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Biomedical subjects

Pitt Supaphol

Publications and source records attributed to Pitt Supaphol.

8 recordsLinked to original sources

In vitro biocompatibility of electrospun poly(3-hydroxybutyrate) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) fiber mats.

In the present contribution, the potential for use of the ultrafine electrospun fiber mats of poly(3-hydroxybutyrate) (PHB) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) as scaffolding materials for skin and nerve regeneration was evaluated in vitro using mouse fibroblasts (L929) and Schwann cells (RT4-D6P2T) as reference cell lines. Comparison was made with PHB and PHBV films that were prepared by solution-casting technique. Indirect cytotoxicity assessment of the as-spun PHB and PHBV fiber mats with mouse fibroblasts (L929) and Schwann cells (RT4-D6P2T) indicated that the materials were acceptable to both types of cells. The attachment of L929 on all of the fibrous scaffolds was significantly better than that on both the film scaffolds and tissue-culture polystyrene plate (TCPS), while RT4-D6P2T appeared to attach on the flat surfaces of TCPS and the film scaffolds much better than on the rough surfaces of the fibrous scaffolds. For L929, all of the fibrous scaffolds were superior in supporting the cell proliferation to the film counterparts, but inferior to TCPS at days 3 and 5, while, for RT4-D6P2T, the rough surfaces of the fibrous scaffolds appeared to be very poor in supporting the cell proliferation when comparing with the smooth surfaces of TCPS and the film scaffolds. Scanning electron microscopy was also used to observe the behavior of both types of cells that were cultured on both the fibrous and the film scaffolds and glass substrate for 24 h.

Animals↗

Preparation and characterization of novel bone scaffolds based on electrospun polycaprolactone fibers filled with nanoparticles.

Novel bone-scaffolding materials were successfully fabricated by electrospinning from polycaprolactone (PCL) solutions containing nanoparticles of calcium carbonate (CaCO(3)) or hydroxyapatite (HA). The diameters of the as-spun fibers were found to increase with the addition and increasing amounts of the nanoparticles. The observed increase in the diameters of the as-spun fibers with the addition and increasing amounts of the nanoparticulate fillers was responsible for the observed increase in the tensile strength of the obtained fiber mats. An increase in the concentration of the base PCL solution caused the average diameter of the as-spun PCL/HA composite fibers to increase. Increasing applied electrical potential also resulted in an increase in the diameters of the obtained PCL/HA composite fibers. Lastly, indirect cytotoxicity evaluation of the electrospun mats of PCL, PCL/CaCO(3), and PCL/HA fibers based on human osteoblasts (SaOS2) and mouse fibroblasts (L929) revealed that these as-spun mats posed no threat to the cells, a result that implied their potential for utilization as bone-scaffolding materials.

Absorbable Implants↗

Stability improvement of electrospun chitosan nanofibrous membranes in neutral or weak basic aqueous solutions.

Further utilization of chitosan nanofibrous membranes that are electrospun from chitosan solutions in trifluoroacetic acid (TFA) with or without dichloromethane (DCM) as the modifying cosolvent is limited by the loss of the fibrous structure as soon as the membranes are in contact with neutral or weak basic aqueous solutions due to complete dissolution of the membranes. Dissolution occurs as a result of the high solubility in these aqueous media of -NH(3)(+)CF(3)COO(-) salt residues that are formed when chitosan is dissolved in TFA. Traditional neutralization with a NaOH aqueous solution only maintained partial fibrous structure. Much improvement in the neutralization method was achieved with the saturated Na(2)CO(3) aqueous solution with an excess amount of Na(2)CO(3)(s) in the solution. We showed that electrospun chitosan nanofibrous membranes, after neutralization in the Na(2)CO(3) aqueous solution, could maintain its fibrous structure even after continuous submersion in phosphate buffer saline (pH = 7.4) or distilled water for 12 weeks.

Animals↗

Electrospinning of hexanoyl chitosan/polylactide blends.

The electrospinning of hexanoyl chitosan (H-chitosan), polylactide (PLA) and their blends was performed using chloroform, dichloromethane or tetrahydrofuran as a spinning solvent. The as-spun PLA fibers appeared to be cross-sectionally round, with rough surface morphology, while the as-spun H-chitosan fibers were flat with smooth surface morphology. Electrospinning of the H-chitosan/PLA blend solutions in chloroform with the H-chitosan solution content of less than or equal to 50% (w/w) produced continuous fibers without the presence of beads, while that of the blend solutions in dichloromethane produced beaded fibers or even just beads at high H-chitosan solution contents. The size of the as-spun fibers from blend solutions with a H-chitosan solution content of less than or equal to 50% (w/w) was found to decrease with increasing the H-chitosan solution content. Thermal characteristics and crystalline structure of selected as-spun fibers from pure and blend solutions in chloroform were characterized by thermogravimetric analysis, differential scanning calorimetry and wide-angle X-ray diffraction (WAXD) techniques.

Biocompatible Materials↗

Electrospun mat of tyrosine-derived polycarbonate fibers for potential use as tissue scaffolding material.

Desaminotyrosyl-tyrosine ethyl ester (DTE) and desaminotyrosyl-tyrosine (DT) were used as monomers in the synthesis of two tyrosine-derived polycarbonates: the slow degrading homopolymer poly(DTE carbonate) and the fast degrading co-polymer poly(DTE-co-20%DT carbonate). Ultrafine fibers of these polymers were successfully fabricated using an electrospinning process. The effects of some solution and process parameters (i.e., polymer concentration, electrostatic field strength and solvent system) on morphological appearance and diameters of the obtained fibers were investigated by scanning electron microscopy (SEM). Smooth fibers were obtained at high enough solution concentrations (i.e., 15 and 20% (w/v)). The average fiber diameter was found to increase with increasing polymer concentration and applied electrostatic field strength. The electrospinnability of poly(DTE-co-20%DT carbonate) in dichloromethane was enhanced when methanol was used as the co-solvent. In all of the conditions investigated, the average diameter of the obtained smooth fibers ranged between 1.9 and 5.8 microm. A qualitative assessment of an as-spun mat of poly(DTE carbonate) fibers as a tissue scaffolding material showed that three different cultured cell lines appeared to adhere and propagate well within the scaffold. For poly(DTE carbonate) exceptionally high cell densities could be achieved after 10 days of cell culture.

Animals↗

Novel bone scaffolds of electrospun polycaprolactone fibers filled with nanoparticles.

Novel bone scaffolding materials were successfully fabricated by electrospinning from polycaprolactone (PCL) solutions containing nanoparticles of calcium carbonate (CaCO3) or hydroxyapatite (HA). The potential use of the electrospun fibrous scaffolds for bone regeneration was evaluated in vitro with human osteoblasts (SaOS2) in terms of attachment, proliferation, and alkaline phosphatase (ALP) activity of the cells that were cultured directly on the scaffolds. The results were compared with those on corresponding solution-cast film scaffolds and tissue-culture polystyrene plate (TCPS). It was found that all of the fibrous scaffolds promoted much better adhesion and proliferation of cells than the corresponding film scaffolds and TCPS. Interestingly, the cells that were seeded on all of the fibrous scaffolds appeared to be well-expanded and attach on the fiber surface very well even only about 1 hr in culture, while those seeded on all of the film scaffolds and the glass substrate were still in round shape. Among the various fibrous scaffolds investigated, the one that was filled with 1.0% HA showed the highest ALP activity. Finally, all of the fibrous scaffolds exhibited much greater tensile strength at yield than all of the corresponding film scaffolds.

Alkaline Phosphatase↗

Fabrication of aligned poly (vinyl alcohol) nanofibers by electrospinning.

Electrospinning has become a versatile tool for fabricating nanofibers from materials of diverse origins. Normally, mats of randomly-aligned fibers were obtained. A number of techniques have been proposed to arrive at uniaxially-aligned fibers. This work reports a new technique, i.e., dual vertical wire technique, for fabrication of uniaxially-aligned fibers. This technique utilized two stainless steel wires that were vertically set in a parallel manner between a charged needle and a grounded collector plate. This technique allowed simultaneous collection of aligned fibers (between the parallel vertical wires) and a randomly-aligned fiber mat (on the collector plate). Application of the technique on poly(vinyl alcohol) (PVA) to prepare uniaxially-aligned fibers was found to be successful at short collection times. Unexpected formation of a large fiber tow consisting of individual as-spun nanofibers that were bound into a bundle was observed at long collection times. Morphological appearance and size of the fiber tow was affected by the change in the distance between the two vertical wire electrodes, while the average diameter of the individual fibers was not (i.e., about 340 to 350 nm). Lastly, mechanical properties and thermal behavior of the fiber tow were also investigated.

Electrochemistry↗

Preparation and characterization of microwave-treated carboxymethyl chitin and carboxymethyl chitosan films for potential use in wound care application.

CM-chitin and CM-chitosan films were successfully crosslinked by microwave treatment. Crosslinking of the microwave-treated CM-chitin films involved mainly the carboxylate and the secondary alcohol groups, while crosslinking of microwave-treated CM-chitosan films involved the carboxylate and the amino groups. In addition, the crystallinity of CM-chitin increased with increasing microwave treatment time, whereas an increase in the crystallinity of the microwave-treated CM-chitosan films was not observed. At a similar percentage of weight loss, the crosslinking of either CM-chitin or CM-chitosan films by microwave treatment required much less stringent condition when compared with the crosslinking by autoclave treatment. Based on both direct and indirect cytotoxicity assays, the cytotoxicity of the microwave-treated CM-chitin films was negative, while that of the microwave-treated CM-chitosan films was positive. Human fibroblasts adhered on the surface of microwave-treated CM-chitosan films much better than on the surface of microwave-treated CM-chitin films.

Animals↗