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Kevin J. McHugh

Researcher at Rice University

Publications -  51
Citations -  1748

Kevin J. McHugh is an academic researcher from Rice University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 16, co-authored 39 publications receiving 1033 citations. Previous affiliations of Kevin J. McHugh include Charles Stark Draper Laboratory & Case Western Reserve University.

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Layer-by-Layer Encapsulation of Probiotics for Delivery to the Microbiome

TL;DR: A layer-by-layer (LbL) approach is reported for probiotic encapsulation to protect probiotics against GI tract insults and improve their adhesion and growth on the intestines, translating to significantly enhanced survival of LbL-probiotics in vivo.
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The topographical effect of electrospun nanofibrous scaffolds on the in vivo and in vitro foreign body reaction

TL;DR: Results indicate that aligned electrospun nanofibers may serve as a promising scaffold for tissue engineering by minimizing host response, enhancing tissue-scaffold integration, and eliciting a thinner fibrous capsule.
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Biocompatible Semiconductor Quantum Dots as Cancer Imaging Agents.

TL;DR: In this article, state-of-the-art biocompatible QDs are compared with current FDA and Drug Administration approved fluorophores used in cancer imaging and a perspective on the pathway to clinical translation is provided.
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Fabrication of fillable microparticles and other complex 3D microstructures

TL;DR: A microfabrication method is described, termed StampEd Assembly of polymer Layers (SEAL), and injectable pulsatile drug-delivery microparticles, pH sensors, and 3D microfluidic devices that the authors could not produce using traditional 3D printing are created.
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Engineered PLGA microparticles for long-term, pulsatile release of STING agonist for cancer immunotherapy.

TL;DR: A single intratumoral injection of STING agonist–loaded microparticles triggered potent local and systemic antitumor immune responses, inhibited tumor growth, and prolonged survival as effectively as multiple soluble doses, but with reduced metastasis in several mouse tumor models.