Hydrogel Formation (hydrogel + formation)

Distribution by Scientific Domains


Selected Abstracts


Irradiation synthesis of biopolymer-based superabsorbent hydrogel: Optimization using the Taguchi method and investigation of its swelling behavior

ADVANCES IN POLYMER TECHNOLOGY, Issue 2 2009
Ghasem R. Bardajee
Abstract In this report, the synthesis of a novel superabsorbent hydrogel via ,-irradiation graft copolymerization of acrylamide onto sodium alginate and kappa-carrageenan hybrid backbones in a homogeneous solution is described. The Taguchi method was used as a powerful experimental design tool for synthesis optimization. A series of superabsorbent hydrogels was synthesized by proposed conditions of Qualitek-4 software. Considering the results of nine trials according to analysis of variance, optimum conditions were proposed. The swelling behavior of optimum superabsorbent hydrogels was studied in various solutions, with pH values ranging from 1 to 13. In addition, swelling kinetics, swelling in various organic solvents, the absorbency under load, and on,off switching behavior were investigated. Also, hydrogel formation was confirmed by Fourier transform infrared spectroscopy. Surface morphology of the synthesized hydrogels was assessed by scanning electron microscopy. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:131,140, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20154 [source]


Dendritic macromers for hydrogel formation: Tailored materials for ophthalmic, orthopedic, and biotech applications

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2008
Mark W. Grinstaff
Abstract Dendritic macromolecules are well-defined highly branched macromolecules synthesized via a divergent or convergent approach. A salient feature of the macromolecules described herein, and a goal of our research effort, is to prepare dendritic macromolecules suitable for in vitro and in vivo use by focusing on biocompatible building blocks and biodegradable linkages. These dendritic macromolecules can be subsequently crosslinked to form hydrogels using a photochemical acrylate-based or a chemical ligation strategy. The properties,mechanical, swelling, degradation, and so forth,of the hydrogels can be tuned by altering the composition, crosslinking chemistry, wt %, generation number and so forth. The utility and diverse applicability is demonstrated through successful use of these hydrogels in three unique applications: hydrogel adhesives for repairing corneal wounds, hydrogel scaffolds for cartilage tissue engineering, and hydrogel reaction chambers for high throughput screening of molecular recognition events. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 383,400, 2008. [source]


Synthesis and hydrogel formation of fluorine-containing amphiphilic ABA triblock copolymers

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 21 2001
Kozo Matsumoto
Abstract Fluorine-containing amphiphilic ABA triblock copolymers, poly(2-hydroxyethyl vinyl ether)- block -poly[2-(2,2,3,3,3-pentafluoropropoxy)ethyl vinyl ether]- block -poly(2-hydroxyethyl vinyl ether) [poly(HOVE- b -PFPOVE- b -HOVE)] (HFH), poly[2-(2,2,3,3,3-pentafluoropropoxy)ethyl vinyl ether]- block -poly(2-hydroxyethyl vinyl ether)- block -poly[2-(2,2,3,3,3-pentafluoropropoxy)ethyl vinyl ether] [poly(PFPOVE- b -HOVE- b -PFPOVE)] (FHF), and poly(n -butyl vinyl ether)- block -poly(2-hydroxyethyl vinyl ether)- block -poly(n -butyl vinyl ether) [poly(NBVE- b -HOVE- b -NBVE)] (LHL), were synthesized, and their behavior in water was investigated. The aforementioned polymers were prepared by sequential living cationic polymerization of 2-acetoxyethyl vinyl ether (AcOVE) and PFPOVE or NBVE, followed by hydrolysis of acetyl groups in polyAcOVE. FHF and LHL formed a hydrogel in water, whereas HFH gave a homogeneous aqueous solution. In addition, the gel-forming concentration of FHF was much lower than that of corresponding LHL. Surface-tension measurements of the aqueous polymer solutions revealed that all the triblock copolymers synthesized formed micelles or aggregates above about 1.0 × 10,4 mol/L. The surface tensions of HFH and FHF solutions above the critical micelle concentration were lower than those of LHL, indicating high surface activity of fluorine-containing triblock copolymers. Small-angle X-ray scattering measurements revealed that HFH formed a core-shell sperical micelle in 1 wt % aqueous solutions, whereas the other block copolymers caused more conplicated assembly in the solutions. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3751,3760, 2001 [source]


Tailoring Polymeric Hydrogels through Cyclodextrin Host,Guest Complexation

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 3 2010
Xuhong Guo
Abstract A close correllation between molecular-level interactions and macroscopic characteristics of polymer networks exists. The characteristics of the polymeric hydrogels assembled from ,-cyclodextrin (,-CD) and adamantyl (AD) substituted poly(acrylate)s can be tailored through selective host,guest complexation between ,-CD and AD substituents and their tethers. Dominantly, steric effects and competitive intra- and intermolecular host,guest complexation are found to control poly(acrylate) isomeric inter-strand linkage in polymer network formation. This understanding of the factors involved in polymeric hydrogel formation points the way towards the construction of increasingly sophisticated biocompatible materials. [source]