重口味SM

Researchers develop new method for delivering RNA and drugs into cells

"This could be a game-changer for treating complex conditions where targeting multiple pathways is beneficial, such as cancer and viral infections"
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PhD candidate Kai Slaughter, left, and University Professor Molly Shoichet are exploring how ionizable drugs can be used to co-formulate small interfering RNA (siRNA) for more effective intracellular delivery (supplied images)

Researchers at the 重口味SM and its hospital partners have developed a method for co-delivering therapeutic RNA and potent drugs directly into cells, potentially leading to a more effective treatment of diseases.

The research, , explores how ionizable drugs can be used to co-formulate small interfering RNA (siRNA) for more effective intracellular delivery.

The team 鈥 including Molly Shoichet, the study鈥檚 corresponding author and a  in U of T鈥檚 department of chemical engineering and applied chemistry in the Faculty of Applied Science & Engineering 鈥 specifically targeted drug-resistant cells with the delivery of a relevant siRNA. The siRNA was discovered study co-author and collaborator David Cescon, a clinician scientist at the Princess Margaret Cancer Centre, University Health Network, and an associate professor in U of T鈥檚 Temerty Faculty of Medicine.

鈥淲e found that our co-formulation method not only potently delivered siRNA to cells but also simultaneously delivered active ionizable drugs,鈥 said research lead author Kai Slaughter, a PhD candidate in Shoichet鈥檚 lab.

鈥淭his could be a game-changer for treating complex conditions where targeting multiple pathways is beneficial, such as cancer and viral infections.鈥

siRNA is a powerful tool in medicine, capable of silencing specific genes responsible for disease, but delivering these molecules into cells without degradation remains a significant challenge. While recent innovations in ionizable lipid design have led to efficiency improvements, traditional nanoparticle formulations are limited in the amount of small molecule drugs they can carry.

When therapeutic formulations are absorbed by cells, small molecule drugs and siRNA are often trapped in small compartments called endosomes, preventing them from reaching their target destination and reducing their effectiveness.

The research team discovered that combining siRNA with ionizable drugs 鈥 compounds that change their charge based on pH levels 鈥 enhances the stability and delivery efficiency of siRNA inside cells, helping both the siRNA and drug escape the endosome and more effectively reach their destination. This novel method utilizes the protective properties of lipids to safeguard siRNA during its journey through the body and ensure the release of RNA and the drug together within the target cells.

鈥淥ne of the biggest hurdles in siRNA therapy has been getting these molecules to where they need to go without losing their potency,鈥 Shoichet says.

鈥淥ur approach using ionizable drugs as carriers marks a significant step forward in overcoming this barrier, while also showing how drugs and RNA can be delivered together in the same nanoparticle formulation.鈥

Donnelly