Drug overdoses in the United States have risen sharply over the past two decades. Nearly 92,000 people died from overdoses of illegal drugs and prescription opioids in 2020 –; more than five times the number of deaths in the year 2000 –; and synthetic opioids like fentanyl are a major culprit.
Naloxone (an injectable drug also marketed as Narcan nasal spray) has saved countless lives, but it only works for opioid overdoses and has other limitations. Now, in an effort to identify a more universal treatment for drug overdoses, a team of scientists from the University of Maryland have tested a chemical compound-;Pillar[6]MaxQ (P6AS)-; as an antidote to methamphetamine and fentanyl. Their findings, published today in the journal Chemistrywere very promising.
Opioids already have a reversing agent in naloxone, but there are a variety of non-opioid drugs of abuse; such as methamphetamine, PCP, mephedrone, ecstasy (MDMA) and cocaine; which have no specific antidote. This is one of the huge opportunities for our complex. »
Lyle Isaacs, Study Lead Author, Professor, Department of Chemistry and Biochemistry at UMD
In vitro et live lab tests have shown that P6AS successfully sequesters fentanyl and methamphetamine, a non-opioid stimulant, and attenuates their life-threatening biological effects. Additional in vitro tests have revealed that P6AS also binds strongly to other drugs, including PCP, ecstasy and mephedrone, suggesting that P6AS could one day be used to counter a wide range of drugs.
The study was conducted by Isaacs’ lab in collaboration with researchers from UMD’s Department of Cell Biology and Molecular Genetics and Department of Psychology. Although the synthesis and chemical properties of P6AS were first documented in 2020 by Isaacs and Weijian Xue, a former postdoc associated with the Department of Chemistry and Biochemistry, this study reports its first live applications.
P6AS functions as a molecular container, meaning it binds and sequesters other compounds in its central cavity.
“When we put molecules in our containers, we can turn off their biological properties and thus reverse any effects they might have,” Isaacs explained. “We measured the interaction between our container and a variety of drugs of abuse; things like meth, fentanyl, ecstasy, PCP and others; and we find that this new container that we have made binds many of them very strongly. »
I live tests revealed that the effects of methamphetamine could be reversed by administering P6AS five minutes later, which is “still a bit short for real-life situations,” Isaacs explained. The effects of fentanyl, however, could be reversed by administering P6AS up to 15 minutes later, which is closer to federal guidelines for drug reversal agents.
Unlike naloxone, which blocks a drug of abuse from binding to receptors in the brain, the UMD team’s molecular container targets drugs directly into the bloodstream.
“Our compound absorbs the drug into the bloodstream and we believe helps promote its excretion in the urine,” Isaacs said. “It’s called a pharmacokinetic process, where we try to minimize the concentration of free drug present in the body. »
Whether this compound helps promote the excretion of a drug from the body needs to be tested experimentally. If it works as the researchers believe, it could be particularly helpful for overdoses of fentanyl, which is up to 50 times stronger than heroin and up to 100 times stronger than morphine. Its potency and lingering effects in the body are why some patients continue to overdose even after receiving naloxone. Isaacs thinks excretion of fentanyl could help prevent this phenomenon, known as renarcotization.
Isaacs said it will likely be years before the new compound is approved for human use. However, he envisions it could be given as an injection, much like naloxone but potentially with wider applications. Isaacs thinks it could even be used to treat overdoses of extremely potent drugs like carfentanil, which has been linked to a string of overdose deaths in recent years.
“There are other synthetic opioids that are much stronger than fentanyl; things like carfentanil, which are hard to reverse with naloxone,” Isaacs said. “Additionally, people are getting so much fentanyl that multiple doses of naloxone are needed, so there is room for a new, improved agent that could help in these situations. »
In addition to Isaacs and Xue, co-authors of this UMD study included Assistant Research Professor of Psychology Adam Brockett and Professor Matthew Roesch, Professor of Cell Biology and Molecular Genetics Volker Briken, and Research Scientist deputy Shivangi Rastogi, former postdoctoral fellows in chemistry and biochemistry Chun-Lin Deng and Canjia Zhai, Ph.D. in biological sciences. student Michael Shuster and doctorate in chemistry. student David King.