نتایج جستجو برای: gastroretentive drug delivery system

تعداد نتایج: 2851854  

2011
AK. Sharma RK. Keservani SC. Dadarwal YL. Choudhary S. Ramteke

BACKGROUND AND THE PURPOSE OF THE STUDY The objective of the present work was to improve bioavailability of cepodoxime proxetil through gastroretentive microballoon formulation. METHODS Microballoons of cefpodoxime proxetil were formulated by solvent evaporation and diffusion method employing hydroxypropylmethyl cellulose (HPMC) and ethyl cellulose (EC) polymers and characterized for particle...

Journal: :iranian journal of pharmaceutical research 0
reza masaeli dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran teherh sadat jafarzadeh kashi dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran rasoul dinarvand nanotechnology research centre, faculty of pharmacy, tehran university of medical sciences, tehran 1417614411, iran mohammadreza tahriri dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran vahid rakhshan department of anatomy, dental branch, islamic azad univesity mehdi esfandyari-manesh nanotechnology research center,tehran university of medical sciences, tehran, iran

microspheres formulated from poly (d,l-lactic-co-glycolide) (plga), a biodegradable polymer, have been extensively evaluated as a drug delivery system. in this study, the preparation, characterization and drug release properties of the plga microspheres were evaluated. simvastatin (sim)-loaded plga microspheres were prepared by oil-in-water emulsion/solvent evaporation method. the microspheres ...

2012
Prashant Upadhyay Jayanta Kumar Pandit

Purpose: Fast-release gastroretentive solid dispersions of glibenclamide using gelucire were prepared to achieve improved bioavailability. Methods: Hot melt granulation technique was adopted to prepare solid dispersions (SDs) of glibenclamide in gelucire 50/13 and were compared with pure glibenclamide and physical mixtures of drug and gelucire using hot stage polarized microscopy, powder x-ray ...

Transdermal drug delivery system is a non-invasive and an efficient method that provides sustained release and delivers therapeutics to target site. This system can improve the therapeutic efficacy and safety of the drugs, keep the plasma level of the drug constant, prevent the hepatic first pass metabolism and is convenient and pain-free self-administration for patients. Despite the many advan...

Journal: :International Journal of Current Research and Academic Review 2016

2016
Anita Ayre Neha Dand K. G. Lalitha

Gastro retentive drug delivery system (GRDDS) is one of the novel approaches in the area of oral sustained release dosage forms. Drugs that are easily absorbed from gastrointestinal tract (GIT) and have short half-lives are eliminated quickly from the systemic circulation require frequent dosing to achieve suitable therapeutic activity. To avoid this limitation, the development of oral sustaine...

Journal: :Advanced pharmaceutical bulletin 2011
Maryam Maghsoodi Elham Hemati Bahram Qadermazi Zahra Yari

PURPOSE A multiparticular floating-pulsatile drug delivery system was developed for time and site specific drug release of piroxicam. A blend of floating and pulsatile principles of drug delivery system would have the advantage that a drug can be released in the upper GI tract after a definite time period. METHODS Hollow microspheres were prepared by the emulsion solvent diffusion method usin...

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