Browsing by Author "Huang, Ying-Pei"

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Directly Thiolated Modification onto the Surface of Detonation Nanodiamonds
(2014-05-28)
Hsu, Ming-Hua
;
Chuang, Hong
;
Cheng, Fong-Yu
;
Huang, Ying-Pei
;
Han, Chien-Chung
An efficient method for modifying the surface of detonation nanodiamonds (5 and 100 nm) with thiol groups (-SH) by using an organic chemistry strategy is presented herein. Thiolated nanodiamonds were characterized by spectroscopic techniques, and the atomic percentage of sulfur was analyzed by elemental analysis and X-ray photoelectron spectroscopy. The conjugation between thiolated nanodiamonds and gold nanoparticles was elucidated by transmission electron microscopy and UV-vis spectrometry. Moreover, the material did not show significant cytotoxicity to the human lung carcinoma cell line and may prospectively be applied in bioconjugated technology. The new method that we elucidated may significantly improve the approach to surface modification of detonation nanodiamonds and build up a new platform for the application of nanodiamonds.
Simple and highly efficient direct thiolation of the surface of carbon nanotubes
(2014)
Hsu, Ming-Hua
;
Chuang, Hong
;
Cheng, Fong-Yu
;
Huang, Ying-Pei
;
Han, Chien-Chung
We established a highly efficient and simple method to directly functionalize the surface of carbon nanotubes (CNTs) with thiol groups (-SH). The -SH groups on the surface of the CNTs were characterized using Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), elemental analysis (EA), and transmission electron microscopy (TEM). The TEM indicated that gold nanoparticles (Au NPs) or other metals can be attached to thiolated CNTs (CNT-SHs) through thiol-metal bonding. Hence, the proposed approach can be used for developing self-assembled materials, sensors, catalysts, and CNT nanodevices.
Synthesis and Evaluation of Aminothiazole-Paeonol Derivatives as Potential Anticancer Agents
(2016-02-01)
Tsai, Chia-Ying
;
Kapoor, Mohit
;
Huang, Ying-Pei
;
Lin, Hui-Hsien
;
Liang, Yu-Chuan
In this study, novel aminothiazole-paeonol derivatives were synthesized and characterized using H-1-NMR, C-13-NMR, IR, mass spectroscopy, and high performance liquid chromatography. All the new synthesized compounds were evaluated according to their anticancer effect on seven cancer cell lines. The experimental results indicated that these compounds possess high anticancer potential regarding human gastric adenocarcinoma (AGS cells) and human colorectal adenocarcinoma (HT-29 cells). Among these compounds, N-[4-(2-hydroxy-4-methoxyphenyl)thiazol-2-yl]-4-methoxybenzenesulfonamide (13c) had the most potent inhibitory activity, with IC50 values of 4.0 mu M to AGS, 4.4 mu M to HT-29 cells and 5.8 mu M to HeLa cells. The 4-fluoro-N-[4-(2-hydroxy-4-methoxyphenyl)thiazol-2-yl]benzenesulfonamide (13d) was the second potent compound, showing IC50 values of 7.2, 11.2 and 13.8 mu M to AGS , HT-29 and HeLa cells, respectively. These compounds are superior to 5-fluorouracil (5-FU) for relatively higher potency against AGS and HT-29 human cancer cell lines along with lower cytotoxicity to fibroblasts. Novel aminothiazole-paeonol derivatives in this work might be a series of promising lead compounds to develop anticancer agents for treating gastrointestinal adenocarcinoma.