Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>

Molecularly imprinted polymers (MIPs) against sialic acid (SA) have been developed as a detection tool to target cancer cells. Before proceeding to <i>in vivo</i> studies, a better knowledge of the overall effects of MIPs on the innate immune system is needed. The aim of this study thus...

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Main Authors: Louise Sternbæk, Martha Kimani, Kornelia Gawlitza, Knut Rurack, Birgit Janicke, Kersti Alm, Anette Gjörloff Wingren, Håkan Eriksson
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/12/12/6091
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author Louise Sternbæk
Martha Kimani
Kornelia Gawlitza
Knut Rurack
Birgit Janicke
Kersti Alm
Anette Gjörloff Wingren
Håkan Eriksson
author_facet Louise Sternbæk
Martha Kimani
Kornelia Gawlitza
Knut Rurack
Birgit Janicke
Kersti Alm
Anette Gjörloff Wingren
Håkan Eriksson
author_sort Louise Sternbæk
collection DOAJ
description Molecularly imprinted polymers (MIPs) against sialic acid (SA) have been developed as a detection tool to target cancer cells. Before proceeding to <i>in vivo</i> studies, a better knowledge of the overall effects of MIPs on the innate immune system is needed. The aim of this study thus was to exemplarily assess whether SA-MIPs lead to inflammatory and/or cytotoxic responses when administered to phagocytosing cells in the innate immune system. The response of monocytic/macrophage cell lines to two different reference particles, Alhydrogel and PLGA, was compared to their response to SA-MIPs. <i>In vitro</i> culture showed a cellular association of SA-MIPs and Alhydrogel, as analyzed by flow cytometry. The reference particle Alhydrogel induced secretion of IL-1β from the monocytic cell line THP-1, whereas almost no secretion was provoked for SA-MIPs. A reduced number of both THP-1 and RAW 264.7 cells were observed after incubation with SA-MIPs and this was not caused by cytotoxicity. Digital holographic cytometry showed that SA-MIP treatment affected cell division, with much fewer cells dividing. Thus, the reduced number of cells after SA-MIP treatment was not linked to SA-MIPs cytotoxicity. In conclusion, SA-MIPs have a low degree of inflammatory properties, are not cytotoxic, and can be applicable for future <i>in vivo</i> studies.
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spelling doaj.art-06ee2552d44c441695b92ff9ae3abd412023-11-23T15:27:37ZengMDPI AGApplied Sciences2076-34172022-06-011212609110.3390/app12126091Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>Louise Sternbæk0Martha Kimani1Kornelia Gawlitza2Knut Rurack3Birgit Janicke4Kersti Alm5Anette Gjörloff Wingren6Håkan Eriksson7Department of Biomedical Sciences, Faculty of Health and Society, Malmö University, SE-205 06 Malmö, SwedenChemical and Optical Sensing Division, Bundesanstalt für Materialforschung und-prüfung (BAM), DE-12489 Berlin, GermanyChemical and Optical Sensing Division, Bundesanstalt für Materialforschung und-prüfung (BAM), DE-12489 Berlin, GermanyChemical and Optical Sensing Division, Bundesanstalt für Materialforschung und-prüfung (BAM), DE-12489 Berlin, GermanyPhase Holographic Imaging AB, SE-223 63 Lund, SwedenPhase Holographic Imaging AB, SE-223 63 Lund, SwedenDepartment of Biomedical Sciences, Faculty of Health and Society, Malmö University, SE-205 06 Malmö, SwedenDepartment of Biomedical Sciences, Faculty of Health and Society, Malmö University, SE-205 06 Malmö, SwedenMolecularly imprinted polymers (MIPs) against sialic acid (SA) have been developed as a detection tool to target cancer cells. Before proceeding to <i>in vivo</i> studies, a better knowledge of the overall effects of MIPs on the innate immune system is needed. The aim of this study thus was to exemplarily assess whether SA-MIPs lead to inflammatory and/or cytotoxic responses when administered to phagocytosing cells in the innate immune system. The response of monocytic/macrophage cell lines to two different reference particles, Alhydrogel and PLGA, was compared to their response to SA-MIPs. <i>In vitro</i> culture showed a cellular association of SA-MIPs and Alhydrogel, as analyzed by flow cytometry. The reference particle Alhydrogel induced secretion of IL-1β from the monocytic cell line THP-1, whereas almost no secretion was provoked for SA-MIPs. A reduced number of both THP-1 and RAW 264.7 cells were observed after incubation with SA-MIPs and this was not caused by cytotoxicity. Digital holographic cytometry showed that SA-MIP treatment affected cell division, with much fewer cells dividing. Thus, the reduced number of cells after SA-MIP treatment was not linked to SA-MIPs cytotoxicity. In conclusion, SA-MIPs have a low degree of inflammatory properties, are not cytotoxic, and can be applicable for future <i>in vivo</i> studies.https://www.mdpi.com/2076-3417/12/12/6091molecularly imprinted polymersdigital holographic cytometrycytotoxicitypro-inflammatory cytokines
spellingShingle Louise Sternbæk
Martha Kimani
Kornelia Gawlitza
Knut Rurack
Birgit Janicke
Kersti Alm
Anette Gjörloff Wingren
Håkan Eriksson
Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
Applied Sciences
molecularly imprinted polymers
digital holographic cytometry
cytotoxicity
pro-inflammatory cytokines
title Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
title_full Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
title_fullStr Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
title_full_unstemmed Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
title_short Molecularly Imprinted Polymers Exhibit Low Cytotoxic and Inflammatory Properties in Macrophages <i>In Vitro</i>
title_sort molecularly imprinted polymers exhibit low cytotoxic and inflammatory properties in macrophages i in vitro i
topic molecularly imprinted polymers
digital holographic cytometry
cytotoxicity
pro-inflammatory cytokines
url https://www.mdpi.com/2076-3417/12/12/6091
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