Drug delivery to the brain using scorpion venom
Posted: 16 November 2018 | European Pharmaceutical Review | 1 comment
IRB researchers have developed a method to use a peptide found in chlorotoxin identified in scorpion venom to deliver drugs through the blood-brain barrier…
The Peptides and Proteins lab at the Institute for Research in Biomedicine (IRB Barcelona) has described the capacity of a small protein (a peptide) derived from chlorotoxin, found in scorpion venom (Giant Yellow Israeli scorpion), to deliver drugs across the blood-brain barrier (BBB).
The barrier serves to protect the brain from toxic substances, but it also prevents many potential drugs for the treatment of neurological diseases and tumours from entering this organ.
“About 98 percent of drugs that could have therapeutic applications cannot be used because they cannot cross this barrier,” explained the head of the lab, Professor Ernest Giralt.
The researchers chemically synthesised chlorotoxin and a series of analogues that retain some of the properties of the parent peptide. They studied the efficiency of these compounds in cell models of the BBB and have demonstrated that the peptide called MiniCTX3 has the capacity to transport compounds of different nature across the BBB “with great efficiency”.
In the same way that traditional medicine uses natural products such as plants and flowers to treat a range of diseases, the IRB Barcelona lab has sought inspiration from venoms with the objective of identifying peptide shuttles.
“Our goal is to enable drugs to enter the brain and to do this we bind them to peptides specifically designed to cross the BBB. The conjugation of these drugs to the shuttles would improve their efficacy,” said Dr Meritxell Teixidó, co-leader of the research.
“There are only two or three groups worldwide devoted to shuttle peptides. We are working on a number of strategies and one of them is venoms,” said Prof Giralt.
In previous studies, these scientists inspired from a peptide from bee venom, namely apamin, had made some chemical modifications and obtained a shuttle with BBB permeability.
After these positive results, the lab wanted to address whether venoms could provide a universal source of peptide shuttles.
“Thousands of venoms that hold millions of peptides with the shuttle potential have been described. We chose chlorotoxin because it has already been reported that it acts like a toxin in the brain,” explained Dr Teixidó.
This study has produced another shuttle that can enhance drug transport into the brain.
The paper was published in Chemical Communications.
Related topics
Drug Delivery Systems, Drug Development, Research & Development (R&D), Therapeutics
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