Water-Soluble Electrostatic Complexes of C60-Anchored Anionic Polymers and Cationic Porphyrins

2007 ◽  
Vol 28 (2) ◽  
pp. 200-204 ◽  
Author(s):  
Chih-Chien Chu ◽  
Tong-Ing Ho ◽  
Leeyih Wang
Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 214 ◽  
Author(s):  
Carla Palomino-Durand ◽  
Marco Lopez ◽  
Frédéric Cazaux ◽  
Bernard Martel ◽  
Nicolas Blanchemain ◽  
...  

Injectable pre-formed physical hydrogels provide many advantages for biomedical applications. Polyelectrolyte complexes (PEC) formed between cationic chitosan (CHT) and anionic polymers of cyclodextrin (PCD) render a hydrogel of great interest. Given the difference between water-soluble (PCDs) and water-insoluble PCD (PCDi) in the extension of polymerization, the present study aims to explore their impact on the formation and properties of CHT/PCD hydrogel obtained from the variable ratios of PCDi and PCDs in the formulation. Hydrogels CHT/PCDi/PCDs at weight ratios of 3:0:3, 3:1.5:1.5, and 3:3:0 were elaborated in a double–syringe system. The chemical composition, microstructure, viscoelastic properties, injectability, and structural integrity of the hydrogels were investigated. The cytotoxicity of the hydrogel was also evaluated by indirect contact with pre-osteoblast cells. Despite having similar shear–thinning and self-healing behaviors, the three hydrogels showed a marked difference in their rheological characteristics, injectability, structural stability, etc., depending on their PCDi and PCDs contents. Among the three, all the best above-mentioned properties, in addition to a high cytocompatibility, were found in the hydrogel 3:1.5:1.5. For the first time, we gained a deeper understanding of the role of the PCDi/PCDs in the injectable pre-formed hydrogels (CHT/PCDi/PCDs), which could be further fine-tuned to enhance their performance in biomedical applications.


2020 ◽  
Vol 31 ◽  
pp. 101947 ◽  
Author(s):  
Ananda Segabinazzi Ries ◽  
Juliana Felipetto Cargnelutti ◽  
Giovana Basso ◽  
Thiago Vargas Acunha ◽  
Bernardo Almeida Iglesias ◽  
...  

2012 ◽  
Vol 51 (26) ◽  
pp. 6447-6451 ◽  
Author(s):  
Astrid J. Olaya ◽  
Delphine Schaming ◽  
Pierre-Francois Brevet ◽  
Hirohisa Nagatani ◽  
Hai-Jun Xu ◽  
...  

2009 ◽  
Vol 9 (10) ◽  
pp. 5795-5802 ◽  
Author(s):  
Pavel Kubát ◽  
Kamil Lang ◽  
Pavel Janda ◽  
Ota Frank ◽  
Irena Matulková ◽  
...  

2012 ◽  
Vol 124 (26) ◽  
pp. 6553-6557 ◽  
Author(s):  
Astrid J. Olaya ◽  
Delphine Schaming ◽  
Pierre-Francois Brevet ◽  
Hirohisa Nagatani ◽  
Hai-Jun Xu ◽  
...  

2013 ◽  
Vol 11 (8) ◽  
pp. 1360-1367 ◽  
Author(s):  
Magdalena Makarska-Bialokoz

AbstractThe association process between two water soluble cationic porphyrins, 5,10,15,20-tetrakis[4-(trimethyl-ammonio)phenyl]-21H,23H-porphine tetra-p-tosylate (H2TTMePP) and 5,10,15,20-tetrakis(1-methyl-4-pyridyl)-21H,23H-porphine tetra-p-tosylate (H2TMePyP), as well as their Cu (II) complexes, with five series of nucleic agents has been studied using UV-VIS spectroscopy in aqueous solutions. During the titration with nucleic compounds the bathochromic effect of porphyrins absorption spectra can be observed as well as the hypochromicity of the Soret maximum. The association constants were calculated using a curve-fitting procedure (KAC of the order of magnitude of 103–105 mol−1). It has been shown that the interactions of H2TTMePP with nucleic agents are much stronger than interactions of H2TMePyP, which is most likely related to the kind and the size of the porphyrin substituent groups partaking in the process of stacking. The strength of the observed associated systems increases generally in a series: nucleic base


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