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Cao, Van Du,Nguyen, Phuong Phong,Khuong, Vo Quoc,Nguyen, Cuu Khoa,Nguyen, Xuan Chuong,Dang, Cap Ha,Tran, Ngoc Quyen Korean Chemical Society 2014 Bulletin of the Korean Chemical Society Vol.35 No.9
In this paper ultrafine copper nanoparticles (CuNPs) were prepared from copper salt via chemical reduction method with sodium citrate dispersant and polyvinylalcol (PVA) capping polymer. The colloidal CuNPs were characterized by using UV-Visible spectroscopy, Transmission Electron Microscopy (TEM), and X-ray Diffraction (XRD) techniques. Our obtained results indicated that the CuNPs were produced ranging from 2 to 4 nm in diameter. The colloidal solution at 7 ppm of CuNPs exhibited a powerful antifungal activity against Corticium salmonicolor (C. Salmonicolor). Fungal killing assays showed colloid solutions containing 10 ppm of CuNPs killed entirely the cultured fungus. A highly killing activity against the fungus was also performed when the CuNPs were sprayed on pink disease-infected rubber trees. These positive results may offer a great potential to produce CuNPs-based eco-fungicide for pink disease.
Van Du Cao,Phuong phong Nguyen,Vo Quoc Khuong,Cuu Khoa Nguyen,Xuan Chuong Nguyen,Cap Ha Dang,Ngoc Quyen Tran 대한화학회 2014 Bulletin of the Korean Chemical Society Vol.35 No.9
In this paper ultrafine copper nanoparticles (CuNPs) were prepared from copper salt via chemical reduction method with sodium citrate dispersant and polyvinylalcol (PVA) capping polymer. The colloidal CuNPs were characterized by using UV–Visible spectroscopy, Transmission Electron Microscopy (TEM), and X-ray Diffraction (XRD) techniques. Our obtained results indicated that the CuNPs were produced ranging from 2 to 4 nm in diameter. The colloidal solution at 7 ppm of CuNPs exhibited a powerful antifungal activity against Corticium salmonicolor (C. Salmonicolor). Fungal killing assays showed colloid solutions containing 10 ppm of CuNPs killed entirely the cultured fungus. A highly killing activity against the fungus was also performed when the CuNPs were sprayed on pink disease-infected rubber trees. These positive results may offer a great potential to produce CuNPs-based eco-fungicide for pink disease.
Thanh Son Cu,Ngoc Quyen Tran,Van Du Cao,Cuu Khoa Nguyen 한국고분자학회 2014 Macromolecular Research Vol.22 No.4
In this paper, we report the preparation and stabilization of colloidal silver nanoparticle solution, with theassistance of chitosan dihydroxyphenyl acetamide (CDHPA), or oligochitosan dihydroxyphenyl acetamide (OCDHPA). The structure of the chitosan derivatives were characterized by nuclear magnetic resonance (1H NMR) spectroscopy. The morphology of the synthesized silver core-chitosan shell nanoparticles were observed by transmission electronmicroscopy (TEM) and X-ray diffraction (XRD) techniques, and showed a well-defined core-shell structure of polymer-coated silver nanoparticles (AgNPs). The core-shell NPs exhibited a strong antibacterial activity against E. coliand S. aureus, at a very low concentration of AgNPs (2.5 ppm). Our studies offer a new method for the preparationand protection of silver nanoparticles for antibacterial applications.
Vo Minh Hoang Do,Long Giang Bach,Diem-Huong Nguyen Tran,Van Du Cao,Thi Nhu Quynh Nguyen,Duc Thuan Hoang,Van Cuong Ngo,Dai Hai Nguyen,Thai Thanh Hoang Thi 한국생물공학회 2020 Biotechnology and Bioprocess Engineering Vol.25 No.2
Polyamidoamine (PAMAM) dendrimer is emerging as an effective nanocarrier for delivering anticancer drugs. Still, unmodified PAMAM dendrimer is hardly used in vivo because of unsatisfied drug release, high tendency of interfering with cellular membranes, and rapid clearance by reticuloendothelial system. In this study, low generation polyamidoamine (PAMAM) dendrimer G3.0 is developed and surface modified with methoxypolyethylene glycol (PAMAM G3.0-mPEG) to overcome its limitations. Specifically, PAMAM G3.0 conjugated with mPEG at different ratios are investigated to effectively eliminate its charge-associated toxicity, in which PAMAM G3.0-mPEG- 8 is chosen for oxaliplatin (OX) loading. Results reveal that OX-loaded PAMAM G3.0-mPEG-8 has desirable size, good entrapment efficiency, and sustained release with minimum drug leakage. In addition, Resazurin assay indicates that the toxicity of loaded OX is reduced as compared to free drug but still maintain substantially anticancer activity on HeLa cells, suggesting the potential application of PAMAM G3.0-mPEG-8 for OX delivery in cancer therapy.