Bio-Acoustic-MEMS in Medicine (BAMM) Laboratory, Center for Bioengineering, Department of Medicine, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, USA.
Nanomedicine (Lond). 2011 Aug;6(6):1115-29. doi: 10.2217/nnm.11.71.
Cell/tissue biopreservation has broad public health and socio-economic impact affecting millions of lives. Cryopreservation technologies provide an efficient way to preserve cells and tissues targeting the clinic for applications including reproductive medicine and organ transplantation. Among these technologies, vitrification has displayed significant improvement in post-thaw cell viability and function by eliminating harmful effects of ice crystal formation compared to the traditional slow freezing methods. However, high cryoprotectant agent concentrations are required, which induces toxicity and osmotic stress to cells and tissues. It has been shown that vitrification using small sample volumes (i.e., <1 µl) significantly increases cooling rates and hence reduces the required cryoprotectant agent levels. Recently, emerging nano- and micro-scale technologies have shown potential to manipulate picoliter to nanoliter sample sizes. Therefore, the synergistic integration of nanoscale technologies with cryogenics has the potential to improve biopreservation methods.
细胞/组织生物保存具有广泛的公共卫生和社会经济效益,影响着数百万人的生命。低温保存技术为细胞和组织的保存提供了一种有效的方法,其目标是应用于生殖医学和器官移植等领域。在这些技术中,与传统的慢速冷冻方法相比,玻璃化技术通过消除冰晶形成的有害影响,显著提高了冻后细胞的活力和功能。然而,需要高浓度的细胞保护剂,这会对细胞和组织产生毒性和渗透压力。已经表明,使用小样本体积(即 <1 µl)进行玻璃化会显著提高冷却速率,从而降低所需的细胞保护剂水平。最近,新兴的纳米和微尺度技术已经显示出在 picoliter 到 nanoliter 样本尺寸方面的潜力。因此,纳米技术与低温学的协同集成有可能改进生物保存方法。