نتایج جستجو برای: modified release

تعداد نتایج: 458567  

Journal: :Yonsei Medical Journal 2004

A. Doustgani E. Ahmadi M. Ghasemnejad S. Hashemikia Z. Mohamadnia

Mesoporous silica nanoparticles with unique structure (SBA-15) were synthesized and modified by [3-(2-Aminoethylamino) propyl] trimethoxysilane (AEAPTMS). The synthesized nanoparticles were characterized by TGA, N‌2‌ adsorption, SEM, FTIR, CHN elemental analysis. The total weight loss for the modified SBA-15 is 15.2% and thermal analysis reveal...

Journal: :international journal of nanoscience and nanotechnology 2015
z. mohamadnia e. ahmadi m. ghasemnejad s. hashemikia a. doustgani

mesoporous silica nanoparticles with unique structure (sba-15) were synthesized and modified by [3-(2-aminoethylamino) propyl] trimethoxysilane (aeaptms). the synthesized nanoparticles were characterized by tga, n­2­ adsorption, sem, ftir, chn elemental analysis. the total weight loss for the modified sba-15 is 15.2% and thermal analysis revealed that 1.5 mmol aeaptms/1g sba-15 had been grafted...

Journal: :Journal of pharmaceutical and biomedical analysis 2005
Yunqi Wu Munir Hussain Reza Fassihi

A simple spectrophotometric method for determination of glucosamine release from sustained release (SR) hydrophilic matrix tablet based on reaction with ninhydrin is developed, optimized and validated. The purple color (Ruhemann purple) resulted from the reaction was stabilized and measured at 570 nm. The method optimization was essential as many procedural parameters influenced the accuracy of...

Journal: :iranian journal of pharmaceutical sciences 0
veerendra s. rajpurohit rajendra institute of technology and sciences, hisar road, sirsa-125055, india pankaj rakha rajendra institute of technology and sciences, hisar road, sirsa-125055, india surender goyal rajendra institute of technology and sciences, hisar road, sirsa-125055, india harish durejab department of pharmaceutical sciences, m. d. university, rohtak- 124001, india gitika arorac ncrd’s sterling institute of pharmacy, navi mumbai- 400706, india manju nagpal school of pharmaceutical sciences, chitkara university, solan-174103, india

in order to enhance in vitro dissolution and content uniformity of poorly soluble drug glimepiride by preparing solid dispersions using modified solvent fusion method, solid dispersions of drug were prepared by modified fusion solvent method using peg 6000 and pvp k25 (as carrier). eight batches (f1-f8) were prepared by factorial design (23) by taking three factors i.e. the concentration of: dr...

The study aimed at determining the effect of acid modified porcine mucin powder on the release and permeation of insulin in transdermal patches. Various batches of insulin patches were prepared by solvent casting method using polysorbate 80 as emulsifying agent and acid treated and untreated mucin powders as base. The patches were evaluated for their physical properties, folding endurance, moi...

ژورنال: مجله دندانپزشکی 2000
رشیدیان, علی , محمودیان, ژاله , کوثری, علی ,

The purpose of this study was to assess the fluoride release of three fluoride- containing materials exposed to fluoride solutions. This study compared the initial fluoride release and release following re-fluoridation (neutral or acidic 2% NaF) of three different filling materials, conventional glass ionomer cement (CG1C), resin- modified glass ionomer cement (RMGIC), polyacid- modified compos...

Journal: :Neuropsychiatric Disease and Treatment 2007
Cynthia Kirkwood Jason Neill Ericka Breden

Zolpidem modified-release (MR) is the first hypnotic agent to be marketed in an extended-release formulation. Zolpidem MR is a two-layered, biphasic release tablet indicated for the management of induction of sleep and sleep maintenance. The pharmacokinetics of the drug are similar to those of immediate-release zolpidem. Two double-blind, placebo-controlled, parallel-group trials demonstrated e...

Gitika Arorac Harish Durejab Manju Nagpal, Pankaj Rakha Surender Goyal Veerendra Rajpurohit

      In order to enhance in vitro dissolution and content uniformity of poorly soluble drug glimepiride by preparing solid dispersions using modified solvent fusion method, solid dispersions of drug were prepared by modified fusion solvent method using PEG 6000 and PVP K25 (as carrier). Eight batches (F1-F8) were prepared by Factorial design (23) by taking three ...

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