GASTRORETENTIVE DRUG DELIVERY SYSTEM OF LEVO-SALBUTAMOL SULPHATE: FORMULATION AND IN VITRO EVALUATION
Journal Title: International Journal of Pharmaceutical Sciences and Drug Research - Year 2016, Vol 8, Issue 2
Abstract
In order to prepare the sustained release tablet with levo-salbutamol sulphate we have used these excipients methylcellulose, PVPK30, magnesium stearate, talc, isopropyl alcohol, microcrystalline cellulose, lactose, HPMCK100, HPMCK4M. Here our approach was for making the sustained released matrix tablet by two ways, one is to make the tablet granules floating and the second one is by retarding the release of the levo-salbutamol sulphate from the matrix. We have already discussed the relationship with delaying the gastric transit time and the active drug absorption, if the tablet granules are floating in our introduction part. Since the above mentioned excipients are floating in nature so formulations with those excipients are supposed to be floating. We also showed a list of excipients those are used in the preparation of floating tablets. Now the second observation which was the release rate, among the three different formulations (mentioned in the introduction) we found different types of release. Since our objective is to prepare a sustained released tablet which will give a prolong release time, in that prospect two among the three formulations were disqualified (though we have not done the kinetic study). We observed desired effect in the formulation-2 during the preparation of experiment.
Authors and Affiliations
Kamanashis Das, Md. Yasin, Ishrak Jahan, Tahira Akter, Saiful Islam, Md. Sagir Mia
QUALITY CONTROL OF A MARINE ORIGIN BASED HERBO-MINERAL UNANI FORMULATION
Kushta Marjan (KM) is one well-known formulation prepared from coral used by Unani physicians for effective treatment of a various ailments. Coral is the calcareous skeleton of the minute marine organism and belongs of p...
BLOCKADE OF EPIDERMAL GROWTH FACTOR RECEPTOR, CYCLOXYGENASE-2 (COX-2) AND MAMMALIAN TARGET OF RAPAMYCIN (M-TOR) IN ANIMAL MODEL OF LUNG CANCER
To explore the effectiveness and possible toxicity of the use of epidermal growth factor receptor inhibitor (EGFR Inhibitor), Celecoxib (COX2 inhibitor) and Sirolimus (m-TOR inhibitor) as single agents and drug combinati...
Formulation and Evaluation of Solid Dispersion Incorporated Fast Disintegrating Tablets of Tenoxicam Using Design of Experiment
The aim of the present work is to develop fast dissolving tablets from the solid dispersion of Tenoxicam for enhancement of solubility. The solid dispersions of Tenoxicam were prepared with Kollidon CL, PVP K30 and Polox...
PROGRESS AND PROSPECTS IN THERAPEUTICS AGAINST HIV INFECTION
Tremendous advances have occurred in recent decades in the development of safe and effective medications for the treatment of viral diseases. Currently there are more than 20 HIV drugs approved for use in humans. Combine...
BIOLOGICALLY ACTIVE TRITERPENES FROM EUGENIA PISIFORMIS CAMBESS. (MYRTACEAE)
In Brazil, Eugenia pisiformis, which belongs to botanical family Myrtaceae occurs in the states of Rio de Janeiro, Espírito Santo, Maranhão and Bahia. A specimen of E. pisiformis collected in Itatiaia National Park, Stat...