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Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery

Due to a lack of safe and effective oral delivery strategies for most protein and peptide therapeutics, pharmaceutical drug developers have focused on parenteral routes to administer these agents. Recent advances in delivery technologies have now shown clinical validation for a few of these biopharm...

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Detalles Bibliográficos
Autores principales: Mrsny, Randall J., Mahmood, Tahir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309183/
https://www.ncbi.nlm.nih.gov/pubmed/34371698
http://dx.doi.org/10.3390/pharmaceutics13071006
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author Mrsny, Randall J.
Mahmood, Tahir A.
author_facet Mrsny, Randall J.
Mahmood, Tahir A.
author_sort Mrsny, Randall J.
collection PubMed
description Due to a lack of safe and effective oral delivery strategies for most protein and peptide therapeutics, pharmaceutical drug developers have focused on parenteral routes to administer these agents. Recent advances in delivery technologies have now shown clinical validation for a few of these biopharmaceuticals following oral administration. While these initial opportunities have provided more than just a glimmer of hope within the industry, there are important aspects of oral biopharmaceutical delivery that do not completely align with pharmacokinetic (PK) parameters and pharmacodynamics (PD) outcomes that have been learned from parenteral administrations. This commentary examines some of these issues with the goal of presenting a rationale for re-assessing methods, models, and success criteria to better measure oral protein or peptide delivery outcomes related to PK/PD events.
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spelling pubmed-83091832021-07-25 Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery Mrsny, Randall J. Mahmood, Tahir A. Pharmaceutics Commentary Due to a lack of safe and effective oral delivery strategies for most protein and peptide therapeutics, pharmaceutical drug developers have focused on parenteral routes to administer these agents. Recent advances in delivery technologies have now shown clinical validation for a few of these biopharmaceuticals following oral administration. While these initial opportunities have provided more than just a glimmer of hope within the industry, there are important aspects of oral biopharmaceutical delivery that do not completely align with pharmacokinetic (PK) parameters and pharmacodynamics (PD) outcomes that have been learned from parenteral administrations. This commentary examines some of these issues with the goal of presenting a rationale for re-assessing methods, models, and success criteria to better measure oral protein or peptide delivery outcomes related to PK/PD events. MDPI 2021-07-02 /pmc/articles/PMC8309183/ /pubmed/34371698 http://dx.doi.org/10.3390/pharmaceutics13071006 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Commentary
Mrsny, Randall J.
Mahmood, Tahir A.
Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title_full Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title_fullStr Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title_full_unstemmed Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title_short Re-Assessing PK/PD Issues for Oral Protein and Peptide Delivery
title_sort re-assessing pk/pd issues for oral protein and peptide delivery
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309183/
https://www.ncbi.nlm.nih.gov/pubmed/34371698
http://dx.doi.org/10.3390/pharmaceutics13071006
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