نتایج جستجو برای: downscaled usp 2 dissolution apparatus

تعداد نتایج: 2587134  

Journal: :The Journal of pharmacy and pharmacology 2008
Rahmat M Talukder Reza Fassihi

The major challenges in targeting drug to various parts of the gastrointestinal tract include control of drug release with respect to its environment and transit time. These two variables should be taken into consideration in designing a rational colonic drug delivery system. To this end, a swelling matrix core containing pectin, hydroxypropyl methylcellulose (HPMC), microcrystalline cellulose ...

Journal: :Acta poloniae pharmaceutica 2013
Atif Ali Muhammad Iqbal Naveed Akhtar Haji Muhamad Shoaib Khan Aftab Ullah Minhaj Uddin Muhammad Tahir Khan

The present study was carried out to develop oral sustained release tablets of propranolol HCl by different ratios of drug : matrix. Tablets were prepared by direct compression technique using xanthan gum and lactose. All the formulations (tablets) were evaluated for thickness, diameter, hardness, friability, weight variation, content of active ingredient, in vitro dissolution using USP dissolu...

2013
Md. Anwar Hossain Shahinul Alam Prasanta Paul

Article history: Received on: 07/04/2013 Revised on: 29/04/2013 Accepted on: 14/05/2013 Available online: 30/05/2013 In the present study an attempt has been taken to develop Indapamide sustained release matrix tablet using Methocel K15M CR by direct compression method. Various amount of polymer was used in the five proposed formulations (F-1to F-5) for the study of release rate retardant effec...

2011
Juha Mönkäre Joakim Riikonen Elina Rauma Jarno Salonen Vesa-Pekka Lehto Kristiina Järvinen

Porous silicon (PSi) is an innovative inorganic material that has been recently developed for various drug delivery systems. For example, hydrophilic and hydrophobic PSi microparticles have been utilized to improve the dissolution rate of poorly soluble drugs and to sustain peptide delivery. Previously, the well-plate method has been demonstrated to be a suitable in vitro dissolution method for...

Journal: :World Journal Of Advanced Research and Reviews 2022

In depressed individuals, Imipramine exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake. hydrochloride having variable bioavailability i.e. ranging from 29-77% due to first pass metabolism, peak plasma concentration is usually attained 2-6 hours. Absorption unaffected by food. It freely soluble in water. The objective this research work improve...

2016

whose empiric formula is C6H12O6 • H2O, and whose molecular weight is 198.17. Dextrose is derived from corn. Nitroglycerin in 5% Dextrose Injection is a sterile, nonpyrogenic solution of nitroglycerin and dextrose in water for injection. The solution is clear and practically colorless. Each 100 mL contains 10 mg, 20 mg, or 40 mg nitroglycerin (added as Diluted Nitroglycerin, USP with propylene ...

2011
J. Varshosaz J. Emami N. Tavakoli M. Minaiyan N. Rahmani F. Dorkoosh P. Mahzouni

BACKGROUND AND THE PURPOSE OF THE STUDY Budesonide is the drug of choice for treatment of active inflammatory bowel disease (IBD). The aim of this study was to develop budesonide pellets based on a novel colon drug delivery system (CODES). METHODS Pellet cores containing lactulose or mannitol were prepared by extrusion/spheronization and coated with an acid soluble polymer (Eudragit E100), hy...

2015
Jatinderpal Singh Rajeev Garg Ghanshyam Das Gupta

Present investigation deals with the preparation and evaluation of orally disintegrating tablets (ODTs) of lamotrigine using β-cyclodextrin and PVP-K30 as polymers for the preparation of solid dispersion which help in enhancement of aqueous solubility of this BCS CLASS-II drug and sodium starch glycolate (SSG) and crospovidone as a superdisintegrating agent, to reduce disintegration time. The O...

2016
Srinivasa Babu A. Madhusudhan Reddy

Bi-layered [1] tablet refers to tablet which contain subunits. In bi-layer [2] tablets, one layer tablet provides immediate release and the other layer acts as sustained release. Sumatriptan is a new class of anti-migraine [3] drugs that selectively activate 5-HT1B/1D receptors and are called triptans. Our objective is to formulate and evaluate the bi-layer tablets of sumatriptan succinate of d...

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