نتایج جستجو برای: Dissolution test

تعداد نتایج: 831608  

Journal: :iranian journal of pharmaceutical research 0
alen shahbazian department of medicinal chemistry, pharmaceutical sciences branch, islamic azad university, tehran, iran. asghar davood department of medicinal chemistry, pharmaceutical sciences branch, islamic azad university, tehran, iran alireza dabirsiaghi department of pharmaceutical sciences, pharmaceutical sciences branch, islamic azad university, tehran, iran.

piroxicam has two different crystalline forms (known as needle and cubic forms), that they are different in physicochemical properties such as biological solubility. in the current research, using taguchi experimental design approach the influences of five operating variables on formation of the piroxicam polymorph shapes in recrystallization were studied. the variables include type of solvent,...

Journal: :Japanese Journal of Hospital Pharmacy 1984

2013
Sree Lakshmi A. V. Badarinath

Dissolution testing of the drug formulation introduced in 1960 since then the importance of dissolution test has grown rapidly as have the number of tests and demands in quality control laboratories. Dissolution testing is an official test used by pharmacopeias for evaluating drug release of solid and semisolid dosage forms. The main applications of the dissolution testing include biopharmaceut...

2009
N. Singla G. D. Gupta A. K. Singla

Biorelevant in vitro dissolution is a useful technique for qualitative forecasting of the in vivo behavior of a formulation. A biorelevant dissolution medium for simvastatin was developed with a lower concentration of surfactant (0.1% sodium lauryl sulfate, SLS) in the medium as compared with the 0.5% SLS concentration stated in the USP monograph. The slower dissolution rate of simvastatin tabl...

2009
Georgeta Ionica F. Radulescu Dalia Miron Valentina Anuta C. Mircioiu Ionela Belu

This paper presents results of a pharmacokinetics study concerning pentoxifylline and its main metabolites after administration of extended release formulation of Trental 400 mg and correlation of this pharmacokinetics with in vitro dissolution test results of parent drug. In order to establish most relevant in vitro test, dissolution was performed in different experimental conditions (stirring...

2005
Piero Armenante Fernando Muzzio

Introduction Dissolution testing is routinely carried out in the pharmaceutical industry to determine the rate of dissolution of solid dosage forms. In addition to being a regulatory requirement, in-vitro dissolution testing is used to assist with formulation design, process development, and the demonstration of batch-to-batch reproducibility in production. The most common of such dissolution t...

Journal: :iranian journal of pharmaceutical research 0
jin bin liao school of chinese materia medica, guangzhou university of chinese medicine, guangzhou, china. yong zhuo liang school of chinese materia medica, guangzhou university of chinese medicine, guangzhou, china. yun long chen school of chinese materia medica, guangzhou university of chinese medicine, guangzhou, china. jian hui xie school of chinese materia medica, guangzhou university of chinese medicine, guangzhou, china. wei hai liu dongguan mathematical engineering academy of chinese medicine, guangzhou university of chinese medicine, dongguan, china jian nan chen institute of higher education, guangzhou university of chinese medicine, guangzhou, china.

the present study investigates the possibility of using poloxamers as solubility and dissolution rate enhancing agents of poorly water soluble bioactive constituent patchouli alcohol (pa) that can be used for the preparation of immediate release pellets formulation. two commercially available grades poloxamer 188 (p 188) and poloxamer 407 (p 407) were selected, and solid dispersions (sds) conta...

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