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Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers
AIM: Cabotegravir long‐acting (LA) intramuscular (IM) injection is being investigated for HIV preexposure prophylaxis due to its potent antiretroviral activity and infrequent dosing requirement. A subset of healthy adult volunteers participating in a Phase I study assessing cabotegravir tissue pharm...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290983/ https://www.ncbi.nlm.nih.gov/pubmed/34240449 http://dx.doi.org/10.1111/bcp.14977 |
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author | Jucker, Beat M. Fuchs, Edward J. Lee, Sarah Damian, Valeriu Galette, Paul Janiczek, Robert Macura, Katarzyna J. Jacobs, Michael A. Weld, Ethel D. Solaiyappan, Meiyappan D'Amico, Ronald Shaik, Jafar Sadik Bakshi, Kalpana Han, Kelong Ford, Susan Margolis, David Spreen, William Gupta, Manish K. Hendrix, Craig W. Patel, Parul |
author_facet | Jucker, Beat M. Fuchs, Edward J. Lee, Sarah Damian, Valeriu Galette, Paul Janiczek, Robert Macura, Katarzyna J. Jacobs, Michael A. Weld, Ethel D. Solaiyappan, Meiyappan D'Amico, Ronald Shaik, Jafar Sadik Bakshi, Kalpana Han, Kelong Ford, Susan Margolis, David Spreen, William Gupta, Manish K. Hendrix, Craig W. Patel, Parul |
author_sort | Jucker, Beat M. |
collection | PubMed |
description | AIM: Cabotegravir long‐acting (LA) intramuscular (IM) injection is being investigated for HIV preexposure prophylaxis due to its potent antiretroviral activity and infrequent dosing requirement. A subset of healthy adult volunteers participating in a Phase I study assessing cabotegravir tissue pharmacokinetics underwent serial magnetic resonance imaging (MRI) to assess drug depot localization and kinetics following a single cabotegravir LA IM targeted injection. METHODS: Eight participants (four men, four women) were administered cabotegravir LA 600 mg under ultrasonographic‐guided injection targeting the gluteal muscles. MRI was performed to determine injection‐site location in gluteal muscle (IM), subcutaneous (SC) adipose tissue and combined IM/SC compartments, and to quantify drug depot characteristics, including volume and surface area, on Days 1 (≤2 hours postinjection), 3 and 8. Linear regression analysis examined correlations between MRI‐derived parameters and plasma cabotegravir exposure metrics, including maximum observed concentration (C (max)) and partial area under the concentration–time curve (AUC) through Weeks 4 and 8. RESULTS: Cabotegravir LA depot locations varied by participant and were identified in the IM compartment (n = 2), combined IM/SC compartments (n = 4), SC compartment (n = 1) and retroperitoneal cavity (n = 1). Although several MRI parameter and exposure metric correlations were determined, total depot surface area on Day 1 strongly correlated with plasma cabotegravir concentration at Days 3 and 8, C (max) and partial AUC through Weeks 4 and 8. CONCLUSION: MRI clearly delineated cabotegravir LA injection‐site location and depot kinetics in healthy adults. Although injection‐site variability was observed, drug depot surface area correlated with both plasma C (max) and partial AUC independently of anatomical distribution. |
format | Online Article Text |
id | pubmed-9290983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92909832022-07-20 Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers Jucker, Beat M. Fuchs, Edward J. Lee, Sarah Damian, Valeriu Galette, Paul Janiczek, Robert Macura, Katarzyna J. Jacobs, Michael A. Weld, Ethel D. Solaiyappan, Meiyappan D'Amico, Ronald Shaik, Jafar Sadik Bakshi, Kalpana Han, Kelong Ford, Susan Margolis, David Spreen, William Gupta, Manish K. Hendrix, Craig W. Patel, Parul Br J Clin Pharmacol Original Articles AIM: Cabotegravir long‐acting (LA) intramuscular (IM) injection is being investigated for HIV preexposure prophylaxis due to its potent antiretroviral activity and infrequent dosing requirement. A subset of healthy adult volunteers participating in a Phase I study assessing cabotegravir tissue pharmacokinetics underwent serial magnetic resonance imaging (MRI) to assess drug depot localization and kinetics following a single cabotegravir LA IM targeted injection. METHODS: Eight participants (four men, four women) were administered cabotegravir LA 600 mg under ultrasonographic‐guided injection targeting the gluteal muscles. MRI was performed to determine injection‐site location in gluteal muscle (IM), subcutaneous (SC) adipose tissue and combined IM/SC compartments, and to quantify drug depot characteristics, including volume and surface area, on Days 1 (≤2 hours postinjection), 3 and 8. Linear regression analysis examined correlations between MRI‐derived parameters and plasma cabotegravir exposure metrics, including maximum observed concentration (C (max)) and partial area under the concentration–time curve (AUC) through Weeks 4 and 8. RESULTS: Cabotegravir LA depot locations varied by participant and were identified in the IM compartment (n = 2), combined IM/SC compartments (n = 4), SC compartment (n = 1) and retroperitoneal cavity (n = 1). Although several MRI parameter and exposure metric correlations were determined, total depot surface area on Day 1 strongly correlated with plasma cabotegravir concentration at Days 3 and 8, C (max) and partial AUC through Weeks 4 and 8. CONCLUSION: MRI clearly delineated cabotegravir LA injection‐site location and depot kinetics in healthy adults. Although injection‐site variability was observed, drug depot surface area correlated with both plasma C (max) and partial AUC independently of anatomical distribution. John Wiley and Sons Inc. 2021-07-31 2022-04 /pmc/articles/PMC9290983/ /pubmed/34240449 http://dx.doi.org/10.1111/bcp.14977 Text en © 2021 ViiV Healthcare. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Jucker, Beat M. Fuchs, Edward J. Lee, Sarah Damian, Valeriu Galette, Paul Janiczek, Robert Macura, Katarzyna J. Jacobs, Michael A. Weld, Ethel D. Solaiyappan, Meiyappan D'Amico, Ronald Shaik, Jafar Sadik Bakshi, Kalpana Han, Kelong Ford, Susan Margolis, David Spreen, William Gupta, Manish K. Hendrix, Craig W. Patel, Parul Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title | Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title_full | Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title_fullStr | Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title_full_unstemmed | Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title_short | Multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
title_sort | multiparametric magnetic resonance imaging to characterize cabotegravir long‐acting formulation depot kinetics in healthy adult volunteers |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290983/ https://www.ncbi.nlm.nih.gov/pubmed/34240449 http://dx.doi.org/10.1111/bcp.14977 |
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