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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...

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Autores principales: Yagoub, Suliman H., Thompson, Jeremy G., Orth, Antony, Dholakia, Kishan, Gibson, Brant C., Dunning, Kylie R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
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.
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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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