Polymers sensitive to external stimuli are intensively studied. They are used for preparation of controlled drug delivery systems for variety of active pharmaceutical ingredients. Poly--isopropyl acrylamide is a temperature sensitive polymer, and its properties have been used to obtain a series of thermally sensitive polymeric structures. The present study evaluates the effect of hydrophilic co-monomer, -(2-hydroxyethyl)acrylamide on the properties of thermosensitive hydrogels with hydroxypropyl methylcellulose and assesses the release rate of the model drug naproxen sodium embedded into the hydrogel. -isopropyl acrylamide derivatives were synthesized by surfactant free precipitation polymerization. The chemical structure of the particles was evaluated via nuclear magnetic resonance spectroscopy, whereas the hydrodynamic diameter was measured by dynamic light scattering method. The molecular weight was determined using the static light scattering. Hydrogel formulations with naproxen sodium were assessed in the terms of model drug release rate at two temperatures: 22 °C and 42 °C, using the pharmacopoeial method. The assessed formulations released lower amounts of drug, as compared to the control formulation, containing only hydroxypropyl methylcellulose as the main hydrophilic component.
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http://dx.doi.org/10.1166/jnn.2019.15848 | DOI Listing |
Molecules
October 2024
Department of Chemical and Process Engineering, Rzeszów University of Technology, 35-959 Rzeszów, Poland.
Protein adsorption behavior was examined on poly(-isopropylacrylamide-co-sodium methacrylate)-based hydrogels at different temperatures: 5, 20, and 37 °C, and pH: 4.5, 7, and 9.2.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2023
Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Adaptable redox-active materials hold great potential for electrochemically mediated separation processes via targeted molecular recognition and reduced energy requirements. This work presents molecularly tunable vinylferrocene metallopolymers (P(VFc-co-X)) with modifiable operating potentials, charge storage capacities, capacity retentions, and analyte affinities in various electrolyte environments based on the hydrophobicity of X. The styrene (St) co-monomer impedes hydrophobic anions from ferrocene access, providing P(VFc-co-St) with specific response capabilities for and greatly improved cyclabilities in hydrophilic anions.
View Article and Find Full Text PDFJ Mater Chem B
September 2023
McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.
Controlled and sustained delivery of therapeutic proteins is crucial for achieving desired effects in wound healing applications. Yet, this remains a challenge in growth factor delivery for bone tissue engineering. Current delivery systems can lead to negative side effects, such as ectopic bone growth and cancer, due to the over administration of growth inducing proteins.
View Article and Find Full Text PDFGels
January 2023
Institute for Organic and Analytical Chemistry, University of Bremen, Leobener Str. 7, 28359 Bremen, Germany.
Poly(-isopropylacrylamide) PNIPAAm hydrogels were modified with a new azobenzene-containing co-monomer. In this work, light responsiveness as an additional functionality, is conceptualized to induce two phase transitions in the same material, which can be controlled by light. For a hydrogel with merely 2.
View Article and Find Full Text PDFDent Mater
March 2023
KU Leuven (University of Leuven), Department of Oral Health Sciences, BIOMAT & UZ Leuven (University Hospitals Leuven), Dentistry, Leuven, Belgium. Electronic address:
Objectives: The mono-functional monomer 2-hydroxyethyl methacrylate (HEMA) is often added to universal adhesives (UAs) to improve surface wetting and prevent phase separation. Nevertheless, HEMA promotes water sorption and hydrolysis at adhesive interfaces, hereby affecting long-term bonding to dentin. This study investigated if two acrylamide monomers could replace HEMA in an UA formulation applied in etch-and-rinse (2E&R) and self-etch (1SE) bonding mode.
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