Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/13931
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dc.contributor.authorBouzas, Luis Fernando da Silva-
dc.contributor.authorBraga, Flavio Henrique Paraguassu-
dc.contributor.authorMotta, Juliana Pessanha Rodrigues-
dc.contributor.authorGomes, Bernadete Evangelho-
dc.contributor.authorPôrto, Luís Cristóvão de Moraes Sobrino-
dc.date.accessioned2023-05-25T13:21:11Z-
dc.date.available2023-05-25T13:21:11Z-
dc.date.issued2010-06-
dc.identifier.issn0011-2240-
dc.identifier.urihttps://ninho.inca.gov.br/jspui/handle/123456789/13931-
dc.description.abstractTransplantation using hematopoietic stem cells from umbilical cord blood (UCB) is a life-saving treat ment option for patients with select oncologic diseases, immunologic diseases, bone marrow failure, and others. Often this transplant modality requires cryopreservation and storage of hematopoietic stem cells (HSC), which need to remain cryopreserved in UCB banks for possible future use. The most widely used cryoprotectant is dimethylsulfoxide (Me2SO), but at 37 C, it is toxic to cells and for patients, infu sion of cryopreserved HSC with Me2SO has been associated with side effects. Freezing of cells leads to chemical change of cellular components, which results in physical disruption. Reactive oxygen species (ROS) generation also has been implicated as cause of damage to cells during freezing. We assessed the ability of two bioantioxidants and two disaccharides, to enhance the cryopreservation of UCB. UCB was processed and subjected to cryopreservation in solutions containing different concentrations of Me2SO, bioantioxidants and disaccharides. Samples were thawed, and then analysed by: flow cytometry analysis, CFU assay and MTT viability assay. In this study, our analyses showed that antioxidants, princi pally catalase, performed greater preservation of: CD34+ cells, CD123+ cells, colony-forming units and cell viability, all post-thawed, compared with the standard solution of cryopreservation. Our present studies show that the addition of catalase improved the cryopreservation outcome. Catalase may act on reducing levels of ROS, further indicating that accumulation of free radicals indeed leads to death in cryopreserved hematopoietic cells.pt_BR
dc.subjectÁcido Ascórbicopt_BR
dc.subjectAscorbic Acidpt_BR
dc.subjectCatalasept_BR
dc.subjectSubunidade alfa de Receptor de Interleucina-3pt_BR
dc.subjectInterleukin-3 Receptor alpha Subunitpt_BR
dc.subjectAntígenos CD34pt_BR
dc.subjectAntigens CD34pt_BR
dc.subjectSangue Fetalpt_BR
dc.subjectFetal Bloodpt_BR
dc.subjectCriopreservaçãopt_BR
dc.subjectCryopreservationpt_BR
dc.subjectSulfato de Atazanavirpt_BR
dc.subjectAtazanavir Sulfatept_BR
dc.subjectSacarosept_BR
dc.subjectSucrosept_BR
dc.subjectTrealosept_BR
dc.subjectTrehalosept_BR
dc.titleEvaluations of bioantioxidants in cryopreservation of umbilical cord blood using natural cryoprotectants and low concentrations of dimethylsulfoxidept_BR
dc.TypeArticlept_BR
Appears in Collections:Hospital do Câncer I (HCI)



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