نتایج جستجو برای: Hydrophilic drug

تعداد نتایج: 602623  

Journal: :iranian journal of pharmaceutical research 0
r aboofazeli

in this study, attempts were made to evaluate the effect of various acrylic acid based carbopols on the release profile of a beta-adrenoreceptor blocking drug, propranolol hcl, from matrix-type tablets invitro. for this purpose, tablets containing 160 mg of propranolol hcl along with various amounts of carbopols 934 (c934), 971 (c971), 974 (c974) and pemulen (pem) were prepared using the wet gr...

Cationic polymeric nanoparticles have great potential for developing drug delivery systemswith limited side effects for tumor medication. The goal of this research is investigation ofcationic dextran-spermine polymer (DS) efficacy for improvement of hydrophilic drug deliveryto negatively charged cancerous cells. Capecitabine (as a hydrophilic antineoplastic drug) wasloaded into the magnetic dex...

Cationic polymeric nanoparticles have great potential for developing drug delivery systemswith limited side effects for tumor medication. The goal of this research is investigation ofcationic dextran-spermine polymer (DS) efficacy for improvement of hydrophilic drug deliveryto negatively charged cancerous cells. Capecitabine (as a hydrophilic antineoplastic drug) wasloaded into the magnetic dex...

Journal: :iranian journal of pharmaceutical sciences 0
saini nish school of pharmaceutical sciences, shoolini university solan (h.p), india george mathew school of pharmaceutical sciences, shoolini university solan (h.p), india joseph lincy school of pharmaceutical sciences, shoolini university solan (h.p), india

the purpose of this review article is to characterize all of the parameters regarding the types, polymers used, and release kinetics of matrix tablets. matrix system was the earliest oral extended release platform for medicinal use. matrix tablets are most commonly used methods to modulate the release profile of drugs. they are much desirable and preferred for such therapy because they offer be...

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 ...

Journal: :SN applied sciences 2021

Abstract Mixed micellar systems have been tried with the aim of achieving higher solubility drugs compared to single systems. Hydrophobic-hydrophilic mixed used for above purpose drug ciprofloxacin in past. In present study, a hydrophilic-hydrophilic binary system comprising pluronic copolymers F127 and L64 has studied its effect on solubilization Ciprofloxacin. The solutions two individual the...

Journal: :research in pharmaceutical sciences 0
vt thakkar pa shah tg soni my parmar mc gohel tr gandhi

the objective of this work was to develop and evaluate the levofloxacin hemihydrate floating formulations (f1-f9). selection of optimized batch was done by model dependent approach and novel mathematical approach. f1-f9 batches were prepared by direct compression method using gelucire 43/01 (hydrophobic) and hydroxypropylmethylcellulose (hydrophilic) polymer in different ratios. the floating ta...

George Mathew Joseph Lincy Saini Nish,

       The purpose of this review article is to characterize all of the parameters regarding the types, polymers used, and release kinetics of matrix tablets. Matrix system was the earliest oral extended release platform for medicinal use. Matrix tablets are most commonly used methods to modulate the release profile of drugs. They are much desirable and preferred for such therapy because they o...

Journal: :iranian journal of pharmaceutical sciences 0
amal a. elkordy university of sunderland, faculty of applied sciences, department of pharmacy, health and well-being, sunderland, sr1 3sd, uk ebtessam a. essa university of tanta, faculty of pharmacy, egypt

the formulation of hydrophobic drugs for oral drug delivery is challenging due to poor solubility, poor dissolution and poor wetting of these drugs. consequently, the aim of this study was to improve the dissolution of a model poorly water soluble drug, ibuprofen. microparticles containing ibuprofen were produced by spray drying and spray chilling technology in the absence/presence of a hydroph...

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