نتایج جستجو برای: in vitro drug release

تعداد نتایج: 17076627  

Kamla Pathak, Monika Joshi, Nida Akhtar, Syed Faisal Ali, Vijay Sharma,

The present investigation was focused to formulate semi-solid capsules (SSCs) of hydrophobic drug telmisartan (TLMS) by encapsulating semi-solid matrix of its solid dispersion (SD) in HPMC capsules. The combinational approach was used to reduce the lag time in drug release and improvise its dissolution. SDs of TLMS was prepared using hot fusion method by varying the combinations of Pluronic-F68...

Journal: :iranian journal of veterinary medicine 0
sakineh khanamani falahatipour department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran ali rasooli department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran yalda hosseinzadeh ardakani .department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran hamid akbari javar associate prof. dept pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran. katayoun kiani dept pharmacology, faculty of vet med, university of tehran, tehran, iran. taghi zahraee salehi prof. and head of dept microbiology, faculty of vet med, university oftehran, tehran, iran.

background: the development of injectable sustained-release products are of great interest to veterinary pharmaceuticals and animal health business. recently, great attention has been paid to in situ gel-forming chitosan/beta-glycerophosphate (chitosan/β-gp) solutions due to their good biodegradability and thermosensitivity. objectives: the general aim of this study was to prepare a novel in si...

Journal: :avicenna journal of dental research 0
zahra jaberi-ansari department of operative dentistry, dental school, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) malihe ekrami department of operative dentistry, dental school, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) hanieh nojehdehian department of dental materials, dental school, shahid beheshti university of medical sciences, tehran, ir iran; department of dental materials, dental school, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122173754 fax: +98-2122173754سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

context biocompatible polymers are potentially effective for dental infections as delivery carriers of disinfectants or antibiotics into the root canal system (rcs). this study aimed to review polymeric microspheres enabling a controlled release of endodontic medicaments. evidence acquisition a literature search was carried out in the pubmed database (may 2013) using the following keywords: “po...

Drug release kinetics plays an important role in determining the mechanism of drug release, which in turn helps in formulating controlled/sustained release formulations.In our study, different concentrations of green tea polyphenols (GTP) were encapsulated into casein nanoparticles which showed a maximum encapsulation efficiency (76.9%) at a GTP concentration of 5 mg/mL. The casein nanopa...

Drug release kinetics plays an important role in determining the mechanism of drug release, which in turn helps in formulating controlled/sustained release formulations.In our study, different concentrations of green tea polyphenols (GTP) were encapsulated into casein nanoparticles which showed a maximum encapsulation efficiency (76.9%) at a GTP concentration of 5 mg/mL. The casein nanopa...

Hedayte Samadi Mitra Jelvehgari, Mohammad Reza Rashidi

       Gel dosage forms are successfully used as drug delivery systems considering their ability to control drug release and to protect medicaments from a hostile environment. The aim of this work was to investigate the properties of carbopol 934P polymeric system in water-misible cosolvents such as glycerin and alcohol. Benzocaine is a local anesthetic and the mucosal gel formulation is appl...

The aim of the present work was to develop immediate release dosage form of the solid dispersion of glimperide (GLIM) for potential enhancement in the bioavailability. The solid dispersions of GLIM were prepared with PEG6000, PVP K30 and Poloxamer 188, in 1:1, 1:3 and 1:5 %w/w ratio by using solvent wetting and solvent melt method. The in vitro dissolution parameters (%DE10min, %DE30min, %DE60m...

Purpose: Enalapril maleate (EPM), was used for hypertension and congestive heart failure. In this way, an innovative delivery system with mPEG–PCL was synthesized and the release profile of the EPM from the drug-loaded polymersomes was evaluated. Methods: Di-block methoxy)-poly (ethylene glycol) - Poly (caprolactone) (mPEG-PCL) copolymers were synthesized and used to prepare of polymersom...

Journal: :iranian journal of pharmaceutical research 0
lingbin meng school of life science, beijing institute of technology, beijing, 100081, p. r. china. zhongqiu teng school of life science, beijing institute of technology, beijing, 100081, p. r. china. nannan zheng sanofi-aventis investment co., ltd., beijing, 100013, p. r. china. weiwei meng school of life science, beijing institute of technology, beijing, 100081, p. r. china. rongji dai school of life science, beijing institute of technology, beijing, 100081, p. r. china. yulin deng school of life science, beijing institute of technology, beijing, 100081, p. r. china.

the aim of this study was to develop a derivative of chitosan as pharmaceutical excipient used in sustained-release matrix tablets of poorly soluble drugs. a water-soluble quaternary ammonium carboxymethylchitosan was synthesized by a two-step reaction with carboxymethylchitosan (cmcts), decylalkyl dimethyl ammonium and epichlorohydrin. the elemental analysis showed that the target product with...

Journal: :research in pharmaceutical sciences 0

candesartan cilexetil (cc) is a newer class of angiotensin ii receptor antagonist used for the treatment of hypertension. the solubility of the cc is very poor and its oral bioavailability is only 15%. the controlled-release polar lipid microparticles of cc (formulations f1, f2, f3 and f4) were prepared using variable erodible lipophilic excipients like hydrogenated castor oil, stearic acid, ce...

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