Maru Department of Pharmaceutics, Loknete Dr.
Gupta, Sandeep Shrivastava Abstract Objective: The aim of present study is to formulate mouth dissolving tablet of omeprazole, the drug will be directly absorbed into systemic circulation through buccal mucosa and lead to produce immediate action. Mouth dissolving tablets of Omeprazole were prepared by wet granulation method.
Required quantity of drug and other excipients were weighed and sieved from sieve no. All the formulated tablets met the pharmacopoeias standard of uniformity of weight, percentage friability, thickness, and drug content.
The in vitro disintegration and dispersion studies were also performed, which shows very good bioavailability and drug release profile.
It may be predicted that formulation will be stable for more than one year. The present investigation successfully formulated mouth dissolving tablets of omeprazole with improved drug release profile.
The formulation was chosen because it showed good results in terms of cumulative drug release, disintegration time, hardness and friability. Drug-delivery products and the Zydis fast-dissolving dosage.
J Pharm Pharmacol ; Fast dissolving drug delivery system: Internet J Pharmcol ;4: Fast-dissolve drug delivery system. A review of mouth dissolving tablet technologies. S Nail, L Galtin. Pharmaceutical dosage forms-parenteral medication, Marcel Dekker Inc.
R Bogner, F Meghan. Fast dissolving tablets, US Pharmacist; Formulation design and optimization of mouth dissolving tablets of nimesulide using vacuum drying technique.
Superdisintegrants for solid dispersion to produce rapidly disintegrating tenoxicam tablets via camphor sublimation. J Remon, S Corveleyn. Formulation and production of rapidly disintegrating tablets by lyophilization using hydrochlorothiazide as a model drug.
Int J Pharm ; Article for carrying chemicals. United States Patent ;4: Preparation of pharmaceutical and another matrix system by solid-state dissolution. United States Patent ;5: Solid pharmaceutical dosage in tablet triturates form and method of producing the same.
Intrabuccally disintegrating preparation and production thereof. The United States ;5: Process and apparatus for making rapidly dissolving dosage unit and product therefrom. J Swarbrick, JC Boylan.Formulation And Evaluation Of Mouth Dissolving Nimesulide Tablets Biology Essay Abstraction: Mouth fade outing tablets has figure of advantage viz., faster oncoming of action, elegance, easiness of disposal, easiness of fabrication, easiness of storage and conveyance.
International Journal of ChemTech Research; 2(1): , ().
Bhanushali Akash, Chaudhari Pallavi, Sonawane Tushar, Solanki Nikita. Formulation and evaluation of mouth dissolving tablets of isosorbide mononitrate. International Research Journal of Pharmacy; 2(3): , ().
Formulation Of Floating Microspheres Of Clarithromycin Biology Essay ?g/ml of clarithromycin is prepared and scanned from the wavelength of to nanometers in UV spectrometry.
The extremum with the highest optical density was taken as the lambda soap of rifampicin for farther surveies. Improved drug soaking up. Techniques for fixing Mouth Dissolving Tablets: There are many techniques that have been reported for the preparation of Mouth fade outing tablets.
Freeze drying / freeze-drying. Freeze drying is the procedure in which H2O is sublimed from the merchandise after it is frozen.
Formulation design and optimization of mouth dissolve tablets of nimesulide using vacuum drying technique Formulation Design and Optimization of Mouth Dissolve Formulation and evaluation. Formulation and evaluation of mouth dissolving tablets of nimesulide by new coprocessed technique Basawaraj S Patil*, Upendra Kulkarni, Parik Bhavik, Srinivas R Soodam, Prakash G Korwar R.M.E.S College of Pharmacy, Gulbarga – Karnataka, India.
ABSTRACT Attempts were made to prepare mouth dissolving tablets of Nimesulide by direct compression method with a view to enhance patient .