Literature DB >> 32703874

The activities of drug inactive ingredients on biological targets.

Joshua Pottel1, Duncan Armstrong2, Ling Zou3, Alexander Fekete2, Xi-Ping Huang4, Hayarpi Torosyan1, Dallas Bednarczyk5, Steven Whitebread2, Barun Bhhatarai5, Guiqing Liang5, Hong Jin2, S Nassir Ghaemi6,7,8, Samuel Slocum4, Katalin V Lukacs9, John J Irwin1, Ellen L Berg10, Kathleen M Giacomini3, Bryan L Roth4, Brian K Shoichet11, Laszlo Urban12.   

Abstract

Excipients, considered "inactive ingredients," are a major component of formulated drugs and play key roles in their pharmacokinetics. Despite their pervasiveness, whether they are active on any targets has not been systematically explored. We computed the likelihood that approved excipients would bind to molecular targets. Testing in vitro revealed 25 excipient activities, ranging from low-nanomolar to high-micromolar concentration. Another 109 activities were identified by testing against clinical safety targets. In cellular models, five excipients had fingerprints predictive of system-level toxicity. Exposures of seven excipients were investigated, and in certain populations, two of these may reach levels of in vitro target potency, including brain and gut exposure of thimerosal and its major metabolite, which had dopamine D3 receptor dissociation constant K d values of 320 and 210 nM, respectively. Although most excipients deserve their status as inert, many approved excipients may directly modulate physiologically relevant targets.
Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2020        PMID: 32703874      PMCID: PMC7960226          DOI: 10.1126/science.aaz9906

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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