Measuring Tissue Back-Pressure - In Vivo Injection Forces During Subcutaneous Injection

Purpose Limited information is available on injection forces of parenterals representing the in vivo situation. Scope of the present study was to investigate the contribution of the subcutaneous (sc) tissue layer to injection forces during in vivo injection. Methods Göttingen minipigs received injec...

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Veröffentlicht in:Pharmaceutical research 2015-07, Vol.32 (7), p.2229-2240
Hauptverfasser: Allmendinger, Andrea, Mueller, Robert, Schwarb, Edward, Chipperfield, Mark, Huwyler, Joerg, Mahler, Hanns-Christian, Fischer, Stefan
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container_end_page 2240
container_issue 7
container_start_page 2229
container_title Pharmaceutical research
container_volume 32
creator Allmendinger, Andrea
Mueller, Robert
Schwarb, Edward
Chipperfield, Mark
Huwyler, Joerg
Mahler, Hanns-Christian
Fischer, Stefan
description Purpose Limited information is available on injection forces of parenterals representing the in vivo situation. Scope of the present study was to investigate the contribution of the subcutaneous (sc) tissue layer to injection forces during in vivo injection. Methods Göttingen minipigs received injections of isotonic dextran solutions (1–100 mPas) into the plica inguinalis using different injection rates and volumes (0.025–0.2 mL/s and 2.5 vs. 4.5 mL). Results The contribution of the sc back-pressure to injection forces was found to increase linearly with viscosity and injection rate ranging from 0.6 ± 0.5 N to 1.0 ± 0.4 N (1 mPas), 0.7 ± 0.2 N to 2.4 ± 1.9 N (10 mPas), and 1.8 ± 0.6 N to 4.7 ± 3.3 N (20 mPas) for injection rates of 0.025 to 0.2 mL/s, respectively. Variability increased with viscosity and injection rate. Values are average values from 10 randomized injections. A maximum of 12.9 N was reached for 20 mPas at 0.2 mL/s; 6.9 ± 0.3 N was determined for 100 mPas at 0.025 mL/s. No difference was found between injection volumes of 2.5 and 4.5 mL. The contribution of the tissue was differentiated from the contribution of the injection device and a local temperature effect. This effect was leading to warming of the (equilibrated) sample in the needle, therefore smaller injection forces than expected compensating tissue resistance to some parts. Conclusions When estimating injection forces representative for the in vivo situation, the contribution of the tissue has to be considered as well as local warming of the sample in the needle during injection.
doi_str_mv 10.1007/s11095-014-1611-0
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Scope of the present study was to investigate the contribution of the subcutaneous (sc) tissue layer to injection forces during in vivo injection. Methods Göttingen minipigs received injections of isotonic dextran solutions (1–100 mPas) into the plica inguinalis using different injection rates and volumes (0.025–0.2 mL/s and 2.5 vs. 4.5 mL). Results The contribution of the sc back-pressure to injection forces was found to increase linearly with viscosity and injection rate ranging from 0.6 ± 0.5 N to 1.0 ± 0.4 N (1 mPas), 0.7 ± 0.2 N to 2.4 ± 1.9 N (10 mPas), and 1.8 ± 0.6 N to 4.7 ± 3.3 N (20 mPas) for injection rates of 0.025 to 0.2 mL/s, respectively. Variability increased with viscosity and injection rate. Values are average values from 10 randomized injections. A maximum of 12.9 N was reached for 20 mPas at 0.2 mL/s; 6.9 ± 0.3 N was determined for 100 mPas at 0.025 mL/s. No difference was found between injection volumes of 2.5 and 4.5 mL. The contribution of the tissue was differentiated from the contribution of the injection device and a local temperature effect. This effect was leading to warming of the (equilibrated) sample in the needle, therefore smaller injection forces than expected compensating tissue resistance to some parts. Conclusions When estimating injection forces representative for the in vivo situation, the contribution of the tissue has to be considered as well as local warming of the sample in the needle during injection.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-014-1611-0</identifier><identifier>PMID: 25537343</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animals ; Biochemistry ; Biomechanical Phenomena - physiology ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Dextrans - administration &amp; dosage ; Dextrans - pharmacokinetics ; Drug Delivery Systems - instrumentation ; Equipment Design ; Hogs ; Injections ; Injections, Subcutaneous ; Male ; Medical Law ; Pharmaceutical sciences ; Pharmacology/Toxicology ; Pharmacy ; Pressure ; Research Paper ; Rheology ; Skin - metabolism ; Swine ; Swine, Miniature ; Tissue Distribution ; Viscosity</subject><ispartof>Pharmaceutical research, 2015-07, Vol.32 (7), p.2229-2240</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>Springer Science+Business Media New York 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-46b4254a00ffc97468bdb70436df76b303d3a7b2c6caee1fe1d021fcf5165f523</citedby><cites>FETCH-LOGICAL-c508t-46b4254a00ffc97468bdb70436df76b303d3a7b2c6caee1fe1d021fcf5165f523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11095-014-1611-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11095-014-1611-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25537343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Allmendinger, Andrea</creatorcontrib><creatorcontrib>Mueller, Robert</creatorcontrib><creatorcontrib>Schwarb, Edward</creatorcontrib><creatorcontrib>Chipperfield, Mark</creatorcontrib><creatorcontrib>Huwyler, Joerg</creatorcontrib><creatorcontrib>Mahler, Hanns-Christian</creatorcontrib><creatorcontrib>Fischer, Stefan</creatorcontrib><title>Measuring Tissue Back-Pressure - In Vivo Injection Forces During Subcutaneous Injection</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Purpose Limited information is available on injection forces of parenterals representing the in vivo situation. Scope of the present study was to investigate the contribution of the subcutaneous (sc) tissue layer to injection forces during in vivo injection. Methods Göttingen minipigs received injections of isotonic dextran solutions (1–100 mPas) into the plica inguinalis using different injection rates and volumes (0.025–0.2 mL/s and 2.5 vs. 4.5 mL). Results The contribution of the sc back-pressure to injection forces was found to increase linearly with viscosity and injection rate ranging from 0.6 ± 0.5 N to 1.0 ± 0.4 N (1 mPas), 0.7 ± 0.2 N to 2.4 ± 1.9 N (10 mPas), and 1.8 ± 0.6 N to 4.7 ± 3.3 N (20 mPas) for injection rates of 0.025 to 0.2 mL/s, respectively. Variability increased with viscosity and injection rate. Values are average values from 10 randomized injections. A maximum of 12.9 N was reached for 20 mPas at 0.2 mL/s; 6.9 ± 0.3 N was determined for 100 mPas at 0.025 mL/s. No difference was found between injection volumes of 2.5 and 4.5 mL. 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Scope of the present study was to investigate the contribution of the subcutaneous (sc) tissue layer to injection forces during in vivo injection. Methods Göttingen minipigs received injections of isotonic dextran solutions (1–100 mPas) into the plica inguinalis using different injection rates and volumes (0.025–0.2 mL/s and 2.5 vs. 4.5 mL). Results The contribution of the sc back-pressure to injection forces was found to increase linearly with viscosity and injection rate ranging from 0.6 ± 0.5 N to 1.0 ± 0.4 N (1 mPas), 0.7 ± 0.2 N to 2.4 ± 1.9 N (10 mPas), and 1.8 ± 0.6 N to 4.7 ± 3.3 N (20 mPas) for injection rates of 0.025 to 0.2 mL/s, respectively. Variability increased with viscosity and injection rate. Values are average values from 10 randomized injections. A maximum of 12.9 N was reached for 20 mPas at 0.2 mL/s; 6.9 ± 0.3 N was determined for 100 mPas at 0.025 mL/s. No difference was found between injection volumes of 2.5 and 4.5 mL. The contribution of the tissue was differentiated from the contribution of the injection device and a local temperature effect. This effect was leading to warming of the (equilibrated) sample in the needle, therefore smaller injection forces than expected compensating tissue resistance to some parts. Conclusions When estimating injection forces representative for the in vivo situation, the contribution of the tissue has to be considered as well as local warming of the sample in the needle during injection.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>25537343</pmid><doi>10.1007/s11095-014-1611-0</doi><tpages>12</tpages></addata></record>
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subjects Animals
Biochemistry
Biomechanical Phenomena - physiology
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Dextrans - administration & dosage
Dextrans - pharmacokinetics
Drug Delivery Systems - instrumentation
Equipment Design
Hogs
Injections
Injections, Subcutaneous
Male
Medical Law
Pharmaceutical sciences
Pharmacology/Toxicology
Pharmacy
Pressure
Research Paper
Rheology
Skin - metabolism
Swine
Swine, Miniature
Tissue Distribution
Viscosity
title Measuring Tissue Back-Pressure - In Vivo Injection Forces During Subcutaneous Injection
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