نتایج جستجو برای: release time

تعداد نتایج: 2072007  

A Gadad A Kulkarni P Dandagi S Kerur V Mastiholimath

The aim of this study is to formulate a novel ophthalmic nanosuspension (ONS), an alternative carrier system to traditional colloidal carriers for controlled release (CR) of acyclovir (ACV). In the present study, ONS is employed to avoid some of major disadvantages of colloidal carriers systems such as instability in cul de sac and short half life by increasing efficiency of drug encapsulation ...

Introduction: It has been reported the alkaline response of pancreas to duodenal acidification is partly mediated through duodenal release of H2S, but till now the effect of duodenal acidification on gastric H2S release has not been investigated. Therefore, the present study designed to evaluate the effects of duodenal acidification on gastric H2S release and level of mRNA expression of cys...

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 ...

Adenilda Honorio-França, Alfredo Pereira-Junior, Bruno L Santos Carlos K B Ferrari Eduardo L França, Luciane A Monteiro

Objective(s): to investigate the chronopharmacological effects of growth hormone on executive function and the oxidative stress response in rats. Materials and Methods: Fifty male Wistar rats (36-40 weeks old) had ad libitum access to water and food and were separated into four groups: diurnal control, nocturnal control, diurnal GH-treated, and nocturnal GH-treated animals. Levels of Cu, Zn sup...

Purpose: The aim of this study is to compare the amount of Bis-GMA, UDMA, and TEGDMA released from four different types of composite resins in three different time periods using the HPLC device. Materials and Methods: Four different composite resin materials with nanofiller content were used in the study. A total of 40 sample discs were prepared and polished to provide 10 pieces for each mater...

Objective(s): Ketotifen fumarate (KF) is a selective and noncompetitive histamine antagonist (H1-receptor) that is used topically in the treatment of allergic conditions of rhinitis and conjunctivitis. The aim of this study was to formulate and improve an ophthalmic delivery system of KF.Ocular nanoparticles were prepared with the objective of reducing the frequency of administration and obtain...

Journal: :jundishapur journal of natural pharmaceutical products 0
abbas akhgari targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran abdolmaohammad ghalambor dezfuli physics department, shahid chamran university, ahvaz, ir iran mohammadebrahim rezaei physics department, shahid chamran university, ahvaz, ir iran mohammad kiarsi nanotechnology research center, school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran mohammadreza abbaspour targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran; targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran. tel/fax: +98-5138823251

results the results showed that the fiber diameter and the amount of loratadine affected the drug release and the disappearance time of nanofibers. the smaller the fiber diameter and drug amount, the faster the solubility and the release time of nanofibers. conclusions it was concluded that electrospinning can be a suitable method for preparing fast-dissolving loratadine nanofibers. materials a...

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