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Biocompatibility Assessment of Polymeric Nanoparticle Carriers for Drug Delivery in Human Osteoblasts

dc.contributor.authorDias, Kamila
dc.contributor.authorLouro, Henriqueta
dc.contributor.authorGonçalves, Lídia
dc.contributor.authorSilva, Maria João
dc.contributor.authorBettencourt, Ana
dc.date.accessioned2018-02-12T15:52:40Z
dc.date.available2018-02-12T15:52:40Z
dc.date.issued2017-05
dc.description.abstractBone infections after prosthetic surgery represent a painful and costly process that should be prevented. The use of nanocarriers as efficient drug-delivery systems represents an innovative strategy to reduce systemic toxicity and avoid antimicrobial resistance. Still, great efforts are required to ensure the biocompatibility and safety of new nanocarriers before their medical application. In this work, the FDA-approved polymers poly(methyl methacrylate) (PMMA), and Eudragit RL 100 (Eud) were used to obtain two sets of nanoparticles, plain PMMA and PMMA-Eud (50:50). Their biocompatibility was assessed in a normal and differentiated human osteoblast cell line. The nanoparticles synthesis was conducted by a previously optimized methodology and their physicochemical properties, including size distribution, surface charge, morphology and aggregation/agglomeration states, were analysed during different preparation steps. Furthermore, the cell uptake and cytotoxicity as well as and their potential to produce reactive oxygen species (ROS) were also studied. Cell assays were performed following exposure of MG63 (ATCC®CRL-1427™) under normal and differentiation culture conditions, to a concentration range of both polymeric nanoparticles. The results of the uptake studies confirmed that both nanoparticles are internalized by osteoblasts. For both formulations, neither a significant decrease in cell viability nor oxidative stress induction was observed. The comparative analysis of data obtained in undifferentiated osteoblast and in those under differentiation conditions showed similar effects being the latter slightly less sensitive to the nanoparticles toxicity. Based on the reported data, PMMA and PMMA-Eud can be described as biocompatible nanomaterials and be further explored in a perspective of potential carriers for drug delivery, reducing adverse effects of conventional treatments. However, another key property i.e., genotoxicity, needs to be assessed before ensuring their safety for human health. This approach isn’t only relevant for understanding the nano-bio interface by disclosing how physicochemical features relate to toxicological events, but also to support the safe-by-design concept.pt_PT
dc.description.sponsorshipTo Portuguese government (Fundação para a Ciência e Tecnologia) for the financial support of this work: research project EXCL/CTM-NAN/0166/2012 (Pest-UID/DTP/04138/2013UID/DTP/04138/2013, EXCL/CTM-NAN/0166/2012, COST Action TD1305 (IPROMEDAI).pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4945
dc.language.isoengpt_PT
dc.peerreviewednopt_PT
dc.subjectNanocarrierspt_PT
dc.subjectPMMA, PMMA-Eudpt_PT
dc.subjectBiosafetypt_PT
dc.subjectOsteoblastspt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.subjectOsteoblastospt_PT
dc.subjectNanopartículaspt_PT
dc.titleBiocompatibility Assessment of Polymeric Nanoparticle Carriers for Drug Delivery in Human Osteoblastspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FDTP%2F04138%2F2013/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/EXCL%2FCTM-NAN%2F0166%2F2012/PT
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.title3rd Innovation Week (which includes the Annual Conferences of the Interdisciplinary Thematic Networks of ULisboa), 3-9 May 2017pt_PT
oaire.fundingStream5876
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isProjectOfPublication8b7dc2e1-c04d-4a11-8fa9-83ead9d8f256
relation.isProjectOfPublication3b03b44b-4527-44bd-a501-a255c86d92f1
relation.isProjectOfPublication.latestForDiscovery3b03b44b-4527-44bd-a501-a255c86d92f1

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