Methods of treating and/or preventing nail conditions and/or improving appearance of nails
A nail and methyl ethyl ketone technology, used in manicure, skin diseases, pharmaceutical formulations, etc., can solve problems such as slow treatment methods, no effect on improving the appearance of nails, and aggravating activities.
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[0083] According to some embodiments of the present invention, the polyiso(thio)cyanate is included in the poly(urea-urethane) polymer. Any suitable polyiso(thio)cyanate may be included in the composition including, for example, aliphatic polyisocyanates, aromatic polyisocyanates, cycloaliphatic polyisocyanates, polyisocyanate heterocycles and heteroaromatic polyisocyanates. Exemplary polyisocyanates include, polyaryl polyisocyanates as defined in US Patent No. 2,683,730; toluene diisocyanate (also known as "TDI"); triphenylmethane-4,4'4" triisocyanate, benzene-1,3,5-triisocyanate; toluene-2,4,6-triisocyanate; diphenyl-2,4,4'-triisocyanate; hexamethylene diisocyanate; xylylene Diisocyanate; Chlorene diisocyanate; Diphenylmethane-4,4'-diisocyanate; Naphthalene-1,5-diisocyanate; Xylene-α,α'diisothiocyanate; 3,3'-diisocyanate Methyl-4,4'-biphenylene diisocyanate; 3-3'dimethoxy-4,4'-biphenylene diisocyanate; 2',3,3'-dimethyl-4, 4'-biphenylene diisocyanate; 5,5'-tetramethyl-4,4'...
Embodiment 1
[0134] Exemplary compositions of the present invention are provided below. The amounts of all components are determined in terms of stoichiometric equilibrium volumetric contents, expressed in milliliters. Liquid thermoset, hydrophobic, elastic, non-toxic polymer solution compositions are prepared by adding reactants in the sequence given by the formula below. The solution was continuously agitated and mixed at 20 revolutions per minute during the continuous addition of the ingredients, and 15 to 20 minutes after the addition of the last components. These parameters of the agitation mixing process, in terms of revolutions and time, are optimal to obtain maximum continuous reactivity of the ingredients during blending. The sequential mixing process was performed at ambient conditions of 70-80°F, approximately 750-760 mm Hg, and 50-65% relative humidity.
[0135] Therapeutic Device Formulation #1 Job Identifier: PMS-P-1000
[0136]
[0137] Therapeutic Device Formulati...
Embodiment 2
[0153]For each of Examples 2-12, the reagents were added in the order indicated and stirred for about 5 minutes between reagent additions. The MDI was added last and was added slowly with stirring. The reactants were kept at room temperature and about 70°C throughout the reaction. After the isocyanate addition was complete, the reaction was stirred for about 10 minutes and then transferred to a sample tank for storage using high performance liquid chromatography (HPLC), gel permeation chromatography (GPC), gel permeation chromatography with multi-angle light prior to storage Scattering Detection (GPC-MALS), Nuclear Magnetic Resonance (NMR) Spectroscopy Fourier Transform Infrared (FT-IR Combination) Spectroscopy was performed to determine molecular weight, confirm chemical structure, and confirm reaction completion. Fourier transform infrared (FT-IR) spectroscopy was performed using high performance liquid chromatography (HPLC), gel permeation chromatography (GPC), gel permeat...
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