A 3D printable and highly stretchable tough hydrogel is developed by combining poly(ethylene glycol) and sodium alginate, which synergize to form a hydrogel tougher than natural cartilage. Encapsulated cells maintain high viability over a 7 d culture period and are highly deformed together with the hydrogel. By adding biocompatible nanoclay, the tough hydrogel is 3D printed in various shapes without requiring support material.
Design and synthesis of efficient drug delivery systems are of vital importance for medicine and healthcare. Materials innovation and nanotechnology have synergistically fueled the advancement of drug delivery. Innovation in material chemistry allows the generation of biodegradable, biocompatible, environment-responsive, and targeted delivery systems. Nanotechnology enables control over size, shape and multi-functionality of particulate drug delivery systems. In this review, we focus on the materials innovation and processing of drug delivery systems and how these advances have shaped the past and may influence the future of drug delivery.
In-network aggregation is an essential primitive for performing queries on sensor network data. However, most aggregation algorithms assume that all intermediate nodes are trusted. In contrast, the standard threat model in sensor network security assumes that an attacker may control a fraction of the nodes, which may misbehave in an arbitrary (Byzantine) manner.We present the first algorithm for provably secure hierarchical in-network data aggregation. Our algorithm is guaranteed to detect any manipulation of the aggregate by the adversary beyond what is achievable through direct injection of data values at compromised nodes. In other words, the adversary can never gain any advantage from misrepresenting intermediate aggregation computations. Our algorithm incurs only O(∆ log 2 n) node congestion, supports arbitrary tree-based aggregator topologies and retains its resistance against aggregation manipulation in the presence of arbitrary numbers of malicious nodes. The main algorithm is based on performing the SUM aggregation securely by first forcing the adversary to commit to its choice of intermediate aggregation results, and then having the sensor nodes independently verify that their contributions to the aggregate are correctly incorporated. We show how to reduce secure MEDIAN, COUNT, and AVERAGE to this primitive.
Abstract. The efficient subdivision of a sensor network into uniform, mostly non-overlapping clusters of physically close nodes is an important building block in the design of efficient upper layer network functions such as routing, broadcast, data aggregation, and query processing. We present ACE, an algorithm that results in highly uniform cluster formation that can achieve a packing efficiency close to hexagonal close-packing. By using the self-organizing properties of three rounds of feedback between nodes, the algorithm induces the emergent formation of clusters that are an efficient cover of the network, with significantly less overlap than the clusters formed by existing algorithms. The algorithm is scale-independent -it completes in time proportional to the deployment density of the nodes regardless of the overall number of nodes in the network. ACE requires no knowledge of geographic location and requires only a small constant amount of communications overhead.
We invent a simple method for fabricating high-aspect-ratio, hierarchical and dynamically tunable surface patterns by harnessing localized-ridge instabilities in gold nanofilms coated on elastomer substrates (a); develop a theoretical model to calculate the critical parameters (e.g. wavelength and amplitude) for designing the new patterns (b); and demonstrate novel applications of the patterns as super-hydrophobic coatings (c) and biomimetic cell-culture substrates (d) capable of on-demand tunability.
An attractive option for tissue engineering is to use of multicellular spheroids as microtissues, particularly with stem cell spheroids. Conventional approaches of fabricating spheroids suffer from low throughput and polydispersity in size, and fail to supplement cues from extracellular matrix (ECM) for enhanced differentiation. In this study, we report the application of microfluidics-generated water-in-oil-in-water (w/o/w) double-emulsion (DE) droplets as pico-liter sized bioreactor for rapid cell assembly and well-controlled microenvironment for spheroid culture. Cells aggregated to form size-controllable (30–80 μm) spheroids in DE droplets within 150 min and could be retrieved via a droplet-releasing agent. Moreover, precursor hydrogel solution can be adopted as the inner phase to produce spheroid-encapsulated microgels after spheroid formation. As an example, the encapsulation of human mesenchymal stem cells (hMSC) spheroids in alginate and alginate-arginine-glycine-aspartic acid (-RGD) microgel was demonstrated, with enhanced osteogenic differentiation further exhibited in the latter case.
Devices that interact with living organisms are typically made of metals, silicon, ceramics, and plastics. Implantation of such devices for long-term monitoring or treatment generally requires invasive procedures. Hydrogels offer new opportunities for human-machine interactions due to their superior mechanical compliance and biocompatibility. Additionally, oral administration, coupled with gastric residency, serves as a non-invasive alternative to implantation. Achieving gastric residency with hydrogels requires the hydrogels to swell very rapidly and to withstand gastric mechanical forces over time. However, high swelling ratio, high swelling speed, and long-term robustness do not coexist in existing hydrogels. Here, we introduce a hydrogel device that can be ingested as a standard-sized pill, swell rapidly into a large soft sphere, and maintain robustness under repeated mechanical loads in the stomach for up to one month. Large animal tests support the exceptional performance of the ingestible hydrogel device for long-term gastric retention and physiological monitoring.
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