نتایج جستجو برای: vivo release

تعداد نتایج: 528607  

Journal: :pharmaceutical and biomedical research 0
sonam singh department of pharmaceutics, rajiv academy for pharmacy, mathura, 281001, india kamla pathak department of pharmaceutics, pharmacy college saifai, uttar pradesh university of medical sciences, saifai, etawah, 206130, india

the aim of the present work was to assess the feasibility of accononmc8-2ep/nf as a bioadhesive material for developing controlled release gastroretentive microsponges of loratadine. modified emulsion-solvent diffusion method was employed for the preparation of microsponges (f1-f9) based on 32 factorial design. the amount of ethyl cellulose (ec) and polyvinyl alcohol (pva) were selected as inde...

Journal: :iranian journal of basic medical sciences 0
mohsen tafaghodi school of pharmacy, mashhad university of medical sciences, mashhad, iran pharmaceutical research center, mashhad university of medical sciences, mashhad, iran abolghasem sajadi tabassi school of pharmacy, mashhad university of medical sciences, mashhad, iran pharmacological research center of medicinal plants, mashhad university of medical sciences, mashhad, iran nafiseh amiri school of pharmacy, mashhad university of medical sciences, mashhad, iran

objective(s) several antigens, adjuvants and delivery systems have been evaluated for induction of protective immune responses against leishmaniasis, but most of them have been inefficient. in this study, plga nanospheres as antigen delivery system cpg-odn as an immunoadjuvant for increasing the immune responses against autoclaved leishmania major (alm) were prepared and characterized. material...

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2008
Banu S Zolnik Diane J Burgess

Two poly(lactic-co-glycolic acid) (PLGA) microsphere formulations, with different polymer molecular weights were investigated to determine whether an in vitro and in vivo relationship could be established for dexamethasone release. A USP apparatus 4 was used for in vitro testing. The in vivo release kinetics and pharmacodynamic effects of dexamethasone were evaluated using a Sprague Dawley rat ...

Journal: :The Journal of pharmacology and experimental therapeutics 2014
Nathan D Schilaty David M Hedges Eun Young Jang Ryan J Folsom Jordan T Yorgason J Michael McIntosh Scott C Steffensen

Electrophysiology and microdialysis studies have provided compelling evidence that moderate to high ethanol concentrations enhance dopamine (DA) neurotransmission in the nucleus accumbens (NAc) through the mesolimbic DA system. However, with fast-scan cyclic voltammetry, short-term exposure to moderate to high doses of ethanol decreases evoked DA release at terminals in the NAc. The aim of this...

2014
Nathan D. Schilaty David M. Hedges Eun Young Jang Ryan J. Folsom Jordan T. Yorgason J. Michael McIntosh Scott C. Steffensen

Electrophysiology and microdialysis studies have provided compelling evidence that moderate to high ethanol concentrations enhance dopamine (DA) neurotransmission in the nucleus accumbens (NAc) through the mesolimbic DA system. However, with fast-scan cyclic voltammetry, short-term exposure to moderate to high doses of ethanol decreases evoked DA release at terminals in the NAc. The aim of this...

In this study a 3-factor, 3-level Box-Behnken design was used to prepare optimized docetaxel (DTX) loaded pegylated poly lactide-co-glycolide (PEG-PLGA) NPs with polymer concentration (X1), drug concentration (X2) and ratio of the organic to aqueous solvent (X3) as the independent variables and particle size (Y1), poly dispersity index (PDI) (Y2) and drug loading (Y3) as the responses. The cyto...

The major challenge to treat Parkinson’s disease (PD) is penetration of target molecule into the brain to improve the efficacy of drugs. To achieve better brain penetration and targeted delivery, 1,9-Pyrazoloanthrone (1,9-P) loaded liposomes were developed by solvent injection technique using ultrasonication and evaluated for particle size, morphology, entrapment efficiency, FT-IR, and in-vitro...

Journal: :International journal of pharmaceutics 2015
Katrin Fuchs Pierre E Bize Alban Denys Gerrit Borchard Olivier Jordan

Drug-eluting microspheres are used for embolization of hypervascular tumors and allow for local controlled drug release. Although the drug release from the microspheres relies on fast ion-exchange, so far only slow-releasing in vitro dissolution methods have been correlated to in vivo data. Three in vitro release methods are assessed in this study for their potential to predict slow in vivo rel...

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2009
Yan Ma Wei-Zhong Li Shi-Xia Guan Xiao-Ping Lai Da-Wei Chen

An approach for the preparation of tetrandrine sustained release calcium alginate gel beads was described. In vitro the release of tetrandrine from sustained release dosage forms went on a time of 12 hours which fitted non-Fickian diffusion with matrix erosion significantly. In vivo the plasma concentration of tetrandrine extended preparation given in dogs reached Cmax 2.67+/-0.69 microg/ml app...

Journal: :مجله علوم اعصاب شفای خاتم 0
behrooz fathi department of pharmacology, school of veterinary medicine, ferdowsi university of mashhad, mashhad, iran alan l harvey strathclyde institute of pharmacy and biomedical sciences, university of strathclyde, 27 taylor street, glasgow g4 0nr, united kingdom edward g rowan strathclyde institute of pharmacy and biomedical sciences, university of strathclyde, 27 taylor street, glasgow g4 0nr, united kingdom fatemeh salami department of physiology, school of veterinary medicine, ferdowsi university of mashhad, mashhad, iran

introduction: in a serious brain disorder like alzheimer's disease, the levels of acetylcholine (ach) drop significantly. the gradual death of cholinergic brain cells leads to a profound loss of memory and learning ability. acetylcholine is the chemical messenger that sends messages from one neuron to another in the area of the brain used for memory. many of the current medications act to ...

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