A reliable procedure for decontamination before thawing of human specimens cryostored in liquid nitrogen Three washes with sterile liquid nitrogen SLN2

Three subsequent washings in certified ultraviolet sterile liquid nitrogen produce an efficient decontamination of vitrification carriers, allowing safe thawing of human specimens.

0
0

Authors

Lodovico Parmegiani, M.Sc., Antonio Accorsi, M.Sc., Silvia Bernardi, B.Sc., Alessandra Arnone, B.Sc., Graciela Estela Cognigni, M.D., Marco Filicori, M.D.

Vol 98, Issue 4, Pages 870-875

Abstract

Objective:

To report a washing procedure, to be performed as frozen specimens are taken out of cryobanks, to minimize the risk of hypothetical culture contamination during thawing.

Design:

Basic research.

Setting:

Private assisted reproduction center.

Intervention(s):

Two batches of liquid nitrogen (LN2) were experimentally contaminated, one with bacteria (Pseudomonas aeruginosa, Escherichia coli, Stenotrophomonas maltophilia) and the other with fungi (Aspergillus niger). Two hundred thirty-two of the most common human gamete/embryo vitrification carriers (Cryotop, Cryoleaf, Cryopette) were immersed in the contaminated LN2 (117 in the bacteria and 25 in the fungi-contaminated LN2). The carriers were tested microbiologically, one group without washing (control) and the other after three subsequent washings in certified ultraviolet sterile liquid nitrogen (SLN2). The carriers were randomly allocated to the "three-wash procedure" (three-wash group, 142 carriers) or "no-wash" (control group, 90 carriers) using a specific software tool.

Mean outcome measure(s):

Assessment of microorganism growth.

Result(s):

In the no-wash control group, 78.6% of the carriers were contaminated by the bacteria and 100% by the fungi. No carriers were found to be contaminated, either by bacteria or fungi, after the three-wash procedure.

Conclusion(s):

The three-wash procedure with SLN2 produced an efficient decontamination of carriers in extreme experimental conditions. For this reason, this procedure could be routinely performed in IVF laboratories for safe thawing of human specimens which are cryostored in nonhermetical cryocontainers, particularly in the case of open or single straw-closed vitrification systems.

Read the full text at: http://www.fertstert.org/article/S0015-0282(12)00681-4/fulltext


Go to the profile of Fertility and Sterility

Fertility and Sterility

Editorial Office, American Society for Reproductive Medicine

Fertility and Sterility® is an international journal for obstetricians, gynecologists, reproductive endocrinologists, urologists, basic scientists and others who treat and investigate problems of infertility and human reproductive disorders. The journal publishes juried original scientific articles in clinical and laboratory research relevant to reproductive endocrinology, urology, andrology, physiology, immunology, genetics, contraception, and menopause. Fertility and Sterility® encourages and supports meaningful basic and clinical research, and facilitates and promotes excellence in professional education, in the field of reproductive medicine.

No comments yet.