2001
DOI: 10.1002/1521-3935(20010401)202:7<1161::aid-macp1161>3.0.co;2-0
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Micellar Behavior of Sugar-Carrying Polystyrene in Aqueous Solution

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Cited by 11 publications
(5 citation statements)
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“…It is reported that the introduction of saccharide residues in the side chain of a polymer increased the water solubility [45], so it is expected that the glucose residue in chitosan-DG will increase its water solubility. The lower DS (9.8%) derivative was dissolved in the water to give a transparent solution.…”
Section: Hydrophobic Modificationsmentioning
confidence: 99%
“…It is reported that the introduction of saccharide residues in the side chain of a polymer increased the water solubility [45], so it is expected that the glucose residue in chitosan-DG will increase its water solubility. The lower DS (9.8%) derivative was dissolved in the water to give a transparent solution.…”
Section: Hydrophobic Modificationsmentioning
confidence: 99%
“…Since amphiphilic PVLA has both hydrophobic backbone and hydrophilic pendant chain, PVLA molecules in aqueous solution form a micelle structure, consisting of a hydrophobic inner core and hydrophilic outer shell. 24 It can be inferred that the lumpy parts shown in Figure 5a,b are the aggregates of micelles. Hepatocyte Adhesion.…”
Section: Resultsmentioning
confidence: 98%
“…In contrast, the surface coated with 5 mg/mL PVLA solution was uneven and divided into two parts (Figure a,b), the PVLA-coated and uncoated parts. Since amphiphilic PVLA has both hydrophobic backbone and hydrophilic pendant chain, PVLA molecules in aqueous solution form a micelle structure, consisting of a hydrophobic inner core and hydrophilic outer shell . It can be inferred that the lumpy parts shown in Figure a,b are the aggregates of micelles.…”
Section: Resultsmentioning
confidence: 99%
“…In this way, the exploration of novel fluoroalkyl end-capped oligomers containing numerous hydroxyl segments is of particular interest, from the developmental viewpoints of new fluorinated functional materials. In a variety of hydroxylated polymers, much attention has been focused on the synthetic sugar-containing polymers (glycopolymers), which possess the pendent gluconic residues (pentaol units), owing to their role as biomimetic analogues and their applications in biomedical and technological fields such as paints and cosmetics [ 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 ]. In fact, poly(allylamine) can react with gluconolactone in water to provide the gluconamide-substituted polymers, successively affording the hydrogel through the interaction of the corresponding polymers with borax [ 20 ].…”
Section: Introductionmentioning
confidence: 99%