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Cryopreservation of very low numbers of spermatozoa from male patients undergoing infertility treatment using agarose capsules. | LitMetric

AI Article Synopsis

  • This study aimed to cryopreserve low numbers of motile spermatozoa from men undergoing infertility treatments using agarose capsules, which were then frozen in liquid nitrogen.
  • A total of 2,142 motile spermatozoa were preserved from 26 patients, with 63% retaining their motility after thawing.
  • The results indicated a strong correlation between the number of motile sperm collected and their motility rates after thawing, suggesting that samples with more motile sperm may freeze better, highlighting the need for further research in different types of sperm.

Article Abstract

This study tried to cryopreserve low numbers of spermatozoa from men undergoing infertility treatments by inserting into agarose capsules. The capsules were transferred into a drop of cryoprotectant solution and injected 3-4 motile spermatozoa that were selected by the swim-up method by conventional intracytoplasmic sperm injection. These capsules were put on a Cryotop and frozen in liquid nitrogen vapor, and then submerged into liquid nitrogen and subsequently thawed and recovered. The motile spermatozoa in the capsules were counted. Eventually, we cryopreserved 2142 motile spermatozoa in 702 agarose capsules from 26 male patients and 1356 (63%) spermatozoa maintained their motility after thawing. The spermatozoa motility rates after thawing (MRAT) ranged from 20.0% (5/25) to 95.1% (58/61) among patients. The median MRAT was 68.3% (interquartile range 46.1-75.7). The total number of motile spermatozoa collected by swim-up method strongly correlated with MRAT (r = 0.746). It was possible to cryopreserve spermatozoa from male patients undergoing infertility treatment using agarose capsules. However, there were wide differences in MRAT among patients. It seems the spermatozoa from semen where there were many motile spermatozoa may have higher freezing resistance. Further studies using this method in cryptozoospermic semen, testicular and epididymal spermatozoa are required.

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Source
http://dx.doi.org/10.1007/s13577-017-0166-xDOI Listing

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