نتایج جستجو برای: release

تعداد نتایج: 214420  

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2015
m. christe sonia mary s. sasikumar

in the present study, floating drug delivery beads (fdds) were prepared with sodium alginate/ starch blend as a matrix, sodium hydrogen carbonate as a pore forming agent, methyl cellulose as a binder and barium chloride solution as a hardening agent. in order to prepare the beads with different porosity and morphology the ratio between pore forming agent to polymer blend and ratio of the consti...

Journal: :nanomedicine journal 0
amir doustgani department of chemical engineering, university of zanjan, zanjan, iranسازمان اصلی تایید شده: دانشگاه زنجان (zanjan university)

objective(s): in this study, drug loaded electrospun nanofibrous mats were prepared and drug release and mechanism from prepared nanofibers were investigated.  materials and methods: paclitaxel (ptx) loaded polylactic acid (pla) nanofibers were prepared by electrospinning. the effects of process parameters, such as ptx concentration, tip to collector distance, voltage, temperature and flow rate...

Journal: :journal of dental school, shahid beheshti university of medical sciences 0
h. nojehdehian dept. of dental materials, school of dentistry, shahid beheshti university of medical sciences, tehran, iran. m. ekrami dept. of operative dentistry, school of dentistry, shahid beheshti university of medical sciences, tehran, iran. z. jaberi ansari dept. of restorative dentistry, school of dentistry, shahid beheshti university of medical sciences, tehran, iran.

objective: in dental treatments, use of carriers for targeted antibiotic delivery would be optimal to efficiently decrease microbial count. in this study, gentamicin was loaded into polylactic co-glycolic acid (plga) microspheres and its release pattern was evaluated for 20 days.   methods: in this experimental study, plga microspheres loaded with gentamycin were produced by the w/o/w method. t...

Journal: :iranian journal of pharmaceutical research 0
r aboofazeli

the influence of various polymers on the release rate of lithium carbonate from matrix-type tablets was investigated in an attempt to formulate a sustained release solid dosage form. for this purpose, tablets containing 450 mg of lithium carbonate along with various amounts of carbopol 934p, 971p, 974p, pemulen and eudragit rlpo as retarding agents and inactive ingredients (e.g. pvp, avicel or ...

Journal: :iranian journal of pharmaceutical research 0
matylda resztak department of physical pharmacy and pharmacokinetics, k. marcinkowski university of medical sciences, święcickiego 6 st., 60-781 poznań, poland tadeusz władysław hermann department of physical pharmacy and pharmacokinetics, k. marcinkowski university of medical sciences, poland wiesław sawicki department of pharmaceutical technology, medical university of gdańsk, poland dorota zuzanna danielak department of physical pharmacy and pharmacokinetics, k. marcinkowski university of medical sciences, poland

the objective of the study was to compare pharmacokinetic and pharmacodynamic parameters of gliclazide after administration of immediate (ir) and modified release (mr) tablets. the experiment included rats with both normoglyceamia and streptozocin (stz)-induced hyperglyceamia. several mr formulations were designed and in vitro drug release profile was assessed by a dissolution test. for the fur...

Journal: :iranian journal of pharmaceutical research 0
j emami m tajeddin f ahmadi

frequent dosing of the potent anti-androgen, flutamide, is necessary to reach a therapeutic level for the treatment of prostatic carcinoma. sustained delivery of the drug could reduce the adverse effects such as gastrointestinal disorders and improve patient compliance. in the present study sustained-release matrix tablets of flutamide were prepared by direct compression method using different ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه رازی - دانشکده علوم 1389

here, we report analysis of in vitro and in vivo drug release from an in situ formulation consisting of triamcinolone acetonide (tr) and poly(d,l-lactide-co-glycolide) (plga) and the additives glycofurol and hydroxyapatite nanoparticles (ha). we found that these additives enhanced drug release rate. we used the taguchi method to predict optimum formulation variables to minimise the initial burs...

Journal: :nanomedicine journal 0
shahryar shakeri department of biotechnology, institute of science and high technology and environmental sciences, graduate university of advanced technology, kerman, iranسازمان اصلی تایید شده: دانشگاه تحصیلات تکمیلی صنعتی کرمان (graduate university of advanced technology) rasoul roghanian department of biology, faculty of sciences, university of isfahan, isfahan, iranسازمان اصلی تایید شده: دانشگاه اصفهان (isfahan university) giti emtiazi department of biology, faculty of sciences, university of isfahan, isfahan, iranسازمان اصلی تایید شده: دانشگاه اصفهان (isfahan university) cesare errico department of chemistry and industrial chemistry, university of pisa, via risorgimento 35, 56126 pisa, italy emo chiellini department of chemistry and industrial chemistry, university of pisa, via risorgimento 35, 56126 pisa, italy federica chiellini department of chemistry and industrial chemistry, university of pisa, via risorgimento 35, 56126 pisa, italy

objective(s):despite of wide range applications of polymeric nanoparticles in protein delivery, there are some problems for the field of protein entrapment, initial burst and controlled release profile.   materials and methods: in this study, we investigated the influence of some changes in plga nanoparticles formulation to improve the initial and controlled release profile. selected parameters ...

Journal: :iranian journal of pharmaceutical sciences 0
thanikachalam sivakumar department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002, prabal kumar manna department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002 thanikachalam sundar rajan kk college of pharmacy, gerugambakkam, chennai-602 101 mahmoud ahmed the madras pharmaceuticals, karapakkam, chennai-600 096, tn, india rajappan manavalan department of pharmacy, faculty of engineering and technology, annamalai university, annamalai nagar-608 002

megaloporous controlled release tablets of diclofenac sodium (ds) were prepared with two kinds of granules. one of them is the restraining-phase matrix granule (rmg) and it controls the release rate of the drug. the other one is the soluble housing-phase matrix granule (hmg) and controls liquid penetration into the system. carnauba wax and eudragit l 100 polymers were used to constitute the res...

Journal: :archives of trauma research 0
ali birjandi nejad orthopedic research center, shahid kamyab hospital, mashhad university of medical sciences, mashhad, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) mohammad hosein ebrahimzadeh orthopedic research center, ghaem hospital, mashhad university of medical sciences, mashhad, ir iran; orthopedic research center, ghaem hospital, mashhad university of medical sciences, p. o. box: 91799-99199, mashhad, ir iran. tel/fax: +98-5118417453سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) ali moradi department of orthopedic surgery, mashhad university of medical sciences, mashhad, ir iran; mass general hospital, harvard medical school, boston, usسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

background loss of motion is a well-known complication after elbow trauma and in severe cases, arthrolysis of elbow is the procedure of choice. the posterior approach might have some advantages especially in post-traumatic patients who have undergone the same surgical approach in the past. objectives the aim of this study was to evaluate the short-term outcomes of elbow arthrolysis through post...

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