2021
DOI: 10.1016/j.polymer.2020.123227
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Loading of doxorubicin into surface-attached stimuli-responsive microgels and its subsequent release under different conditions

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Cited by 22 publications
(22 citation statements)
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“…In the field of the controlled release of active compounds, the role of nanotechnology has driven the development of micro/nanoscopic polymeric systems (polymer–drug conjugates, micelles, dendritic structures) among which microgels have a highlighted role. The possibility to tune the microgel mesh size, that is, porosity, in addition to the composition, colloidal stability, and elasticity, has significantly contributed to the development of microgels as drug delivery or active compound carriers [ 50 , 51 , 52 , 53 ]. These systems are the basis of what is now known as nanomedicine, whose research in the last decade has been mainly directed toward the development of theragnostic systems, a combination of a therapeutic and diagnostic functions.…”
Section: Applications Of Microgelsmentioning
confidence: 99%
“…In the field of the controlled release of active compounds, the role of nanotechnology has driven the development of micro/nanoscopic polymeric systems (polymer–drug conjugates, micelles, dendritic structures) among which microgels have a highlighted role. The possibility to tune the microgel mesh size, that is, porosity, in addition to the composition, colloidal stability, and elasticity, has significantly contributed to the development of microgels as drug delivery or active compound carriers [ 50 , 51 , 52 , 53 ]. These systems are the basis of what is now known as nanomedicine, whose research in the last decade has been mainly directed toward the development of theragnostic systems, a combination of a therapeutic and diagnostic functions.…”
Section: Applications Of Microgelsmentioning
confidence: 99%
“…In another work, Pergushov et al controlled the uptake on and release of DOX from P(NIPAm-co-AA) microgel films in solutions at different ionic strengths: when deposited at high temperature, the microgels formed a uniform densely packed film, wherein the AA moieties adsorbed cationic DOX via electrostatic interactions at neutral pH. [231] The addition of NaCl or a polycation (i.e., quaternized poly(4-vinylpyridine)) to the surrounding solution disrupted DOX binding; it triggered its immediate release from the swollen microgels, affording 90% release in under 30 min.…”
Section: Controlled Releasementioning
confidence: 99%
“…Regarding the use of microgels as drug-delivery vehicles, many different studies have been performed with varying drugs, ranging from lysozyme [ 24 ] over the more hydrophilic drugs dopamine, naproxen, desipramine, dibucaine, acetaminophen [ 25 ], and -aescin [ 26 ] to the hydrophobic doxorubicin (DOX) [ 27 , 28 , 29 , 30 , 31 , 32 , 33 ]. Just from these representative examples, it can be stated that the structure of microgels, which often exhibit a rather hydrophobic, cross-linker rich core region and a rather hydrophilic corona [ 34 ], enables these particles to act as carriers for a variety of hydrophilic and hydrophobic drugs.…”
Section: Introductionmentioning
confidence: 99%