Chain Exchange in Binary Copolymer Micelles at Equilibrium: Confirmation of the Independent Chain Hypothesis.

The mechanism of chain exchange in block polymer micelles at equilibrium is investigated using time-resolved small-angle neutron scattering (TR-SANS). The binary micelles are formed from blends of two poly(styrene-b-ethylene-alt-propylene) (PS-PEP) copolymers with different PS core block lengths, only one of which is contrast-matched with the solvent, squalane, so that the monitored scattering intensity only reflects the other species. Micelles prepared with an excess of deuterated PS chains (of the visible species) and those with the equivalent protonated PS chains are blended ("postmixed") at room temperature, where the exchange of chains is suppressed. At several elevated temperatures these samples were monitored by TR-SANS, in which mixing of isotope-labeled visible species gives systematic reduction of scattering signals with time and provides a quantitative way to characterize the micelle exchange kinetics. Within experimental error, the results for each labeled chain (i.e., longer or shorter) in the binary micelles are identical to those recently reported for the same labeled chains in the corresponding single block copolymer component micelles, thus proving that chain exchange in these micelles involves independent chain motion. This reinforces the important conclusions that the single-chain exchange mechanism dominates in the studied micelle solutions and that micelle fusion or fission events are rare.

Molecular Exchange in Diblock Copolymer Micelles: Bimodal Distribution in Core-Block Molecular Weights.

The role of core block size dispersity on the rate of molecular exchange in spherical micelles formed from 1% by volume poly(styrene-b-ethylenepropylene) (PS-PEP) diblock copolymers in squalane (C30H62) was investigated using time-resolved small-angle neutron scattering (TR-SANS). Separate copolymer solutions (total polymer 1% by volume) containing either deuterium labeled (dPS) or normal (hPS) poly(styrene) core blocks were prepared and mixed at room temperature, below the core glass transition temperature. Each preparation (dPS or hPS) contained equal volume fractions of Mn = 26 and 42 kg/mol (h-equivalent) poly(styrene) blocks. Heating to temperatures between 87 and 146 °C resulted in block copolymer exchange as evidenced by a systematic reduction in the SANS intensity; C30H62 and C30D62 were blended so as to contrast match the fully exchanged cores. Following a protocol established in a previous report, the time-dependent intensity data were shifted with respect to time and temperature, leading to a master curve covering nearly 7 orders of magnitude in reduced time. These results are quantitatively accounted for by summing the weighted relaxation functions obtained from the individual components, consistent with a previously published model that accounts for the dramatic sensitivity of the molecular exchange dynamics to core block dispersity.

Electromechanical limits of polymersomes.

Self-assembled membranes of amphiphilic diblock copolymers enable comparisons of cohesiveness with lipid membranes over the range of hydrophobic thicknesses d = 3-15 nm. At zero mechanical tension the breakdown potential V(c) for polymersomes with d = 15 nm is 9 V, compared to 1 V for liposomes with d = 3 nm. Nonetheless, electromechanical stresses at breakdown universally exhibit a V(c)(2) dependence, and membrane capacitance shows the expected strong d dependence, conforming to simple thermodynamic models. The viscous nature of the diblock membranes is apparent in the protracted postporation dynamics.

Shear-induced nano-macro structural transition in a polymeric bicontinuous microemulsion.

Bicontinuous microemulsions arise in a narrow concentration range for ternary blends containing two immiscible homopolymers and the corresponding diblock copolymer. Steady shear reveals four distinct regimes of response as a function of shear rate, corresponding to flow-induced transitions in fluid structure. In situ neutron scattering shows flow-induced anisotropy in the nanometer-scale microemulsion structure at moderate shear rates, while higher rates induce bulk phase separation, with micron-size morphology, which is characterized with in situ light scattering and optical microscopy.

Preparation, stability, and in vitro performance of vesicles made with diblock copolymers.

Vesicles made completely from diblock copolymers-polymersomes-can be stably prepared by a wide range of techniques common to liposomes. Processes such as film rehydration, sonication, and extrusion can generate many-micron giants as well as monodisperse, approximately 100 nm vesicles of PEO-PEE (polyethyleneoxide-polyethylethylene) or PEO-PBD (polyethyleneoxide-polybutadiene). These thick-walled vesicles of polymer can encapsulate macromolecules just as liposomes can but, unlike many pure liposome systems, these polymersomes exhibit no in-surface thermal transitions and a subpopulation even survive autoclaving. Suspension in blood plasma has no immediate ill-effect on vesicle stability, and neither adhesion nor stimulation of phagocytes are apparent when giant polymersomes are held in direct, protracted contact. Proliferating cells, in addition, are unaffected when cultured for an extended time with an excess of polymersomes. The effects are consistent with the steric stabilization that PEG-lipid can impart to liposomes, but the present single-component polymersomes are far more stable mechanically and are not limited by PEG-driven micellization. The results potentiate a broad new class of technologically useful, polymer-based vesicles.

Polymersomes: tough vesicles made from diblock copolymers.

Vesicles were made from amphiphilic diblock copolymers and characterized by micromanipulation. The average molecular weight of the specific polymer studied, polyethyleneoxide-polyethylethylene (EO40-EE37), is several times greater than that of typical phospholipids in natural membranes. Both the membrane bending and area expansion moduli of electroformed polymersomes (polymer-based liposomes) fell within the range of lipid membrane measurements, but the giant polymersomes proved to be almost an order of magnitude tougher and sustained far greater areal strain before rupture. The polymersome membrane was also at least 10 times less permeable to water than common phospholipid bilayers. The results suggest a new class of synthetic thin-shelled capsules based on block copolymer chemistry.

Polymer-polymer phase behavior.

Different polymers can be combined into a single material in many ways, which can lead to a wide range of phase behaviors that directly influence the associated physical properties and ultimate applications. Four factors control polymer-polymer phase behavior: choice of monomers, molecular architecture, composition, and molecular size. Current theories and experiments that deal with the equilibrium thermodynamics and non-equilibrium dynamics of polymer mixtures are described in terms of these experimentally accessible parameters. Two representative molecular architectures, binary linear homopolymer mixtures and diblock copolymers, exhibiting macrophase separation and microphase segregation, respectively, are examined in some detail. Although these model systems are fairly well understood, a myriad of mixing scenarios, with both existing and unrealized materials applications, remain unexplored at a fundamental level.