Daily Times

In the United State, all drugs approved by the Food and Drug Administration (FDA) have to be tested for bacterial contaminants. Endotoxin is a common bacterial contaminant in drugs which might lead to toxic shock or life-threatening fever if it is injected into our body.

Fortunately for horseshoe crabs, this practice may be dying out. Researchers discovered that a molecule in LAL called factor C was responsible for its clotting action. Researchers genetically modified the guts of insects—who belong to the same phylum as horseshoe crabs, Arthropoda—to produce factor C. As a result, the insects began pumping out factor C, which could then be sold as recombinant factor C (rFC) on the market as a viable substitute to horseshoe crab blood.

Though rFC has been on the market since 2003, it’s been slow to gain traction. Initially, it was only being produced by one manufacturer, the Lonza Group. Pharmaceutical companies are wary to rely on a single manufacturer in case an emergency occurs, and their supply is cut off. The Food and Drug Administration’s (FDA’s) regulatory process was quite slow as well. But these obstacles are gradually being overcome. Hyglos GmbH, another pharmaceutical manufacturer, began producing rFC in 2013. European regulatory bodies have approved its use, which lays the groundwork for future approval by the FDA. Major pharmaceutical companies who have used rFC have confirmed that it works just as well as LAL. Today, experts believe that rFC will become the dominant method of detecting endotoxins, letting horseshoe crabs off the hook.