Announcing a recent publication for Acta Materia Medica journal. The compound 7-ethyl-10-hydroxy-camptothecin (SN38) is a broad-spectrum antitumor agent whose applications are greatly limited by its poor solubility. Subsequently, irinotecan, the hydrophilic derived prodrug of SN38, has been developed because the business formulation Campto® for colorectal cancer.

Nonetheless, only one% to 0.1% of irinotecan is converted to energetic SN38 in vivo, thus resulting in unsatisfactory antitumor activity in clinical settings. The authors of this text report a sensible stimuli-responsive SN38 prodrug nanoassembly for efficient cancer therapy. First, SN38 was conjugated with an endogenous lipid, cholesterol (CST), via a redox dual-responsive disulfide bond (namely SN38-SS-CST). The prodrug self-assembled into uniform prodrug nanoassemblies with good colloidal stability and ultrahigh drug loading. SN38-SS-CST NPs released sufficient SN38 within the redox environments of tumor cells but remained intact in normal tissues.

Finally, SN38-SS-CST NPs potently inhibited the expansion of colon cancer without causing systemic toxicity, thus indicating their promise as a translational chemotherapeutic nanomedicine.