Thin films of the polysaccharide chitosan and several chitosan derivatives, including conjugates of l-cysteine, thioglycolic acid, and 2-iminothiolane, were produced from dilute acidic solutions. Attempts to produce a fourth conjugate using lipoic acid resulted in the synthesis of partially N-acetylated chitosan ethanoate. These biopolymer films were exposed to solutions containing 50 ppm concentrations of various metal ion and counterion analytes. Analyte-induced changes in film thicknesses and refractive indices were measured using a spectroscopic ellipsometer, and shifts in film color were quantified using a reflectance spectrometer. The modified chitosans were generally more sensitive to change in response to pure water but also showed varied response to several ions of interest, including Cr(III) and Cr(VI), Hg(II), Ni(II), and others. The potential for tuning film response was demonstrated by varying the concentration of sulfur groups in the thioglycolic acid conjugate, leading to increased specificity for Hg(II).
Electrospinning is a cost effective and facile method to manufacture fiber mats appropriate for biomedical applications. Due to its high molecular weight and charged backbone, hyaluronic acid (HA) fiber mats with consistent fiber morphology have been difficult to electrospin from neutral pH solutions. Here, we present that the electrospinning of HA fibers in aqueous dimethylformamide solutions is facilitated by the addition of three phosphate salts. The salts-glycerol phosphate (GP), sodium phosphate (SP), and tripolyphosphate (TPP)-facilitated electrospinning of the solutions as characterized by conductivity measurements and fiber morphology. From tensile experiments, HA mats electrospun with SP demonstrated improved Young's modulus (12 MPa) over HA mats spun with either GP or TPP (5 and 3 MPa, respectively). This work demonstrates that a new neutral solvent system can be employed to spin HA fibers, which offers the potential for using the fibers for biomedical applications, such as a bone biomimetic.
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