Nanotechnology boosts cancer drug potency 20,000-fold, eliminating side effects: Recent research shows

5-Fu is traditionally limited by poor solubility and low cellular uptake, resulting in suboptimal cancer cell targeting and significant toxicity to healthy cells. To overcome these challenges, Professor Chad A. Mirkin’s team synthesized spherical nucleic acid (SNA) nanostructures by integrating chemotherapy molecules directly into the DNA strands coating tiny spherical nanoparticles. These SNAs exploit natural scavenger receptors, particularly abundant on myeloid leukemia cells, to enable highly selective and efficient drug internalization.

The researchers employed sophisticated chemical synthesis to attach 5-Fu molecules to oligonucleotides, which were then assembled onto phospholipid core liposomes, forming the SNA architecture. The new formulation was rigorously tested in animal models of acute myeloid leukemia (AML), a rapidly progressing and difficult-to-treat blood cancer.

Remarkably, SNA-5-Fu entered leukemia cells 12.5 times more efficiently than conventional 5-Fu, exhibited up to 20,000-fold greater cytotoxicity, and slowed cancer advancement by a factor of 59. Importantly, this potent therapeutic effect occurred with no detectable damage to healthy tissues or overt side effects, a significant improvement over standard chemotherapy’s harsh profile.

Professor Mirkin described the breakthrough as a potential paradigm shift that transforms weak, toxic chemotherapy agents into precision nanomedicines with improved outcomes. With multiple SNA drugs already in clinical trials, this pioneering approach may soon extend beyond cancer to tackle infections, neurodegenerative diseases, and autoimmune disorders—ushering in a safer, more effective era of drug design and delivery.

REFERENCE: Taokun Luo, Young Jun Kim, Zhenyu Han, Jeongmin Hwang, Sneha Kumari, Vinzenz Mayer, Alex Cushing, Roger A. Romero, Chad A. Mirkin. Chemotherapeutic Spherical Nucleic Acids. ACS Nano, 2025; DOI: 10.1021/acsnano.5c16609