نتایج جستجو برای: eudragit s 100

تعداد نتایج: 1080878  

Journal: :European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 2004
Nathalie Huyghebaert An Vermeire Jean Paul Remon

The aim of this study was to develop an alternative method for enteric coating of HPMC capsules that avoids the sealing step before coating, resulting in ready-to-use enteric-coated capsules for the use in retail or hospital pharmacy or R&D sections of pharmaceutical industry and for the production of enteric-coated heat and moisture sensitive biomaterials. HPMC caps and bodies 00 (Vcaps, Capsu...

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2006
Mamoru Fukuda Nicholas A Peppas James W McGinity

The purpose of this study was to investigate the influence of sodium bicarbonate on the physicochemical properties of controlled release hot-melt extruded (HME) tablets containing Eudragit RS PO and/or Eudragit E PO. Acetohydroxamic acid and chlorpheniramine maleate were used as model drugs. Sodium bicarbonate was incorporated into the tablet formulations and the drug release properties and buo...

2008
Yvonne Tan Tze Fung

The prolonged release gliclazide matrix tablets were prepared using polymeric materials, namely, HPMC, Kollidon SR, Carbopol with Xanthan gum, Eudragit RSPO and Eudragit RLPO. HPMC, Kollidon SR and Carbopol with Xanthan gum were able to retard gliclazide release from matrix tablets in a concentration dependent manner, but the rate of retardation differed among the polymers. On the other hand, d...

Journal: :International journal of pharmaceutics 2011
Xue-qing Wang Jie-ming Fan Ya-ou Liu Bo Zhao Zeng-rong Jia Qiang Zhang

Sorafenib is slightly absorbed in the gastrointestinal tract due to its poor solubility in water. To improve its absorption, a novel nanoparticulate formulation-nanomatrix was used in the study. The nanomatrix was a system prepared from a porous material Sylysia(®) 350 and a pH sensitive polymer Eudragit(®). The formulations were optimized by orthogonal design (L(9)(3(4))) and their bioavailabi...

Journal: :Acta poloniae pharmaceutica 2006
Burcu Devrim Kandemir Canefe

The aim of this study was to prepare and evaluate microspheres containing ibuprofen. Microspheres were prepared by modified quasi-emulsion solvent diffusion method. The influence of formulation factors (drug-polymer ratio, volumes of solvent, polyvinyl alcohol concentration and type of polymer) on the morphology, particle size distribution, drug loading capacity, micromeritical properties and t...

Journal: :Nanofabrication 2022

The purpose of this study was to synthesize duloxetine (DLX)- loaded Eudragit-Chitosan (Eud-CHT) nanoparticles enclosed in an oral gelatin capsule and evaluate the potential transport DLX blood-brain barrier (BBB)for improved neuro-availability. utilization Eudragit® with chitosan offers a pH-dependent controlled drug release. physicochemical properties formulated DLX-loaded Eud-CHT nanosystem ...

Journal: :Coatings 2021

The preparation of the metal surface before coating application is fundamental in determining properties coatings, particularly roughness, adhesion, and corrosion resistance. In this work, chitosan/Eudragit E 100 (chit/EE100) were fabricated by electrophoretic deposition (EPD) both their microstructure investigated. present research aimed at characterizing effects pretreatment titanium substrat...

Journal: :iranian journal of pharmaceutical sciences 0
thanikachalam sivakumar department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002, prabal kumar manna department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002 thanikachalam sundar rajan kk college of pharmacy, gerugambakkam, chennai-602 101 mahmoud ahmed the madras pharmaceuticals, karapakkam, chennai-600 096, tn, india rajappan manavalan department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002

megaloporous controlled release tablets of diclofenac sodium (ds) were prepared with two kinds of granules. one of them is the restraining-phase matrix granule (rmg) and it controls the release rate of the drug. the other one is the soluble housing-phase matrix granule (hmg) and controls liquid penetration into the system. carnauba wax and eudragit l 100 polymers were used to constitute the res...

Journal: :journal of reports in pharmaceutical sciences 0
rahim bahri-najafi gholam reza asghari hamid reza dehlavi

buccal mucoadhesive films have attracted great attention among mucoadhesive systems due to their ability to adhere and remain on the oral mucosa and to release their drug content gradually. the aim of the current study was to formulate the ziziphus jujuba aqueous extract as buccal bioadhesive film, which continiously releases the drug at sufficient concentration for reducing the frequency of th...

Journal: :research in pharmaceutical sciences 0

buccal mucoadhesive systems among novel drug delivery systems have attracted great attention in recent years due to their ability to adhere and remain on the oral mucosa and to release their drug content gradually. buccal mucoadhesive films can improve the drug therapeutic effect by enhancement of drug absorption through oral mucosa increasing the drug bioavailability via reducing the hepatic f...

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