Pharmacokinetic Properties of Fast-acting Insulin Aspart Administered in Different Subcutaneous Injection Regions: Response to the commentary by Nuggehally R. Srinivas
[...]there have been some discussions about the validity of pharmacodynamic results with the euglycemic glucose clamp technique in healthy people, mostly related, however, to the assessment of duration of action and late metabolic activity of basal insulins [2, 3]. Because of the high metabolic acti...
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Veröffentlicht in: | Clinical drug investigation 2017-09, Vol.37 (9), p.885-887 |
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description | [...]there have been some discussions about the validity of pharmacodynamic results with the euglycemic glucose clamp technique in healthy people, mostly related, however, to the assessment of duration of action and late metabolic activity of basal insulins [2, 3]. Because of the high metabolic activity of prandial insulins, endogenous insulin in healthy people is largely suppressed under glucose clamp conditions and should not contribute significantly to the observed pharmacodynamic effects. While the differences between injection sites did not reach statistical significance in the study by Sfisstrunk et al. (which is hardly surprising considering a sample size of n = 4), the tendency to a delayed and lower absorption was consistent across the two studies. [9] that Dr. Srinivas referred to, but also in other investigations [10, 11]. [...]a slower and impaired absorption from the thigh has been reported for other injectable drugs such as growth hormone [12] or exenatide [13]. Insulin absorption from the abdomen and the thigh in healthy subjects during rest and exercise: blood glucose, plasma insulin, growth hormone, adrenaline and noradrenaline levels. |
doi_str_mv | 10.1007/s40261-017-0539-7 |
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While the differences between injection sites did not reach statistical significance in the study by Sfisstrunk et al. (which is hardly surprising considering a sample size of n = 4), the tendency to a delayed and lower absorption was consistent across the two studies. [9] that Dr. Srinivas referred to, but also in other investigations [10, 11]. [...]a slower and impaired absorption from the thigh has been reported for other injectable drugs such as growth hormone [12] or exenatide [13]. Insulin absorption from the abdomen and the thigh in healthy subjects during rest and exercise: blood glucose, plasma insulin, growth hormone, adrenaline and noradrenaline levels.</description><identifier>ISSN: 1173-2563</identifier><identifier>EISSN: 1179-1918</identifier><identifier>DOI: 10.1007/s40261-017-0539-7</identifier><identifier>PMID: 28597216</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Abdomen ; Blood Glucose ; Commentary ; Diabetes ; Glucose ; Humans ; Hypoglycemic Agents ; Injections, Subcutaneous ; Insulin ; Insulin Aspart ; Internal Medicine ; Medicine ; Medicine & Public Health ; Metabolism ; Pharmacokinetics ; Pharmacology/Toxicology ; Pharmacotherapy ; Studies</subject><ispartof>Clinical drug investigation, 2017-09, Vol.37 (9), p.885-887</ispartof><rights>Springer International Publishing Switzerland 2017</rights><rights>Copyright Springer Science & Business Media Sep 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c324t-1187c8f9ba48af84cfcf62ef6a30a00f5390255823f6439bf1406d4b5396da823</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/s40261-017-0539-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40261-017-0539-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28597216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heise, Tim</creatorcontrib><creatorcontrib>Hövelmann, Ulrike</creatorcontrib><creatorcontrib>Nosek, Leszek</creatorcontrib><creatorcontrib>Sassenfeld, Bettina</creatorcontrib><creatorcontrib>Thomsen, Karen Margrete Due</creatorcontrib><creatorcontrib>Haahr, Hanne</creatorcontrib><title>Pharmacokinetic Properties of Fast-acting Insulin Aspart Administered in Different Subcutaneous Injection Regions: Response to the commentary by Nuggehally R. Srinivas</title><title>Clinical drug investigation</title><addtitle>Clin Drug Investig</addtitle><addtitle>Clin Drug Investig</addtitle><description>[...]there have been some discussions about the validity of pharmacodynamic results with the euglycemic glucose clamp technique in healthy people, mostly related, however, to the assessment of duration of action and late metabolic activity of basal insulins [2, 3]. Because of the high metabolic activity of prandial insulins, endogenous insulin in healthy people is largely suppressed under glucose clamp conditions and should not contribute significantly to the observed pharmacodynamic effects. While the differences between injection sites did not reach statistical significance in the study by Sfisstrunk et al. (which is hardly surprising considering a sample size of n = 4), the tendency to a delayed and lower absorption was consistent across the two studies. [9] that Dr. Srinivas referred to, but also in other investigations [10, 11]. [...]a slower and impaired absorption from the thigh has been reported for other injectable drugs such as growth hormone [12] or exenatide [13]. Insulin absorption from the abdomen and the thigh in healthy subjects during rest and exercise: blood glucose, plasma insulin, growth hormone, adrenaline and noradrenaline levels.</description><subject>Abdomen</subject><subject>Blood Glucose</subject><subject>Commentary</subject><subject>Diabetes</subject><subject>Glucose</subject><subject>Humans</subject><subject>Hypoglycemic Agents</subject><subject>Injections, Subcutaneous</subject><subject>Insulin</subject><subject>Insulin Aspart</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolism</subject><subject>Pharmacokinetics</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacotherapy</subject><subject>Studies</subject><issn>1173-2563</issn><issn>1179-1918</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kc1u1TAQhSMEoqXwAGyQJTZsUvyT2Am7q9LSShWtWlhbjmPn-pLYwXaQ7hP1NZmSFiGkruZo_J0Z26co3hJ8TDAWH1OFKSclJqLENWtL8aw4JES0JWlJ8_yPZiWtOTsoXqW0w5hwwunL4oA2dSso4YfF3fVWxUnp8MN5k51G1zHMJmZnEgoWnamUS6Wz8wO68GkZnUebNKuY0aafnHcpm2h6BO3PzlrQPqPbpdNLVt6EJYFrZ8AfPLoxA5T0CUSaQRiUA8pbg3SYJvCpuEfdHn1dhsFs1Tju0c0xuo2w5JdKr4sXVo3JvHmoR8X3s9NvJ-fl5dWXi5PNZakZrXJJSCN0Y9tOVY2yTaWttpwayxXDCmMLv4RpXTeUWV6xtrOkwryvOujzXkH7qPiwzp1j-LmYlOXkkjbjuD5HkhY3FatFwwB9_x-6C0v0cDugBGO4JawGiqyUjiGlaKyco5vgrZJgeZ-iXFOUkKK8T1EK8Lx7mLx0k-n_Oh5jA4CuQIIjP5j4z-onp_4GYQWqAQ</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Heise, Tim</creator><creator>Hövelmann, Ulrike</creator><creator>Nosek, Leszek</creator><creator>Sassenfeld, Bettina</creator><creator>Thomsen, Karen Margrete Due</creator><creator>Haahr, Hanne</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20170901</creationdate><title>Pharmacokinetic Properties of Fast-acting Insulin Aspart Administered in Different Subcutaneous Injection Regions: Response to the commentary by Nuggehally R. 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subjects | Abdomen Blood Glucose Commentary Diabetes Glucose Humans Hypoglycemic Agents Injections, Subcutaneous Insulin Insulin Aspart Internal Medicine Medicine Medicine & Public Health Metabolism Pharmacokinetics Pharmacology/Toxicology Pharmacotherapy Studies |
title | Pharmacokinetic Properties of Fast-acting Insulin Aspart Administered in Different Subcutaneous Injection Regions: Response to the commentary by Nuggehally R. Srinivas |
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