Related Experiment Video
Updated: Jan 22, 2026

Inkjet-printed Polyvinyl Alcohol Multilayers
Published on: May 11, 2017
Hydrophilic modification on polyvinyl alcohol membrane by hyaluronic acid
Yan Liu1, Huiyuan Hu1, Xinlin Yang1
1College of Chemistry and Environmental Engineering, Shenzhen University, No. 3688 Nanhai Road, Nanshan District, Shenzhen, Guangdong Province, People's Republic of China.
Abstract:
PVA was dissolved in mixed solvent (DMSO and water) and followed by several freeze-thaw cycles in a mold to produce PVA membrane. Surface modification of PVA membranes by HA molecules was investigated to improve the hydrophilicity of the membrane surface thereby reducing adsorption of the proteins onto the membrane. The surface composition, water contact angle, optical and mechanical properties, surface morphology, cell compatibility and protein adhesion were systematically investigated. ATR-FTIR spectra, XPS, SEM and AFM indicated that PVA membranes were successfully modified by grafting of the HA. The modified membranes showed increased hydrophilicity and cytocompatibility, decreased surface roughness and mechanical properties, and suppressed cell and protein adhesion compared to the pristine membrane. In general, the achievement of the HA coating with anti-adhesive property can potentially be widely used on surface modification of artificial cornea and other biomedical implants.
More Related Videos
Related Concept Videos
Acidity and Basicity of Alcohols and Phenols
Acid Halides to Alcohols: Grignard Reaction
Grignard reagents are a source of carbanions and function as nucleophiles. The mechanism begins with the nucleophilic attack by the carbanion at the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs,...
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Carboxylic Acids to Primary Alcohols: Hydride Reduction
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Nonenolizable Aldehydes to Acids and Alcohols: The Cannizzaro Reaction

