Adsorption of hydrophobically end-capped poly(ethylene glycol) on cellulose.

Adsorption of poly(ethylene glycol), hydrophobically end-capped with octadecenylsuccinic anhydride (OSA-PEG-OSA), on an ultrathin film of cellulose has been studied by quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM). Normally, PEG does not adsorb on cellulosic surfaces, but the use of the telechelic hydrophobic modification was found to promote adsorption. The influence of the conformation of the polymer in solution prior to adsorption and the subsequent properties of the adsorbed layer were investigated.

CMC-modified cellulose biointerface for antibody conjugation.

In this Article, we present a new strategy for preparing an antihemoglobin biointerface on cellulose. The preparation method is based on functionalization of the cellulose surface by the irreversible adsorption of CMC, followed by covalent linking of antibodies to CMC. This would provide the means for affordable and stable cellulose-based biointerfaces for immunoassays.

Arrangements of cationic starch of varying hydrophobicity on hydrophilic and hydrophobic surfaces.

Arrangements of cationic starches hydrophobized by acetylation (CS-acet) deposited from aqueous electrolyte solutions onto hydrophilized and hydrophobized silica surfaces were investigated by atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and contact angle measurements. The influence of electrolyte composition, acetylation degree of cationic starch (DS(ACET)), and deposition method was examined. On a hydrophobic substrate, CS-acet formed an open film with structure strongly dependent on DS(ACET) and electrolyte composition of the solution.

Effect of polycation length on its complexation with DNA and with poly(oxyethylene-block-sodium methacrylate).

Polyelectrolyte complexes of a synthetic polycation with either a genomic DNA or a synthetic poly(oxyethylene-block-sodium methacrylate), POE-b-PMANa, have been studied in aqueous solutions as a function of cation:anion ratio, the degree of polymerization of the polycation, the ionic strength, and temperature using dynamic light scattering and turbidity measurements. The polycation was a copolymer of methacryl oxyethyl trimethylammonium chloride and poly(oxyethylene) monomethyl ether monomethacrylate with 4-5 oxyethylene repeating units, PMOTAC-g-POE. The molar masses of the polycations in a homological series were 0.

Overcharging of polyelectrolyte complexes by the guest polyelectrolyte studied by fluorescence spectroscopy.

Polyion complexes (PICs) of anionic block copolymer poly(ethylene oxide)-block-poly(sodium methacrylate), PEO-block-(PMA)Na, and a cationic homopolymer, poly((methacryloyloxyethyl)trimethylammonium chloride), PMOTAC, have been studied by fluorescence spectroscopy. Pyrene and naphthalene singly labeled block copolymers were used with two different sodium methacrylate block lengths. The chain exchange between the stoichiometric PICs at the equilibrium state and the formation of the negatively charged PICs on addition of excess PEO-block-(PMA)Na to stoichiometric PIC solution were of interest.