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A tissue snap-freezing apparatus without sacrificial cryogens

机译:没有牺牲冷冻液的组织卡扣冻结装置

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Molecular technologies in cancer diagnosis require a fresh and frozen tissue, which is obtained by means of snap-freezing. Currently, coolants such as solid carbon dioxide and liquid nitrogen are used to preserve good morphology of the tissue. Using these coolants, snap freezing of tissues for diagnostic and research purposes is often time consuming, laborious, even hazardous and not user friendly. For that reason snap-freezing is not routinely applied at the location of biopsy acquisition. Furthermore, the influence of optimal cooling rate and cold sink temperature on the viability of the cells is not well known. In this paper, a snap-freezing apparatus powered by a small cryocooler is presented that will allow bio-medical research of tissue freezing methods and is safe to use in a hospital. To benchmark this apparatus, cooldown of a standard aluminum cryo-vial in liquid nitrogen is measured and the cooling rate is about -25 K/s between 295 K and 120 K. Sufficient cooling rate is obtained by a forced convective helium gas flow through a gap formed between the cryo-vial and a cold surface and is therefore chosen as the preferred cooling method. A conceptual design of the snap-apparatus with forced flow is discussed in this paper.
机译:癌症诊断中的分子技术需要一种新鲜和冷冻的组织,该组织通过卡扣渗透而获得。目前,诸如固体二氧化碳和液氮的冷却剂用于保持组织的良好形态。使用这些冷却剂,快速冻结组织进行诊断和研究目的通常是耗时,费力,危险,而不是用户友好。因此,在活检采集的位置,不常规应用捕获量。此外,最佳冷却速率和冷槽温度对细胞的活力的影响是不公知的。在本文中,提出了一种由小冷冻机供电的凝固装置,这将允许组织冷冻方法生物医学研究,并且在医院使用安全。为了基准测试该装置,测量液氮中的标准铝低温小瓶的冷却,冷却速率约为-25k / s在295k和120k之间。通过强制对流氦气流过a,获得足够的冷却速率在低温小瓶和冷表面之间形成的间隙,因此选择作为优选的冷却方法。本文讨论了具有强制流程的概念性设计。

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