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Nicholas A. Peppas

Researcher at University of Texas at Austin

Publications -  840
Citations -  101193

Nicholas A. Peppas is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Self-healing hydrogels & Polymer. The author has an hindex of 141, co-authored 825 publications receiving 90533 citations. Previous affiliations of Nicholas A. Peppas include National Technical University & University of Texas System.

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Modular Fabrication of Intelligent Material-Tissue Interfaces for Bioinspired and Biomimetic Devices.

TL;DR: This review is a comprehensive evaluation and critical analysis of the design and fabrication of environmentally responsive cell-material constructs for bioinspired machinery and biomimetic devices for peptide delivery, cancer theranostics, biomonitoring, neuroprosthetics, soft robotics, and biological machines.
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Polymer chain entanglements and brittle fracture

TL;DR: In this paper, a stochastic model is presented to predict the molecular weight dependence of the polymer fracture energy and strength for polymers with molecular weights higher than the critical value corresponding to the onset of entanglements.
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Penetrant transport in crosslinked polystyrene

TL;DR: In this paper, cross-linked polystyrene was examined at 50 and 70 o C. Dynamic swelling studies were performed in several penetrants including aromatic and aliphatic compounds.
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Macromolecular structure of coals: 2. Molecular weight between crosslinks from pyridine swelling experiments

TL;DR: In this article, the effective macromolecular structure of ten coals was investigated by application of a modified Gaussian network equation to the results of equilibrium vapour-swelling studies using pyridine as the penetrant.
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pH-Responsive poly(itaconic acid-co-N-vinylpyrrolidone) hydrogels with reduced ionic strength loading solutions offer improved oral delivery potential for high isoelectric point-exhibiting therapeutic proteins.

TL;DR: Hydrogels synthesized and tested as carriers for the oral delivery of high isoelectric point (pI) exhibiting therapeutic proteins exhibit significantly greater delivery potential than methacrylic acid-based hydrogels and it is shown that utilizing a lower ionic strength solution during drug loading significantly improves drug delivery potential for high pI therapeutics.