P-glycoprotein inhibitors: synthesis and in vitro evaluation of a preactivated thiomer

Abstract

The aim of this study was to synthesize the preactivated thiomer poly(acrylic acid)-cyteine-2-mercaptonicotinic acid (PAA-Cys-2MNA) and to evaluate its P-glycoprotein (P-gp) inhibitory properties. The thiomer (PAA-Cys) was synthesized by covalent immobilization of thiol groups on poly(acrylic acid) (PAA) with a molecular mass of 250 kDa followed by immobilization of 2-mercaptonicotinic acid (2MNA) to thiol groups via disulfide bond formation resulting in PAA-Cys-2MNA. P-gp inhibitory effect of this preactivated thiomer was evaluated on Caco-2 cells. Transports of rhodamine 123 at 37 °C with and without verapamil and at 4 °C were performed to evaluate P-gp function of cells. In total, 1571.81 ± 156.18 µmol thiol groups were immobilized per gram of polymer that were in the next step by 99.88% preactivated. The enhancement ratios of P_app calculated from the ratio between P_app of rhodamine 123 in the presence of P-gp inhibitors and P_app of rhodamine 123 alone were 2.36, 2.09, and 1.84-fold in the presence of PAA-Cys-2MNA, PAA-Cys, and PAA, respectively. Because of its pronounced P-gp inhibitory effect, PAA-Cys-2MNA could be considered as promising macromolecular P-gp inhibitor for various drug delivery systems.

• Caco-2 cell
• efflux
• poly(acrylic acid)
• rhodamine 123
• transport

Declaration of interest

The authors would like to acknowledge the Technology Grants East Asia financed by the Austrian Federal Ministry for Science and Research and administered/executed by the OeAD (Austrian Agency for International Cooperation in Education and Research, OeAD-GmbH).