Abstract:Biopolymeric continuous core-sheath fibres, with an inner core of chitosan and alginate as the sheath, were fabricated for the first time without using a template. Hereby, the necessary conditions to achieve chitosanalginate core-sheath fibre via a wet-spinning process are presented. SEM micrographs show the cylindershaped monofilament structure of the chitosan core surrounded by the alginate sheath. The coaxial fibres exhibit a 260% increase in ultimate stress and more than 300% enhancement in the Young's mod… Show more
“…The uniaxial tensile testing was performed by moving the bottom stage down at a fixed velocity (0.2 mm s –1 ) until the fibers split. The tensile testing of individual fibers has also been reported previously for synthetic, as well as simple and composite hydrogel fibers …”
A new class of smart alginate microfibers with asymmetric oil encapsulates is introduced. These fibers are produced by injecting an aqueous alginate solution into an outer aqueous calcium chloride solution to form alginate fibers, which are asymmetrically loaded with oil entities through eccentrically aligned inner capillaries. The fiber morphology and its degree of asymmetry can be tuned via altering the size, location, and frequency of the oil encapsulates. These asymmetric fibers reveal significant potential for applications where conventional symmetric fibers fail to perform. It is shown how asymmetric oil-encapsulated fibers can become dehydration-sensitive, and trigger the release of encapsulates if their hydration level drops below a critical value. It is also shown how the triggered response could be switched off on demand by stabilizing the oil encapsulates. The capability of asymmetric fibers to carry and release multiple cargos in parallel is demonstrated. The fibers loaded with equal-sized spheres are more asymmetric than those containing unequal drops, have a higher tensile strength, and show better potential for a triggered response.
“…The uniaxial tensile testing was performed by moving the bottom stage down at a fixed velocity (0.2 mm s –1 ) until the fibers split. The tensile testing of individual fibers has also been reported previously for synthetic, as well as simple and composite hydrogel fibers …”
A new class of smart alginate microfibers with asymmetric oil encapsulates is introduced. These fibers are produced by injecting an aqueous alginate solution into an outer aqueous calcium chloride solution to form alginate fibers, which are asymmetrically loaded with oil entities through eccentrically aligned inner capillaries. The fiber morphology and its degree of asymmetry can be tuned via altering the size, location, and frequency of the oil encapsulates. These asymmetric fibers reveal significant potential for applications where conventional symmetric fibers fail to perform. It is shown how asymmetric oil-encapsulated fibers can become dehydration-sensitive, and trigger the release of encapsulates if their hydration level drops below a critical value. It is also shown how the triggered response could be switched off on demand by stabilizing the oil encapsulates. The capability of asymmetric fibers to carry and release multiple cargos in parallel is demonstrated. The fibers loaded with equal-sized spheres are more asymmetric than those containing unequal drops, have a higher tensile strength, and show better potential for a triggered response.
“…Using alginate-chitosan mixtures can be obtained fi bers with advanced useful properties, compared to individual polymers. Wet spinning technique [69][70][71][72][73][74][75] is the most common method for manufacturing these fi bers. Using this method, it can be obtained fi bers consisting entirely of alginate-chitosan mixture [70,75], alginate coated with chitosan [69,[71][72][73] (Figure 5) or vice versa -chitosan coated with alginate [74] (Figure 6).…”
Section: Fibersmentioning
confidence: 99%
“…Wet spinning technique [69][70][71][72][73][74][75] is the most common method for manufacturing these fi bers. Using this method, it can be obtained fi bers consisting entirely of alginate-chitosan mixture [70,75], alginate coated with chitosan [69,[71][72][73] (Figure 5) or vice versa -chitosan coated with alginate [74] (Figure 6). Due to chitosan and antimicrobial compounds (sulfathiazole [71]), alginate-chitosan fi bers show antimicrobial activity -inhibit the growth of various bacteria that inhabit the skin of mammals, such as Staphylococcus aureus [69,70,72], Escherichia coli [70,71], Micrococcus luteus, Staphylococcus epidermidis [69].…”
Section: Fibersmentioning
confidence: 99%
“…Due to chitosan and antimicrobial compounds (sulfathiazole [71]), alginate-chitosan fi bers show antimicrobial activity -inhibit the growth of various bacteria that inhabit the skin of mammals, such as Staphylococcus aureus [69,70,72], Escherichia coli [70,71], Micrococcus luteus, Staphylococcus epidermidis [69]. This property together with the ability to carry cationic [74] and anionic [75] drugs, allow antimicrobial alginate-chitosan fi bers to be a potential candidate for wound dressing materials.…”
Abstract. Natural polysaccharides alginate and chitosan have been used extensively, separately or in mixtures (systems), in manufacturing of pharmaceutical products (antimicrobial) and not only. Alginates usually serve as basis for antimicrobial systems, while chitosan, in certain proportions, enhances their physicochemical and antimicrobial properties. Focusing on the recent literature (mostly since 2000), this review outlines the main synthetic approaches for the preparation of systems based on both polymers as well as identify potential areas of their application as antimicrobial agents. Various techniques used for systems preparation like microparticles, fi lms, fi bers, nanoparticles, sponges, applications and usefulness of these systems as carriers of antimicrobial compounds will also be discussed.
“…Sodium alginate (SA) is a polysaccharide material extracted from the cell walls of brown algae by β‐ d ‐mannuronic acid and n ‐ l ‐guluronic acid via glycosidic linkages. It has excellent biocompatibility and film‐forming properties and has been widely used in the fields of medical and health materials, such as in medical dressings, tissue engineering repair materials, drug‐release materials and fiber materials . However, SA has a low strength, poor toughness, and poor water resistance, so the modification of SA has become a hotspot in recent years.…”
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