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This work describes the synthesis and characterization of a new series of semifluorinated sulfonated polytriazole copolymers (PTATSH‐XX) with varying degree of sulfonation and higher IEC. The copolymers have been prepared by click reaction using a combination of diazide monomers; a newly synthesized diazide monomer namely 4,4‐bis[3‐trifluoromethyl‐4(4‐azidophenoxy)phenyl]benzene (TAZ) and a commercially available diazide monomer namely 4,4′‐diazido‐2,2′‐stilbenedisulfonic acid disodium salt (DADSDB) with a bis‐alkyne monomer namely 4,4′‐(propane‐2,2‐diyl)bis((prop‐2‐ynyloxy)benzene) (BPEBPA). The copolymers are well characterized by FTIR and NMR spectroscopy and have exhibited good solubility and film forming abilities along with good thermal and chemical stability, low water uptake, good dimensional stability and high mechanical properties. The TEM micrographs of the copolymer membranes show good phase separated morphology with cluster size in the range 10–60 nm. The proton conductivity values of the copolymer membranes are found in the range of 15–90 mS cm−1 at 80°C and 16–97 mS cm−1 at 90°C. POLYM. ENG. SCI., 57:312–323, 2017. © 2016 Society of Plastics Engineers

A series of polytriazole copolymers were synthesized by the click polymerization of fluorinated dialkyne with a mixture of two different diazide monomers and the proton exchange membrane properties of the copolymers were investigated.

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Objectives Fetuin-A is a circulating glycoprotein, formed in the liver. It regulates bone remodelling and calcium metabolism. Fetuin-A has adipogenic properties, so fat accumulation in the liver may be associated with higher levels of fetuin-A. Fetuin-A is an inhibitor of the phosphorylation of the insulin receptor tyrosine kinase. Key findings High concentrations of fetuin-A in humans causes insulin resistance. Insulin sensitivity is also found to be increased in fetuin-A knockout mice. Fetuin-A has been shown to cause insulin resistivity in type-2 diabetes mellitus and worsens the pro-atherogenic milieu. Summary Fetuin-A should be considered as a hepatic bio-marker. Vascular diseases like atherosclerosis are major causes of disability in patients with diabetes mellitus.