Succinate dehydrogenase inhibitors are essential fungicides used in agriculture. To explore new pyrazole-carboxamides with high fungicidal activity, a series of N-substitutedphenyl-3-di/trifluoromethyl-1-methyl-1H-pyrazole-4-carboxamides bearing a branched alkyl ether moiety were designed and synthesized. The in vitro bioassay indicated that some target compounds displayed appreciable fungicidal activity.
View Article and Find Full Text PDFIn nature, the combination of composition, structure, and shape determines the matter's functional performance to a large extent. Inspired by which, two electrospun Janus nanofiber formulations were created using side-by-side electrospinning in this work. Tamoxifen citrate (TAM) was used as a model drug and ethyl cellulose (EC) and polyvinylpyrrolidone K60 (PVP) as the polymer carrier matrices.
View Article and Find Full Text PDFMater Sci Eng C Mater Biol Appl
August 2020
Complex nanostructures are increasingly becoming important in the development of novel functional nanomaterials. Nano drug depots, characterized by core-shell structures with core drug reservoirs, are drawing increasing attention because of its potential applications in furnishing drug-sustained release profiles. In the present study, two kinds of nano drug depots, one containing a crystal drug reservoir and the other having a medicated composite drug reservoir, were prepared through modified triaxial electrospinning.
View Article and Find Full Text PDFBerberine hydrochloride (BH), an important alkaloid, can be captured from water and released in organic solution circularly by a charged porous polymer (TPB-HCP), which is hypercross-linked using the cost-effective Friedel-Crafts reaction using sodium tetraphenylborate as the monomer. With high BET surface area, hierarchical porous structure and charged characteristics, TPB-HCP displays excellent adsorption capacity for BH owing to the synergistic effects of size matching and electrostatic interaction.
View Article and Find Full Text PDFGuang Pu Xue Yu Guang Pu Fen Xi
April 2006
To look for new MRI (magnetic resonance imaging) contrast agents with higher relaxivity as well as liver-selecsivity, four novel ester-amino ligands were synthesized by bis-acylation of octadecanyl, hexadecanyl, tetradecanyl and dedecanyl L-lysine with diethylenetriaminepentaacetic acid mono-anhydride (DTPA-MA), respectively. The corresponding dimeric Gd(III) complexes were gained by the reaction of these ligands with GdCl3 x 6H2O. All ligands and complexes were characterized by FTIR, 1H NMR and elemental analysis.
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