Inexpensive and non-toxic water repellent coatings comprising SiO2 nanoparticles and long chain fatty acids

Special wettability durable coatings, with average water contact angles exceeding 140°, have been fabricated utilising functionalised hydrophobic-SiO2(H-SiO2) particles embedded in fatty acids. The inexpensive and non-toxic H-SiO2particles imparted delicate lotus leaf inspired hierarchical surface nano-morphologies while the fatty acid modification afforded a suitable drop in surface energy. Comparison studies were carried out to explore the effects of fatty acid chain length and pipette as opposed to spray coating deposition methods on the coatings hydrophobicity. It was determined that the longest chain length fatty acid coatings showed enhanced hydrophobic properties due to their extended hydrophobic alkyl chain. A pipette deposited suspension containing H-SiO2nanoparticles and octadecanoic acid generated a coating with the most favourable average water contact and tilting angles of 142 ± 6° and 16 ± 2° respectively

Role of MC1R variants in uveal melanoma

Variants of the melanocortin-1 receptor (MC1R) gene have been linked to sun-sensitive skin types and hair colour, and may independently play a role in susceptibility to cutaneous melanoma. To assess the role of MC1R variants in uveal melanoma, we have analysed a cohort of 350 patients for the changes within the major region of the gene displaying sequence variation. Eight variants were detected – V60L, D84E, V92M, R151C, I155T, R160W, R163Q and D294H – 63% of these patients being hetero- or homozygous for at least one variant. Standard melanoma risk factor data were available on 119 of the patients. MC1R variants were significantly associated with hair colour (P¼0.03) but not skin or eye colour. The frequency of the variants detected in the 350 patients was comparable with those in the general population, and comparison of the cumulative tumour distribution by age at diagnosis in carriers and noncarriers provided no evidence that MC1R variants confer an increased risk of uveal melanoma. We interpret the data as indicating that MC1R variants do not appear to be major determinants of susceptibility to uveal melanoma. © 2003 Cancer Research U