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American Journal of PharmTech Research

S. Keerthi

Author Profile
2
Publications
2
Years Active
5
Collaborators
53
Citations

Publications by S. Keerthi

2 publications found • Active 2012-2014

2014

1 publication

Formulation and Evaluation of Pulsatile Drug Delivery System of Anti-Asthmatic Drug

with Vijay bhaskar reddy, Gopal muralidharan, L.V.G Nargund
2/1/2014

Aim of the present work was to formulate and evaluate an oral, time controlled drug delivery system to achieve timed release of Montelukast sodium, for the treatment of nocturnal asthma. An asthmatic attack mainly takes place early in the morning. Time controlled delivery system is capable of delivering drug when and where it is required most. Time-delayed tablets, designed to release drug after a predictable lag time, are intended for oral chronotherapy. A time dependant pulsed release system consisting of a core surrounded by coat layer of different ratios of swellable erodible hydrophilic layer HPMC K100M and rupturable hydrophobic layer Eudragit L 100 and Eudragit S 100 were prepared. These pulsatile tablets were evaluated for the drug content, thickness and in-vitro release profile, etc. and  two optimized formulation were selected and subjected to further studies. .

2012

1 publication

Design and Characterization of Microspheres of Anti Hypertensive Drug Using Biodegradable Natural Polymers

with T. S. Keerthi, S. K. Senthilkumar
8/1/2012

  Present investigation describes preparation of microspheres by solvent evaporation followed by in vitro characterization of microspheres to evaluate the effect of method of preparation on physical properties and drug release profile of microspheres. The microspheres were found to be discrete, spherical with free flowing properties. The morphology (Scanning Electron Microscopy), particle size distribution, entrapment efficiency and their release profiles were investigated. The yield was found to be maximum in case of solvent evaporation method. The microsphere prepared by solvent evaporation method was found in ranges of 250-50 μm, respectively. The microspheres formulation prepared by solvent evaporation method the drug carrier interactions were investigated in solid state by Fourier Transform Infrared (FT-IR) spectroscopy study. In vitro drug release rate for A microsphere was found to be sustained over 12 hours. Hence, it can be concluded that the Formulation prepared by solvent evaporation method, has potential to deliver Losartan Potassium in a controlled manner in a regular fashion over extended period of time in Comparison to all other formulations and can be adopted for a successful oral delivery of Losartan potassium for safe management of hypertension.

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