Drug deliveryNSAIDTargeted applicationBiodistributionPharmacokineticsPhospholipid bilayerTransfenac, a lotion-like formulation of diclofenac, is described. It consists...
Drug deliveryNSAIDTargeted applicationBiodistributionPharmacokineticsPhospholipid bilayerTransfenac, a lotion-like formulation of diclofenac, is described. It consists...
CG Blume - Biochimica et Biophysica Acta (BBA) - Biomembranes
The rationale behind developing sustained release microsphere formulations of non-steroidal anti-inflammatory drugs (NSAIDs) administered via the intra-art...
The nonsteroidal anti-inflammatory drugs (NSAIDs) are found to be potential chemopreventive agents of colorectal cancer. Celecoxib, an NSAID with selective...
The nonsteroidal anti-inflammatory drugs (NSAIDs) are found to be potential chemopreventive agents of colorectal cancer. Celecoxib, an NSAID with selective...
The present invention is directed to drug dosage forms that release an agent that raises the pH of a patient's gastrointestinal tract, followed by a non-steroidal anti-inflammatory drug. The dosage form is designed so that the NSAID is n...
NSAIDs are a widely used class of analgesic and anti-inflammatory drugs that act by inhibiting the cyclo-oxygenase (COX) enzyme. However, because of their ...
The objective of this investigation was to develop novel colon specific drug delivery. Aceclofenac, a NSAID, was successfully encapsulated into chitosan mi...
For the treatment of pain and inflammation Non-steroidal anti-inflammatory drugs are themost frequently used medications, but because of number of side effects limit their uses.Transdermal drug delivery system (TDDS) provides sustain dru...
Over 230 million surgical procedures are conducted worldwide each year with numbers increasing. Pain, undesirable inflammation and infection are common com...
Swellable matrix systems with anomalous release kinetics are suitable solutions for drug release control for oral administration. Generally, the release ra...
Swellable matrix systems with anomalous release kinetics are suitable solutions for drug release control for oral administration. Generally, the release ra...
CDDS Molecular weight or size Small molecules may pass through pores of amembrane by convective transport. This applies to both, the drug release from thed...
in addition to the active ingredient of the capsules a genetic surfactant, a ways to esters or ether is and, at the same time, hydrophilic and lipophi u00adle shares and contains an organic polymer, containing the active substance and th...
During last 25 years, a large number of coating materials are introduced for sustained release dosage form. In spite of availability of large number of coating materials, an ideal coating is still a dream of formulator and hence search f...
Drugs that have narrow absorption window in the gastrointestinal tract (GIT) will have poor absorption. For these drugs, gastroretentive drug delivery systems offer the advantage in prolonging the gastric emptying time. Metoprolol tartra...
The objective of the present study was to prepare nanofibers of Lornoxicam by Electro spinning technique and to increase the drug bioavailability using different polymers such as PMMA, Ethyl Cellulose, Polyethylene oxide, Gelatin. Totall...