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Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection
PURPOSE: Intracytoplasmic sperm injection (ICSI) addresses male sub-fertility by injecting a spermatozoon into the oocyte. This challenging procedure requires the use of dual micromanipulators, with success influenced by inter-operator expertise. We hypothesized that minimizing oocyte handling durin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365896/ https://www.ncbi.nlm.nih.gov/pubmed/35552947 http://dx.doi.org/10.1007/s10815-022-02485-1 |
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author | Yagoub, Suliman H. Thompson, Jeremy G. Orth, Antony Dholakia, Kishan Gibson, Brant C. Dunning, Kylie R. |
author_facet | Yagoub, Suliman H. Thompson, Jeremy G. Orth, Antony Dholakia, Kishan Gibson, Brant C. Dunning, Kylie R. |
author_sort | Yagoub, Suliman H. |
collection | PubMed |
description | PURPOSE: Intracytoplasmic sperm injection (ICSI) addresses male sub-fertility by injecting a spermatozoon into the oocyte. This challenging procedure requires the use of dual micromanipulators, with success influenced by inter-operator expertise. We hypothesized that minimizing oocyte handling during ICSI will simplify the procedure. To address this, we designed and fabricated a micrometer scale device that houses the oocyte and requires only one micromanipulator for microinjection. METHODS: The device consisted of 2 components, each of sub-cubic millimeter volume: a Pod and a Garage. These were fabricated using 2-photon polymerization. Toxicity was evaluated by culturing single-mouse presumptive zygotes (PZs) to the blastocyst stage within a Pod, with several Pods (and embryos) docked in a Garage. The development was compared to standard culture. The level of DNA damage/repair in resultant blastocysts was quantified (γH2A.X immunohistochemistry). To demonstrate the capability to carry out ICSI within the device, PZs were microinjected with 4-μm fluorescent microspheres and cultured to the blastocyst stage. Finally, the device was assessed for oocyte traceability and high-throughput microinjection capabilities and compared to standard microinjection practice using key parameters (pipette setup, holding then injecting oocytes). RESULTS: Compared to standard culture, embryo culture within Pods and a Garage showed no differences in development to the blastocyst stage or levels of DNA damage in resultant blastocysts. Furthermore, microinjection within our device removes the need for a holding pipette, improves traceability, and facilitates high-throughput microinjection. CONCLUSION: This novel device could improve embryo production following ICSI by simplifying the procedure and thus decreasing inter-operator variability. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10815-022-02485-1. |
format | Online Article Text |
id | pubmed-9365896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93658962022-08-12 Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection Yagoub, Suliman H. Thompson, Jeremy G. Orth, Antony Dholakia, Kishan Gibson, Brant C. Dunning, Kylie R. J Assist Reprod Genet Technological Innovations PURPOSE: Intracytoplasmic sperm injection (ICSI) addresses male sub-fertility by injecting a spermatozoon into the oocyte. This challenging procedure requires the use of dual micromanipulators, with success influenced by inter-operator expertise. We hypothesized that minimizing oocyte handling during ICSI will simplify the procedure. To address this, we designed and fabricated a micrometer scale device that houses the oocyte and requires only one micromanipulator for microinjection. METHODS: The device consisted of 2 components, each of sub-cubic millimeter volume: a Pod and a Garage. These were fabricated using 2-photon polymerization. Toxicity was evaluated by culturing single-mouse presumptive zygotes (PZs) to the blastocyst stage within a Pod, with several Pods (and embryos) docked in a Garage. The development was compared to standard culture. The level of DNA damage/repair in resultant blastocysts was quantified (γH2A.X immunohistochemistry). To demonstrate the capability to carry out ICSI within the device, PZs were microinjected with 4-μm fluorescent microspheres and cultured to the blastocyst stage. Finally, the device was assessed for oocyte traceability and high-throughput microinjection capabilities and compared to standard microinjection practice using key parameters (pipette setup, holding then injecting oocytes). RESULTS: Compared to standard culture, embryo culture within Pods and a Garage showed no differences in development to the blastocyst stage or levels of DNA damage in resultant blastocysts. Furthermore, microinjection within our device removes the need for a holding pipette, improves traceability, and facilitates high-throughput microinjection. CONCLUSION: This novel device could improve embryo production following ICSI by simplifying the procedure and thus decreasing inter-operator variability. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10815-022-02485-1. Springer US 2022-05-12 2022-07 /pmc/articles/PMC9365896/ /pubmed/35552947 http://dx.doi.org/10.1007/s10815-022-02485-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Technological Innovations Yagoub, Suliman H. Thompson, Jeremy G. Orth, Antony Dholakia, Kishan Gibson, Brant C. Dunning, Kylie R. Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title | Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title_full | Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title_fullStr | Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title_full_unstemmed | Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title_short | Fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
title_sort | fabrication on the microscale: a two-photon polymerized device for oocyte microinjection |
topic | Technological Innovations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365896/ https://www.ncbi.nlm.nih.gov/pubmed/35552947 http://dx.doi.org/10.1007/s10815-022-02485-1 |
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