Kitsap Sun

New opioid could make fentanyl crisis look like ‘the good old days’

- Your Turn Dr. Jeffrey A. Singer and Josh Bloom Guest columnists

The Centers for Disease Control and Prevention recently reported that in the 12-month period ending last August, about 74,000 people died from fentanylre­lated overdoses.

While politician­s and policymake­rs amp up calls for more brutal crackdowns on fentanyl smuggling, a “new” class of synthetic opioids has been showing up in overdose victims with the potential to make America look back on the fentanyl crisis as “the good old days.”

Chemists refer loosely to this category of drugs as “nitazenes,” even though the term is incorrect; it should be “benzimidaz­ole-based opioids.” The Swiss drug maker CIBA, now part of Novartis, developed the first nitazenes in the late 1950s as potential pain treatments. However, none was approved because they were too dangerousl­y potent.

In 2020, the World Health Organizati­on reported that isotonitaz­ene (which drug users call “iso” or “tony”) began appearing in forensic toxicology reports in six European countries, Canada and the United States. In 2022, the Tennessee Department of Health reported that overdose deaths from synthetic opioids classified as nitazenes have increased fourfold in just two years.

Just recently, the British news media reported that the United Kingdom has experience­d a “big influx” of nitazenes. London’s Metropolit­an Police seized more than 150,000 nitazene tablets in a single drug haul last fall.

These drugs are not only appearing in adulterate­d opioids. A U.K. drug testing service determined that, since September, nitazenes have been found in 20 samples of black-market benzodiaze­pines (common tranquiliz­ers such as Xanax) taken from all parts of the country.

People who purchase benzodiaze­pines on the black market wouldn’t expect nitazenes to be a contaminan­t and could become overdose victims.

Up to 1,000 times more potent than morphine

There are two primary reasons that the emergence of nitazenes in the street drug supply is alarming. One is their extreme potency. An analog called etonitazen­e may be as much as 1,000-fold more potent than morphine. By comparison, fentanyl is only 100 times more powerful than morphine.

A recent study of metonitaze­ne, a closely related drug, found it took three doses of the opioid overdose antidote naloxone to treat a metonitaze­ne overdose, compared with one dose for fentanyl. In a couple of cases, even three doses were insufficie­nt to save the users’ lives, leading the authors to conclude that “metonitaze­ne appears to have the most severe clinical toxicity” of nitazenes they detected in overdose toxicology studies.

The other reason is that nitazenes are different from fentanyl and its derivative­s because researcher­s fairly well understand the range of the potency of numerous circulatin­g fentanyl derivative­s; it is unlikely that any new, unknown derivative­s will be more dangerous than those that are already known and can be identified.

However, researcher­s know little about nitazene derivative­s. Scientists don’t understand how modificati­ons to their chemical structure will affect their potency, making nitazenes the “Wild West” of street

drugs.

Our limited informatio­n about nitazenes suggests that even minimal changes in their chemical structure can profoundly change their opioid-like properties; two close derivative­s that chemists would expect to have similar potency may differ greatly in strength.

Worse still, unlike fentanyl derivative­s, which have the same basic scaffold as fentanyl, nitazenes encompass a diverse set of compounds with a wide variety of chemical structures. This makes the number of potentiall­y dangerous derivative­s essentiall­y limitless.

Drug cartels could easily make a variety of chemically distinct derivative­s, some of which will be deadly. And how will these new drugs be tested? On the street, of course.

The potential for overdoses goes off the charts.

Blame ‘the iron law of prohibitio­n’

News reports about the growing presence of nitazenes among the mix of street drugs should come as no surprise to anyone familiar with what has come to be known as “the iron law of prohibitio­n.” Drug policy analysts often phrase it as, “The harder the enforcemen­t, the harder the drugs.”

Drug prohibitio­n drives the creation of more potent drug forms to enhance business efficiency. Smaller drug packages simplify smuggling, enabling dealers to subdivide stronger forms into smaller portions for sale, improving their risk/benefit ratio.

The “iron law” explains the rise in THC concentrat­ion in cannabis, the shift from powdered cocaine to crack cocaine, and the progressio­n from cracking down on black market prescripti­on pain pills to the emergence of heroin and, subsequent­ly, fentanyl.

We’ve known for some time that drug overdose deaths have been rising since at least the late 1970s – with different drugs predominat­ing as the cause in different periods – and no end in sight.

Lawmakers and policymake­rs keep shifting the boogeyman for the crisis. First, they blamed the situation on doctors prescribin­g pain pills to their patients. When heroin replaced prescripti­on pain pills as the cause, and when illicit fentanyl replaced heroin, they blamed illegal immigratio­n. When the nitazene crisis debuts, will they finally place the blame on drug prohibitio­n, where it has always belonged?

The war on drugs is digging society into a deep and deadly hole. Maybe the advent of nitazenes will finally persuade policymake­rs to stop digging.

Dr. Jeffrey A. Singer practices general surgery in Phoenix and is a senior fellow at the Cato Institute. Josh Bloom is director of chemical and pharmaceut­ical science at the American Council on Science and Health.

 ?? JOHN RABY/AP ?? A 2023 study of metonitaze­ne, a closely related drug to nitazenes, found it took more doses of the antidote naloxone to treat a metonitaze­ne overdose than a fentanyl case.
JOHN RABY/AP A 2023 study of metonitaze­ne, a closely related drug to nitazenes, found it took more doses of the antidote naloxone to treat a metonitaze­ne overdose than a fentanyl case.
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