Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/13931
Title: Evaluations of bioantioxidants in cryopreservation of umbilical cord blood using natural cryoprotectants and low concentrations of dimethylsulfoxide
Authors: Bouzas, Luis Fernando da Silva
Braga, Flavio Henrique Paraguassu
Motta, Juliana Pessanha Rodrigues
Gomes, Bernadete Evangelho
Pôrto, Luís Cristóvão de Moraes Sobrino
Keywords: Ácido Ascórbico
Ascorbic Acid
Catalase
Subunidade alfa de Receptor de Interleucina-3
Interleukin-3 Receptor alpha Subunit
Antígenos CD34
Antigens CD34
Sangue Fetal
Fetal Blood
Criopreservação
Cryopreservation
Sulfato de Atazanavir
Atazanavir Sulfate
Sacarose
Sucrose
Trealose
Trehalose
Issue Date: Jun-2010
Abstract: Transplantation 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.
URI: https://ninho.inca.gov.br/jspui/handle/123456789/13931
ISSN: 0011-2240
Appears in Collections:Hospital do Câncer I (HCI)



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.