نتایج جستجو برای: drug targeting

تعداد نتایج: 718057  

Journal: :research on history of medicine 0
arman zargaran student research committee, shiraz university of medical sciences, shiraz, iran mohammad m. zarshenas research office for the history of persian medicine, shiraz university of medical sciences, shiraz, iran alireza mehdizadeh research office for the history of persian medicine, shiraz university of medical sciences, shiraz, iran gholamreza kordafshari faculty of traditional medicine, tehran university of medical sciences, tehran, iran abdolali mohagheghzadeh department of traditional pharmacy, faculty of pharmacy and pharmaceutical sciences research center, shiraz university of medical sciences, shiraz, iran

avicenna (980 – 1037 ad) known as the prince of physicians in the west was one of the most prominent persian thinkers, philosophers, and physicians. owing to his interests in cardiology, he authored considerable works on different aspects of cardiology. “resaley-e-ragshenasi” (book on pulsology) and”kitab al-adviyt- ol-qalbiye” (the book on drugs for cardiovascular diseases) are avicenna’s grea...

Journal: :iranian journal of pharmaceutical research 0
hamid r. moghimi school of pharmacy, shahid beheshti university of medical sciences, tehran, iran mostafa saffari department of pharmaceutics, school of pharmacy, islamic azad university, tehran, iran crispin r. dass school of pharmacy, faculty of health sciences, curtin university, perth 6845, australia

abstractgene therapy is a therapeutic approach to deliver genetic material into cells to alter their function in entire organism. one promising form of gene delivery system (dds) is liposomes. the success of liposome-mediated gene delivery is a multifactorial issue and well-designed liposomal systems might lead to optimized gene transfection particularly in vivo. liposomal gene delivery systems...

Journal: :research in pharmaceutical sciences 0
j k patel n v patel s h shah

a controlled release matrix formulation for mesalamine was designed and developed to achieve a 24 h release profile. using compritol 888 ato (glyceryl behenate) as an inert matrix-forming agent to control the release of mesalamine, formulation granules containing the solid dispersions were investigated. pectin, a polysaccharide, was used as bacterial dependent polymer for colon targeting. the m...

Journal: :jundishapur journal of microbiology 0
mansoureh shahbazi dastjerdeh department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran shirin kouhpayeh department of immunology, school of medicine, isfahan university of medical sciences, isfahan, ir iran faezeh sabzehei department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran hossein khanahmad department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran; department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran. tel: +98-031337922487, fax: +98-031-3668859 mansour salehi department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran zahra mohammadi department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran

conclusions our findings revealed that the zfn technology could be employed to overcome ampicillin resistance by the targeted disruption of the ampicillin resistance gene, which leads to inactivation of β-lactam synthesis. therefore, zfn technology could be engaged to decrease the antibiotic resistance issue with the construction of a zfn archive against different args. to tackle the resistance...

Journal: :basic and clinical neuroscience 0
mina ranjbaran neuroscience research center, baqiyatallah (a.s.) university of medical sciences, tehran, iran. * corresponding author: hedayat sahraei1, phd. neuroscience research center, baqiyatallah (a.s.) university of medical sciences, tehran, iran. tel: +98-21- 26127286 e-mail: [email protected] in the 1960s, discovery of pleasure system (defined as reward system) in the brain that may underlie drug reward and addiction encouraged many scientists to investigate the mechanisms by which drug abuse affects central nervous system function. in this regard, investigators developed several drugs targeting the brain reward system for drug dependence therapy. however, no positive results obtained in drug addiction treatment. it seems that more brain systems other than brain reward system must be considered in this regard. article info: hedayat sahraei neuroscience research center, baqiyatallah (a.s.) university of medical sciences, tehran, iran. * corresponding author: hedayat sahraei1, phd. neuroscience research center, baqiyatallah (a.s.) university of medical sciences, tehran, iran. tel: +98-21- 26127286 e-mail: [email protected] in the 1960s, discovery of pleasure system (defined as reward system) in the brain that may underlie drug reward and addiction encouraged many scientists to investigate the mechanisms by which drug abuse affects central nervous system function. in this regard, investigators developed several drugs targeting the brain reward system for drug dependence therapy. however, no positive results obtained in drug addiction treatment. it seems that more brain systems other than brain reward system must be considered in this regard. article info:

in the 1960s, discovery of pleasure system (defined as reward system) in the brain that may underlie drug reward and addiction encouraged many scientists to investigate the mechanisms by which drug abuse affects central nervous system function. in this regard, investigators developed several drugs targeting the brain reward system for drug dependence therapy. however, no positive results obtain...

Journal: :research in pharmaceutical sciences 0
mn singh ksy hemant hg shivakumar hg shivakumar

microparticles offer various significant advantages as drug delivery systems, including: (i) an effective protection of the encapsulated active agent against (e.g. enzymatic) degradation, (ii) the possibility to accurately control the release rate of the incorporated drug over periods of hours to months, (iii) an easy administration (compared to alternative parenteral controlled release dosage ...

The potential of PLGA-nanoparticles as a carrier of amphotericin B and doxorubicin against visceral leishmaniasis was evaluated by macrophage-mediated drug targeting approach. PLGA-nanoparticles were modified by coating them with macrophage-specific ligand-lectin. Prior to in-vitro studies, characterization studies were carried out systematically include particle size, surface morphology, perce...

Journal: :research in pharmaceutical sciences 0

in this study, the folate decorated biodegradable poly (lactide-co-glycolide) (plga) nanoparticles were developed for tumor targeting of anticancer agents. due to the overexpression of the folate receptor on tumor surface, the folate has been efficiently employed as a targeting moiety for various anticancer agents to avoid their non-specific attacks on normal tissues and also to increase their ...

Journal: :Open Schools Journal for Open Science 2020

Hedayat Sahraei, Mina Ranjbaran,

In the 1960s, discovery of pleasure system (defined as reward system) in the brain that may underlie drug reward and addiction encouraged many scientists to investigate the mechanisms by which drug abuse affects central nervous system function. In this regard, investigators developed several drugs targeting the brain reward system for drug dependence therapy. However, no positive results obtain...

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