by using a ternary solvent system consisting of 1,3-dioxolane as a good solvent, 2-butanone as mid-solvent, and water as a poor solvent, the diameter of PLLA microspheres can be easily controlled by changing the ratio of 1,3-dioxolane and water. The diameter of PLLA microspheres prepared ranged from 28.8 ± 5.9 μm to 63.8 ± 12.5 μm. Moreover, the evolution of PLLA spherulitic structures grown from polymer solution was confirmed as well through varying solvent ratios and PLLA concentrations. The presence of water as a non-solvent governed the phase separation mechanism of the phase separation process. At the same time, the diameter of the spherulites is affected by the ratio of 1,3-dioxolane controlling the polymer crystallization process in the polymer-rich region. Interestingly, the surface of these spherulites contains nanopores due to the stacking of lamellar crystals of PLLA during polymer crystallization which contributed to its superhydrophobicity and superoleophilicity. Hence, the prepared PLLA spherulites were utilized as PLLA microspheres with nanoporous surfaces for the adsorption and removal of oil in oil/water and oil-in-water emulsion. This facile method provides a novel pathway to prepare nanoporous PLLA microspheres with controllable diameters for eco-friendly oil/water and oil-in-water separation applications.

Revealing nanoscale structure and interfaces of protein and polymer condensates via cryo-electron microscopy.

Liquid-liquid phase separation (LLPS) is a ubiquitous demixing phenomenon observed in various molecular solutions, including in polymer and protein solutions. Demixing of solutions results in condensed, phase separated droplets which exhibit a range of liquid-like properties driven by transient intermolecular interactions. Understanding the organization within these condensates is crucial for deciphering their material properties and functions. This study explores the distinct nanoscale networks and interfaces in the condensate samples using a modified cryo-electron microscopy (cryo-EM) method. The method involves initiating condensate formation on electron microscopy grids to limit droplet growth as large droplet sizes are not ideal for cryo-EM imaging. The versatility of this method is demonstrated by imaging three different classes of condensates. We further investigate the condensate structures using cryo-electron tomography which provides 3D reconstructions, uncovering porous internal structures, unique core-shell morphologies, and inhomogeneities within the nanoscale organization of protein condensates. Comparison with dry-state transmission electron microscopy emphasizes the importance of preserving the hydrated structure of condensates for accurate structural analysis. We correlate the internal structure of protein condensates with their amino acid sequences and material properties by performing viscosity measurements that support that more viscous condensates exhibit denser internal assemblies. Our findings contribute to a comprehensive understanding of nanoscale condensate structure and its material properties. Our approach here provides a versatile tool for exploring various phase-separated systems and their nanoscale structures for future studies.

Synthesis and performance study of biomass-based suppressant and its application in radioactive aerosol sedimentation

The decommissioning of nuclear facilities and nuclear accidents may release a various amount of radioactive aerosols, which could pose a serious threat to the natural environment and human health. Therefore, there is a need to develop an eco-friendly aerosol suppressant to control the radioactive aerosol. In this paper, carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), rhamnolipid and sophorajaponica glycolipid were selected as the raw material, and the aerosol suppressant was prepared by solution polymerization. The sample was characterized by FTIR, TGA, viscosity, surface tension and contact angle analysis. The results indicated that the grafted reaction was successful. Rhamnolipid and sophorajaponica glycolipid effectively reduced the surface tension of the copolymer solution to 27.7 mN/m, and the contact angle between the polymer solution and experimental dust was decreased to 27.36°. The aerosol sedimentation experiment showed that the suppressant had a significant effect on aerosol. The sedimentation efficiency of concrete aerosols was 87.7%, and the sedimentation efficiency of radioactive aerosols reached 90.8%. It provided an eco-friendly and effective method to quickly and easily control and remove high-concentration radioactive aerosol.

Extensional rheology of elastoviscous aqueous PEO/PEG or DMS Boger fluids and weakly elastic alternatives for investigating viscoelastic flows and instabilities

Boger fluids that exhibit a rate-independent shear viscosity (typically ∼ 1 Pa∙s = 1000x water viscosity) and elasticity measurable using torsional rheometers (modulus, relaxation time, or first normal stress difference) are considered as the realization of viscoelastic fluids described by the Oldroyd-B model. However, Boger fluids, conventionally formulated as dilute solutions of high molecular weight (Mw) polymers in relatively high viscosity solvents (or solutions of oligomers or lower Mw polymer), are unsuitable for emulating polymeric fluids used in coating formulations that are lower in viscosity, appear inelastic in torsional shear rheometry, and yet appear prone to viscoelastic instabilities. Therefore, Dontula, Macosko, and Scriven (DMS) (AIChE J, 1998) chose to create an alternative model of elastic fluids by dissolving ultrahigh molecular weight (UHMw) poly(ethylene oxide) (PEO) in an aqueous solution of its lower Mw analog, often referred to as poly(ethylene glycol) or PEG. Even though numerous studies of printing and coating flow instabilities use this aqueous PEO/PEG or DMS Boger fluids as model viscoelastic fluids, only a few explicitly measured elastic properties, especially using relaxation time, and hardly any characterized extensional rheology. In this contribution, we recreate the DMS Boger fluids to examine their elasticity and extensional rheology response using dripping-onto-substrate (DoS) rheometry that relies on an analysis of capillarity-driven pinching dynamics. Though the aqueous PEG solution is often treated as a viscous and Newtonian solvent, we discover that in DoS rheometry, both the PEG solution and the DMS Boger fluid display power law response followed by elastocapillary, in contradiction with the assumptions and the response expected of the Oldroyd-B model. Furthermore, the solution of entangled PEG chains influences specific viscosity, pinching dynamics, and measured extensional rheology response in striking contrast with Newtonian solvents of the same viscosity. Lastly, we describe the possibility of using dilute, aqueous solutions of UHMw PEO as model viscoelastic fluids for coating flows, for both elasticity and extensional viscosity can be determined using DoS rheometry. Due to their water-like viscosity, the aqueous PEO solutions appeal as model fluids that have elasticity, emulate Newtonian fluids in the early stages of pinching, and have a relaxation time tunable by changing polymer Mw or concentration.

Study of the impact of polymeric solution preparation parameters on the production of nanofibers based on PAN and PVA

Study of the impact of polymeric solution preparation parameters on the production of nanofibers based on PAN and PVA

Application of drag-reducing polymers in forest firefighting: Effects on wood properties and mechanism study

Based on the successful utilization of polymer additives in drag reduction for long-distance transportation and the intricacies of their application in firefighting contexts, this study investigated the impact of additives on wood properties in forest fire suppression through a combination of experiments and molecular dynamics simulations, focusing on wettability, fluidity, and combustibility. Optimal concentrations of polymer solutions were determined through contact angle measurements and surface flow experiments. The effects of polymers on wood water retention, thermal stability, and microstructure were analyzed using thermogravimetric analysis, infrared spectroscopy, and wood impregnation experiments. Wetting and flow models of polymers on cellulose surfaces were simulated to elucidate the wetting mechanism and dynamic behavior of polymers during flow. The results revealed that polyacrylamide (PAM) and polyethylene oxide (PEO) promoted wood surface wetting, improved flowability, enhanced water retention, and delayed decomposition at optimal concentrations. PAM exhibited superior effects in flow stability, thermal stability, and liquid absorption enhancement, attributed to strong hydrogen bonding between PAM and surfaces, primarily through amide groups. During flow, PAM molecules gradually aggregated and moved as aggregates along the X-axis. In contrast, the PEO system relied on electrostatic forces between water and surfaces, with dynamic processes involving repeated stretching and shrinking of PEO molecular chains to facilitate water flow and enhance wetting. This research contributes to delineating the application conditions and benefits of polymer on wood surfaces, enhancing the efficacy and potential of drag-reducing agents in firefighting applications.

Electrospinning of cellulose nanocrystals; procedure and optimization

Cellulose nanocrystals (CNCs) and cellulose microfibrils (CMFs) are promising materials with the potential to significantly enhance the mechanical properties of electrospun nanofibers. However, the crucial aspect of optimizing their integration into these nanofibers remains a challenge. In this work, we present a method to prepare and electrospin a cellulosic solution, aiming to overcome the existing challenges and realize the optimized incorporation of CNCs into nanofibers. The solution parameters of electrospinning were explored using a combined experimental and simulation (molecular dynamics) approach. Experimental results emphasize the impact of polymer solution concentration on fiber morphology, reinforcing the need for further optimization. Simulations highlight the intricate factors, including the molecular weight of cellulose acetate (CA) polymer chains, electrostatic fields, and humidity, that impact the alignment of CNCs and CMFs. Furthermore, efforts were made to study CNCs/CMFs alignment rate and quality optimization. It is predicted that pure CNCs benefit more from electrostatic alignment, while lower molecular weight CA enables better CNC/CMF alignment.

Preparation and Characterization of Zein-Metformin/Gelatin Nanofibers by Coaxial Electrospinning.

Metformin is a drug commonly used for the treatment of type 2 diabetes. However, it has been associated with damaging side effects when used over a long period of time. A potential solution to this problem is the implementation of a prolonged-release system for metformin, which would enhance the efficiency of the doses administered to patients. To achieve this, it is necessary to use materials compatible with humans. Electrospinning is an efficient technique that can be employed for this purpose, utilizing solvents that are safe for human use. Therefore, the objective of this study was to prepare and characterize a system for the prolonged release of metformin from zein and gelatin through coaxial electrospinning as well as to investigate its in vitro release. Metformin-loaded zein/gelatin coaxial nanofibers were prepared using the coaxial electrospinning technique and then characterized by morphological, structural, and thermal analysis. Morphologically, metformin-loaded zein/gelatin coaxial nanofibers were obtained with an average diameter of 322.6 ± 44.5 nm and a smooth surface. Fourier transform infrared spectroscopy (FTIR) analysis showed band shifts at a higher wavenumber due to drug-protein interactions by hydrogen bonding between N-H and C=O groups. Thermal gravimetric analysis (TGA) results suggested a possible interaction between materials due to an increase in the degradation temperatures of zein and gelatin when metformin was included. The transition of the crystallinity of metformin to the amorphous form was also confirmed by differential scanning calorimetry (DSC). Coaxial nanofibers exhibited an encapsulation efficiency of 66% and a profile release that showed an initial release of metformin (40%) in the first hour, followed by a gradual release until it reached equilibrium at 60 h and a cumulative release of 97% of metformin. It was concluded that using the coaxial electrospinning technique, it is possible to obtain nanofibers from polymeric solutions of zein and gelatin to encapsulate metformin, with a potential application as a prolonged-release system.

Porous Spindle-Knot Fiber by Fiber-Microfluidic Phase Separation for Water Collection and Nanopatterning.

Porous spindle-knot structures have been found in many creatures, such as spider silk and the root of the soybean plant, which show interesting functions such as droplet collection or biotransformation. However, continuous fabrication of precisely controlled porous spindle-knots presents a big challenge, particularly in striking a balance among good structural controllability, low-cost, and functions. Here, we propose a concept of a fiber-microfluidics phase separation (FMF-PS) strategy to address the above challenge. This FMF-PS combines the advantages of a microchannel regulated Rayleigh instability of polymer solution coated onto a fiber with the nonsolvent-induced phase separation of the polymer solution, which enables continuous and cost-effective production of porous spindle-knot fiber (PSKF) with well-controlled size and porous structures. The critical factors controlling the geometry and the porous structures of the spindle-knot by FMF-PS have been systematically investigated. For applications, the PSKF exhibited faster water droplet nucleation, growth, and maximum water collection capability, compared to the control samples, as revealed by in situ water collection growth curves. Furthermore, high-level fabrics of the PSKFs, including a two-dimensional network and three-dimensional architecture, have been demonstrated for both large-scale water collection and art performance. Finally, the PSKF is demonstrated as a programmable building block for surface nanopatterning.