Author, as appears in the article.: Baulin, V.; Stefanic, M.; Ward, K.; Tawfik, H.; Seemann, R.; Guo, Y.; Fleury, J.-B.; Drouet, C.
Department: Enginyeria Química
URV's Author/s: BAULIN, VLADIMIR; Stefanic, M.; Ward, K.; Tawfik, H.; Seemann, R.; GUO, YACHONG; Fleury, J.-B.; Drouet, C.
Keywords: Lipid bilayer Cryopreservation Apatite
Abstract: Cryopreservation of red blood cells (RBC) is an important method for maintaining an inventory of rare RBC units and managing special transfusion circumstances. Currently, in a clinical setting, glycerol is used as cryoprotectant against freezing damage. After thawing and before transfusion, glycerol must however be removed to avoid intravascular hemolysis, via a complex and time-consuming deglycerolization process which requires specialized equipment. Improved cryopreservation methods using non-toxic agents are required to increase biocompatibility and decrease processing time. Biocompatible cryoprotectants (e.g. trehalose) were proposed, but their low permeation through RBC membranes limits their cryoprotection efficacy. Herein, we report for the first time a glycerol-free cryopreservation approach, using colloidal bioinspired apatite nanoparticles (NP) as bioactive promoters of RBC cryopreservation mediated by trehalose. Addition of apatite NP in the medium tremendously increases RBC cryosurvival, up to 91% (42% improvement compared to a control without NP) which is comparable to FDA-approved cryoprotection protocol employing glycerol. NP concentration and incubation conditions strongly modulate the NP bioactivity. Complementary experimental and computational analyses of the interaction between apatite NP and model lipid bilayers revealed complex events occurring at the NP-bilayer interface. Apatite NP do not cross the bilayer but momentarily modulate its physical status. These changes affect the membrane behavior, and promote the permeation of trehalose and a model fluorescent molecule (FITC). This approach is a new alternative to using toxic glycerol for cells cryopreservation, and the identification of this enhancing no-pore permeation mechanism of apatite NP appears as an original delivery pathway for cryoprotectant agents and beyond.
Research group: Molecular simulation I: Complex Systems
Thematic Areas: Chemical engineering Ingeniería química Enginyeria química
licence for use: https://creativecommons.org/licenses/by/3.0/es/
ISSN: 0142-9612
Author identifier: 0000-0003-2086-4271; ; ; ; ; ; ;
Record's date: 2017-10-23
Last page: 149
Journal volume: 140
Papper version: info:eu-repo/semantics/acceptedVersion
Link to the original source: https://www.sciencedirect.com/science/article/pii/S0142961217304179
Funding program: european; Marie Curie; DFG; SFB1027 european; Marie Curie; ITN; SNAL 608184
Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
Article's DOI: 10.1016/j.biomaterials.2017.06.018
Entity: Universitat Rovira i Virgili
Journal publication year: 2017
First page: 138
Publication Type: Article Artículo Article