The synthesis of amphiphilic diblock copolymers: An investigation into the formation of micelles as a function of hydrophobic block length

Acrylate-based amphiphilic diblock copolymers show great potential for anti-cancer drug transport due to their ability to aggregate into protective core-shell micelles. Using RAFT polymerization, copolymers containing poly(acrylic acid) and poly(methyl acrylate) blocks were made with high monomer conversion and narrow distributions of molecular weight for eventual use in medicinal applications. Based on previous findings of copolymers with low weight hydrophobic blocks failing to micellize, it was hypothesized that increasing the poly(methyl acrylate) block length would allow for micelle formation. 1H-NMR experiments conducted in the presence of an aqueous solution yielded diminished and broadened resonances of the lengthened hydrophobic block, which confirmed effects of micellization. As a result, a rigid hydrophobic core may be substituted with a longer flexible acrylate block for biological use. The adoption of longer core chain lengths in a micellar system may be useful in other transport applications when precipitation of drugs in vivo remains an issue

Vitamin A levels in patients with CF are influenced by the inflammatory response

Background: Serum vitamin A, normally depressed in inflammatory conditions, is frequently low in people with CF. Vitamin A is important in respiratory epithelial regeneration and repair. We hypothesised that serum vitamin A would be associated with inflammation and disease severity. Methods: Serum vitamin A (as retinol), C-reactive protein (CRP), vitamin E, 25-hydroxy vitamin D (25OHD), 1,25-dihydroxy vitamin D (1,25(OH)D), weight, and lumbar spine bone mineral density (LSBMD) were measured in 138 subjects with CF (5-56 years) and 138 control subjects (5-48 years). FEV, presence of CF liver disease (CFLD) and hospital admissions were recorded in those with CF. Results: Serum vitamin A level was lower in CF subjects than in controls (mean, 95% CI: 1.29, 1.0-1.37 vs. 1.80, 1.7-1.87 μmol/l,

Height and weight fail to detect early signs of malnutrition in children with cystic fibrosis

Background: Many children with cystic fibrosis grow poorly and are malnourished. This study was undertaken to determine whether extensive anthropometry could detect early signs of malnutrition in prepubertal children with cystic fibrosis to prevent deficits in height and weight