A DSC study of the miscibility of poly(ethylene oxide)-block-poly( -lactide) copolymers with poly( -lactide)

The purpose of this study was to examine the miscibility of poly(ethylene oxide)-block-poly( -lactide) copolymers with poly ( -lactide). The copolymers L7E73L7 and L17E78L17 (L=carbonyloxymethylmethylene unit, OCOCH(CH3); E=oxyethylene unit, OCH2CH2) were synthesised by non-catalysed anionic polymerisation and characterised by gel permeation chromatography and 13C NMR. Blends of each of the copolymers with poly( -lactide) with compositions over the range from 10 to 90 wt% copolymer were cast as thin films and examined by differential scanning calorimetry (DSC) to determine glass transition temperatures (Tg) and melting temperatures (Tm). The phase diagram showed a region of miscibility above the melting point of the copolymer in the system (approx. 35–40°C). Within this region the system was glassy at low mass fractions of oxyethylene in the copolymer (wE 0.1) and rubbery at higher mass fractions. Below Tm a mechanically compatible glassy blend existed at low wE whilst quenching of systems of higher wE led to phase separation, the biphasic region consisting of crystalline Em-sequences of copolymer separated from non-crystalline poly( -lactide). The phase diagram resulting from this study provides the means for the design of drug delivery systems based on blends of poly( -lactide) and poly(ethylene oxide)-containing components. The crystal melt boundary can be lowered by the use of block copolymers with short poly(ethylene oxide) blocks permitting the preparation of blends which are miscible at room temperature and rubbery or glassy according to composition.