Comprehensive Biomaterials II 2017
DOI: 10.1016/b978-0-12-803581-8.09291-2
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4.23 Polymers in Oral Drug Delivery

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Cited by 25 publications
(28 citation statements)
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“…1 ), promoting unfolding and enhancing viscosity by electrostatic repulsion. 18–22 This work reveals 1 H MAS NMR to provide suitable sensitivity and resolution to detect structural changes induced in organic polymers during their hydration. Magnetohydrodynamic mixing was shown to not only induce less structural damage during the mixing process, as compared to high shear mixing, magneto-hydrodynamic mixing also generates long-lived charge stabilization on the polymer, giving rise to enhanced properties of the hydrated carbomer dispersion.…”
mentioning
confidence: 97%
“…1 ), promoting unfolding and enhancing viscosity by electrostatic repulsion. 18–22 This work reveals 1 H MAS NMR to provide suitable sensitivity and resolution to detect structural changes induced in organic polymers during their hydration. Magnetohydrodynamic mixing was shown to not only induce less structural damage during the mixing process, as compared to high shear mixing, magneto-hydrodynamic mixing also generates long-lived charge stabilization on the polymer, giving rise to enhanced properties of the hydrated carbomer dispersion.…”
mentioning
confidence: 97%
“…In vitro tests showed good biocompatibility on normal L929 murine fibroblast cells and anti-cancer properties against A431 human skin carcinoma cell lines [ 139 ]. Furthermore, Jangde et al [ 140 ] incorporated quercetin into a multiphase hydrogel consisting of Carbopol ® (the trade name for carbomers, high molecular weight cross-linked poly(acrylic acid) polymers) and varying gelatin ratio. The most suitable hydrogel was obtained at a ratio of gelatin to Carbopol ® of 6 to 4, which exhibited accelerated wound healing and reduced wound closure time albino rat models [ 141 ].…”
Section: Wound Dressings In Skin Cancermentioning
confidence: 99%
“…PMAA was the first polymethacrylate used in oral dosage form for drug delivery [ 24 ]. Two copolymers of PMAA have been applied with gastrointestinal (GI) tract targeting for drug delivery: (i) poly(methacrylic acid-co-ethyl acrylate) dissolved in duodenum at pH > 5.5, and (ii) poly(methacrylic acid-co-methyl methacrylate) dissolved in jejunum at pH > 6.0 or in colon at pH > 7.0 [ 25 ]. These copolymers are supplied under the trade name Eudragit for pharmaceutical applications.…”
Section: Introductionmentioning
confidence: 99%
“…The synthesis was carried out by IEP, under free-radical polymerization using water as continuous media, through a “grafting from” approach. In contrast to previously published in other works for drug delivery systems prepared with PMAA [ 24 , 25 ], in this work, BA co-monomer and functionalized CNTs were used in the preparation. It is expected that the last two components of the studied PNs increase their capacity to deliver drugs.…”
Section: Introductionmentioning
confidence: 99%