Droplet-Assisted Microfluidic Fabrication and Characterization of Multifunctional Polysaccharide Microgels Formed by Multicomponent Reactions

dc.bibliographicCitation.firstPage1055
dc.bibliographicCitation.issue10
dc.bibliographicCitation.journalTitlePolymerseng
dc.bibliographicCitation.volume10
dc.contributor.authorHauck, Nicolas
dc.contributor.authorSeixas, Nalin
dc.contributor.authorCenteno, Silvia P.
dc.contributor.authorSchlüßler, Raimund
dc.contributor.authorCojoc, Gheorghe
dc.contributor.authorMüller, Paul
dc.contributor.authorGuck, Jochen
dc.contributor.authorWöll, Dominik
dc.contributor.authorWessjohann, Ludger A.
dc.contributor.authorThiele, Julian
dc.date.accessioned2023-01-26T09:27:03Z
dc.date.available2023-01-26T09:27:03Z
dc.date.issued2018
dc.description.abstractPolysaccharide-based microgels have broad applications in multi-parametric cell cultures, cell-free biotechnology, and drug delivery. Multicomponent reactions like the Passerini three-component and the Ugi four-component reaction are shown in here to be versatile platforms for fabricating these polysaccharide microgels by droplet microfluidics with a narrow size distribution. While conventional microgel formation requires pre-modification of hydrogel building blocks to introduce certain functionality, in multicomponent reactions one building block can be simply exchanged by another to introduce and extend functionality in a library-like fashion. Beyond synthesizing a range of polysaccharide-based microgels utilizing hyaluronic acid, alginate and chitosan, exemplary in-depth analysis of hyaluronic acid-based Ugi four-component gels is conducted by colloidal probe atomic force microscopy, confocal Brillouin microscopy, quantitative phase imaging, and fluorescence correlation spectroscopy to elucidate the capability of microfluidic multicomponent reactions for forming defined polysaccharide microgel networks. Particularly, the impact of crosslinker amount and length is studied. A higher network density leads to higher Young’s moduli accompanied by smaller pore sizes with lower diffusion coefficients of tracer molecules in the highly homogeneous network, and vice versa. Moreover, tailored building blocks allow for crosslinking the microgels and incorporating functional groups at the same time as demonstrated for biotin-functionalized, chitosan-based microgels formed by Ugi four-component reaction. To these microgels, streptavidin-labeled enzymes are easily conjugated as shown for horseradish peroxidase (HRP), which retains its activity inside the microgels.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/11075
dc.identifier.urihttp://dx.doi.org/10.34657/10101
dc.language.isoeng
dc.publisherBasel : MDPI
dc.relation.doihttps://doi.org/10.3390/polym10101055
dc.relation.essn2073-4360
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540
dc.subject.otherDroplet microfluidicseng
dc.subject.otherMulticomponent reactioneng
dc.subject.otherPasserini three-component reactioneng
dc.subject.otherPolysaccharide microgelseng
dc.subject.otherUgi four-component reactioneng
dc.titleDroplet-Assisted Microfluidic Fabrication and Characterization of Multifunctional Polysaccharide Microgels Formed by Multicomponent Reactionseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorIPF
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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