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Hsing-Wen Sung

Researcher at National Tsing Hua University

Publications -  301
Citations -  24531

Hsing-Wen Sung is an academic researcher from National Tsing Hua University. The author has contributed to research in topics: Genipin & Glutaraldehyde. The author has an hindex of 86, co-authored 290 publications receiving 21594 citations. Previous affiliations of Hsing-Wen Sung include Industrial Technology Research Institute & Georgia Institute of Technology.

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Diverse Applications of Nanomedicine

Beatriz Pelaz, +91 more
- 14 Mar 2017 - 
TL;DR: An overview of recent developments in nanomedicine is provided and the current challenges and upcoming opportunities for the field are highlighted and translation to the clinic is highlighted.
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A novel pH-sensitive hydrogel composed of N,O-carboxymethyl chitosan and alginate cross-linked by genipin for protein drug delivery.

TL;DR: The results clearly suggested that the genipin-cross-linked NOCC/alginate hydrogel could be a suitable polymeric carrier for site-specific protein drug delivery in the intestine.
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In vitro evaluation of cytotoxicity of a naturally occurring cross-linking reagent for biological tissue fixation

TL;DR: Genipin, a naturally occurring cross-linking reagent which has been used in herbal medicine and in the fabrication of food dyes, was used by this group to fix biological tissues to assess the cytotoxicity of genipin in vitro using 3T3 fibroblasts and suggested that the cellular compatibility of thegenipin-fixed tissue was superior to its glutaraldehyde-fixed counterpart.
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Highly cited research articles in Journal of Controlled Release: Commentaries and perspectives by authors

TL;DR: A compilation of commentaries gives a historical perspective and current status of research covered in some of the most cited research articles in the history of the Journal of Controlled Release.
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Physically crosslinked alginate/N,O-carboxymethyl chitosan hydrogels with calcium for oral delivery of protein drugs.

TL;DR: The calcium-alginate-NOCC beads with distinct total concentrations developed in the study may be used as a potential system for oral delivery of protein drugs to different regions of the intestinal tract.