Reversibly Reconfigurable Cross-Linking Induces Fusion of Separate Chitosan Hydrogel Films

2018 ◽  
Vol 1 (5) ◽  
pp. 1695-1704 ◽  
Author(s):  
Huimin He ◽  
Jinyang Li ◽  
Xiaodong Cao ◽  
Changshun Ruan ◽  
Qi Feng ◽  
...  
Author(s):  
Qiong Jiang ◽  
Wei zhou ◽  
Jun Wang ◽  
Rupei Tang ◽  
Di Zhang ◽  
...  

2019 ◽  
Vol 50 (4) ◽  
pp. 526-542
Author(s):  
Isabel Solé ◽  
Susana Vílchez ◽  
Núria Montanyà ◽  
Maria José García-Celma ◽  
Marcela Ferrándiz ◽  
...  

Cosmeto-textiles, which allow the administration of molecules when in contact with the skin, are increasingly being developed by cosmetic industries. We have designed an innovative approach for cosmeto-textile products, based on the impregnation of textile fibers with chitosan hydrogels, which have been cross-linked with genipin and loaded with dihydroxyacetone, which is an active component that induces sunless tanning. Dihydroxyacetone-loaded chitosan hydrogels have been prepared and characterized by means of cryogenic scanning electron microscopy (cryo-SEM). The images showed that genipin cross-linking decreases the mesh distance of hydrogels. The release of dihydroxyacetone from these cross-linked genipin chitosan hydrogels has been studied by a dialysis membrane method. These dihydroxyacetone-loaded chitosan hydrogels have been incorporated to polyamide textiles by a simple padding technique. The presence of dihydroxyacetone on these textiles has been detected by hyperspectral imaging on a dark field high resolution optical microscope. Finally, the performance of fabrics as cosmeto-textiles, with a tanning effect, has been evaluated by skin-colorimetry measured with an evaluation panel of 10 people. The results have demonstrated that dihydroxyacetone-loaded textiles produce a tanning effect on skin, and incorporation of dihydroxyacetone-loaded chitosan hydrogels into polyamide fabrics represents a friendly and appropriate strategy to obtain a cosmeto-textile with tanning effect.


2009 ◽  
Vol 114 (3) ◽  
pp. 1902-1907 ◽  
Author(s):  
Hiroaki Tanuma ◽  
Hiroki Kiuchi ◽  
Weihua Kai ◽  
Koji Yazawa ◽  
Yoshio Inoue

2015 ◽  
Vol 125 ◽  
pp. 189-199 ◽  
Author(s):  
Di Zhang ◽  
Wei Zhou ◽  
Bing Wei ◽  
Xin Wang ◽  
Rupei Tang ◽  
...  

Marine Drugs ◽  
2021 ◽  
Vol 19 (9) ◽  
pp. 479
Author(s):  
Jingjing Zhang ◽  
Wenqiang Tan ◽  
Qing Li ◽  
Xiaorui Liu ◽  
Zhanyong Guo

Hydrogels, possessing high biocompatibility and adaptability to biological tissue, show great usability in medical applications. In this research, a series of novel cross-linked chitosan quaternary ammonium salt loading with gentamicin sulfate (CTMCSG) hydrogel films with different cross-linking degrees were successfully obtained by the reaction of chitosan quaternary ammonium salt (TMCS) and epichlorohydrin. Fourier transform infrared spectroscopy (FTIR), thermal analysis, and scanning electron microscope (SEM) were used to characterize the chemical structure and surface morphology of CTMCSG hydrogel films. The physicochemical property, gentamicin sulphate release behavior, cytotoxicity, and antibacterial activity of the CTMCSG against Escherichia coli and Staphylococcus aureus were determined. Experimental results demonstrated that CTMCSG hydrogel films exhibited good water stability, thermal stability, drug release capacity, as well as antibacterial property. The inhibition zone of CTMCSG hydrogel films against Escherichia coli and Staphylococcus aureus could be up to about 30 mm. Specifically, the increases in maximum decomposition temperature, mechanical property, water content, swelling degree, and a reduction in water vapor permeability of the hydrogel films were observed as the amount of the cross-linking agent increased. The results indicated that the CTMCSG-4 hydrogel film with an interesting physicochemical property, admirable antibacterial activity, and slight cytotoxicity showed the potential value as excellent antibacterial wound dressing.


2017 ◽  
Vol 176 ◽  
pp. 195-202 ◽  
Author(s):  
Yongxiang Xu ◽  
Shenpo Yuan ◽  
Jianmin Han ◽  
Hong Lin ◽  
Xuehui Zhang

2007 ◽  
Vol 561-565 ◽  
pp. 1455-1458
Author(s):  
Zuo Wei Li ◽  
Li Yan Zhang ◽  
Qing Xiao Zeng

N-carboxyethyl chitosan (ACS) was formed by a Micheal reaction. Through the analysis of IR and 1H-NMR spectra, the Micheal reaction was carried out between - NH2 of chitosan and - C = C - of acrylic acid. ACS hydrogel (ACSG) was prepared by cross-linking with glutaraldehyde. ACSG show pH-sensitive swelling behavior, and the smallest swelling rate (SR) of ACSG is in pH5.0 buffer solution.With dosage of glutaraldehyde increasing, the SR of ACSG decreased. With grafting degree (GD) increasing, the SR of ACSG increased first and decreased afterward. Using bovine serum albumin (BSA) as a model medicine, the releasing behaviors of ACSG were investigated in vitro. In simulated gastric and intestinal fluid, the ACSG loading BSA (GD=20.45%) has better releasing behaviors.


Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2185
Author(s):  
Mohamed Dellali ◽  
Camelia Elena Iurciuc (Tincu) ◽  
Corina Lenuța Savin ◽  
Nawel Spahis ◽  
M’hamed Djennad ◽  
...  

Cross-linked chitosan (CS) films with aldehyde groups obtained by oxidation of carboxymethyl cellulose (CMC) with NaIO4 were prepared using different molar ratios between the CHO groups from oxidized carboxymethyl cellulose (CMCOx) and NH2 groups from CS (from 0.25:1 to 2:1). Fourier-transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopy demonstrated the aldehyde groups’ presence in the CMCOx. The maximum oxidation degree was 22.9%. In the hydrogel, the amino groups’ conversion index value increased when the -CHO/-NH2 molar ratio, cross-linking temperature, and time increased, while the swelling degree values decreased. The hydrogel films were characterized by scanning electron microscopy (SEM) and FTIR analysis. The curcumin encapsulation efficiency decreases from 56.74% to 16.88% when the cross-linking degree increases. The immobilized curcumin release efficiency (REf%) and skin membrane permeability were evaluated in vitro in two different pH solutions using a Franz diffusion cell, and it was found to decrease when the molar ratio -CH=O/NH2 increases. The curcumin REf% in the receptor compartment was higher at pH = 7.4 (18%- for the sample with a molar ratio of 0.25:1) than at pH = 5.5 (16.5%). The curcumin absorption in the skin membrane at pH = 5.5 (47%) was more intense than at pH = 7.4 (8.6%). The curcumin-loaded films’ antioxidant activity was improved due to the CS presence.


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