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Other formulations have been developed over time. In 1916, Marcel Daufresne substituted sodium bicarbonate for Dakin's boric acid as buffering agent. [7] [17] This formulation is the basis of current commercial products. [18] The concentration chosen by Dakin (0.5%) was the maximum highest concentration found tolerable to the skin.
Boric acid is a weak acid, with pK a (the pH at which buffering is strongest because the free acid and borate ion are in equal concentrations) of 9.24 in pure water at 25 °C. But apparent p K a is substantially lower in swimming pool or ocean waters because of interactions with various other molecules in solution.
Burow's solution is an aqueous solution of aluminium triacetate.It is available in the U.S. as an over-the-counter drug for topical administration, with brand names including Domeboro (Moberg Pharma), Domeboro Otic (ear drops), Star-Otic, and Borofair. [1]
The following is a sample recipe for BBS: 10 mM Sodium borate; 150 mM NaCl; Adjust pH to pH 8.2 The simplest way to prepare a BBS solution is to use BBS tablets. They are formulated to give a ready to use borate buffered saline solution upon dissolution in 500 ml of deionized water.
Figure 1.0 - Basic anatomical features of the human eye. Ophthalmic drug administration is the administration of a drug to the eyes, most typically as an eye drop formulation. Topical formulations are used to combat a multitude of diseased states of the eye. These states may include bacterial infections, eye injury, glaucoma, and dry eye. [1]
Boroline is an over-the-counter antiseptic cream sold in India by G. D. Pharmaceuticals. The cream is marketed as a natural and ayurvedic solution for various skin issues such as cuts, cracked lips, rough skin, and infections. The product traces its origins to the Swadeshi movement prevalent in India in the 1920s. First produced in 1929 by Gour ...
Fluoroboric acid is corrosive and attacks the skin. It is available commercially as a solution in water and other solvents such as diethyl ether. It is a strong acid with a weakly coordinating, non-oxidizing conjugate base. [2] It is structurally similar to perchloric acid, but lacks the hazards associated with oxidants.
At a meeting of the Society of Arts, on March 29, 1882, Professor Barff delivered a lecture, in which he announced his discovery of boro-glycerine. Barff had been attempting to find a way in which boric acid, a known antiseptic, could be used to preserve meats, at a time when beef prices were considered high.