New BioIVT Research on Botanical-Drug Interactions Published in Applied In Vitro Toxicology
Study compares two in vitro liver methods to determine which one best predicts BDIs
Westbury, NY – May 2, 2019 – BioIVT, a leading provider of research models and services for drug and diagnostic development, today announced that its ADME-Tox team has co-authored a second peer-reviewed paper investigating the potential for clinically-relevant botanical-drug interactions (BDIs) with toxicology colleagues at The Procter & Gamble Company (P&G).1 The paper describes a research collaboration by BioIVT and P&G based on studies conducted in BioIVT’s laboratory in Durham, NC.
This new study investigates potential BDIs with Boswellia serrata (Indian Frankincense), a botanical that is used as an anti-inflammatory supplement. The popularity of products containing B. serrata extract is growing. US retail sales of B. serrata reached $14.6 million in 20172 and it continues to move up the top 40 list of best-selling herbal supplements; it is currently ranked number 19.2
“As the use of botanicals, such as B. serrata, increases so does the need to investigate the potential for BDIs. This is especially true because the use of botanical supplements is highest amongst the elderly (those aged 65 years and older), who are more likely to have comorbidities and take multiple medications,”3-5 said Amy Roe, PhD, DABT, lead author and principal toxicologist at P&G. “Our primary goal with this study was to help determine the most reliable in vitro method for predicting BDIs.”
BioIVT and P&G’s study compared two in vitro methods – conventional pooled human liver microsomes and a whole cell model using TRANSPORTER CERTIFIED™ hepatocytes in sandwich culture – to evaluate the inhibitory effects of B. serrata on CYP enzymatic activity. It focused specifically on CYP2C9 and CYP3A4/5 as those enzymes had been shown in in vitro studies to be the most potently inhibited by B. serrata. CYP enzymes play an important role in drug metabolism, so inhibiting them can change the effectiveness and safety of some drugs. For example, CYP2C9 is the primary CYP isoform involved in the clearance of the nonsteroidal anti-inflammatory drug (NSAID), ibuprofen.6
While the microsomal liver method predicted potent CYP inhibition by B. serrata, the sandwich-cultured whole cell model predicted much less inhibition potential.
“Although we are not aware of any clinical studies investigating potential BDIs with B. serrata, the large volume of sales of this botanical, seemingly without adverse events, tends to suggest that the microsomal model may be overly conservative, potentially leading to false positives,” said Kenneth Brouwer, VP, ADME-Tox at BioIVT and a study co-author. “The microsomal studies may overestimate the interaction potential because they lack the full complement of metabolic enzyme and transporter functions. Therefore, we believe that the sandwich-cultured human hepatocytes model, which incorporates cellular uptake, efflux, metabolism, and regulatory function, serves as a more accurate predictor of in vivo effects. It can also be employed to investigate both potential drug-drug interactions and BDIs.”
Although the sandwich-cultured human hepatocyte data suggested that the risk of BDIs with B. serrata was generally low, the authors urged caution when combining it with drugs that have a narrow therapeutic window, such as warfarin, or drugs that are sensitive substrates for CYP2C9, such as the NSAID diclofenac.
The US Food and Drug Administration (FDA) is also focusing on botanicals and the potential risk for BDIs. In February 2019, FDA announced increased efforts to strengthen regulatory oversight of dietary supplements. Included in this initiative was the formation of the Botanical Safety Consortium, a public-private partnership that will investigate “novel ways to use cutting-edge toxicology tools, including alternatives to animal testing, to promote the goals of safety and effectiveness we share with consumers and other stakeholders.7”
BioIVT supports this initiative and is committed to developing products and methods that will help researchers predict potential risks and benefits of dietary supplements and enable consumers to make informed decisions about these products.
1. Amy L. Roe, Rachel Wilcox, Jason M. Price, Lijuan Li, Hong Dai, Kimberly M. Freeman, Weslyn W. Friley, Ashley G. Herman, Christopher B. Black, Kenneth R. Brouwer, and Jonathan P. Jackson. An Evaluation of Potential Inhibition of CYP3A4/5 and CYP2C9 Enzymatic Activity by Boswellia serrata Extract. Applied In Vitro Toxicology. Mar 2019. http://doi.org/10.1089/aivt.2018.0023.
2. Smith T, Kawa K, Eckl V, et al. Herbal supplement sales in US increase 8.5% in 2017, topping $8 billion. HerbalGram 2018:119;62–71. Google Scholar
3. National Center for Health Statistics. Health, United States, 2014: With Special Feature on Adults Aged 55–64. Hyattsville, MD: National Center for Health Statistics (US); 2015 Google Scholar
4. Council for Responsible Nutrition, CRN 2017. Annual survey on dietary supplements. Council for Responsible Nutrition, Washington, DC. www.crnusa.org/survey. Google Scholar
5. Agbabiaka T, Wider B, Waston L, et al. Concurrent use of prescription drugs and herbal medicinal products in older adults: a systemic review. Drug Aging 2017:34;891–905. Crossref, Medline, Google Scholar
6. Mazaleuskaya LL, Theken KN, Gong L, et al. PharmGKB summary: ibuprofen pathways. Pharmacogenet Genomics 2015:25;96–106. Crossref, Medline, Google Scholar
7. Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s new efforts to strengthen regulation of dietary supplements by modernizing and reforming FDA’s oversight. Feb.11, 2019. https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm631065.htm.
BioIVT, formerly BioreclamationIVT, is a leading global provider of research models and value-added research services for drug discovery and development. We specialize in control and disease-state biospecimens including human and animal tissues, cell products, blood, and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research and the effort to improve patient outcomes by coupling comprehensive clinical data with donor samples. Our PHASEZERO® Research Services team works collaboratively with clients to provide target and biomarker validation, phenotypic assays to characterize novel therapeutics, clinical assay development and in vitro hepatic modeling solutions. And as the premier supplier of hepatic products, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly-discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service, and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in elevating science. For more information, please visit www.bioivt.com or follow the company on Twitter @BioIVT.