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冷冻载体Cryotop降温速率的测量及系统优化 被引量:2

Cooling Rate Measurement and System Optimization for Cryotop Device
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摘要 Cryotop法是玻璃化保存卵母细胞较有效的方法之一。当Cryotop载体插入液氮时,降温速度极高,几乎瞬间完成,常规的方法无法测量。实验使用数字示波器、线径25μm的T型热电偶建立起高速测温系统,测量了Cryotop法用于卵母细胞低温保存时的降温速率。通过改变载体材料、厚度、冷源温度等条件,提高Cryotop的降温速率。结果发现当使用60μm的铜质载板,使用浆状液氮作为冷源时,降温速度最高,可达到(37130±1336)K/min,较商品化的Cryotop的降温速度((11982±1936)K/min)提高了2倍。 Cryotop is one of the best effective methods for ooeytes cryopreservation. When Cryotop is inserted into liquid nitrogen, the cooling speed is extremely high, which is difficult to measure by conventional method. In this study, digital oscilloscopes and type T thermocouple of 25 .王海松.m diameter were employed to establish a high speed temperature measurement system. The cooling rates of Cryotop device at different cartier material, thickness and cold source temperature were measured. The results showed that when 60.王海松.m copper was used as carrier and slush nitrogen was used as cold source, the cooling rate was increased. It could reach (37130 ± 1336)K/min, which was twice higher than that of commercially available Cryotop ( (11982 ± 1936)K/min).
出处 《制冷学报》 CAS CSCD 北大核心 2013年第5期95-98,共4页 Journal of Refrigeration
基金 国家自然科学基金(50906057 51076108)资助项目 上海市重点学科(S30503)项目资助~~
关键词 CRYOTOP 降温速率 高速测温 Cryotop cooling rate ultra-fast temperature measurement
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  • 1Kuwayama M. Highly efficient vitrification for cryopreser- vation of human oocytes and embryos : The Cryotop method [J].Theriogenology, 2007, 67 ( 1 ) : 73-80.
  • 2Cobo A, Domingo J, Perez S, et al. Vitrification : an ef- fective new approach to oocyte banking and preserving fer- tility in cancer patients [ J ]. Clinical & Translational Oncol- ogy, 2008, 10(5) :268-273.
  • 3Li W, Zhou X, Wang H, et al. Numerical analysis to de- termine the performance of different oocyte vitrification de- vices for cryopreservation [ J]. Cryoletters, 2012,33 ( 2 ) : 143-149.
  • 4Sansinena M, Santos M V, Zaritzky N, et al. Numerical simulation of cooling rates in vitrification systems used for oocyte cryopreservation [ J ]. Cryobiology,2011,63 ( 1 ) : 32- 37.
  • 5Kleinhans F W, Shinsuke S, Peter Mazur. Simple, inex- pensive attainment and measurement of very high cooling and warming rates[J]. Cryobiology, 2010, 61 (2) :231- 233.
  • 6Omega Engineering Inc., Stamibrd, Connecticut, USA. mV vs. Temperature reference charts[ EB/OL]. (2011-09- 13 ) [ 2012-6-04 ]. http ://www. omega, com/temperature/ Z/pdf/z207. pdf.
  • 7WILKES C E,SUMMERS J W,DANIELS C A.乔辉,丁筠,盛平厚,等译.聚氯乙烯手册[M].北京:化学工业出版社,2008:70-80.
  • 8Santos M V, Sansinena M, Zaritzky N, et al. Assessment of external heat transfer coefficient during oocyte vitrifica- tion in liquid and slush nitrogen using numerical simula- tions to determine cooling rates [ J ]. Cryoletters, 2011,33 ( 1 ) :31-34.

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  • 1王欣,华泽钊,刘宝林,杨光辉,崔磊,曹谊林.Me_2SO浓度及预处理条件对组织工程化真皮活性的影响[J].上海理工大学学报,2007,29(4):311-314. 被引量:3
  • 2Franks F. Biophysics and biochemistry at low temperatures [ M]. Cambridge Press, 1985.
  • 3Shaw J M, Oranratnachai A, Trounson A O. Fundamental cryobiology of mammalian oocytes and ovarian tissue [ J ].Theriogenology, 2000, 53 ( 1 ) : 59-72.
  • 4Cobo A, Meseguer M, Remohi J, et al. Use of cryobanked oocytes in an ovum donation program: a prospective, ran- domized, controlled clinical trial editorial comment [ J ]. Obstetrical & Gynecological Survey, 2010, 65 (12): 775- 777.
  • 5Jondet M, Dominique S, Scholler R. Effects of freezing and thawing on mammalian oocyte [ J ]. Cryobiology, 1984, 21(2) : 192-199.
  • 6Landa V, Tepla O. Cryopreservation of mouse 8-cell em- bryos in microdrops [ J ]. Folia Biologica, 1990, 36 ( 3/4 ) : 153-158.
  • 7Riesco M F, Martinez-Pastor F, Chereguini O, et al. E- valuation of zebrafish (danio rerio) pgcs viability and DNA damage using different cryopreservation protocols [ J ]. The- riogenology, 2012, 77(1) : 122-130.
  • 8Vajta G, Kuwayama M, Booth P J, et al. Open pulled straw (ops) vitrification of cattle oocytes [ J ]. Theriogenol- ogy, 1998, 49(1) : 176.
  • 9Liang Y Y, Srirattana K, Phermthai T, et al. Effects of vitrifieation cryoprotectant treatment and cooling method on the viability and development of buffalo ooeytes after intra- cytoplasmic sperm injection [ J ]. Cryobiology, 2012, 65 (2) : 151-156.
  • 10Martino A, Songsasen N, Leibo S P. Development into blastocysts of bovine oocytes cryopreserved by ultra-rapid cooling [ J ]. Biology of Reproduction, 1996, 54 ( 5 ) : 1059-1069.

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