2020
DOI: 10.1016/j.polymer.2020.123045
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Surface hydrophilization of highly porous poly(ether imide) microparticles by covalent attachment of poly(vinyl pyrrolidone)

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Cited by 5 publications
(3 citation statements)
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“…The reason why the hydrophobic nature of polyesters does not impede their utilization as scaffolds is that there are many, readily available techniques that can alter the surface characteristics of polyesters. The list of examples includes plasma treatment, UV irradiation, coating, or blending with other polymers [26][27][28]. Each method can be used for the hydrophilization of the surface of the macromolecular matrix, which paves the way before the application of polyesters as scaffolds.…”
Section: Introductionmentioning
confidence: 99%
“…The reason why the hydrophobic nature of polyesters does not impede their utilization as scaffolds is that there are many, readily available techniques that can alter the surface characteristics of polyesters. The list of examples includes plasma treatment, UV irradiation, coating, or blending with other polymers [26][27][28]. Each method can be used for the hydrophilization of the surface of the macromolecular matrix, which paves the way before the application of polyesters as scaffolds.…”
Section: Introductionmentioning
confidence: 99%
“…One solution to tackle this problem is to replace them by low molar mass PVP (i.e., oligomers). Chain transfer agents, such as hydrogen peroxide or mercaptoethanol, can be used to control their molar mass during radical polymerization. For instance, Kratz et al synthesized amino-terminated PVP oligomers ( M n = 5400 g/mol) by using cysteamine as a chain-transfer agent . Other methods can be used to obtain low molar mass PVP such as fractionation techniques used by Ranucci et al for oligomeric drug carrier application or ultrafiltration techniques reported by Baldoli et al , Nonetheless, these methods limit the range of end-groups accessible and give no access to well-defined PVP with low molar mass dispersity.…”
Section: Introductionmentioning
confidence: 99%
“…11−16 For instance, Kratz et al synthesized amino-terminated PVP oligomers (M n = 5400 g/mol) by using cysteamine as a chain-transfer agent. 17 Other methods can be used to obtain low molar mass PVP such as fractionation techniques used by Ranucci et al for oligomeric drug carrier application or ultrafiltration techniques reported by Baldoli et al 18,19 Nonetheless, these methods limit the range of endgroups accessible and give no access to well-defined PVP with low molar mass dispersity.…”
Section: ■ Introductionmentioning
confidence: 99%