How a Drug's Charge Alters Its Path Under the Skin express

Original: "Effect of Electric Charge on Biotherapeutic Transport, Binding and Absorption: A Computational Study"
arXiv:2601.00505 · 2026-01-01 · CC BY 4.0 · 1 min
The electric charge of antibodies influences how deep and how fast a drug spreads after an injection.

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After an injection under the skin, a drug doesn't just spread out like ink in water. Antibody molecules carry an electric charge, and that charge makes them interact with surrounding tissues — much like a magnet attracts or repels iron filings. Some antibodies are positively charged, others negatively, and this determines how quickly they reach blood vessels and start working.

The authors built a mathematical model that, for the first time, combines fluid movement in porous tissue with electric forces between charged particles. They tested the model on two types of antibodies with different charges and compared the calculations with real data from lab experiments. It turned out that charge affects not only speed but also penetration depth: some antibodies linger near the injection site, while others travel deeper into the tissue.

An antibody's charge can be adjusted by tweaking the solution's acidity. It's like tuning the strength of a magnet to guide the drug where you want it to go.

The model also accounts for other factors: solution acidity, patient weight, needle depth, and drug concentration. Together, these determine what fraction of the drug reaches the bloodstream and how quickly. For doctors and pharmacists, this offers a way to predict in advance how much of a drug will reach its target without extra human trials.

This approach is akin to tuning a musical instrument: change one parameter, and the whole 'sound' of the treatment shifts. Antibody charge turns out to be one of those strings that was rarely touched before.

Original abstract

as written by the authors arXiv:2601.00505

This study explores the effects of electric charge on the dynamics of drug transport and absorption in subcutaneous injections of monoclonal antibodies (mAbs). We develop a novel mathematical and computational model, based on the Nernst-Planck equations and porous media flow theory, to investigate the complex interactions between mAbs and charged species in subcutaneous tissue. The model enables us to study short-term transport dynamics and long-term binding and absorption for two mAbs with different electric properties. We examine the influence of buffer pH, body mass index, injection depth, and formulation concentration on drug distribution and compare our numerical results with experimental data from the literature.

Monoclonal antibodies are proteins that the immune system naturally produces to fight specific targets; in medicine, they are created in the lab and used against cancer, autoimmune diseases, and infections.

Concepts
charge transfer drug delivery light absorption electron charge electrolyte transport energy transfer atp current molecular interaction coulomb chemotherapy picocoulomb millivolt per meter microelectrode array capacity voltage charged particles faraday constant microorganism swimming dynamics metabolism