dc.creator | Baieli, María Fernanda | |
dc.creator | Urtasun, Nicolás | |
dc.creator | Hirsch, Daniela Belén | |
dc.creator | Miranda, María Victoria | |
dc.creator | Cascone, Osvaldo | |
dc.creator | Wolman, Federico Javier | |
dc.date.accessioned | 2021-05-11T15:28:11Z | |
dc.date.accessioned | 2022-10-15T11:19:06Z | |
dc.date.available | 2021-05-11T15:28:11Z | |
dc.date.available | 2022-10-15T11:19:06Z | |
dc.date.created | 2021-05-11T15:28:11Z | |
dc.date.issued | 2020-11 | |
dc.identifier | Baieli, 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.identifier | 0168-1656 | |
dc.identifier | http://hdl.handle.net/11336/131817 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4380030 | |
dc.description.abstract | Equine 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.language | eng | |
dc.publisher | Elsevier Science | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0168165620302157 | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jbiotec.2020.08.004 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | CHITOSAN | |
dc.subject | CHROMATOGRAPHY | |
dc.subject | EQUINE CHORIONIC GONADOTROPHIN | |
dc.subject | WHEAT GERM AGGLUTININ | |
dc.title | Single-step purification of equine chorionic gonadotrophin directly from plasma using affinity chromatography | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:ar-repo/semantics/artículo | |
dc.type | info:eu-repo/semantics/publishedVersion | |