Susanna Holappa

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. The preparation and characterization of the biointerface were studied on Langmuir-Schaefer cellulose model surfaces in real time using the quartz crystal microbalance with dissipation and surface plasmon resonance techniques. The stable attachment of antihemoglobin to adsorbed CMC was achieved, and a linear calibration of hemoglobin was obtained. CMC modification was also observed to prevent nonspecific protein adsorption. The antihemoglobin-CMC surface regenerated well, enabling repeated immunodetection cycles of hemoglobin on the same surface.

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. The adsorption experiments were done at concentrations below and above the critical association concentration. The adsorption of OSA-PEG-OSA on cellulose was observed to occur in four distinct stages. Because of the amphiphilic nature of cellulose, further adsorption experiments were performed on hydrophobic (polystyrene) and hydrophilic (silica) model substrates to illuminate the contribution of hydrophobic and hydrophilic factors in the adsorption phenomenon. As expected, the kinetics and the mechanism of adsorption were strongly dependent on the chemical composition of the substrate.

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. On a hydrophilic substrate, acetylation increased the hydrophobicity of the film when the starch was deposited by adsorbing. When deposition was made by spin coating, i.e., the CS-acet was forced onto the substrate, the hydrophobic tuning by acetylation was lost. The films deposited by spin coating were thicker and considerably rougher than those deposited by adsorbing.