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Remote Drug Loading — Ammonium-Sulfate Liposome Gradient (2D)

A 2D cross-section model of remote (active) liposomal drug loading: a real Henderson-Hasselbalch membrane-flux equation and single-exponential internal-pH curve drive a draggable, zoomable particle field showing a weakly-basic drug crossing the bilayer and getting trapped as the interior acidifies.

Nanomedicine & Drug Delivery Materials2DAdvanced60 FPS📱 Mobile-adapted⇄ 3D version
2d-nanotech-topic-105 ↗ Open standalone

This 2D cross-section simulator draws a single liposome as a disk: a lipid-bilayer ring 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 at the centre. Adjust the ammonium load, drug dose and temperature and watch the loading-efficiency readout plateau exactly where the chemistry says it should — the same remote-loading mechanism used to manufacture liposomal doxorubicin and similar clinical nanomedicines, here rendered as a pannable, zoomable flat diagram instead of a 3D scene.

⚙ Under the hood

A 2D cross-section model of remote (active) liposomal drug loading: a real Henderson-Hasselbalch membrane-flux equation and single-exponential internal-pH curve drive a draggable, zoomable particle field showing a weakly-basic drug crossing the bilayer and getting trapped as the interior acidifies.

nanomedicineliposomedrug deliverypH gradientpharmacokineticsnanotechnology

2D · HTML5 Canvas 2D · 60 FPS target · runs fully client-side, no install

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