Abstract:
Vitrification is a simple and cost-effective method for the storage of human spermatozoa without the use of conventional
cryoprotectants, by plunging the sperm suspension directly into liquid nitrogen. As a result, solidification of living cells
without the formation of ice crystals is achieved during cooling. This study aimed to compare cryoprotectant-free
vitrification to conventional cryopreservation protocols. Semen samples (n = 35) were collected from patients seeking
diagnostic assistance at the Reproductive and Endocrine Unit at Steve Biko Academic Hospital. Samples were processed
using a discontinu-ous density-gradient centrifugation method. Washed samples were split into two aliquots and
cryopreserved either by means of cryoprotectant-free vitrifica-tion (sucrose + 1% albumin) or conventional slow freezing
(TEST-yolk buf-fer). Post-thawing, the sperm motion parameters, mitochondrial membrane potential (Dwm) and DNA
fragmentation were compared between the two groups. No significant differences were observed in the sperm motility
parame-ters (P > 0.05). Significantly higher percentages of Dwm (11.99% 4.326%versus 6.58% 1.026%; P < 0.001) and
lower percentages of DNA fragmenta-tion (2.79% 1.017% versus 3.86% 1.38%; P < 0.01) were observed when
comparing cryoprotectant-free vitrification to conventional cryopreservation. Cryoprotectant-free vitrification is a rapid and
promising alternative to conventional methods resulting in good-quality spermatozoa post-thaw.
