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Controlled Release Of Cryoprotectants By Near Infrared Irradiation For Improved Cell Cryopreservation

Posted on:2021-04-24Degree:MasterType:Thesis
Institution:UniversityCandidate:Faryal Farooq CheepaFull Text:PDF
GTID:2404330602997450Subject:Biomedical engineering
Abstract/Summary:PDF Full Text Request
Cryopreservation is essential to bank living cells and tissues for future use while maintaining the proper levels of cell functions.The use of cryoprotectants(CPAs)to inhibit intracellular ice formation during cryopreservation is vital for cell survival,but the addition and removal of CPAs and ice recrystallization during rewarming will cause fatal injury to cells.The conventional CPA loading and unloading methods generate osmotic shocks and cause mechanical injury for biological samples,and the conventional method of rewarming using a water bath also leads to ice recrystallization and devitrification.To overcome these difficulties,a new CPAs loaded microparticles based method for loading and photothermal rewarming under near-infrared(NIR)laser irradiation was proposed.We have successfully achieved the controlled release of cryoprotectants(2 M EG,2 M PG,and 0.5 M trehalose)with graphene oxide(GO,0.04%w/v)from 1.5%(w/v)sodium alginate to the human umbilical vein endothelial cells(HUVECs)within 60 s using near-infrared(NIR)laser irradiation(808 nm Lasever(?)at a 5000 mW/cm2),and successfully recovered the CPAs-loaded cells with 0.04%(w/v)GO in 8 to 10 s using the same NIR irradiation.The results show that this method achieved 25%higher viability of HUVECs compared to the conventional method.In short,this study proposes a new approach for achieving controlled CPAs loading to cells with the photothermal induced strategy for cells cryopreservation.
Keywords/Search Tags:CPAs loading, Alginate hydrogel, Encapsulation, Core-shell structure, Vitrification
PDF Full Text Request
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