نتایج جستجو برای: sustain release

تعداد نتایج: 235270  

Journal: :British medical journal 1984
R Canepa-Anson M Williams J Marshall T Mitsuoka S Lightman R Sutton

A woman with tachycardia associated with polyuria was investigated. Electrophysiological analysis showed that the tachycardia was an atrioventricular nodal re-entrant tachycardia. Programmed stimulation was then used to provoke and sustain the tachycardia for 40 minutes. Polyuria, with an appreciable increase in free water clearance, was observed. This was associated with reduction in plasma an...

2015
Rishi Kumar Rishabha Malviya Promod Kumar Sharma

Natural polymers have shown an increasing interest in the field of medical science. These have been used in the different dosage form that helps in the sustain and control release of drug. Now a day natural polymers are used in novel and conventional dosage form directly or indirectly. Natural polymers used in various formulations like microspheres, nanoparticles, tablets, gels, implants, nioso...

2005
Esteban Maestre Emilia Gómez

We describe a method to automatically extract a set of features from the audio signal that are related to musical expressivity, more concretely to dynamics and articulation. We define a description scheme based on intra-note segmentation into attack, sustain, release and transition segments, and a subsequent amplitude and pitch contour characterization. Then, we present a series of algorithms t...

2018
Vinay K Belwal KP Singh

This study encompasses the development and comparison of nanosilica-supported liposome (protocells), conventional liposome, and polyethylene glycol (PEG)-liposome. An effort was made to study the drug encapsulation efficiency and the in vitro release of the drug, and whether protocells (nanovesicles) could sustain the release of the drug by increasing the residence time, which could reduce the ...

2009
Ravi Kumar M. B. Patil Sachin R. Patil Mahesh S. Paschapur

Famotidine has been the most widely used drug for the treatment of peptic ulcer for many decades. The present investigation concerns the development and evaluation of floating tablets of famotidine which, after oral administration, are designed to prolong the gastric residence time, increase drug bioavailability and target the gastric ulcer. A floating drug delivery system (FDDS) was developed ...

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: :Nanotechnology, science and applications 2012
Karen C Dos Santos Maria Fatima Gf da Silva Edenir R Pereira-Filho Joao B Fernandes Igor Polikarpov Moacir R Forim

This present investigation deals with the development and optimization of polymeric nanoparticle systems loaded with 3,5,3'-triiodothyroacetic acid (Triac). A 2(11-6) fractional factorial design and another 2(2) factorial design were used to study the contrasts on particle size distribution, morphology, surface charge, drug content, entrapment efficiency, and in vitro drug release profiles. The...

Journal: :Journal of molecular and cellular cardiology 2005
Gina Sánchez Zully Pedrozo Raúl J Domenech Cecilia Hidalgo Paulina Donoso

We have shown previously that electrically induced tachycardia effectively produces myocardial preconditioning. Among other effects, tachycardia increases calcium release rates in microsomal fractions enriched in sarcoplasmic reticulum (SR) isolated from dog cardiac ventricular muscle. Here, we report that preconditioning tachycardia increased twofold the NADPH oxidase activity of isolated SR-e...

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