We report on two types of poly(methacrylic acid) (PMAA)-based hydrogel microcontainers (capsules) of cubical shape with distinctly different shape responses upon pH variations. The microcontainers were prepared as replicas of cubical inorganic templates through chemical cross-linking of hydrogenbonded layer-by-layer (LbL) films. The two types of hollow hydrogels, a single-component (PMAA) and PMAA-poly(N-vinylpyrrolidone) (PMAA-PVPON), showed drastic differences in their shape response to pH variations. Cubical (PMAA) 20 capsules turned into bulged sphere-like structures of the same size when transitioned from pH 3 to pH 8. In contrast, cubical (PMAA-PVPON) 5 capsules retained their cubical shape at pH 3 while increasing in size at pH 8. The pH-triggered size change of cubical capsules was completely reversible. The difference in pH-triggered shape responses was rationalized through the difference in hydrogel rigidity expressed as the ratio of the polymer contour length between the neighboring cross-links to the persistence polymer length. The ratios of 22.7 and 2 for (PMAA) and (PMAA-PVPON) systems, respectively, suggested that the dual-component system is more rigid and therefore expands uniformly in all directions. We believe that the results provide new prospects for developing polymeric materials with predictable shape and size-changing properties for controlled drug delivery, cellular uptake, and pH-regulating transport behavior in microfluidic devices.

We present a novel type of ultrathin hydrogel microcapsules with pH-triggered shape switch. The capsules are produced as hollow hydrogel replicas of cubical inorganic templates and capable of keeping cubical geometries at neutral pH but transform into bulged structures at basic pH.

We report on the evolution of the internal structure of dry and hydrated poly(methacrylic acid) (PMAA) hydrogels by quantifying the extent of layer interdiffusion in hydrogen-bonded (HB) films and upon subsequent cross-linking and hydration. These hydrogels are produced by ethylenediamine (EDA)-assisted cross-linking of PMAA in spinassisted (SA) and dipped HB PMAA/poly(N-vinylpyrrolidone) (PVPON) multilayers followed by complete release of PVPON at pH 8 due to severing of hydrogen bonds with the PMAA network. Internal hydrogel architecture was monitored by neutron reflectometry using deuterated dPMAA marker layers. We found that even in the highly stratified SA HB films, layer interdiffusion extends over three (PMAA/PVPON) bilayers. Cross-linking of this film induces marker layer interpenetration more deeply into the surrounding material, extending over five layers. The volume fraction of dPMAA at the nominal center of a marker layer decreased from 0.65 to 0.51 after cross-linking. Hydrated SA hydrogels preserve well-organized layering and exhibit a persistent differential swelling with two distinct swelling ratios corresponding to MAA cross-link-rich and cross-link-poor strata. In contrast, layer organization in dipped films decays rapidly with distance from the silicon substrate. Both types of hydrogel swelled by factors of two and four times their dry total thicknesses at pH 5 and 7, respectively, and exhibited elevated surface roughness upon hydration. To fit the neutron reflectometry data, a self-consistent model was developed wherein the amount of PMAA initially deposited was preserved through subsequent chemical modification and hydration. Our results open opportunities for the development of thin hydrogels with a regulated structure, which can be utilized for efficient sensing, protection, activation, and rapid response in an aqueous environment. The internal morphological hierarchy of these multilayer hydrogels affords a means of fine-tuning their response to pH, temperature, or light to a degree rarely possible for randomly cross-linked responsive networks or brushes.

Figure S1. Neutron reflectivity (NR) data (left panels) and corresponding SLD profiles (right panels) for spin-assisted dry single-stack (PVCL) 20 (a,b) and (PVPON) 20 (c,d) hydrogels. Open symbols and solid lines show NR data and fit, respectively. D 2 O 6.200E-06 4.75E-11 2.00E-12 500.0 230.2

Local modulation of oxidative stress is crucial for a variety of biochemical events including cellular differentiation, apoptosis, and defense against pathogens. Currently employed natural and synthetic antioxidants exhibit a lack of biocompatibility, bioavailability, and chemical stability, resulting in limited capability to scavenge reactive oxygen species (ROS). To mediate these drawbacks, we have developed a synergistic manganoporphyrin-polyphenol polymeric nanothin coating and hollow microcapsules with efficient antioxidant activity and controllable ROS modulation. These materials are produced by multilayer assembly of a natural polyphenolic antioxidant, tannic acid (TA), with a synthesized copolymer of polyvinylpyrrolidone containing a manganoporphyrin modality (MnP-PVPON) which mimics the enzymatic antioxidant superoxide dismutase. The redox activity of the copolymer is demonstrated to dramatically increase the antioxidant response of MnP-PVPON/TA capsules versus unmodified PVPON/TA capsules through reduction of a radical cationic dye and to significantly suppress the proliferation of superoxide via cytochrome C competition. Inclusion of MnP-PVPON as an outer layer enhances radical-scavenging activity as compared to localization of the layer in the middle or inner part of the capsule shell. In addition, we demonstrate that TA is crucial for the synergistic radical-scavenging activity of the MnP-PVPON/TA system which exhibits a combined superoxide dismutase-like ability and catalase-like activity in response to the free radical superoxide challenge. The MnP-PVPON/TA capsules exhibit a negligible, 8% loss of shell thickness upon free radical treatment, while PVPON/TA capsules lose 39% of their shell thickness due to the noncatalytic free-radical-scavenging of TA, as demonstrated by small angle neutron scattering (SANS). Finally, we have found the manganoporphyrin-polyphenol capsules to be nontoxic to splenocytes from NOD mice after 48 h incubation. Our study illustrates the strong potential of combining catalytic activity of manganoporphyrins with natural polyphenolic antioxidants to design efficient free-radical-scavenging materials that may eventually be used in antioxidant therapies and as free radical dissipating protective carriers of biomolecules for biomedical or industrial applications.