2022
DOI: 10.1016/j.ijpharm.2022.121838
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Quantifying how drug-polymer interaction and volume phase transition modulate the drug release kinetics from core-shell microgels

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Cited by 12 publications
(2 citation statements)
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“…Furthermore, at pH 7, 10, and 11, the κC-Sa/ZnO biopolymer was less soluble, resulting in low permeability, a higher water content, as well as a higher permeability of HCQ (Fahmy et al 2021;Sethi et al 2022). Figure 10D shows the effect of the different concentrations of salts on the release of the drug on the surface of the polymer, as it was found that the highest point of release was at a salt concentration (0.1g NaCl) and the highest release rate was 54% within 8 hours (Lim et al 2022).…”
Section: Drug Loading In Vitromentioning
confidence: 97%
“…Furthermore, at pH 7, 10, and 11, the κC-Sa/ZnO biopolymer was less soluble, resulting in low permeability, a higher water content, as well as a higher permeability of HCQ (Fahmy et al 2021;Sethi et al 2022). Figure 10D shows the effect of the different concentrations of salts on the release of the drug on the surface of the polymer, as it was found that the highest point of release was at a salt concentration (0.1g NaCl) and the highest release rate was 54% within 8 hours (Lim et al 2022).…”
Section: Drug Loading In Vitromentioning
confidence: 97%
“…The interactions between drugs and polymers exert the considerable influence on the drug release, such as ionic bonds, hydrogen bonds, and van der Waals forces [146 , 147] . The interaction nature and strength of these interactions are related to the types of donor and acceptor [148] .…”
Section: Roles and Mechanismsmentioning
confidence: 99%