Abstract: A method and kit for treating a nail surface. The method includes brushing or spraying an adhesive on a coated or uncoated nail surface to form an adhesive-coated surface. A covering (e.g., a curable nail gel, evaporative nail polish, or artificial nail) is then applied to the adhesive-coated surface. The covering is removable by soaking in solvent for less than 20 minutes, peeling, or a combination thereof.

Abstract: A method and kit for treating a nail surface. The method includes brushing or spraying an adhesive on a coated or uncoated nail surface to form an adhesive-coated surface. A covering (e.g., a curable nail gel, evaporative nail polish, or artificial nail) is then applied to the adhesive-coated surface. The covering is removable by soaking in solvent for less than 20 minutes, peeling, or a combination thereof.

Abstract: A method and kit for treating a nail surface. The method includes brushing or spraying an adhesive on a coated or uncoated nail surface to form an adhesive-coated surface. A covering (e.g., a curable nail gel, evaporative nail polish, or artificial nail) is then applied to the adhesive-coated surface. The covering is removable by soaking in solvent for less than 20 minutes, peeling, or a combination thereof.

Abstract: Provided is a slow-release delivery vehicle for delivering at least one active ingredient into a film coating, comprising a population of stable, homogeneously-dispersed, porous polymeric or co-polymeric beads having a network of pores, wherein the at least one active ingredient is held within the bead particles and within the network of pores and slowly released by internal flow, and wherein the network of pores is substantially non-collapsible upon removal of the active ingredient. The porous co-polymer bead preparation comprises a continuous aqueous phase solution containing a monomeric mixture of at least one polyvinylaromatic monomer and at least one porogen forming a network that comprising (i) macropores; (ii) mesopores; (iii) micropores; and (iv) gel porosity. Also provided are methods of preparing the porous co-polymer bead preparation; and for its use as a slow-release delivery vehicle.

Abstract: A toothbrush having brush means and a means to support the brush means; and a one or two part therapeutic tooth treatment composition which becomes activated when wet incorporated on the brush means or within the toothbrush means to support the brush means in a manner such that the composition remains inactive during storage and is only activated when contacted with water or saliva; and a method comprising brushing a tooth with the toothbrush so that the brush means become wet with saliva, optionally wetting the brush means with water immediately prior to brushing a tooth, and the composition becomes activated to form a therapeutic composition to provide remineralization, whitening, and/or fluoridation.

Abstract: A toothbrush having brush means and a means to support the brush means; and a one or two part therapeutic tooth treatment composition which becomes activated when wet incorporated on the brush means or within the toothbrush means to support the brush means in a manner such that the composition remains inactive during storage and is only activated when contacted with water or saliva; and a method comprising brushing a tooth with the toothbrush so that the brush means become wet with saliva, optionally wetting the brush means with water immediately prior to brushing a tooth, and the composition becomes activated to form a therapeutic composition to provide remineralization, whitening, and/or fluoridation.

Abstract: A method of preparing colored UV-curable artificial nail gel compositions comprising dispersing a pigment in an organic liquid to form a pigment concentrate and mixing the pigment concentrate with a polyfunctional acrylic monomer and/or a polyfunctional acrylic oligomer, and the resultant highly colored artificial nail gel are disclosed.

Abstract: A method of preparing colored UV-curable artificial nail gel compositions comprising dispersing a pigment in an organic liquid to form a pigment concentrate and mixing the pigment concentrate with a polyfunctional acrylic monomer and/or a polyfunctional acrylic oligomer, and the resultant highly colored artificial nail gel are disclosed.

Abstract: Provided is a slow-release delivery vehicle for delivering at least one active ingredient into a film coating, comprising a population of stable, homogeneously-dispersed, porous polymeric or co-polymeric beads having a network of pores, wherein the at least one active ingredient is held within the bead particles and within the network of pores and slowly released by internal flow, and wherein the network of pores is substantially non-collapsible upon removal of the active ingredient. The porous co-polymer bead preparation comprises a continuous aqueous phase solution containing a monomeric mixture of at least one polyvinylaromatic monomer and at least one porogen forming a network that comprising (i) macropores; (ii) mesopores; (iii) micropores; and (iv) gel porosity. Also provided are methods of preparing the porous co-polymer bead preparation; and for its use as a slow-release delivery vehicle.

Abstract: Quick drying coating compositions, preferably but not exclusively for application to natural or artificial nails are provided. The quick-drying coating composition comprises a base or lacquer component and an optional pigment component. The base component can dry in less than about 70 seconds under ambient conditions, yet is free of undesirable solvents and components such as acetone, toluene, chlorinated hydrocarbons, and formaldehyde-containing resins. The base component includes film-forming polymers, a monomer component compatible with the polymers, and a free radical source.

Abstract: Materials and methods for increasing the adhesion of adhesives and coatings to proteinaceous substrates are provided wherein a liquid substantially acid-free hydrophilic acrylate monomer composition is employed to treat the substrate before application of adhesives and coating thereto.

Abstract: New bile acid sequestrant polymer compositions and a process for preparing the polymers in particulate form, preferably in spherical form, are described. The polymer particles are prepared by crosslinking an amine-containing polymer with an amount of a polyfunctional amine-reactive compound sufficient to crosslink the polymer so that it is essentially water insoluble and has bile acid sequestering efficacy greater than that of cholestyramine, preferably greater than about three times the efficacy of cholestyramine. A preferred polymerization process revolves suspension polymerization of water-soluble amine-containing monomers, such as dialkylaminoalkyl (meth)acrylate esters and dialkylaminoalkyl (meth)acrylamides, in the presence of polyfunctional amine-reactive compounds, such as substituted dihaloalkanes. Pharmaceutical compositions containing the bile acid sequestrant polymer particles and a method for lowering blood cholesterol levels using the pharmaceutical compositions are also described.

Abstract: A process is provided for suspension polymerization of water-soluble monomers in aqueous suspension to form spherical, unagglomerated polymer beads. The polymerization is conducted in the presence of a nonionic, substituted hydroxyalkylcellulose dispersant which is especially effective in protecting the monomer droplets from coalescence prior to their forming stable polymer particles.

Abstract: New bile acid sequestrant polymer compositions and a process for preparing the polymers in particulate form, preferably in spherical form, are described. The polymer particles are prepared by crosslinking an amine-containing polymer with an amount of a polyfunctional amine-reactive compound sufficient to crosslink the polymer so that it is essentially water insoluble and has bile acid sequestering efficacy greater than that of cholestyramine, preferably greater than about three times the efficacy of cholestyramine. A preferred polymerization process involves suspension polymerization of water-soluble amine-containing monomers, such as dialkylaminoalkyl (meth)acrylate esters and dialkylaminoalkyl (meth)acrylamides, in the presence of polyfunctional amine-reactive compounds, such as substituted dihaloalkanes. Pharmaceutical compositions containing the bile acid sequestrant polymer particles and a method for lowering blood cholesterol levels using the pharmaceutical compositions are also described.

Abstract: A bile acid sequestrant having a crosslinked polymeric matrix and having branches supported on the polymeric matrix and providing bonding sites for binding bile acid conjugates to the sequestrant, pharmaceutical compositions containing the sequestrant for treatment of elevated plasma cholesterol level are described.

Abstract: New bile acid sequestrant polymer compositions and a process for preparing the polymers in particulate form, preferably in spherical form, are described. The polymer particles are prepared by crosslinking an amine-containing polymer with an amount of a polyfunctional amine-reactive compound sufficient to crosslink the polymer so that it is essentially water insoluble and has bile acid sequestering efficacy greater than that of cholestyramine, preferably greater than about three times the efficacy of cholestyramine. A preferred polymerization process involves suspension polymerization of water-soluble amine-containing monomers, such as dialkylaminoalkyl (meth)acrylate esters and dialkylaminoalkyl (meth)acrylamides, in the presence of polyfunctional amine-reactive compounds, such as substituted dihaloalkanes. Pharmaceutical compositions containing the bile acid sequestrant polymer particles and a method for lowering blood cholesterol levels using the pharmaceutical compositions are also discribed.