نتایج جستجو برای: drug lipid micromatrices

تعداد نتایج: 735525  

Journal: :research in pharmaceutical sciences 0

amodiaquine is an antimalarial drug used in the prophylaxis and treatment of this disease. however, hepatotoxicity as a life‑threatening adverse effect is associated with its clinical use. we evaluated amodiaquine-induced toxicity in isolated rat hepatocytes as an in vitro model for studying drug‑induced hepatotoxicity. this study attempts to investigate the protective effects of taurine and n-...

Journal: :Digital discovery 2022

Lipid membranes are vital in a wide range of biological and biotechnical systems; underpinning functions from modulation protein activity to drug uptake delivery. Rapid situ determination phase behaviour is key experimental objective.

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2012
Sok Bee Lim Amrita Banerjee Hayat Önyüksel

Drug toxicity is an important factor that contributes significantly to adverse drug events in current healthcare practice. Application of lipid-based nanocarriers in drug formulation is one approach to improve drug safety. Lipid-based delivery systems include micelles, liposomes, solid lipid nanoparticles, nanoemulsions and nanosuspensions. These carriers are generally composed of physiological...

Journal: :iranian journal of pharmaceutical research 0
ak seth a misra

the aim of this study was to prepare liposomes of acyclovir (acy) by thin layer evaporation (tle) and reverse phase evaporation (rev) methods. twenty-seven batches of liposomes from each method were prepared using technique of three variables at three levels (33) factorial design. drug/lipid (molar ratio), hydration volume and hydration time were considered three independent variables in tle me...

Journal: :International journal of pharmaceutics 2016
Hanpeng Chen Arcadia Woods Ben Forbes Stuart Jones

Nanocarriers can aid therapeutic agent administration to the lung, but controlling drug delivery from these systems after deposition in the airways can be problematic. The aim of this study was to evaluate if chemically mediated shell permeabilisation could help manipulate the rate and extent of nanocarrier drug release. Rifampicin was loaded into lipid shell (loading efficiency 41.0±11.4%, siz...

2012
M. Shah Y. K. Agrawal K. Garala A. Ramkishan

The aim of this study was to understand and investigate the relationship between experimental factors and their responses in the preparation of ciprofloxacin hydrochloride based solid lipid nanoparticles. A quadratic relationship was studied by developing central composite rotatable design. Amount of lipid and drug, stirring speed and stirring time were selected as experimental factors while pa...

2015
R. S. R. Murthy

Development of delivery systems for new drug for its safe and effective delivery it into the body is an integral part of drug research program. This is particularly true due to increased incidence of adverse pharmacokinetic behavior of new drugs developed recently. Alternative delivery systems have been researched extensively not only to modulate their kinetic behavior in the body but also to a...

Journal: :Advanced drug delivery reviews 2007
Paolo Blasi Stefano Giovagnoli Aurélie Schoubben Maurizio Ricci Carlo Rossi

The present review discusses the potential use of solid lipid nanoparticles for brain drug targeting purposes. The state of the art on surfactant-coated poly(alkylcyanoacrylate) nanoparticles specifically designed for brain targeting is given by emphasizing the transfer of this technology to solid lipid matrices. The available literature on solid lipid nanoparticles and related carriers for bra...

2012
Patrícia Severino Tatiana Andreani Ana Sofia Macedo Joana F. Fangueiro Maria Helena A. Santana Amélia M. Silva Eliana B. Souto

Lipids and lipid nanoparticles are extensively employed as oral-delivery systems for drugs and other active ingredients. These have been exploited for many features in the field of pharmaceutical technology. Lipids usually enhance drug absorption in the gastrointestinal tract (GIT), and when formulated as nanoparticles, these molecules improve mucosal adhesion due to small particle size and inc...

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