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In the pharmaceutical industry, drug dissolution testing is routinely used to provide critical in vitro drug release information for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict in vivo drug release profiles. [1]
In pharmaceutics, sink condition is a term mostly related to the dissolution testing procedure.. It means using a sheer volume of solvent, usually about 5 to 10 times greater than the volume present in the saturated solution of the targeted chemical (often the API, and sometimes the excipients) contained in the dosage form being tested.
The USP is published in a combined volume with the National Formulary (a formulary) as the USP-NF. [2] If a drug ingredient or drug product has an applicable USP quality standard (in the form of a USP-NF monograph), it must conform in order to use the designation "USP" or "NF".
Partition coefficients can be measured experimentally in various ways (by shake-flask, HPLC, etc.) or estimated by calculation based on a variety of methods (fragment-based, atom-based, etc.). If a substance is present as several chemical species in the partition system due to association or dissociation , each species is assigned its own K ow ...
Diammonium phosphate (DAP; IUPAC name diammonium hydrogen phosphate; chemical formula (NH 4) 2 (HPO 4)) is one of a series of water-soluble ammonium phosphate salts that can be produced when ammonia reacts with phosphoric acid. Solid diammonium phosphate shows a dissociation pressure of ammonia as given by the following expression and equation: [2]
A quantitative method to determine the amount of phosphate present in samples, such as boiler feedwater, is as follows. A measured amount of boiler water is poured into a mixing tube and ammonium heptamolybdate reagent is added. The tube is then stoppered and vigorously shaken.
Another method by which sustained release is achieved is through an osmotic controlled-release oral delivery system, where the active compound is encased in a water-permeable membrane with a laser drilled hole at one end. As water passes through the membrane the drug is pushed out through the hole and into the digestive tract where it can be ...
In the present day, the method is applied, among other areas, in measuring osmolarity in lens care solutions as well as eye drops. [8] It is further used in clinical chemistry, pharmaceutical, and quality control laboratories, where it facilitates different processes. As compared to the other methods, the freezing point depression osmometer has ...