Modification of thermoplastic polyurethane nanofiber membranes by in situ polydopamine coating for tissue engineering

To improve the interaction between cells and scaffolds, the appropriate surface chemical property is very important for tissue engineering scaffolds. In this work, the dopamine (DA) was first introduced into thermoplastic polyurethane (TPU) matrix to obtain TPU/DA nanofibers by electrospinning. Subsequently, the TPU@polydopamine (PDA) composite nanofibers with core/shell structure were fabricated by in situ polymerization of PDA. In comparison with TPU nanofibers, the uniformization of PDA coating layer on the surface of TPU/DA composite nanofibers significantly increased due to the addition of DA, which used as the active sites to guide the PDA particles accumulated along with the fiber direction. The hydrophilicity and water uptake ability of TPU@PDA composite nanofibers were larger than those of TPU nanofibers. The TPU@PDA composite nanofibers possess excellent comprehensive mechanical properties of high strength, stiffness, elasticity, and recoverability because of the hydrogen bonding occurrence between PDA and DA, as well as between PDA and TPU matrix. The attachment and viability of mouse embryonic osteoblasts cells (MC3T3-E1) cultured on TPU@PDA composite nanofibers were obviously enhanced compared with TPU nanofibers. Those results suggested that the modified TPU@PDA composite nanofibers have superior mechanical and biological properties, which promoting them potentially useful for tissue engineering scaffolds.     

Poly(ethylene glycol)-interpenetrated genipin-crosslinked chitosan hydrogels: Structure,pH responsiveness,gelation kinetics,and rheology

In the development of pH-responsive chitosan-based hydrogels, achieving reproducible porosity and swelling behavior is essential for the design of hydrogel networks. Herein, we enhance the level of control in hydrogel microarchitecture by incorporating poly(ethylene glycol) (PEG) into the chitosan–genipin matrix. Hydrogels, varied in composition, were synthesized under mild conditions (37°C, 1 atm, 24 hr), yielding microporous structures with a pore diameter ranging from 11 to 57 μm and an average cross-sectional porosity of approximately 40–64%. Compared to chitosan–genipin hydrogels without PEG, presence of PEG in concentrations up to 1.9 mM generated the same effect as would increase in genipin content, yielding structures with a smaller pore diameter, a lower swelling degree in pH 2 buffer and a higher elastic modulus. Considering cost effectiveness and scale-up, reducing genipin content by the addition of PEG is favorable. Importantly, hydrogel samples containing higher concentrations of PEG (2.9 mM and above) showed a sudden increase in the swelling degree accompanied with a decrease in the elastic modulus. Findings showcase the potential variation in the composition of these hydrogels has in yielding scaffolds with significantly different physico-chemical behaviors.     

Swelling behavior of expandable poly(methyl methacrylate-acrylic acid)/polymethyl methacrylate bio-composites with different crosslinking densities

The volume shrinkage of poly(methyl methacrylate-acrylic acid) (PMMA) bone cement was mainly tackled by the different types and contents of the hydrophilic additives. While the crosslinking density was assumed to regulate the hydrophilic group amounts and 3D network structures in the additives, which influenced the absorption and swelling capacity of the PMMA-based bone cement. In this study, the expandable PMMA/polymethyl methacrylate bio-composites (EBC) with different N, N-methylenebisacrylamide (MBA) contents were synthesized to investigate the relationship between the crosslinking density and swelling performance, and also promoted the absorption and swelling properties before the solidification of EBC. The results demonstrated that the equilibrium absorption ratio and the equilibrium swelling ratio both exhibited a normal distribution with the various MBA content. In addition, the controlled absorption ratio (7.3–60.2%) and swelling ratio (8.5–61.8%) of EBC could be obtained by altering crosslinking density in the system. Furthermore, EBC could obtain a similar equilibrium absorption ratio and equilibrium swelling ratio with different mechanical properties, which provided more options for meeting the requirements of EBC in different clinical settings.     

Mechanophysical Cues in Extracellular Matrix Regulation of Cell Behavior

The extracellular matrix (ECM) is a macromolecular network that can provide biochemical and structural support for cell adhesion and formation. It regulates cell behavior by influencing biochemical and physical cues. It is a dynamic structure whose components are modified, degraded, or deposited during connective tissue development, giving tissues strength and structural integrity. The physical properties of the natural ECM environment control the design of naturally or synthetically derived biomaterials to guide cell function in tissue engineering. Tissue engineering is an important field that explores physical cues of the ECM to produce new viable tissue for medical applications, such as in organ transplant and organ recovery. Understanding how the ECM exerts physical effects on cell behavior, when cells are seeded in synthetic ECM scaffolds, is of utmost importance. Herein we review recent findings in this area that report on cell behaviors in a variety of ECMs with different physical properties, i.e., topology, geometry, dimensionality, stiffness, and tension.     

Alcohol-triggered silk fibroin hydrogels having random coil and β-turn structures enhanced for cytocompatible cell response

Alcohol additive is one of the stimulants that induces the fast gelation of silk fibroin solution. Based on our previous report, different alcohol types influence the gelation kinetic and the properties of resulting silk fibroin hydrogels. Here, the effects of alcohol concentrations on the silk fibroin gelation and cell response were reported. All fibroin hydrogels prepared with various alcohol additives showed cell biocompatibility, especially the fibroin hydrogel prepared with 10 wt % n-butanol. Results on the mechanical properties of hydrogels, n-butanol additive enhanced a higher compressive modulus up to ~ 22 times in comparison to non-alcoholic fibroin hydrogel. Fourier transform infrared analysis and peak deconvolution showed a possible formation of more β-turn linkage and random coil structure of fibroin segments in alcoholic fibroin hydrogel. So, the micro-segmental structure of fibroin hydrogel caused the higher compressive modulus, prolonged deformation of the hydrogels, and efficient cell growth on the fibroin hydrogel. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48731.     

PDMS microfluidics: A mini review

Polydimethylsiloxane (PDMS) is hailed as one of the foundational materials for microfluidics. Though a silicone-based elastomer of many desirable properties, the emergence of microfluidic fabrication techniques, especially soft lithography, has elevated its status to an exceptional one. In this mini review, we look at the salient aspects that make PDMS so special in achieving such a coveted status in the microfluidics community. A methodical approach is followed to touch upon the application of PDMS in various aspects of microfluidics with the advantages, limitations, and some future directions. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48958.     

Microencapsulation of sulfur by calcium alginate

The sulfur blooms on surface of rubber compounds cause loss of the needed tack for formation of multiply articles like tires. Although insoluble sulfur can be used to mitigate this problem, it is expensive to manufacture with a complex and hazardous process. This work examines an alternative approach that involves microencapsulation of soluble sulfur in alginate-based matrix. The formulations and procedures are developed and evaluated. Alginate crosslinking time, controlled temperature change (e.g., from 10 to 36°C), and the drying method were found to be critical to achieving high encapsulation efficiencies. The higher temperature (36°C) helped with the mass transfer limited removal of CS₂ used for dissolving sulfur, and treatment of crosslinked beads with oil prior to air-drying improved sulfur encapsulation. Formulated beads had higher than 65% sulfur content (>80%, oil-free basis) with almost 90% of the beads being <150 μm. The process parameters can be adjusted to make even smaller beads.     

Regenerated cellulose aerogel: Morphology control and the application as the template for functional cellulose nanoparticles

This article focuses on controlling the morphology of regenerated cellulose aerogel (RCA) and its application as a template for the preparation of functional cellulose nanoparticles (FCNPs). RCA is prepared by lyophilizing cellulose hydrogel which is fabricated through a sol–gel method in sodium hydroxide (NaOH)/urea aqueous solution. The morphology of RCA is adjusted by varying the gelation temperature and time. With the gelation temperature and time increasing, lamellar RCA transforms into strings of cellulose nanoparticles. Subsequently, RCA with the morphology of "strings of nanoparticles" is modified through the bulk condensation of l -lactic acid and RCA. Eventually, the prepared functionalized RCA (FRCA) is dispersed in an organic solvent to obtain purified FCNPs. The results demonstrate that single FCNP can be obtained by dispersing FRCA in dimethyl sulfoxide. Moreover, the prepared FCNPs have uniform size, good thermal-stability, and increasing hydrophobicity, which are ideal candidates for polymer composites in terms of fillers.