In vitro tagging of embryos with nanoparticles

被引:15
作者
Fynewever, Tricia L.
Agcaoili, Evelyn S.
Jacobson, John D.
Patton, William C.
Chan, Philip J.
机构
[1] Loma Linda Univ, Sch Med, Ctr Fertil & IVF, Dept Gynecol & Obstet, Loma Linda, CA 92354 USA
[2] Loma Linda Univ, Sch Med, Dept Physiol & Pharmacol, Loma Linda, CA 92354 USA
关键词
mouse preimplantation embryos; ID tagging; ICSI ART; nanoparticles; microspheres;
D O I
10.1007/s10815-006-9084-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: To develop an in vitro method for tagging embryos and to compare the development of the embryos after nanoparticles injection versus externally-applied nanoparticles derived from either polystyrene or polyacrylonitrile. Methods: Each mouse 1-cell embryo (the selected test-model) was either: (a) injected by intracytoplasmic injection or (b) co-incubated with different nanoparticles at 37 degrees C, 5% CO2 in air. The embryos were assessed after 2 and 6 days of culture. Results: Embryo development was similar for externally-applied polystyrene nanoparticles and control (97.6 +/- 2.7 versus 100.0 +/- 0%) but different for polyacrylonitrile nanoparticles (90.0 +/- 2.8 %) on day 2. However, the results were similar on Day 6. Injected embryos were linked to lower percent development on Day 2. Few injected embryos reached blastocyst stage on Day 6 after a brief UV-fluorescence exposure. Conclusions: Tagging embryos by external polystyrene-based nanoparticles was the better method when compared with injected nanoparticles. Larger nanoparticles in microsphere range were easier to qualitate. Inhibited hatching limited their use beyond the blastocyst stage.
引用
收藏
页码:61 / 65
页数:5
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