Characterization and mechanical support of asymmetric hydrogel membranes based on the interfacial cross-linking of poly(vinyl alcohol) with toluene diisocyanate

1996 ◽  
Vol 111 (1) ◽  
pp. 115-122 ◽  
Author(s):  
R.H. Li ◽  
T.A. Barbari
2021 ◽  
Vol 22 (8) ◽  
pp. 3901
Author(s):  
Mohsen Setayeshmehr ◽  
Shahzad Hafeez ◽  
Clemens van Blitterswijk ◽  
Lorenzo Moroni ◽  
Carlos Mota ◽  
...  

Various hydrogel systems have been developed as biomaterial inks for bioprinting, including natural and synthetic polymers. However, the available biomaterial inks, which allow printability, cell viability, and user-defined customization, remains limited. Incorporation of biological extracellular matrix materials into tunable synthetic polymers can merge the benefits of both systems towards versatile materials for biofabrication. The aim of this study was to develop novel, cell compatible dual-component biomaterial inks and bioinks based on poly(vinyl alcohol) (PVA) and solubilized decellularized cartilage matrix (SDCM) hydrogels that can be utilized for cartilage bioprinting. In a first approach, PVA was modified with amine groups (PVA-A), and mixed with SDCM. The printability of the PVA-A/SDCM formulations cross-linked by genipin was evaluated. On the second approach, the PVA was functionalized with cis-5-norbornene-endo-2,3-dicarboxylic anhydride (PVA-Nb) to allow an ultrafast light-curing thiol-ene cross-linking. Comprehensive experiments were conducted to evaluate the influence of the SDCM ratio in mechanical properties, water uptake, swelling, cell viability, and printability of the PVA-based formulations. The studies performed with the PVA-A/SDCM formulations cross-linked by genipin showed printability, but poor shape retention due to slow cross-linking kinetics. On the other hand, the PVA-Nb/SDCM showed good printability. The results showed that incorporation of SDCM into PVA-Nb reduces the compression modulus, enhance cell viability, and bioprintability and modulate the swelling ratio of the resulted hydrogels. Results indicated that PVA-Nb hydrogels containing SDCM could be considered as versatile bioinks for cartilage bioprinting.


2012 ◽  
Vol 29 (8) ◽  
pp. 1108-1113 ◽  
Author(s):  
Mi Sun Lee ◽  
Eun Young Mok ◽  
Won Cheol Shin ◽  
Jong Dai Kim ◽  
Jin-Chul Kim

2009 ◽  
Vol 46 (1-2) ◽  
pp. 379-383 ◽  
Author(s):  
Elena V. Basiuk ◽  
Arfat Anis ◽  
Sri Bandyopadhyay ◽  
Edgar Alvarez-Zauco ◽  
Sammy L.I. Chan ◽  
...  

Biomaterials ◽  
1994 ◽  
Vol 15 (3) ◽  
pp. 231-238 ◽  
Author(s):  
Krystyna Burczak ◽  
Toshiya Fujisato ◽  
Motoyoshi Hatada ◽  
Yoshito Ikada

2016 ◽  
Vol 36 (9) ◽  
pp. 891-898
Author(s):  
Sadao Araki ◽  
Yuko Shirakura ◽  
Harufumi Suzuki ◽  
Hideki Yamamoto

Abstract Spherical glutaraldehyde cross-linked poly(vinyl alcohol) (PVA) hydrogels (G-PVA) were prepared in three steps: gelatification, cross-linking, and removal of alginate. Gelatification was carried out by dropping a solution of alginate, PVA, and glutaraldehyde into a calcium chloride solution to form calcium alginate. Calcium alginate gels were prepared at 20°C, 40°C, 60°C, and 80°C to study the effect of gelatification temperature on the formation of pores on the surface of G-PVA. The effect of the alginate content was studied. PVA and glutaraldehyde were cross-linked by immersion of the gels in a solution of H2SO4 and Na2SO4. The effect of sodium alginate and inorganic salts, such as MgSO4 and K2SO4, on the formation of pores on the surface of G-PVA was confirmed.


2015 ◽  
Vol 7 (35) ◽  
pp. 19691-19699 ◽  
Author(s):  
Juho Antti Sirviö ◽  
Samuli Honkaniemi ◽  
Miikka Visanko ◽  
Henrikki Liimatainen

RSC Advances ◽  
2016 ◽  
Vol 6 (47) ◽  
pp. 41428-41438 ◽  
Author(s):  
Jingmei Xu ◽  
Hongzhe Ni ◽  
Xueyan Luo ◽  
Zhe Wang ◽  
Huixuan Zhang

The cross-linking structures and introduced PVA effectively blocked the transmission channel of methanol and inhibited the infiltration of methanol.


1992 ◽  
Vol 46 (8) ◽  
pp. 1449-1451 ◽  
Author(s):  
Toshihiro Hirai ◽  
Hidetoshi Maruyama ◽  
Takashi Suzuki ◽  
Sadao Hayashi

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