dc.creatorBaieli, María Fernanda
dc.creatorUrtasun, Nicolás
dc.creatorHirsch, Daniela Belén
dc.creatorMiranda, María Victoria
dc.creatorCascone, Osvaldo
dc.creatorWolman, Federico Javier
dc.date.accessioned2021-05-11T15:28:11Z
dc.date.accessioned2022-10-15T11:19:06Z
dc.date.available2021-05-11T15:28:11Z
dc.date.available2022-10-15T11:19:06Z
dc.date.created2021-05-11T15:28:11Z
dc.date.issued2020-11
dc.identifierBaieli, María Fernanda; Urtasun, Nicolás; Hirsch, Daniela Belén; Miranda, María Victoria; Cascone, Osvaldo; et al.; Single-step purification of equine chorionic gonadotrophin directly from plasma using affinity chromatography; Elsevier Science; Journal of Biotechnology; 323; 11-2020; 174-179
dc.identifier0168-1656
dc.identifierhttp://hdl.handle.net/11336/131817
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4380030
dc.description.abstractEquine chorionic gonadotrophin (eCG) is a hormone widely used in superovulation protocols because of its follicle-stimulating action, which increases reproductive efficiency in animals of productive interest. It contains 45% carbohydrate, 10% of which is N-acetylneuraminic acid (sialic acid). The eCG purification procedures from equine serum or plasma are mainly based on chromatographic methods. However, before these procedures, it is necessary to follow sample pre-conditioning steps, such as several precipitation stages and/or ultrafiltration/diafiltration processes. In this work, an efficient affinity chromatographic matrix for eCG purification directly from plasma was developed. The matrix consisted of chitosan mini-spheres with immobilized wheat germ agglutinin (WGA). The matrix allowed 98% adsorption of eCG directly from plasma without any pre-treatment with an overall yield of around 60%. The matrix chosen was able to maintain the efficient performance of the purification process for three consecutive cycles. Also, the process was scaled-up 500 times in volume and tested over seven consecutive cycles maintaining its chromatographic performance. The results presented here suggest the potential application of this matrix to one-step purification of eCG from plasma.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0168165620302157
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jbiotec.2020.08.004
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCHITOSAN
dc.subjectCHROMATOGRAPHY
dc.subjectEQUINE CHORIONIC GONADOTROPHIN
dc.subjectWHEAT GERM AGGLUTININ
dc.titleSingle-step purification of equine chorionic gonadotrophin directly from plasma using affinity chromatography
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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