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dc.creatorMedina-Rivero, Emilioes_ES
dc.creatorVallejo-Castillo, Luises_ES
dc.creatorVázquez-Leyva, Saides_ES
dc.creatorPérez-Sánchez, Gilbertoes_ES
dc.creatorFavari, Lilianaes_ES
dc.creatorVelasco-Velázquez, Marcoes_ES
dc.creatorEstrada-Parra, Sergioes_ES
dc.creatorPavón, Lenines_ES
dc.creatorPérez-Tapia, Sonia Mayraes_ES
dc.date2016
dc.date.accessioned2023-10-26T15:37:38Z
dc.date.available2023-10-26T15:37:38Z
dc.date.issued2016
dc.identifier.issn2314-6133 
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/7797
dc.identifier.urihttp://dx.doi.org/10.1155/2016/7935181
dc.descriptionTransferon, a biotherapeutic agent that has been used for the past 2 decades for diseases with an inflammatory component, has been approved by regulatory authorities in Mexico (COFEPRIS) for the treatment of patients with herpes infection. The active pharmaceutical ingredient (API) of Transferon is based on polydispersion of peptides that have been extracted from lysed human leukocytes by a dialysis process and a subsequent ultrafiltration step to select molecules below 10 kDa. To physicochemically characterize the drug product, we developed chromatographic methods and an SDS-PAGE approach to analyze the composition and the overall variability of Transferon. Reversed-phase chromatographic profiles of peptide populations demonstrated batch-to batch consistency from 10 representative batches that harbored 4 primary peaks with a relative standard deviation (RSD) of less than 7%. Aminogram profiles exhibited 17 proteinogenic amino acids and showed that glycine was the most abundant amino acid, with a relative content of approximately 18%. Further, based on their electrophoretic migration, the peptide populations exhibited a molecular mass of about 10 kDa. Finally, we determined the Transferon fingerprint using a mass spectrometry tool. Because each batch was produced from independent pooled buffy coat samples from healthy donors, supplied by a local blood bank, our results support the consistency of the production of Transferon and reveal its peptide identity with regard to its physicochemical attributes.
dc.formatPDF
dc.language.isoeng
dc.publisherHindawi Pub. Co.
dc.relation2016:7935181
dc.rightsAcceso Cerrado
dc.titlePhysicochemical Characteristics of Transferon™ Batcheses_ES
dc.contributor.affiliationUnidad de Desarrollo e Investigacion en Bioprocesos (UDIBI), Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Colonia Santo Tomás, 11340 Ciudad de México, México
dc.contributor.emaillkuriaki@imp.edu.mx (Lenin Pavón)
dc.contributor.emailcipft.encb@gmail.com (Sonia Mayra Pérez Tapia)
dc.relation.jnabreviadoBIOMED RES INT
dc.relation.journalBioMed Research International
dc.identifier.placeEstados Unidos
dc.date.published2016
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñiz
dc.identifier.eissn2314-6141
dc.identifier.doi10.1155/2016/7935181


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