Katia Rodriguez

Biomimetic calcium phosphate crystal mineralization on electrospun cellulose-based scaffolds.

Novel cellulose based-scaffolds were studied for their ability to nucleate bioactive calcium phosphate crystals for future bone healing applications. Cellulose-based scaffolds were produced by electrospinning cellulose acetate (CA) dissolved in a mixture of acetone/dimethylacetamide (DMAc). The resulting nonwoven CA mats containing fibrils with diameters in the range of 200 nm to 1.5 μm were saponified by NaOH/ethanol for varying times to produce regenerated cellulose scaffolds. Biomimetic crystal growth nucleated from the fiber surface was studied as a function of surface chemistry. Regenerated cellulose scaffolds of varying treatments were soaked in simulated body fluid (SBF) solution. Scaffolds that were treated with CaCl(2), a mixture of carboxymethyl cellulose (CMC) and CaCl(2), and NaOH and CaCl(2), were analyzed using X-ray photoelectron spectroscopy, X-ray powder diffraction, and scanning electron microscopy to understand the growth of bioactive calcium phosphate (Ca-P) crystals as a function of surface treatment. The crystal structure of the nucleated Ca-P crystals had a diffraction pattern similar to that of hydroxyapatite, the mineralized component of bone. The study shows that the scaffold surface chemistry can be manipulated, providing numerous routes to engineer cellulosic substrates for the requirements of scaffolding.

Environmental science and engineering applications of nanocellulose-based nanocomposites

Compared with cellulose, the primary component of the paper we use every day, nanocellulose has a much smaller diameter (typically <10 nm) that renders it many unique properties. Amongst many others, these properties include high mechanical strength, large surface area and low visual light scattering. Nanocellulose can be obtained by disintegration of plant cellulose pulp or by the action of specific types of bacteria. Once produced, nanocellulose can be used to make transparent films, fibers, hydrogels, or aerogels that exhibit extraordinary mechanical, thermal, and optical properties. Each of these substrates is a suitable template or carrier for inorganic nanoparticles (NPs), thus enabling production of nanocomposites that possess properties of the two constituents. In this review, we focus on the preparation of nanocellulose, nanocellulose films, and nanocellulose papers, and introduce nanocellulose-based nanocomposites and their environmental applications.

Superhydrophobic behaviour of plasma modified electrospun cellulose nanofiber-coated microfibers

In this work, a method is presented for production of a textile cellulose fiber with non-wetting properties suitable for applications ranging from wound care and tissue engineering to clothing and other textile applications. Non-wettability is achieved by coating a textile cellulose microfiber with electrospun cellulose nanofibers, creating a large and rough surface area that is further plasma treated with fluorine plasma. High surface roughness and efficient deposition of covalently bound fluorine groups results in the fiber exhibiting non-wetting properties with contact angle measurements indicating superhydrophobicity (>150° water contact angle). It is an environmentally friendly method and the flexibility of the electrospinning process allows for careful design of material properties regarding everything from material choice and surface chemistry to fiber morphology and fiber assembly, pointing to the potential of the method and the developed fibers within a wide range of applications.

Electrospun nanofibrous cellulose scaffolds with controlled microarchitecture

Introducing porosity in electrospun scaffolds is critical to improve cell penetration and nutrient diffusion for tissue engineering. Nanofibrous cellulose scaffolds were prepared by electrospinning cellulose acetate (CA) followed by saponification to regenerate cellulose. Using a computer-assisted design approach, scaffolds underwent laser ablation resulting in pores with diameters between 50 and 300 μm without damaging or modifying the surrounding scaffold area. A new mineralization method was employed in conjunction with microablation using commercial phosphate buffered saline (PBS) to soak carboxymethylcellulose surface-modified electrospun scaffolds. The resulting crystals within the scaffold on the interior of the pore had a calcium to phosphate ratio of 1.56, similar to hydroxyapatite. It was observed that porosity of the cellulose scaffolds enhanced osteoblast cell attachment at the edge of the pores, while mineralization enhanced overall cell density.

Improved thermal stability of polylactic acid (PLA) composite film via PLA-β-cyclodextrin-inclusion complex systems.

The effects of the incorporation of PLA-β-cyclodextrin-inclusion complex (IC) and β-cyclodextrin (β-CD) on biopolyester PLA films were investigated. Thermal stability, surface morphology, barrier, and mechanical properties of the films were measured at varying IC (1, 3, 5, and 7%) and β-CD (1 and 5%) concentrations. The PLA-IC-composite films (IC-PLA-CFs) showed uniform morphological structure, while samples containing β-CD (β-CD-PLA-CFs) showed high agglomeration of β-CD due to poor interfacial interaction between β-CD and PLA moieties. According to the thermal property analysis, the 5% IC-PLA-CFs showed 6.6 times lower dimensional changes (6.5%) at the temperature range of 20-80°C than that of pure PLA film (43.0%). The increase of IC or β-CD content in the PLA-composite films shifted the glass transition and crystallization temperature to higher temperature regions. The crystallinity of both composite films improved by increasing IC or β-CD content. Both composite films had higher oxygen and water vapor permeability as IC or β-CD content increased in comparison to pure PLA film. All the composite films had less flexibility and lower tensile strength than the pure PLA film. In conclusion, this study shows that the IC technique is valuable to improve the thermal expansion stability of PLA-based films.

Biocomposite adhesion without added resin: understanding the chemistry of the direct conversion of wood into adhesives

In this work we revealed how the controlled degradation of wood surfaces with infrared light from a CO2 pulsed laser facilitated adhesion between two biobased substrates without the use of additional resins. Laser modification physically and chemically altered the natural biopolymer organization of lignocellulosic materials enabling adhesion when subsequently hot pressed using typical industrial equipment. Surface analysis of the modified material revealed that laser modification changed the native wood morphology as it appeared to coalesce, while the hemicelluloses were depolymerized and vaporized, and the surface was enriched with cellulose II and lignin. The latter two materials made up over 90% of the solid surface. The lignin itself was partially depolymerized resulting in enrichment of cinnamyl alcohol end groups, which are structures arising from homolytic cleavage of the β-O-4 linkages. An adhesion mechanism related to heat induced coupling in the presence of structural polysaccharides was discussed. Laser modification of wood followed by hot pressing provided a bio-based alternative for petroleum and natural gas derived wood adhesives and provides a path towards utilizing cellulose and lignin directly as structural adhesives.