Drainage dynamics of thin liquid foam films containing soft PNiPAM microgels: influence of the cross-linking density and concentration.

We investigate the drainage dynamics of thin liquid foam films containing PNiPAM microgel suspensions with two cross-linking densities (1.5 and 5 mol% BIS) and at two microgel concentrations (0.1 and 1% wt). For this purpose, we use a thin-film pressure balance apparatus that can apply a controlled and sudden hydrostatic pressure on a film, and record the subsequent film thinning as a function of time. Once the film thickness has reached a stationary value, we test the adhesion between the interfaces of the film by reducing the pressure and measuring the angle between the film and the meniscus. This angle increases on reduction of pressure for adhesive films, which resists the separation of their interfaces. Non-adhesive films separate easily, and the meniscus angle stays constant. At a low microgel concentration, the more densely cross-linked microgels (5 mol% BIS) tend to drain into more adhesive films than the more loosely cross-linked particles (1.5 mol% BIS). The adhesion results from particles that bridge the two air-water interfaces of the film and are shared between them. In these cases, the film, which is initially stabilized by a bilayer of microgel particles, rearrange to a state where the microgels bridge the interfaces. These results are discussed and compared with previous studies at a low concentration of microgels, which have shown that emulsions stabilized with densely cross-linked microgels are more adhesive and less resistant to mechanical stresses than those obtained with lower cross-linking densities. In addition, micron-scale depleted zones with no microgels are observed in the films stabilized with the 5 mol% BIS particles, which eventually lead to the rupture of the films. At 1% wt, the films drain slowly, are not adhesive and have the thickness of a bilayer of microgel; while at 0.1% wt, the films have the thickness of a monolayer of microgel, are adhesive and show bridging. From the thin liquid foam film thicknesses we extract a rough estimation of the radii of adsorbed particles in the thick films before applying the pressure. Our results are consistent with particles being adsorbed in a spread conformation for the 0.1% wt sample and in a compressed conformation for the 1% wt sample. In line with previous studies on emulsions, we conclude that a larger surface coverage may reduce rearrangements, thus preventing bridging.

Saccharide-induced modulation of photoluminescence lifetime in microgels.

Sugar-responsive microgels were prepared by the covalent grafting of a poly(N-isopropylacrylamide) (pNIPAM) matrix with phenylboronic acid (PBA) as a saccharide sensing unit and a [Ru(bpy)3](2+) derivative (2,2'-bipyridine) as a luminescent reporter. Time-resolved emission studies reveal that the ruthenium complex has an unusually long lifetime (1.6 µs) and high quantum yield (∼0.17) in the PBA-microgel environment. In the presence of sugars, the microgels swell due to the formation of a sugar-boronate ester, leading to a more hydrophilic polymer chain. The swelling is accompanied by a decrease of the lifetime and the photoluminescence quantum yield, which cannot be explained solely by the swelling of the hydrogel. The emission properties of the ruthenium complex in PBA-functionalized microgels are compared to those in pNIPAM microgels lacking PBA moieties in various swelling states. The presence of PBA in the vicinity of [Ru(bpy)3](2+) is shown to have a predominant impact on its luminescence properties, mainly through a decrease of the polarity. Sugar-induced triggering of the boronate state thus leads to strong variations of the polarity and the luminescence characteristics.

Synthesis of conducting asymmetric hydrogel particles showing autonomous motion.

In the present work, we introduce a new approach for the synthesis of asymmetric particles made from electrically conducting polyaniline-alginate hydrogels by using bipolar electrochemistry. Such an intrinsic break of symmetry allows the soft beads to exhibit tunable motion at the air/water interface when loaded with ethanol due to controllable directed release of the solvent.

Oil-in-microgel strategy for enzymatic-triggered release of hydrophobic drugs.

Polymer microgels have received considerable attention due to their great potential in the biomedical field as drug delivery systems. Hyaluronic acid (HA) is a naturally occurring glycosaminoglycan composed of N-acetyl-d-glucosamine and d-glucuronic acid. This polymer is biodegradable, nontoxic, and can be chemically modified. In this work, a co-flow microfluidic strategy for the preparation of biodegradable HA microgels encapsulating hydrophobic drugs is presented. The approach relies on: (i) generation of a primary oil-in-water (O/W) nanoemulsion by the ultrasonication method, (ii) formation of a double oil-in-water-in-oil emulsion (O/W/O) using microfluidics, and (iii) cross-linking of microgels by photopolymerization of HA precursors modified with methacrylate groups (HA-MA) present in the aqueous phase of the droplets. The procedure is used for the encapsulation and controlled release of progesterone. Degradability and encapsulation/release studies in PBS buffer at 37°C in presence of different concentrations of hyaluronidase are performed. It is demonstrated that enzymatic degradation can be used to trigger the release of progesterone from microgels. This method provides precise control of the release system and can be applied for the encapsulation and controlled release of different types of hydrophobic drugs.