EMBARGOED FOR RELEASE: Tuesday, March 18, 2014, 11 a.m. Eastern Time Note to journalists: Please report that this research was presented at a meeting of the American Chemical Society.
Newswise — DALLAS, March 18, 2014 — As some countries and companies roll out new rules to limit animal testing in pharmaceutical products designed for people, scientists are stepping in with a new way to test therapeutic drug candidates and determine drug safety and drug interactions — without using animals. The development of “chemosynthetic livers,” which could dramatically alter how drugs are made, was presented at the 247th National Meeting & Exposition of the American Chemical Society (ACS), the world’s largest scientific society.
The meeting features more than 10,000 presentations on a wide range of science topics and is being held here through Thursday.
Mukund Chorghade, Ph.D., noted that the European Union enacted new regulations in 2010, known as REACH, that aim to dramatically reduce the use of animals in testing. But the development of new pharmaceuticals still depends heavily on the time-consuming and expensive process of animal testing.
“Researchers in drug discovery make small quantities of new potential drug compounds and then test them in animals,” said Chorghade, who is chief scientific officer of Empiriko Corporation and president of THINQ Pharma. “It is a very painstaking, laborious and costly process. Frequently, scientists have to sacrifice many animals, and even after all that, the results are not optimal.”
Typically, when researchers are onto a new compound that could address an unmet human health need, they test it on animals to see if it’s toxic before taking it into clinical trials with human subjects. They figure this out by doing something called metabolic profiling. That is, after giving an animal a test drug, the experimental compound does its designated job in the body until the liver breaks it down. Then researchers try to detect the resulting, minute amounts of molecular byproducts, or metabolites. It’s these metabolites that are often responsible for causing nasty side effects that can derail an otherwise promising therapeutic candidate.
This is where Empiriko’s patented chemosynthetic liver technology (Biomimiks™) comes in. Chorghade has developed these stand-ins, which are catalysts that act similarly to a group of enzymes known as cytochrome P450. Catalysts are substances that speed up processes that otherwise wouldn’t happen or would occur slowly. Many of these cytochrome P450 enzymes break down drugs in the liver.
So rather than using lab animals, researchers could figure out metabolic profiles of drugs by mixing them in test tubes with chemosynthetic livers. Chorghade’s team at Empiriko has already demonstrated how Biomimiks™ works with several pharmaceutical compounds.
“These chemosynthetic livers not only produce the same metabolites as live animals in a fraction of the time,” Chorghade said, “but they also provide a more comprehensive metabolic profile, in far larger quantities for further testing and analysis.”
Other possible applications are cropping up for these chemosynthetic livers. One of Empiriko’s scientific advisors suggested the use of Biomimiks™ to detoxify blood for liver transplant patients. Biomimiks™ could also be used in the near future to predict side effects when multiple drugs are taken together.
“The average American above 60 years of age is taking multiple drugs a day,” Chorghade explained. “Side effects from drug-to-drug interactions could be substantial.” In a case study, Chorghade and collaborators looked at two drugs commonly taken together, one for high cholesterol and the other for type 2 diabetes. They found that the cholesterol drug sped up the breakdown of the other one, which could potentially lower its effectiveness.
The chemosynthetic livers aren’t yet approved to take the place of animal tests. But Chorghade is optimistic. His group has tested more than 50 drugs so far to show that the catalysts accurately mimic how the human body processes them. He said that they’re working to get that number up to 100, which is what the U.S. Food and Drug Administration requires for regulatory approval.
Chorghade acknowledges funding from a private investor responsible for supporting this technology to date.
The American Chemical Society is a nonprofit organization chartered by the U.S. Congress. With more than 161,000 members, ACS is the world’s largest scientific society and a global leader in providing access to chemistry-related research through its multiple databases, peer-reviewed journals and scientific conferences. Its main offices are in Washington, D.C., and Columbus, Ohio.
A press conference on this topic will be held Tuesday, March 18, at 11:30 a.m. Central time in Room A122/A123 of the Dallas Convention Center. Reporters can attend in person or access live video of the event and ask questions at the ACS Ustream channel http://www.ustream.tv/channel/acslive.
Title Chemosynthetic livers: A new paradigm for drug discovery
Abstract Several problems are associated with use of biological systems in studying drug metabolism. • In vitro studies produce small quantities of primary metabolites that are hydrophilic and difficult to isolate. • Animals studies necessitate sacrifice of animals and are expensive. Liver slice preparations of variable potency make it difficult to quantitate oxidant stoichiometry. • Many metabolites are not amenable to synthesis by conventional routes. We present examples of porphyrin-mediated oxidations of sophisticated pharmaceutical entities. The reactions are generally applicable and have been used on numerous substrates. This is an efficient method for the systematic identification of the entire spectrum of metabolites. Our proprietary in vitro chemical technology (“synthetic livers”) allows us to mimic the in vivo metabolism of chemical entities used in pharmaceuticals, cosmetics, polymers, agricultural and synthetic dyes. Biomimiks™ enables prediction of metabolism patterns, pathways and profiles and introduces a new paradigm for drug discovery and mimicking drug-drug interactions for clinical diagnostics.