نتایج جستجو برای: drug carrier

تعداد نتایج: 655357  

Journal: :iranian journal of pharmaceutical sciences 0
fatemah atyabi department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran afsaneh mohammadi department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran rassoul dinarvand department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran

the purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl cellulose (ec) as a carrier polymer through an emulsion solvent evaporation method. these evaluations characterized the pattern of drug release from prepared microspheres. nimodipin loaded microspheres were prepared using an emulsification solvent evaporation method. the effect of process variab...

Journal: :research in pharmaceutical sciences 0
ma shahtalebi sa mostafavi a moghaddas

niosomes are non-ionic surfactant vesicles that have potential applications in the delivery of hydrophilic and hydrophobic drugs. the topical form of n-acetyl glucosamine (nag) recently has been considered in the treatment of hyperpigmentation disorders due to its inhibitory effect on thyrosinase enzymes in melanocytes. to improve nag penetration into the skin we formulated the drug in niosomes...

ژورنال: کومش 2020

Introduction: One of the effective drugs in the treatment of cancer is dexamethasone. Dexamethasone is known as one of the safest glucocorticoid, but there is still side-effects, due to its hydrophobicity and low bioavailability. The purpose of the present study is to design a controlled release carrier for dexamethasone in order to overcome constraints and reduce side effects. Materials and Me...

For many years, dexamethasone has been used as an anti-inflammatory drug and is still one of the safest glucocorticoids for treating various diseases. Due to the wide range of the side effects of this drug, it is essential to find a suitable delivering system for reduction in dosage with increased effectiveness. Electrospinning is one of the fiber fabrication methods which is widely used to dev...

In this study, tretinoin microemulsion has been formulated based on phase diagram studies by changing the amounts and proportions of inactive ingredients, such as surfactants, co-surfactants and oils. The effects of these variables have been determined on microemulsion formation, particle size of the dispersed phase and release profile of tretinoin from microemulsion through dialysis membrane. ...

In this study, tretinoin microemulsion has been formulated based on phase diagram studies by changing the amounts and proportions of inactive ingredients, such as surfactants, co-surfactants and oils. The effects of these variables have been determined on microemulsion formation, particle size of the dispersed phase and release profile of tretinoin from microemulsion through dialysis membrane. ...

Journal: :Physical Chemistry Chemical Physics 2023

Release of drug or vaccine molecules from macro-, micro-, and nano-sized carriers is usually considered to be limited by diffusion and/or carrier dissolution erosion. The corresponding experimentally observed kinetics...

A Barzegar-Jalali GH Mohammadi H Valizadeh KH Adibkia M Barzegar-Jalali MR Siahi Shadbad S Dastmalchi

Carbamazepine belongs to the class II biopharmaceutical classification system (BCS) which is characterized by a high per-oral dose, a low aqueous solubility and a high membrane permeability. The bioavailability of such a drug is limited by the dissolution rate. In order to increase the drug dissolution, its solid dispersions were prepared by the cogrinding technique using an insoluble but highl...

A Barzegar-Jalali GH Mohammadi H Valizadeh KH Adibkia M Barzegar-Jalali MR Siahi Shadbad S Dastmalchi

Carbamazepine belongs to the class II biopharmaceutical classification system (BCS) which is characterized by a high per-oral dose, a low aqueous solubility and a high membrane permeability. The bioavailability of such a drug is limited by the dissolution rate. In order to increase the drug dissolution, its solid dispersions were prepared by the cogrinding technique using an insoluble but highl...

Journal: :Journal of pharmaceutical research international 2021

Background: Solid dispersions (SDs) are the dispersion of hydrophobic drugs in an inert hydrophilic carrier. SDs prepared to improve dissolution properties and bioavailability slightly water-soluble drug molecules by dispersing them into carrier.
 Aims Objective: Evaluate solubility Dispersion Lercanidipine Hydrochloride (LER).
 Materials Methods: To study effect polymer, studies were...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید