نتایج جستجو برای: dissolution reprecipitation

تعداد نتایج: 21070  

2017
Lukas Uebbing Lukas Klumpp Gregory K Webster Raimar Löbenberg

Drug product performance testing is an important part of quality-by-design approaches, but this process often lacks the underlying mechanistic understanding of the complex interactions between the disintegration and dissolution processes involved. Whereas a recent draft guideline by the US Food and Drug Administration (FDA) has allowed the replacement of dissolution testing with disintegration ...

2009
S. M. H. Rahman T. C. Telny T. K. Ravi S. Kuppusamy

Curcumin is a phytoconstituent with wide range of biological activity. It is poorly soluble in water. In the present study a new dissolution medium was developed, as there is no validated dissolution method available in the literature. The composition of the dissolution medium was selected on the basis of solubility data at 37 degrees . Solubility data revealed that addition of surfactant may b...

2016

The aims of the study were to observe the dissolution profile of four types of selected fruit powder fast dissolve tablet and apply different dissolution profile comparison methods, in order to select most applicable method. Spray dried powder of pitaya, pineapple, guava and mango were used as raw material. Each type of fruit powder tablet has identical dissolution profile. Dissolution profiles...

Jafar Akbari, Katayoun Morteza-Semnani, Majid Saeedi, Reza Enayatifard, Samira Rajabi,

Naproxen is a poor water soluble, non-steroidal analgesic and anti-inflammatory drug. The enhancement of oral bioavailability of poor water soluble drugs remains one of the most challenging aspects of drug development. Although salt formation, solubilization and particle size reduction have commonly been used to increase dissolution rate and thereby oral absorption and bioavailability of low wa...

2010
Bashar A. Alkhalidi Hatim S. Alkhatib Ayman A. Khdair

Drug dissolution studies are commonly conducted using compendial methods employing USP Paddle and Basket apparatuses. In many cases, dissolution studies can be of limited benefit especially for product-dependent dissolution procedures like in extended release (ER) formulations. The high variability in dissolution testing, that is not productrelated, emphasizes the need for developing new method...

Journal: :iranian journal of pharmaceutical sciences 0
maryam maghsoodi school of pharmacy and drug applied research center, tabriz university of medical sciences, tabriz, iran sara esmaeilzadeh school of pharmacy and drug applied research center, tabriz university of medical sciences, tabriz, iran

in this study, the effect of recrystallization of naproxen in the presence of hydroxypropyl cellulose (hpc) on the release rate of drug was investigated. crystals were generated by the anti-solvent approach using the hpc solution in water as the anti-solvent. the samples were subjected to various physicochemical evaluations such as crystal size, scanning electron microscopy, fourier transform i...

Journal: :pharmaceutical and biomedical research 0
hossein danafar zanjan pharmaceutical nanotechnology research center, zanjan university of medical sciences, zanjan, iran

ezetimide belongs to a class of lipid lowering compounds that selectively inhibits intestinal absorption of cholesterol and related phytosterols. the purpose of this study is to establish a reliable and quick method for the assignment of ezetimibe in tablets form by high performance liquid chromatography with ultraviolet detection (hplc-uv). a rapid and sensitive hplc method has been developed ...

Journal: :pharmaceutical and biomedical research 0
hossein danafar zanjan pharmaceutical nanotechnology research center, zanjan university of medical sciences, zanjan, iran

tolterodine tartrate, is a new, potent and competitive muscarinic receptor antagonist in clinical development for the treatment of urge incontinence and other symptoms of unstable bladder. the purpose of this study is to establish a reliable and quick method for the assignment of tolterodine tartrate by high performance liquid chromatography with ultraviolet detection (hplc-uv). a rapid and sen...

Journal: :the iranian journal of pharmaceutical research 0
singh satya prakash division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india. ch. niranjan patra division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india. chakraborty santanu division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india. pandit hemant kumar division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india. v. jagannath patro division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india. m vimala devi division of formulation and development, pg department of pharmaceutics, college of pharmaceutical sciences, berhampur, orissa, india.

the dried fruit of terminalia chebula is widely used for its laxative properties. the objective of the present study was to examine the flowability and compressibility of terminalia chebula fruit powder, subsequently developing its tablet formulations by utilizing wet granulation and direct compression technology. initial studies on flowability and compressibility revealed that the fruit powder...

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