نتایج جستجو برای: self microemulsifying drug delivery system
تعداد نتایج: 3268999 فیلتر نتایج به سال:
Piroxicam is a non-steroidal anti-inflammatory drug (NSAID) that commonly used for arthritis, gout, and other musculoskeletal disorders. poorly soluble in water according to the biopharmaceutical classification system (BCS) classified as Class II with good permeability but poor dissolution. The self-nanoemulsifying delivery (SNEDDS) has been extensively employed improve dissolution absorption o...
the present work was aimed to design and develop self-nanoemulsifying drug delivery systems (snedds) with the objective to overcome the problems associated with the delivery of talinolol, a hydrophobic and poorly bioavailable drugs having ph dependant solubility. the solubility of talinolol in various oils, surfactants, cosurfactants and aqueous phases were determined to identify and select the...
Transdermal drug delivery system is a non-invasive and an efficient method that provides sustained release and delivers therapeutics to target site. This system can improve the therapeutic efficacy and safety of the drugs, keep the plasma level of the drug constant, prevent the hepatic first pass metabolism and is convenient and pain-free self-administration for patients. Despite the many advan...
nanoparticles have been at the center of research focus as a new promising material for the treatment of cancer in recent years. although many chemotherapy drugs for cancer treatment are available, their potential toxicity is the main point of concern. on the other hand, the conventional chemotherapeutic approach has not been found to be very efficient in colorectal cancer (crc) as the drug mol...
background: several multiphase flow analyses have been developed to predict the fate of particles used in inhalation drug delivery; however, the collapse of droplets during their passage through respiratory tract has not been investigated. objective: to assess the probability of droplet collapse in the upper respiratory tract. methods: a 3d model of mouth-to-second generation airway after the t...
conclusions it was shown that combination of pectin and eudragits can relatively control drug release in the upper gi. on the other hand, pectin degraded in the presence of pectinase and formulations were susceptible to the colonic media. results it was shown that in the presence of pectin, formulations without erl had a relative resistance to drug release in sgf. pellets containing pectin and ...
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