نتایج جستجو برای: initial release

تعداد نتایج: 573577  

Journal: :اکو هیدرولوژی 0

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Journal: :ادیان و عرفان 0

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2017
Maria Porta-i-Batalla Elisabet Xifré-Pérez Chris Eckstein Josep Ferré-Borrull Lluis F. Marsal

The use of nanoporous anodic alumina (NAA) for the development of drug delivery systems has gained much attention in recent years. The release of drugs loaded inside NAA pores is complex and depends on the morphology of the pores. In this study, NAA, with different three-dimensional (3D) pore structures (cylindrical pores with several pore diameters, multilayered nanofunnels, and multilayered i...

Journal: :Acta pharmaceutica 2007
Chinam Niranjan Patra Arethi Bharani Kumar Hemant Kumar Pandit Satya Prakash Singh Meduri Vimala Devi

The objective of the present research was to develop a bilayer tablet of propranolol hydrochloride using superdisintegrant sodium starch glycolate for the fast release layer and water immiscible polymers such as ethylcellulose, Eudragit RLPO and Eudragit RSPO for the sustaining layer. In vitro dissolution studies were carried out in a USP 24 apparatus I. The formulations gave an initial burst e...

2011
Swati Jain Neelesh Kumar Mehra Akhlesh Kumar Singhai Gaurav Kant Saraogi Lakshmi Narayan

The study was obtained to develop oral controlled release matrix tablets of Lamivudine having different proportion of Guar gum (retardant polymer) and to study the effect of formulation factor such as polymer proportion on the invitro release. The prepared granules were evaluated such as angle of repose, loose bulk density, tapped bulk density and compressibility index and satisfactory results ...

Objective(s): Nanoparticles (NPs) are known for their specific accumulation in the inflamed tissues of the colon and thus allow a selective delivery to the site of inflammation with minimum adverse effects. The main objective of this work is to attain mesalamine loaded chitosan nanoparticles as a carrier for oral delivery. Methods: In this study, me...

A Box-Behnken design with three replicates was used for preparation and evaluation of Eudragit vancomycin (VCM) nanoparticles prepared by double emulsion. The purpose of this work was to optimize VCM nanoparticles to improve the physicochemical properties. Nanoparticles were formed by using W1/O/W2 double-emulsion solvent evaporation method using Eudragit RS as a retardant material. Full factor...

Journal: :Water research 2012
M G A Keuten F M Schets J F Schijven J Q J C Verberk J C van Dijk

Pollutants, brought into a swimming pool by bathers, will react with chlorine to form disinfection by-products (DBPs). Some of these DBPs are found to be respiratory and ocular irritant and might be associated with asthma, or might even be carcinogenic. As DBPs in swimming pools are formed from bather-shed-pollutants, a reduction of these pollutants will lead to a reduction of DBPs. Until now, ...

2014
Sanjay Dey Sankha Chattopadhyay Bhaskar Mazumder

The objective of the present study was to develop bilayer tablets of atorvastatin and atenolol that are characterized by initial fast-release of atorvastatin in the stomach and comply with the release requirements of sustained-release of atenolol. An amorphous, solvent evaporation inclusion complex of atorvastatin with β -cyclodextrin, present in 1 : 3 (drug/cyclodextrin) molar ratio, was emplo...

2008
Y. Ramgopal S. S. Venkatraman W. T. Godbey

The controlled delivery of low-molecular weight drugs and proteins from biodegradable polymers has received considerable attention. However, controlled release studies of pDNA from such polymers have not been reported to date. In this study, a plasmid DNA was complexed with the cationic polymer called polyethylenimine (PEI). This gene vector has been shown to be very effective in transfecting c...

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