Lipid bilayer membrane Trapped drug core
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Remote Drug Loading — Ammonium-Sulfate Liposome Gradient

This simulator renders a single liposome in cutaway: a lipid-bilayer shell holding a concentrated ammonium-sulfate interior, bathed in an external buffer carrying a weakly basic drug. Neutral drug molecules diffuse across the membrane; as escaping NH₃ acidifies the interior, crossed molecules protonate and become trapped, building up as a dense core. Adjust the ammonium load, drug dose and temperature and watch the loading-efficiency curve plateau exactly where the chemistry says it should — this is the remote-loading mechanism used to manufacture liposomal doxorubicin and similar clinical nanomedicines.