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Ming-Kung Yeh

Researcher at National Defense Medical Center

Publications -  35
Citations -  1183

Ming-Kung Yeh is an academic researcher from National Defense Medical Center. The author has contributed to research in topics: Microparticle & Gelatin. The author has an hindex of 20, co-authored 35 publications receiving 1072 citations. Previous affiliations of Ming-Kung Yeh include South Korean Ministry for Health, Welfare and Family Affairs & National Taiwan University of Science and Technology.

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Salmonella detection using 16S ribosomal DNA/RNA probe-gold nanoparticles and lateral flow immunoassay.

TL;DR: An ultrasensitive, simple, and fast lateral flow immunoassay for Salmonella detection using gold nanoparticles conjugated with a DNA probe, which is complementary to the 16S ribosomal RNA and DNA of Salmoneella, has been developed.
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Novel protein-loaded chondroitin sulfate-chitosan nanoparticles: Preparation and characterization

TL;DR: In this paper, the potential of chondroitin sulfate (ChS)-chitosan (CS) nanoparticles for the delivery of proteins was investigated by ionic cross-linking of CS solution with ChS.
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Formulation factors in preparing BTM-chitosan microspheres by spray drying method.

TL;DR: Betamethasone disodium phosphate (BTM)-loaded microspheres demonstrated good drug stability, high entrapped efficiency, and positive surface charge and the in vitro drug release from themicrospheres was related to gelatin content.
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Novel RGD-lipid conjugate-modified liposomes for enhancing siRNA delivery in human retinal pigment epithelial cells.

TL;DR: The results of this study suggest that RGD-PEGylated liposomes might be useful for siRNA delivery into retinal pigment epithelial cells by integrin receptor-medicated endocytosis.
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Improving anticancer efficacy of (-)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells.

TL;DR: EGCG-pNG showed improved anti-cancer efficacy in B16F10 murine melanoma cells and the pNG surface conjugated with EGCG is most likely the key factor that contributes to the decreased release of hemoglobin from human red blood cells in the hemolysis assay.