Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/37715
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dc.contributor.authorMagalhães, Flávia F.pt_PT
dc.contributor.authorAlmeida, Mafalda R.pt_PT
dc.contributor.authorSoares, Sofia F.pt_PT
dc.contributor.authorTrindade, Titopt_PT
dc.contributor.authorFreire, Mara G.pt_PT
dc.contributor.authorDaniel-da-Silva, Ana Luísapt_PT
dc.contributor.authorTavares, Ana P. M.pt_PT
dc.date.accessioned2023-05-15T11:18:03Z-
dc.date.available2023-05-15T11:18:03Z-
dc.date.issued2020-05-01-
dc.identifier.issn0141-8130pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/37715-
dc.description.abstractImmunoglobulin G (IgG) has been used in the treatment of cancer, autoimmune diseases and neurological disorders, however, the current technologies to purify and recover IgG from biological media are of high-cost and time-consuming, resulting in high-cost products. In this sense, the search for cost-effective technologies to obtain highly pure and active IgG is highly required. The present work proposes a simple and efficient method for the purification and recovery of IgG from rabbit serum using magnetic iron oxide nanoparticles (magnetite, Fe3O4) coated with hybrid shells of a siliceous material modified with the anionic polysaccharide κ-carrageenan. Experimental parameters such as pH, contact time between the hybrid magnetic nanoparticles (HMNPs) and rabbit serum, and total protein concentration or dilution factor of serum were evaluated. The best results were achieved at pH 5.0, with a contact time of 60 min and using a rabbit serum with a total protein concentration of 4.8 mg·mL-1. Under these conditions, it was obtained an IgG purification factor and adsorption yield onto the HMNPs of 3.0 and 90%, respectively. The desorption of IgG from the HMNPs was evaluated using two strategies: a KCl aqueous solution and buffered aqueous solutions. Comparing to the initial rabbit serum, an IgG purification factor of 2.7 with a recovery yield of 74% were obtained using a buffered aqueous solution at pH 7.0. After desorption, the secondary structure of IgG and other proteins was evaluated by circular dichroism and no changes in the secondary structure were observed, meaning that the IgG integrity is kept after the adsorption and desorption steps. In summary, the application of HMNPs in the purification of IgG from serum samples has a high potential as a new downstream platform.pt_PT
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50011%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50011%2F2020/PTpt_PT
dc.relationPOCI-01-0145-FEDER-031268pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/Investigador FCT/IF%2F01634%2F2015%2FCP1302%2FCT0023/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/Investigador FCT/IF%2F00405%2F2014%2FCP1222%2FCT0007/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F121366%2F2016/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectImmunoglobulin Gpt_PT
dc.subjectAdsorptionpt_PT
dc.subjectκ-Carrageenanpt_PT
dc.subjectMagnetic nanoparticlespt_PT
dc.subjectRecoverypt_PT
dc.titleRecovery of immunoglobulin G from rabbit serum using κ-carrageenan-modified hybrid magnetic nanoparticlespt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage914pt_PT
degois.publication.lastPage921pt_PT
degois.publication.titleInternational journal of biological macromoleculespt_PT
degois.publication.volume150pt_PT
dc.identifier.doi10.1016/j.ijbiomac.2020.02.135pt_PT
Appears in Collections:CICECO - Artigos
DQ - Artigos

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