Biodegradable Sodium Alginate Research Articles

Transient security transistors self-supported on biodegradable natural-polymer membranes for brain-inspired neuromorphic applications.

Transient electronics, a new generation of electronics that can physically or functionally vanish on demand, are very promising for future "green" security biocompatible electronics. At the same time, hardware implementation of biological synapses is highly desirable for emerging brain-like neuromorphic computational systems that could look beyond the conventional von Neumann architecture. Here, a hardware-security physically-transient bidirectional artificial synapse network based on a dual in-plane-gate Al-Zn-O neuromorphic transistor was fabricated on free-standing laterally-coupled biopolymer electrolyte membranes (sodium alginate). The excitatory postsynaptic current, paired-pulse-facilitation, and temporal filtering characteristics from high-pass to low-pass transition were successfully mimicked. More importantly, bidirectional dynamic spatiotemporal learning rules and neuronal arithmetic were also experimentally demonstrated using two lateral in-plane gates as the presynaptic inputs. Most interestingly, excellent physically-transient behavior could be achieved with a superfast water-soluble speed of only ∼120 seconds. This work represents a significant step towards future hardware-security transient biocompatible intelligent electronic systems.

Biosynthesis of Silver Nanoparticles from Persimmon Byproducts and Incorporation in Biodegradable Sodium Alginate Thin Film.

Fruit industrial wastes such as persimmon seed, peel, and calyx were used to synthesize silver nanoparticles (AgNPs) which were incorporated in sodium alginate thin films. This study evaluated the antioxidant activities and mechanical properties of the films that could be useful in the manufacture of food packaging using biodegradable films.

Biodegradable sodium alginate based semi-interpenetrating polymer network hydrogels for antibacterial application

A series of biodegradable, semi-interpenetrating polymer network (semi-IPN) hydrogels were synthesized from a combination of carbohydrate polymer and sodium alginate (NaAlg) with acrylamide and dimethyl aminoethyl methacrylate, and crosslinked with N,N-methylenebisacrylamide via radical redox polymerization. The cytocompatibility of the hydrogels with respect to their monomers and semi-IPN hydrogels was evaluated in vitro using cultures of mouse fibroblast cell lines. This study allowed the entrapment of silver nanoparticles (NPs) into semi-IPN hydrogel networks by the in situ reduction of Ag+ ions using NaBH4 as a reducing agent. UV–visible spectroscopy confirmed the formation of silver NPs in the semi-IPN hydrogel matrix. The formation of silver NPs was also confirmed from a themogravimetric analysis weight loss difference between hydrogel and silver nanocomposite as 32%. The morphology and structure of the AgNPs present in the hydrogel networks were examined by scanning electron microscopy. Transmission electron microscopy revealed silver NPs with a size of ∼5 nm. The silver nanocomposite hydrogel exhibited good antibacterial activity against both gram positive (Staphylococcus aureus) and gram negative (Escherichia coli) bacteria. These results suggest that the hydrogel can be applied as wound dressings and for water purification purposes. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 3196–3206, 2014.

Biodegradable sodium alginate and lignosulphonic acid blends: characterization and swelling studies

In this article, Sodium alginate and Lignosulphonic acid blends were prepared in different weight ratios by solution casting method. Swelling experiments were conducted for Sodium alginate and its blends by adding calcium chloride for various intervals in a pH 7.4 medium. The strength of the films increases after their treatment with CaCl2 at higher intervals forming an alginate network. The SA/LS blend (80/20) is subjected for sorption studies at variable pH 1.2 & 7.4, in order to test the suitability of the blends for controlled drug delivery. Further, experiments were conducted for de-crosslinking using 0.1M HCl. The solvent uptake for the blends decreased with increasing LS content in the blends. Blends were investigated by X-ray diffraction and Fourier Transform Infra-Red spectroscopy in order to study the crystallinity and molecular interactions. XRD confirms the reduction in cluster space in blends leading to lower uptake of solvent.

Formulation and Characterization of Sodium Alginate g-Hydroxy Ethylacrylate Bio-Degradable Polymeric Beads: In Vitro Release Studies

Novel type of highly swollen beads were prepared by grafting 2-hydroxyethylacrylate onto biodegradable Sodium alginate (SA) via free-radical polymerization using potassium persulphate as an initiator and Triprolidine hydrochloride as a model drug. Evidence of grafting was obtained by fourier transform infrared spectroscopic technique. Morphological properties of the beads were studied by SEM analysis. Thermal properties and crystallinity of the beads were characterized using differential scanning calorimetry and thermogravimetric analysis and X-ray diffraction techniques, respectively. Dissolution experiments were performed to study the release profiles at 37 °C in phosphate buffer solution (pH-7.4). Effect of monomer content, crosslinking agent and drug/polymer ratio on swelling properties and release profiles were also comparatively studied. A dissolution result concludes that drug release decreases with increasing crosslinker content. The highest release (96%) was obtained for the beads prepared with 0.5 mL crosslinking agent. Equilibrium swelling degree also supports the drug release profiles confirming SA-g-HEA beads showed better release profiles compare to plain SA beads.