Improved tissue cryopreservation using inductive heating of magnetic nanoparticles.
Navid ManuchehrabadiZhe GaoJinjin ZhangHattie L RingQi ShaoFeng LiuMichael McDermottAlex FokYoed RabinKelvin G M BrockbankMichael GarwoodChristy L HaynesJohn C BischofPublished in: Science translational medicine (2017)
Vitrification, a kinetic process of liquid solidification into glass, poses many potential benefits for tissue cryopreservation including indefinite storage, banking, and facilitation of tissue matching for transplantation. To date, however, successful rewarming of tissues vitrified in VS55, a cryoprotectant solution, can only be achieved by convective warming of small volumes on the order of 1 ml. Successful rewarming requires both uniform and fast rates to reduce thermal mechanical stress and cracks, and to prevent rewarming phase crystallization. We present a scalable nanowarming technology for 1- to 80-ml samples using radiofrequency-excited mesoporous silica-coated iron oxide nanoparticles in VS55. Advanced imaging including sweep imaging with Fourier transform and microcomputed tomography was used to verify loading and unloading of VS55 and nanoparticles and successful vitrification of porcine arteries. Nanowarming was then used to demonstrate uniform and rapid rewarming at >130°C/min in both physical (1 to 80 ml) and biological systems including human dermal fibroblast cells, porcine arteries and porcine aortic heart valve leaflet tissues (1 to 50 ml). Nanowarming yielded viability that matched control and/or exceeded gold standard convective warming in 1- to 50-ml systems, and improved viability compared to slow-warmed (crystallized) samples. Last, biomechanical testing displayed no significant biomechanical property changes in blood vessel length or elastic modulus after nanowarming compared to untreated fresh control porcine arteries. In aggregate, these results demonstrate new physical and biological evidence that nanowarming can improve the outcome of vitrified cryogenic storage of tissues in larger sample volumes.
Keyphrases
- aortic valve
- gene expression
- high resolution
- magnetic nanoparticles
- mitral valve
- physical activity
- mental health
- endothelial cells
- iron oxide nanoparticles
- heart failure
- left ventricular
- aortic stenosis
- cell cycle arrest
- transcatheter aortic valve replacement
- risk assessment
- mesenchymal stem cells
- mass spectrometry
- pulmonary hypertension
- pulmonary arterial hypertension
- coronary artery
- cell proliferation
- fluorescence imaging
- pluripotent stem cells
- finite element
- signaling pathway
- heavy metals
- human health
- finite element analysis