In vitro digestion of emulsions: diffusion and particle size distribution using diffusing wave spectroscopy and diffusion using nuclear magnetic resonance

Soft Matter ◽  
2012 ◽  
Vol 8 (42) ◽  
pp. 10994 ◽  
Author(s):  
Sébastien Marze ◽  
Maëla Choimet ◽  
Loïc Foucat
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Particle Size ◽  
Magnetic Resonance ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
In Vitro Digestion ◽  
Diffusing Wave Spectroscopy ◽  
And Diffusion ◽  
Nuclear Magnetic

scholarly journals Kinetics of In Vitro Digestion of Starches Monitored by Time-Resolved1H Nuclear Magnetic Resonance

2009 ◽  
Vol 10 (3) ◽  
pp. 638-644 ◽  
Author(s):  
Anthony C. Dona ◽  
Guilhem Pages ◽  
Robert G. Gilbert ◽  
Marianne Gaborieau ◽  
Philip W. Kuchel
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
In Vitro Digestion ◽  
Kinetics Of ◽  
Nuclear Magnetic

Effect of particle size distribution on the in vitro digestion of calcium alginate‐starchy model foods

2019 ◽  
Vol 42 (5) ◽  
Author(s):  
Cristian Ramírez ◽  
Camila Millón ◽  
Helena Nuñez ◽  
Valeria Campo ◽  
Sergio Almonacid ◽  
...  
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Calcium Alginate ◽  
In Vitro Digestion ◽  
Effect Of Particle Size

scholarly journals N-[7-Chloro-4-[4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl] quinoline]-acetamide

Molbank ◽  
10.3390/m1213 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1213
Author(s):  
Paolo Coghi ◽  
Jerome P. L. Ng ◽  
Ali Adnan Nasim ◽  
Vincent Kam Wai Wong
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Quantum Coherence ◽  
Biologically Active ◽  
Proton Nuclear Magnetic Resonance ◽  
Dipolar Cycloaddition ◽  
Heteronuclear Single Quantum Coherence ◽  
Pharmacokinetic Properties ◽  
Nuclear Magnetic

The 1,2,3-triazole is a well-known biologically active pharmacophore constructed by the copper-catalyzed azide–alkyne cycloaddition. We herein reported the synthesis of 4-amino-7-chloro-based [1,2,3]-triazole hybrids via Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of 4-azido-7-chloroquinoline with an alkyne derivative of acetaminophen. The compound was fully characterized by Fourier-transform infrared (FTIR), proton nuclear magnetic resonance (1H-NMR), carbon-13 nuclear magnetic resonance (13C-NMR), heteronuclear single quantum coherence (HSQC), ultraviolet (UV) and high-resolution mass spectroscopies (HRMS). This compound was screened in vitro with different normal and cancer cell lines. The drug likeness of the compound was also investigated by predicting its pharmacokinetic properties.

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