نتایج جستجو برای: phase diagram brinzolamide ophthalmic delivery biological studies release efficiency

تعداد نتایج: 3001818  

2011
Ines Lanzl Thomas Raber

INTRODUCTION The purpose of this study was to document the efficacy and tolerability of the new fixed-combination (FC) brinzolamide 1%/timolol 0.5% as used in daily practice throughout Germany. METHODS An open-label, multicenter, observational study of patients was performed that evaluated the transition from prior medication to brinzolamide/timolol FC for the reduction of intraocular pressur...

Journal: :Acta pharmaceutica 2005
Shyam Shimpi Bhaskar Chauhan Prajakta Shimpi

The objective of this review article is to explain the use of cyclodextrin in the different routes of drug administration. The article gives the chemistry of cyclodextrins and addresses the issue of the mechanism of drug release from cyclodextrin complexes. Dilution, competitive displacement, protein binding, change in ionic strength and temperature and drug uptake by tissues are the different ...

Journal: :Biomaterials 2001
G H Hsiue J A Guu C C Cheng

This work investigates pilocarpine trapped in a matrix diffusion-controlled drug delivery system using hydrophilic inserts of Poly(2-hydroxyethyl methacrylate) (pHEMA) to ensure an increased bioavailability of pilocarpine and prolong the length of time in which the medication remains in the eyes of the test subjects. The physical and chemical properties of pilocarpine were investigated to eluci...

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...

Asal Mir Mohammad Sadeghi Mohammad Reza Avadi Naser Mohammadpour Nastaran Farhangi Nazanin Forouhar Orkideh Ghorban Dadras

Many strategies have been developed to improve vaccine delivery in the past decade. The aim of the current study was to develop a nanoparticulate system based on ionic gelation between chitosan and tripolyphosphate in order to load Androctonus Crassicauda scorpion venom. The best formulation was selected according to the highest association efficiency, loading capacity, optimum particle size an...

2018
Viviana Vergaro Monica Civallero Cinzia Citti Maria Cosenza Francesca Baldassarre Giuseppe Cannazza Samantha Pozzi Stefano Sacchi Francesco Paolo Fanizzi Giuseppe Ciccarella

Owing to their nano-sized porous structure, CaCO₃ nanocrystals (CaCO₃NCs) hold the promise to be utilized as desired materials for encapsulating molecules which demonstrate wide promise in drug delivery. We evaluate the possibility to encapsulate and release NVP-BEZ235, a novel and potent dual PI3K/mTOR inhibitor that is currently in phase I/II clinical trials for advanced solid tumors, from th...

2013
K. H. Ramteke

Hydrogels are the 3 dimensional cross linked polymeric networks which absorb the water 10-20 times of its molecular weight. Hydrogels are sensitive to different environmental stimuli like pH, temperature, ion, electric signals, light, pressure, antigen specific, enzyme sensitive, and glucose levels. When the environment is get change they get swell, and swelling is the most important characteri...

2018
Fazhan Wang Xingting Bao Aiping Fang Huili Li Yang Zhou Yongmei Liu Chunling Jiang Jinhui Wu Xiangrong Song

Novel ocular drug delivery systems (NODDSs) remain to be explored to overcome the anatomical and physiological barriers of the eyes. This study was to encapsulate brinzolamide (BRZ)-hydropropyl-β-cyclodextrin (HP-β-CD) inclusion complex (HP-β-CD/BRZ) into nanoliposomes and investigate its potential as one of NODDS to improve BRZ local glaucomatous therapeutic effect. HP-β-CD/BRZ was firstly pre...

Journal: :Pharmaceutics 2021

Protamine is a natural cationic peptide mixture mostly known as drug for the neutralization of heparin and compound in formulations slow-release insulin. also used cellular delivery nucleic acids due to opposite charge-driven coupling. This year marks 60 years since first use transfection enhancement agent. Since then, has been broadly stabilization agent RNA delivery. It involved several compo...

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