The cytisine-enriched poly(3-hydroxybutyrate) fibers for sustained-release dosage form.

The polymeric cytisine-enriched fibers based on poly(3-hydroxybutyrate) were obtained using electrospinning method. The biocompatibility study, advanced thermal analysis and release of cytisine from the poly(3-hydroxybutyrate) fibers were carried out. The nanofibers' morphology was evaluated by scanning electron microscopy. The formation and description of phases during the thermal processes of fibers by the advanced thermal analysis were examined. The new quantitative thermal analysis of polymeric fibers with cytisine phases based on vibrational, solid and liquid heat capacities was presented. The apparent heat capacity of fibers was measured using the standard differential scanning calorimetry. The quantitative analysis allowed for the study of the glass transition and melting/crystallization process. The mobile amorphous fraction, degree of crystallinity and rigid amorphous fraction were determined depending on the thermal history of semicrystalline polymeric fibers. Furthermore, the cytisine dissolution behaviour was studied. It was observed that the kinetic of the release from polymeric nanofiber is delayed than for the marketed product. The immunosafety of the tested polymeric nanofibers with cytisine was confirmed by the Food and Drug Agency Guidance as well as the European Medicines Agency. The polymeric matrix with cytisine seems to be a promising candidate for the prolonged release formulation.

Investigation of arsenic removal from aqueous solution through selective sorption and nanofiber-based filters.

BACKGROUND: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH). MATERIALS AND METHODS: Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined. RESULTS: It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %. CONCLUSIONS: The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium.

The adsorption, kinetics, and interaction mechanisms of various types of estrogen on electrospun polymeric nanofiber membranes.

This study focuses on the adsorption kinetics of four highly potent sex hormones (estrone (E1), 17ß-estradiol (E2), 17α-ethinylestradiol (EE2), and estriol (E3)), present in water reservoirs, which are considered a major cause of fish feminization, low sperm count in males, breast and ovarian cancer in females induced by hormonal imbalance. Herein, electrospun polymeric nanostructures were produced from cellulose acetate, polyamide, polyethersulfone, polyurethanes (918 and elastollan), and polyacrylonitrile (PAN) to simultaneously adsorbing these estrogenic hormones in a single step process and to compare their performance. These nanofibers possessed an average fiber diameter in the range 174-330 nm and their specific surface area ranged between 10.2 and 20.9 m2g-1. The adsorption-desorption process was investigated in four cycles to determine the effective reusability of the adsorption systems. A one-step high-performance liquid chromatography technique was developed to detect and quantify concurrently each hormone present in the solution. Experimental data were obtained to determine the adsorption kinetics by applying pseudo-first-order, pseudo-second-order and intraparticle diffusion models. Findings showed that E1, E2 and EE2 best fitted pseudo-second-order kinetics, while E3 followed pseudo-first-order kinetics. It was found that polyurethane Elastollan nanofibers had maximum adsorption capacities of 0.801, 0.590, 0.736 and 0.382 mg g-1for E1, E2, EE2 and E3, respectively. In addition, the results revealed that polyurethane Elastollan nanofibers had the highest percentage efficiency of estrogens removal at ∼58.9% due to its strong hydrogen bonding with estrogenic hormones, while the least removal efficiency for PAN at ∼35.1%. Consecutive adsorption-desorption cycles demonstrated that polyurethane maintained the best efficiency, even after being repeatedly used four times compared to the other polymers. Overall, the findings indicate that all the studied nanostructures have the potential to be effective adsorbents for concurrently eradicating such estrogens from the environment.

An Estimate of the Onset of Beadless Character of Electrospun Nanofibers Using Rheological Characterization.

Electrospinning represents the very effective process of producing nanofibrous mats. This process is influenced by a number of mutually and strongly interlaced entry parameters (characteristics of polymer, solvent, process parameters) and their participation in the resulting nanofiber quality. The appearance of nanofibers is a result of the necessary primary experimental parameter setting within an acceptable range. However, finer analysis of nanofiber quality depends on the proper choice of these individual factors. The aim of this contribution is to evaluate one of the key factors-polymer concentration-with respect to the presence or absence of bead formation. This passage can be approximated by rheological oscillatory measurements when a sudden decrease in phase angle indicates this change. It replaces otherwise time- and cost-consuming trial-and-error experiments. This approach was tested using three different materials: solutions of poly(vinylidene fluoride-co-hexafluoropropylene), poly(vinyl butyral), and poly(ethylene oxide).