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Investigating the Relationship Between Structure, Ice Recrystallization Inhibition Activity and Cryopreservation Ability of Various Galactopyranose Derivatives

The goal of our research is to generate cryopreservation agents derived from antifreeze
glycoproteins. One postulated mechanism of cell cryo-injury is ice recrystallization. It is known that simple saccharides and cryopreservation agents (DMSO) display ice recrystallization inhibition (IRI). This study assessed the cytotoxicity and cryopreservation ability of these sugars in relation to their IRI. It was determined that compounds with greater IRI have increased cytotoxicity yet confer cryoprotection. To further investigate how structure is affecting IRI activity, several galactopyranoside derivatives were synthesized. A series of deoxy and α-Callyl-
deoxy galactopyranoses were prepared. Testing determined that removal of any hydroxyl
group removes IRI. 3-deoxy-β-thiophenyl galactose was also synthesized and had surprisingly better IRI than β-thiophenylgalactose. Also, 6-azido galactose had similar IRI to 6-deoxy galactose. Lastly, a series of β- thioalkylgalactosides was synthesized and testing gave contradicting results which suggest that predicting IRI based on hydrophilicity is more complicated than initially hypothesized.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:OOU./en#10393/20040
Date31 May 2011
CreatorsTokarew, Jacqueline
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeThèse / Thesis

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