Divergent synthesis of dendrimer-like pH-responsive macromolecules through a combination of ATRP and ROP for controlled release of anti-cancer drug.

Abstract

This work is focused on the synthesis and controlled drug release behavior of 8-arm and 12-arm amphiphilic pH-responsive dendrimer-like block copolymers. To study the role of architecture and the number of arms at the critical micelle concentration (CMC) value, differential scanning calorimetry (DSC), micelle size and in vitro controlled release of drug, we investigated a series of 8-arm and 12-arm block copolymers. The poly(acrylic acid) (PAA)-carrying dendrimer-like block copolymers were synthesized in two main steps. First, a second-generation dendrimer-like poly(ε-caprolactone) (PCL) was obtained by ring-opening polymerization (ROP) of ε-caprolactone (CL) from a bis and tris-hydroxylated core. For this goal, a conventional selective AB2-type branching agent for the PCL chain ends was designed: the latter includes a carboxyl (A) group for its attachment to the PCL arm ends and two geminal hydroxyls (B2) for the reiteration of the PCL growth as second generation using ROP. Subsequently, the hydroxyl-end groups quantitatively converted into bromoester groups as atom transfer radical polymerization (ATRP) initiating sites. The second step is the ATRP which thus served to grow poly(tBA) chains. After the hydrolysis of the t-butyl ester groups, amphiphilic, pH-responsive dendrimer-like block copolymers were obtained. Transmission electron microscopy (TEM) and dynamic light scattering (DLS) demonstrated that the micelles exhibit a spherical shape with a size range of 43-64 nm in diameter. As a model drug, quercetin was loaded into the obtained 2G3(PAA)8 and 3G3(PAA)12 micelles via a dialysis method for in vitro release studies and their response to pH variation was investigated. The in vitro cytotoxicity evaluation of the polymers clearly showed that both compounds are safe in a wide range of concentrations (several times above the CMC value).