Keng-Shiang Huang

Prof. Keng-Shiang Huang

The School of Chinese Medicine for Post-Baccalaureate, I-Shou University, Kaohsiung 840301, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
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Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
CYChih-Hui Yang
Chih-Hui Yang
Shu-Ling HuangShu-Ling Huang
Shu-Ling Huang
CCCheng-You Chen
Cheng-You Chen
YLYuan-Yi Lu
Yuan-Yi Lu
YLYung-Sheng Lin
Yung-Sheng Lin
Human safety and well-being is threatened by microbes causing numerous infectious diseases resulting in a large number of deaths every year. Despite substantial progress in antimicrobial drugs, many infectious diseases remain difficult to treat. Antimicrobial polymers offer a promising antimicrobial strategy for fighting pathogens and have received considerable attention in both academic and industrial research. This mini-review presents the advances made in antimicrobial polymers since 2013. Antimicrobial mechanisms exhibiting either passive or active action and polymer material types containing bound or leaching antimicrobials are introduced. This article also addresses the applications of these antimicrobial polymers in the medical, food, and textile industries.

5 April 2018 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
WKWEN-SHUO KUO
WEN-SHUO KUO
YSYu-Ting Shao
Yu-Ting Shao
Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
TCTing-Mao Chou
Ting-Mao Chou
CYChih-Hui Yang
Chih-Hui Yang

22 September 2009 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
KHKuo-Wei Hu
Kuo-Wei Hu
TLTzu-Ming Liu
Tzu-Ming Liu
KCKuei-Yi Chung
Kuei-Yi Chung
Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
CHChien-Tai Hsieh
Chien-Tai Hsieh
Chen-Sheng YehChen-Sheng Yeh
Chen-Sheng Yeh

18 May 2006 in Lab on a Chip
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Journal Article
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Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
TLTzung-Heng Lai
Tzung-Heng Lai
YLYu-Cheng Lin
Yu-Cheng Lin
In this paper the manipulation of Ca-alginate microspheres, using a microfluidic chip, for the encapsulation of gold nanoparticles is presented. Our strategy is based on hydrodynamic-focusing on the forming of a series of self-assembling sphere structures, the so-called water-in-oil (w/o) emulsions, in the cross-junction microchannel. These fine emulsions, consisting of aqueous Na-alginates, are then dripped into a solution of 20% calcium salt to accomplish Ca-alginate microspheres in an efficient manner. Experimental data show that microspheres with diameters ranging from 50 µm to 2000 µm with a variation less than 5% were precisely generated. The size and gap of the droplets are tunable by adjusting the relative sheath/sample flow rate ratio. Furthermore, we applied them to encapsulated gold nanoparticles, and this one shot operation performs the ‘Lab on a Chip’.

19 December 2008 in Lab on a Chip
Verified
Journal Article
Closed access
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CYChih-Hui Yang
Chih-Hui Yang
Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
YLY.-S. Lin
Y.-S. Lin
KLK. Lu
K. Lu
CTC.-C. Tzeng
C.-C. Tzeng
JCJia-Yaw Chang
Jia-Yaw Chang
This paper demonstrates a proof-of-concept approach for encapsulating the anticancer drug tamoxifen, Fe3O4nanoparticles (NPs) and CdTe quantum dots (QDs) into size-controlled polycaprolactone (PCL) microcapsules utilizing microfluidic emulsification, which combined magnetic targeting, fluorescence imaging and drug controlled release properties into one drug delivery system. Cross-linking the composite PCL microcapsules with poly(vinyl alcohol) (PVA) tailored their size, morphology, optical and magnetic properties and drug release behaviors. The flow conditions of the two immiscible solutions were adjusted in order to successfully generate various sizes of polymer droplets. The result showed superparamagnetic and fluorescent properties, and was used as a controlled drug release vehicle. The composite magnetic and fluorescent PCL microcapsules are potential candidates for a smart drug delivery system.

1 August 2016 in International Journal of Pharmaceutics
Verified
Journal Article
Open access
CYChih-Hui Yang
Chih-Hui Yang
LWLung-Shuo Wang
Lung-Shuo Wang
SCSzu-Yu Chen
Szu-Yu Chen
MHMao-Chen Huang
Mao-Chen Huang
YLYa-Hua Li
Ya-Hua Li
Keng-Shiang HuangKeng-Shiang Huang
Keng-Shiang Huang
Silver nanoparticle (Ag NP)-loaded chitosan composites have numerous biomedical applications; however, fabricating uniform composite microparticles remains challenging. This paper presents a novel microfluidic approach for single-step and in situ synthesis of Ag NP-loaded chitosan microparticles. This proposed approach enables obtaining uniform and monodisperse Ag NP-loaded chitosan microparticles measuring several hundred micrometers. In addition, the diameter of the composites can be tuned by adjusting the flow on the microfluidic chip. The composite particles containing Ag NPs were characterized using UV-vis spectra and scanning electron microscopy-energy dispersive X-ray spectrometry data. The characteristic peaks of Ag NPs in the UV-vis spectra and the element mapping or pattern revealed the formation of nanosized silver particles. The results of antibacterial tests indicated that both chitosan and composite particles showed antibacterial ability, and Ag NPs could enhance the inhibition rate and exhibited dose-dependent antibacterial ability. Because of the properties of Ag NPs and chitosan, the synthesized composite microparticles can be used in several future potential applications, such as bactericidal agents for water disinfection, antipathogens, and surface plasma resonance enhancers.