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Maximum volume of nasal administration using a mucosal atomization device without aspiration in Japanese White rabbits
Recently, a mucosal atomization device (MAD) has been applied in veterinary medicine. In the present study, the maximum volume of nasal atomization without aspiration using MAD was examined in eight healthy female Japanese White (JW) rabbits. Each rabbit had their head and neck examined by computed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246693/ https://www.ncbi.nlm.nih.gov/pubmed/35400673 http://dx.doi.org/10.1292/jvms.21-0648 |
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author | WEI, Yixian HORI, Ai CHEN, I-Ying TAMOGI, Haruka HIROKAWA, Taku KATO, Keiko ITAMI, Takaharu SANO, Tadashi YAMASHITA, Kazuto |
author_facet | WEI, Yixian HORI, Ai CHEN, I-Ying TAMOGI, Haruka HIROKAWA, Taku KATO, Keiko ITAMI, Takaharu SANO, Tadashi YAMASHITA, Kazuto |
author_sort | WEI, Yixian |
collection | PubMed |
description | Recently, a mucosal atomization device (MAD) has been applied in veterinary medicine. In the present study, the maximum volume of nasal atomization without aspiration using MAD was examined in eight healthy female Japanese White (JW) rabbits. Each rabbit had their head and neck examined by computed tomography before and after nasal atomization with four different doses (0.15, 0.3, 0.45, and 0.6 ml per nostril) of diluted contrast medium (1:2 mixture of iohexol and saline). This was done under general anesthesia by an intramuscular administration of alfaxalone 2.5 mg/kg, medetomidine 40 μg/kg, and butorphanol 0.4 mg/kg, with a 7-day washout period between each treatment. The diluted contrast medium was distributed in the nasal cavity, external nares, and/or oral cavity in all rabbits receiving each treatment. The intranasal distribution volumes of the contrast medium were 287 (250–333) mm(3) [median (interquartile range)] for 0.15 ml, 433 (243–555) mm(3) for 0.3 ml, 552 (356–797) mm(3) for 0.45 ml, and 529 (356–722) mm(3) for 0.6 ml of treatment. The intranasal distribution volume for 0.15 ml treatment tended to be lower than that for 0.6 ml treatment (P=0.083). The contrast medium was deposited in the trachea in one rabbit (12.5%) and four rabbits (50%) receiving treatments of 0.45 and 0.6 ml per nostril, respectively. The maximum volume of nasal atomization without aspiration into the trachea was 0.3 ml per nostril for the JW rabbits. |
format | Online Article Text |
id | pubmed-9246693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92466932022-07-09 Maximum volume of nasal administration using a mucosal atomization device without aspiration in Japanese White rabbits WEI, Yixian HORI, Ai CHEN, I-Ying TAMOGI, Haruka HIROKAWA, Taku KATO, Keiko ITAMI, Takaharu SANO, Tadashi YAMASHITA, Kazuto J Vet Med Sci Surgery Recently, a mucosal atomization device (MAD) has been applied in veterinary medicine. In the present study, the maximum volume of nasal atomization without aspiration using MAD was examined in eight healthy female Japanese White (JW) rabbits. Each rabbit had their head and neck examined by computed tomography before and after nasal atomization with four different doses (0.15, 0.3, 0.45, and 0.6 ml per nostril) of diluted contrast medium (1:2 mixture of iohexol and saline). This was done under general anesthesia by an intramuscular administration of alfaxalone 2.5 mg/kg, medetomidine 40 μg/kg, and butorphanol 0.4 mg/kg, with a 7-day washout period between each treatment. The diluted contrast medium was distributed in the nasal cavity, external nares, and/or oral cavity in all rabbits receiving each treatment. The intranasal distribution volumes of the contrast medium were 287 (250–333) mm(3) [median (interquartile range)] for 0.15 ml, 433 (243–555) mm(3) for 0.3 ml, 552 (356–797) mm(3) for 0.45 ml, and 529 (356–722) mm(3) for 0.6 ml of treatment. The intranasal distribution volume for 0.15 ml treatment tended to be lower than that for 0.6 ml treatment (P=0.083). The contrast medium was deposited in the trachea in one rabbit (12.5%) and four rabbits (50%) receiving treatments of 0.45 and 0.6 ml per nostril, respectively. The maximum volume of nasal atomization without aspiration into the trachea was 0.3 ml per nostril for the JW rabbits. The Japanese Society of Veterinary Science 2022-04-11 2022-06 /pmc/articles/PMC9246693/ /pubmed/35400673 http://dx.doi.org/10.1292/jvms.21-0648 Text en ©2022 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Surgery WEI, Yixian HORI, Ai CHEN, I-Ying TAMOGI, Haruka HIROKAWA, Taku KATO, Keiko ITAMI, Takaharu SANO, Tadashi YAMASHITA, Kazuto Maximum volume of nasal administration using a mucosal atomization device without aspiration in Japanese White rabbits |
title | Maximum volume of nasal administration using a mucosal atomization device
without aspiration in Japanese White rabbits |
title_full | Maximum volume of nasal administration using a mucosal atomization device
without aspiration in Japanese White rabbits |
title_fullStr | Maximum volume of nasal administration using a mucosal atomization device
without aspiration in Japanese White rabbits |
title_full_unstemmed | Maximum volume of nasal administration using a mucosal atomization device
without aspiration in Japanese White rabbits |
title_short | Maximum volume of nasal administration using a mucosal atomization device
without aspiration in Japanese White rabbits |
title_sort | maximum volume of nasal administration using a mucosal atomization device
without aspiration in japanese white rabbits |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246693/ https://www.ncbi.nlm.nih.gov/pubmed/35400673 http://dx.doi.org/10.1292/jvms.21-0648 |
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