Hydrogen bonds in silk fibroin-poly (acrylonitrile-co-methyl acrylate) blends: FT-IR study

Author(s):  
Yuyu Sun ◽  
Zhengzhong Shao ◽  
Ping Hu ◽  
Tongyin Yu
2014 ◽  
Vol 33 (10) ◽  
pp. 2641-2652 ◽  
Author(s):  
Nina N. Chipanina ◽  
Nataliya F. Lazareva ◽  
Tamara N. Aksamentova ◽  
Alexey Yu. Nikonov ◽  
Bagrat A. Shainyan

Cellulose ◽  
2006 ◽  
Vol 13 (2) ◽  
pp. 131-145 ◽  
Author(s):  
Karin Hofstetter ◽  
Barbara Hinterstoisser ◽  
Lennart Salmén

2013 ◽  
Vol 25 (5) ◽  
pp. 2447-2450
Author(s):  
Chen Qiao-Yan ◽  
Chen Guang-Mei ◽  
Zhang Feng-Jun ◽  
Li Rong ◽  
Huang Yi-Ping

2003 ◽  
Vol 198 (1-2) ◽  
pp. 185-194 ◽  
Author(s):  
Emmanuelle Breysse ◽  
François Fajula ◽  
Annie Finiels ◽  
Georges Frémy ◽  
Jean Lamotte ◽  
...  

1993 ◽  
Vol 71 (9) ◽  
pp. 1334-1339 ◽  
Author(s):  
R.A. Shaw ◽  
H.H. Mantsch ◽  
B.Z. Chowdhry

Infrared spectra of the cyclic peptide cyclosporin A and three analogues have been measured in a number of organic solvents (CCl4, CDCl3, acetonitrile, DMSO, and 50:50 acetonitrile:D2O). Seven of the eleven amide groups of cyclosporin A are methylated, the remaining four N-H protons forming strong intramolecular hydrogen bonds in the crystal and in CDCl3 solution. These hydrogen bonds give rise to amide I (C=O stretching) bands at positions characteristic of β-turns, γ-turns, and β-sheet domains in proteins and model polypeptides. Increasing the polarity of the solvent eliminates some of these features; however, the spectra in DMSO and acetonitrile–D2O retain strong amide I absorptions characteristic of hydrogen-bonded carbonyl groups. The conformation of cyclosporin A in water cannot be observed directly due to low solubility; these findings suggest that the structure likely retains strong intramolecular hydrogen bonding. Spectra of the three analogues are consistent with this interpretation. Implications respecting the mechanism of pharmacological action of cyclosporin A are discussed.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Reza Eivazzadeh-Keihan ◽  
Fateme Radinekiyan ◽  
Hooman Aghamirza Moghim Aliabadi ◽  
Sima Sukhtezari ◽  
Behnam Tahmasebi ◽  
...  

AbstractHerein, a novel nanobiocomposite scaffold based on modifying synthesized cross-linked terephthaloyl thiourea-chitosan hydrogel (CTT-CS hydrogel) substrate using the extracted silk fibroin (SF) biopolymer and prepared Mg(OH)2 nanoparticles was designed and synthesized. The biological capacity of this nanobiocomposite scaffold was evaluated by cell viability method, red blood cells hemolytic and anti-biofilm assays. According to the obtained results from 3 and 7 days, the cell viability of CTT-CS/SF/Mg(OH)2 nanobiocomposite scaffold was accompanied by a considerable increment from 62.5 to 89.6% respectively. Furthermore, its low hemolytic effect (4.5%), and as well, the high anti-biofilm activity and prevention of the P. aeruginosa biofilm formation confirmed its promising hemocompatibility and antibacterial activity. Apart from the cell viability, blood biocompatibility, and antibacterial activity of CTT-CS/SF/Mg(OH)2 nanobiocomposite scaffold, its structural features were characterized using spectral and analytical techniques (FT-IR, EDX, FE-SEM and TG). As well as, given the mechanical tests, it was indicated that the addition of SF and Mg(OH)2 nanoparticles to the CTT-CS hydrogel could improve its compressive strength from 65.42 to 649.56 kPa.


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