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Novel cannula design improves large volume auto-injection rates for high viscosity solutions

A prototype reusable large-volume (2 mL) autoinjector (LVAI) was designed to compare injection performance of a novel 27 gauge ultra-thin wall (UTW) pre-filled syringe (PFS) cannula (8 mm external cannula length, 14.4 mm total needle length) against an existing 27 gauge special thin wall (STW) PFS c...

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Autores principales: Roberts, Bruce C., Rini, Christopher, Klug, Rick, Sherman, Douglas B., Morel, Didier, Pettis, Ronald J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725910/
https://www.ncbi.nlm.nih.gov/pubmed/34962225
http://dx.doi.org/10.1080/10717544.2021.2018069
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author Roberts, Bruce C.
Rini, Christopher
Klug, Rick
Sherman, Douglas B.
Morel, Didier
Pettis, Ronald J.
author_facet Roberts, Bruce C.
Rini, Christopher
Klug, Rick
Sherman, Douglas B.
Morel, Didier
Pettis, Ronald J.
author_sort Roberts, Bruce C.
collection PubMed
description A prototype reusable large-volume (2 mL) autoinjector (LVAI) was designed to compare injection performance of a novel 27 gauge ultra-thin wall (UTW) pre-filled syringe (PFS) cannula (8 mm external cannula length, 14.4 mm total needle length) against an existing 27 gauge special thin wall (STW) PFS cannula (12.7 mm external cannula length, 19 mm total needle length) across a range of injectate viscosities (2.3–30 cP) in a series of in vivo feasibility studies in swine. The UTW cannula had an approximately 30% greater cross-sectional lumen area than the STW cannula. The target exposed needle length was adjusted to ensure appropriate needle penetration depth and achieve injectate deposition in the subcutaneous (SC) tissue. Delivery time and volume, injection site leakage, injectate depot location, and local tissue effects were examined. The STW and UTW cannulae both provided effective SC delivery of contrast placebo solutions, and were able to accommodate injectate viscosity up to 30 cP without quantifiable leakage from the tissue and with minor tissue effects which resolved within 1–2 hours. Delivery times at each viscosity were significantly different between PFS types with the UTW PFS producing faster delivery times. In a histological substudy of the UTW cannula using injectate viscosities up to 50 cP, injection site reactions were rare and, when present, were of minimal severity. This series of studies demonstrates the feasibility of LVAI SC injection and informs autoinjector and PFS design considerations. Use of a UTW cannula may enable more rapid LVAI injections with minimal tissue effects, especially for higher viscosity formulations.
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spelling pubmed-87259102022-01-05 Novel cannula design improves large volume auto-injection rates for high viscosity solutions Roberts, Bruce C. Rini, Christopher Klug, Rick Sherman, Douglas B. Morel, Didier Pettis, Ronald J. Drug Deliv Research Article A prototype reusable large-volume (2 mL) autoinjector (LVAI) was designed to compare injection performance of a novel 27 gauge ultra-thin wall (UTW) pre-filled syringe (PFS) cannula (8 mm external cannula length, 14.4 mm total needle length) against an existing 27 gauge special thin wall (STW) PFS cannula (12.7 mm external cannula length, 19 mm total needle length) across a range of injectate viscosities (2.3–30 cP) in a series of in vivo feasibility studies in swine. The UTW cannula had an approximately 30% greater cross-sectional lumen area than the STW cannula. The target exposed needle length was adjusted to ensure appropriate needle penetration depth and achieve injectate deposition in the subcutaneous (SC) tissue. Delivery time and volume, injection site leakage, injectate depot location, and local tissue effects were examined. The STW and UTW cannulae both provided effective SC delivery of contrast placebo solutions, and were able to accommodate injectate viscosity up to 30 cP without quantifiable leakage from the tissue and with minor tissue effects which resolved within 1–2 hours. Delivery times at each viscosity were significantly different between PFS types with the UTW PFS producing faster delivery times. In a histological substudy of the UTW cannula using injectate viscosities up to 50 cP, injection site reactions were rare and, when present, were of minimal severity. This series of studies demonstrates the feasibility of LVAI SC injection and informs autoinjector and PFS design considerations. Use of a UTW cannula may enable more rapid LVAI injections with minimal tissue effects, especially for higher viscosity formulations. Taylor & Francis 2021-12-28 /pmc/articles/PMC8725910/ /pubmed/34962225 http://dx.doi.org/10.1080/10717544.2021.2018069 Text en © 2021 Becton Dickinson and Company https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Roberts, Bruce C.
Rini, Christopher
Klug, Rick
Sherman, Douglas B.
Morel, Didier
Pettis, Ronald J.
Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title_full Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title_fullStr Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title_full_unstemmed Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title_short Novel cannula design improves large volume auto-injection rates for high viscosity solutions
title_sort novel cannula design improves large volume auto-injection rates for high viscosity solutions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725910/
https://www.ncbi.nlm.nih.gov/pubmed/34962225
http://dx.doi.org/10.1080/10717544.2021.2018069
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