Results 1 to 10 of about 475,693 (306)
Developing and evaluation of orodispersible tablets containing caffeine [PDF]
Romanian Journal of Pharmaceutical Practice, 2021 Starting from the premise that a reduced number of active pharmaceutical ingredients (APIs) are used to treat hypotension, the aim of this study consisted of developing new formulations of caffeine-orodispersible tablets (CAFODTs).
Robert-Alexandru Vlad +7 more
doaj +1 more source
Dissolution Test for Mianserin Hydrochloride in Tablets
Drug Analytical Research, 2019 A dissolution test for mianserin hydrochloride in coated tablets containing 30 mg was developed and validated using a fast ultraviolet spectrophotometric method.
Letícia Lenz Sfair +3 more
doaj +9 more sources
Alternative Methods for Dissolution Profile Comparison in the Dissolution Test
Разработка и регистрация лекарственных средств, 2021 Introduction. The article discusses the problem of assessing the similarity of the dissolution profiles of two batches of the nebivolol. The use of a generally accepted similarity factor for assessing equivalence is unacceptable in some cases, for ...
D. P. Romodanovsky, D. V. Goryachev
doaj +1 more source
Edible Gels with Cranberry Extract: Evaluation of Anthocyanin Release Kinetics
Gels, 2023 The bioactive compounds found in cranberry fruit are natural antioxidants, and their consumption reduces the risk of diabetes, cardiovascular disease, cancers, and urinary tract infections.
Rima Šedbarė +2 more
doaj +1 more source
Validation of a UV spectrophotometric method to quantify losartan potassium in tablets from the dissolution test at pH 1.2, 4.5 and 6.8 [PDF]
Journal of Pharmacy & Pharmacognosy Research, 2022 Context: The validation of a method is synonymous with the quality of the obtained results. The dissolution test is an analytical technique to evaluate the quality and stability of drugs during their development.
Antonella S. Araujo-Fernandez +5 more
doaj
Dissolution test for glibenclamide tablets
Química Nova, 2007 The aim of this work is to develop and validate a dissolution test for glibenclamide tablets. Optimal conditions to carry out the dissolution test are 500 mL of phosphate buffer at pH 8.0, paddles at 75 rpm stirring speed, time test set to 60 min and ...
Elisabeth Aparecida dos Santos Gianotto +4 more
doaj +1 more source
Fast and Efficient Monitoring of Diclofenac Dissolution Profile by CE [PDF]
, 2014 Capillary electrophoresis (CE) was used to follow Diclofenac tablet dissolution, in very short times and allowing dissolution testing without volume replacement. By using Student´s t test and F-test, this CE method was compared with HPLC.
Delfino, Mario Raul +3 more
core +1 more source
Automation of Dissolution Tests [PDF]
Dissolution Technologies, 2000 Dissolution testing of drug formulations was introduced in the 1960s and accepted by health regulatory authorities in the 1970s. Since then, the importance of dissolution has grown rapidly as have the number of tests and demands in quality‐control laboratories.
openaire +2 more sources
Bubble dissolution in horizontal turbulent bubbly flow in domestic central heating system [PDF]
, 2013 In a domestic central heating system, the phenomenon of microbubble nucleation and detachment on the surface of a boiler heat exchanger finds its origins in the high surface temperature of the wall and consequential localised super saturation ...
Brunel University +4 more
core +1 more source
Química Nova, 2010 A simple liquid chromatographic method was optimized for the quantitative determination of terbinafine in pharmaceutical hydroalcoholic solutions and tablets, and was also employed for a tablet dissolution test.
Monika P. Tagliari +5 more
doaj +1 more source