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The self-assembly of the amphiphilic block copolymer poly(n-butyl methacrylate)-block-poly[2-(dimethylamino)ethyl methacrylate] at the air-water interface has been investigated at different pH values. Similar to Rehfeldt et al. (J. Phys. Chem. B 2006, 110, 9171), the subphase pH strongly affects the monolayer properties. The formation of calcium phosphate beneath the monolayer can be tuned by the subphase pH and hence the monolayer charge. After 12 h of mineralization at pH 5, the polymer monolayers are still transparent, but transmission electron microscopy (TEM) shows that very thin calcium phosphate fibers form, which aggregate into cotton ball-like features with diameters of 20 to 50 nm. In contrast, after 12 h of mineralization at pH 8, the polymer film is very slightly turbid and TEM shows dense aggregates with sizes between 200 and 700 nm. The formation of calcium phosphate is further confirmed by Raman and energy dispersive X-ray spectroscopy. The calcium phosphate architectures can be assigned to the monolayer charge, which is high at low pH and low at high pH. The study demonstrates that the effects of polycations should not be ignored if attempting to understand the colloid chemistry of biomimetic mineralization. It also shows that basic block copolymers are useful complementary systems to the much more commonly studied acidic block copolymer templates.

The self-assembly of the amphiphilic block copolymer poly(butadiene)-block-poly[2-(dimethylamino)ethyl methacrylate] at the air-water interface and the mineralization of the monolayers with calcium phosphate was investigated at different pH values. As expected for polyelectrolytes, the subphase pH strongly affects the monolayer properties. The focus of the current study, however, is on the effect of an oscillating (instead of a static) polymer monolayer on calcium phosphate mineralization. Monitoring of the surface pressure vs. mineralization time shows that the monolayer is quite stable if the mineralization is performed at pH 8. In contrast, the monolayer at pH 5 shows a measurable decrease of the surface pressure already after ca. 2 h of mineralization. Transmission electron microscopy reveals that mineralization at low pH under constant oscillation leads to small particles, which are arranged in circular features and larger entities with holes of ca. 200 nm. The larger features with the holes disappear as the mineralization is continued in favor of the smaller particles. These grow with time and form necklace-like architectures of spherical particles with a uniform diameter. In contrast, mineralization at pH 8 leads to very uniform particle morphologies already after 2 h. The mineralization products consist of a circular feature with a dark dot in the center. The increasing contrast of the precipitates in the electron micrographs with mineralization time indicates an increasing degree of mineralization vs. reaction time. The study therefore shows that mechanical effects on mineralization at interfaces are quite complex.

The hydrolytic and enzymatic degradation behavior of poly(epsilon-caprolactone) (PCL) is investigated using the Langmuir monolayer technique, and an improved data acquisition and data reduction procedure is presented. Hydrolytic and enzymatic monolayer degradation experiments of PCL with various molecular weights by Pseudomonas cepacia lipase have been carried out to analyze the influence of subphase pH, subphase temperature, enzyme concentration, and the packing density of polymer chains on the degradation kinetics. The enzymatic monolayer degradation results in an exponential increase in the number of dissolved degradation fragments with increasing degradation time, which confirms random chain scission to be the dominant scission mechanism. The increase in the enzymatic scission rate constant with decreasing initial average molecular weight of the polymers is assigned to the influence of the area density of polar terminal groups on the substrate-enzyme complex formation.

The understanding of the simultaneous transport and chain-scission phenomena involved in the hydrolysis of bulk-degrading polymers requires the experimental separation of chain cleavage and water diffusion. The hydrolytic chain cleavage of poly(rac-lactide) rac-(PLA) and poly[(rac-lactide)-co-glycolide] (PLGA) is analysed on the basis of monolayer degradation experiments combined with an improved data reduction procedure. Different, partly contradictory models of the hydrolytic degradation and erosion mechanism of PLA and PLGA, namely random chain scission and chain-end scission, are discussed in the literature. The instantaneous linear area reduction observed for the polymer Langmuir films indicates a chain-end scission mechanism. As monolayers of end-capped and non-end-capped polymers degrade with exactly the same rate, the observed differences in the degradation kinetics of bulk samples do clearly result from differences in the water penetration into these polymers. A pronounced 'auto-inhibition' effect is observed for the polymers degraded at initially high pH of the aqueous subphase in the absence of buffers.