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1.
J Colloid Interface Sci ; 423: 48-53, 2014 Jun 01.
Article in English | MEDLINE | ID: mdl-24703667

ABSTRACT

Achieving a stable and robust dispersion of ultrafine particles in concentrated electrolytes is challenging due to the shielding of electrostatic repulsion. Stable dispersion of ultrafine particles in concentrated electrolytes is critical for several applications, including electro-codeposition of ceramic particles in protective metal coatings. We achieved the steric stabilization of SiC micro- and nano-particles in highly concentrated electroplating Watts solutions using their controlled coating with linear and branched polyethyleneimines (PEI) as dispersants. Branched polyethyleneimine of 60,000 MW effectively disperses both microparticles and nanoparticles at a concentration of 1000 ppm. However, lower polymer dosages and smaller polymers fail to disperse, presumably due to insufficient coverage and bridging flocculation. Dispersion stability correlates well with the adsorption density of PEI on microparticles. We discuss the results in the framework of DLVO theory and suggest possible dispersion mechanisms. However, though the dispersion is enhanced with extended adsorption time, the residual PEI in solution adversely affects electroplating. We overcome this drawback by precoating the particles with the polymer and resuspending them in Watts solution. With this novel approach, we obtained robust dispersions. These results offer new possibilities to control dispersion at high electrolyte concentration, as well as bring new insights into the dispersion phenomenon.


Subject(s)
Carbon Compounds, Inorganic/chemistry , Electrolytes/chemistry , Nanoparticles/chemistry , Polyethyleneimine/chemistry , Silicon Compounds/chemistry , Nanoparticles/ultrastructure , Osmolar Concentration , Solubility
2.
AAPS PharmSciTech ; 12(4): 1186-92, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21918918

ABSTRACT

Microparticle powders for nasal delivery were formulated to contain the model drug, zolmitriptan, and varying proportions of different polymers. The objective of the study was to investigate the effects of these formulative parameters on the surface chemistry of the spray-dried microparticles and their potential for adhesion to the tested substrates, porcine mucin, and nasal tissue. The polymers used were chitosans of varying ionization states and molecular weights and hydroxypropyl methyl cellulose. The surface energies of the surfaces of the microparticles were determined using contact angle measurements and the van Oss model. The theory of surface thermodynamics was applied to determine the theoretical potential for the different materials to adhere to the substrates. It was found that the drug or polymers alone, as well as the various formulations, were more likely to adhere to mucin than to nasal tissue. Further, there was a trend for higher molecular weight chitosans to adhere better to the substrates than lower molecular weight chitosans. Similarly, adhesion was improved for formulations with a higher content of polymers. These theoretical predictions may be compared with further experimental results and be of use in making informed decisions on the choice of formulations for future expensive bio-studies.


Subject(s)
Chitosan/chemistry , Drug Carriers , Methylcellulose/analogs & derivatives , Mucins/chemistry , Oxazolidinones/chemistry , Serotonin 5-HT1 Receptor Agonists/chemistry , Tryptamines/chemistry , Adhesiveness , Animals , Chemistry, Pharmaceutical , Chitosan/metabolism , Drug Compounding , Hypromellose Derivatives , Methylcellulose/chemistry , Methylcellulose/metabolism , Molecular Weight , Nasal Mucosa/metabolism , Oxazolidinones/metabolism , Powders , Serotonin 5-HT1 Receptor Agonists/metabolism , Surface Properties , Sus scrofa , Technology, Pharmaceutical/methods , Thermodynamics , Tryptamines/metabolism
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