Modification of Branched Poly(ethylene imine) with d‐Fructose for Selective Delivery of siRNA into Human Breast Cancer Cells

Abstract

AbstractBranched poly(ethylene imine) (bPEI) is frequently used in RNA interference (RNAi) experiments as a cationic polymer for the delivery of small interfering RNA (siRNA) because of its ability to form stable polyplexes that facilitate siRNA uptake. However, the use of bPEI in gene delivery is limited by its cytotoxicity and a need for target specificity. In this work, bPEI is modified with d‐fructose to improve biocompatibility and target breast cancer cells through the overexpressed GLUT5 transporter. Fructose‐substituted bPEI (Fru−bPEI) is accessible in three steps starting from commercially available protected fructopyranosides and bPEI. Several polymers with varying molecular weights, degrees of substitution, and linker positions on d‐fructose (C1 and C3) are synthesized and characterized with NMR spectroscopy, size exclusion chromatography, and elemental analysis. In vitro biological screenings show significantly reduced cytotoxicity of 10 kDa bPEI after fructose functionalization, specific uptake of siRNA polyplexes, and targeted knockdown of green fluorescent protein (GFP) in triple‐negative breast cancer cells (MDA‐MB‐231) compared to noncancer cells (HEK293T).