No abstract

Abstract-We consider the problem of communicating information over a network secretly and reliably in the presence of a hidden adversary who can eavesdrop and inject malicious errors. We provide polynomial-time, rate-optimal distributed network codes for this scenario, improving on the rates achievable in [1]. Our main contribution shows that as long as the sum of the adversary's jamming rate ZO and his eavesdropping rate ZI is less than the network capacity C, (i.e., ZO + ZI < C), our codes can communicate (with vanishingly small error probability) a single bit correctly and without leaking any information to the adversary. We then use this to design codes that allow communication at the optimal source rate of C − ZO − ZI , while keeping the communicated message secret from the adversary. Interior nodes are oblivious to the presence of adversaries and perform random linear network coding; only the source and destination need to be tweaked. In proving our results we correct an error in prior work [2] by a subset of the authors in this work.

No abstract

No abstract

Abstract-The network communication scenario where one or more receivers request all the information transmitted by different sources is considered. We introduce distributed polynomialtime network codes in the presence of malicious nodes. Our codes can achieve any point inside the rate region of multiple-source multicast transmission scenarios both in the cases of coherent and non-coherent network coding. For both cases the encoding and decoding algorithm runs in poly(|E|)exp(s) time, where poly(|E|) is a polynomial function of the number of edges |E| in the network and exp(s) is an exponential function of the number of sources s. Our codes are fully distributed and different sources require no knowledge of the data transmitted by their peers. Our codes are "end-to-end", that is, all nodes apart from the sources and the receivers are oblivious to the adversaries present in the network and simply implement random linear network coding.

In this work, a novel strategy was developed to fabricate prevascularized cell-layer blood vessels in thick tissues and small-diameter blood vessel substitutes using three-dimensional (3D) bioprinting technology. These thick vascularized tissues were comprised of cells, a decellularized extracellular matrix (dECM), and a vasculature of multilevel sizes and multibranch architectures. Pluronic F127 (PF 127) was used as a sacrificial material for the formation of the vasculature through a multi-nozzle 3D bioprinting system. After printing, Pluronic F127 was removed to obtain multilevel hollow channels for the attachment of human umbilical vein endothelial cells (HUVECs). To reconstruct functional small-diameter blood vessel substitutes, a supporting scaffold (SE1700) with a double-layer circular structure was first bioprinted. Human aortic vascular smooth muscle cells (HA-VSMCs), HUVECs, and human dermal fibroblasts–neonatal (HDF-n) were separately used to form the media, intima, and adventitia through perfusion into the corresponding location of the supporting scaffold. In particular, the dECM was used as the matrix of the small-diameter blood vessel substitutes. After culture in vitro for 48 h, fluorescent images revealed that cells maintained their viability and that the samples maintained structural integrity. In addition, we analyzed the mechanical properties of the printed scaffold and found that its elastic modulus approximated that of the natural aorta. These findings demonstrate the feasibility of fabricating different kinds of vessels to imitate the structure and function of the human vascular system using 3D bioprinting technology.

A large number of opportunities for biomedical hydrogel design and functionality through photo-processing have stretched the limits of innovation. As both photochemical understanding and engineering technologies continue to develop, more complicated geometries and spatiotemporal manipulations can be realized through photo-exposure, producing multifunctional hydrogels with specific chemical, biological and physical characteristics for the achievement of biomedical goals. This report describes the role that light has recently played in the synthesis and functionalization of biomedical hydrogels and primarily the design of photoresponsive hydrogels via different chemical reactions (photo crosslinking and photo degradation) and conventional light curing processes (micropatterning, stereolithography and two/multiphoton techniques) as well as typical biomedical applications of the hydrogels (cell culture, differentiation and in vivo vascularization) and their promising future.

We consider a simple multiple access network in which a destination node receives information from multiple sources via a set of relay nodes. Each relay node has access to a subset of the sources, and is connected to the destination by a unit capacity link. Arbitrary errors may be introduced by up to z of the relay nodes. We propose an efficient distributed error correction coding scheme, where the relay nodes encode independently such that the overall codewords received at the destination are codewords from a single Reed-Solomon code. We show that it achieves the full capacity region for up to three sources.