<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tirgar P</submitter><funding>National Institute for Genetic Engineering and Biotechnology</funding><pagination>034104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8133792</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(3)</volume><pubmed_abstract>Embryo vitrification is a fundamental practice in assisted reproduction and fertility preservation. A key step of this process is replacing the internal water with cryoprotectants (CPAs) by transferring embryos from an isotonic to a hypertonic solution of CPAs. However, this applies an abrupt osmotic shock to embryos, resulting in molecular damages that have long been a source of concern. In this study, we introduce a standalone microfluidic system to automate the manual process and minimize the osmotic shock applied to embryos. This device provides the same final CPA concentrations as the manual method but with a gradual increase over time instead of sudden increases. Our system allows the introduction of the dehydrating non-permeating CPA, sucrose, from the onset of CPA-water exchange, w</pubmed_abstract><journal>Biomicrofluidics</journal><pubmed_title>Toward embryo cryopreservation-on-a-chip: A standalone microfluidic platform for gradual loading of cryoprotectants to minimize cryoinjuries.</pubmed_title><pmcid>PMC8133792</pmcid><funding_grant_id>677</funding_grant_id><pubmed_authors>Shoushtari Zadeh Naseri A</pubmed_authors><pubmed_authors>AzizMohseni S</pubmed_authors><pubmed_authors>Ehrlicher A</pubmed_authors><pubmed_authors>Zandi G</pubmed_authors><pubmed_authors>Tirgar P</pubmed_authors><pubmed_authors>Ziaie N</pubmed_authors><pubmed_authors>Najafi M</pubmed_authors><pubmed_authors>Kazemi P</pubmed_authors><pubmed_authors>Fayazi S</pubmed_authors><pubmed_authors>Dashtizad M</pubmed_authors><pubmed_authors>Sarmadi F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Toward embryo cryopreservation-on-a-chip: A standalone microfluidic platform for gradual loading of cryoprotectants to minimize cryoinjuries.</name><description>Embryo vitrification is a fundamental practice in assisted reproduction and fertility preservation. A key step of this process is replacing the internal water with cryoprotectants (CPAs) by transferring embryos from an isotonic to a hypertonic solution of CPAs. However, this applies an abrupt osmotic shock to embryos, resulting in molecular damages that have long been a source of concern. In this study, we introduce a standalone microfluidic system to automate the manual process and minimize the osmotic shock applied to embryos. This device provides the same final CPA concentrations as the manual method but with a gradual increase over time instead of sudden increases. Our system allows the introduction of the dehydrating non-permeating CPA, sucrose, from the onset of CPA-water exchange, w</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-07-09T11:23:04.612Z</modification><creation>2026-07-09T10:46:47.582Z</creation></dates><accession>S-EPMC8133792</accession><cross_references><pubmed>34025896</pubmed><doi>10.1063/5.0047185</doi></cross_references></HashMap>