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Development of sustained release tablets

SURFACE RESPONSE METHODOLOGY FOR DEVELOPMENT AND OPTIMIZATION OF NAPROXEN SUSTAINED RELEASE TABLETS

SURFACE RESPONSE METHODOLOGY FOR DEVELOPMENT AND OPTIMIZATION OF NAPROXEN SUSTAINED RELEASE TABLETS

... the development and optimization of Naproxen 800mg sustained release tablets using surface response ...drug release was controlled by formulating it into a sustained ...

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Synergistic Homopolysaccharide:Heteropolysaccharide Interactions- Rheological Investigation and Development of Sustained Release Tablets

Synergistic Homopolysaccharide:Heteropolysaccharide Interactions- Rheological Investigation and Development of Sustained Release Tablets

... Matrix tablets were formulated using Metoprolol tartarte as a model drug and evaluated for erosion and swelling indices to correlate with the in vitro dissolution ...drug release is that relatively smaller ...

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Formulation Development and Evaluation of Sustained Release Tablets of Aceclofenac

Formulation Development and Evaluation of Sustained Release Tablets of Aceclofenac

... Aceclofenac sustained release tablets using different polymers as release retarding ...as tablets. Tablets were tested for weight variation, thickness, hardness and friability as ...

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Formulation Development of Metformin Hydrochloride Sustained Release Tablets

Formulation Development of Metformin Hydrochloride Sustained Release Tablets

... oral sustained release Metformin hydrochloride matrix tablets by using hydroxyl methyl cellulose polymer (HPMC) as rate controlling factor and to evaluate drug release parameters as per ...

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FORMULATION DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE TABLETS OF LORNOXICAM

FORMULATION DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE TABLETS OF LORNOXICAM

... KEYWORDS: Lornoxicam, Sustained release, Dissolution, HPMC. INTRODUCTION Oral route of drug administration is the most important method of administering drugs for systemic effects. Nevertheless, it is ...

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Formulation Development and Evaluation of Valsartan Sodium Sustained Release Tablets

Formulation Development and Evaluation of Valsartan Sodium Sustained Release Tablets

... superdisintegrant. Tablets were formulated by direct compression, slugging and wet granulation ...drug release were ...drug release and selected as an optimized formulation and it was concluded that ...

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DEVELOPMENT AND EVALUATION OF A DIRECTLY COMPRESSIBLE CO PROCESSED MULTIFUNCTION SUSTAINED RELEASE AGENT FOR ISOSORBIDE MONONITRATE SUSTAINED RELEASE TABLETS

DEVELOPMENT AND EVALUATION OF A DIRECTLY COMPRESSIBLE CO PROCESSED MULTIFUNCTION SUSTAINED RELEASE AGENT FOR ISOSORBIDE MONONITRATE SUSTAINED RELEASE TABLETS

... Available online on www.ijpsr.com 104 INTRODUCTION: Co-processed excipients are combinations of two or more excipients that possess performance advantages when compared to a physical mixture of the same combination of ...

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Formulation Development and  In-vitro Evaluation of Sustained Release Tablets of Carvedilol Solid Dispersion

Formulation Development and In-vitro Evaluation of Sustained Release Tablets of Carvedilol Solid Dispersion

... formulate sustained release tablets of Carvedilol by solid dispersion technique for improving solubility of Carvedilol using Poloxamer 407 and PVP ...carvedilol tablets were prepared by direct ...

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DEVELOPMENT AND OPTIMIZATION OF SUSTAINED RELEASE ABACAVIR MATRIX TABLETS

DEVELOPMENT AND OPTIMIZATION OF SUSTAINED RELEASE ABACAVIR MATRIX TABLETS

... Abacavir sustained release ...prepared tablets were characterized for hardness, thickness, disintegration time and drug release ...drug release studies and physical ...

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DESIGN AND DEVELOPMENT OF ORAL SUSTAINED RELEASE MATRIX TABLETS OF DIDANOSINE

DESIGN AND DEVELOPMENT OF ORAL SUSTAINED RELEASE MATRIX TABLETS OF DIDANOSINE

... design sustained-release tablets containing Didanosine using natural gums like Xanthan gum, Guar gum and Karaya ...The sustained-release tablets containing Didanosine prepared by ...

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Formulation and Development of Sustained Release Matrix Tablets Containing Metformin Hydrochloride

Formulation and Development of Sustained Release Matrix Tablets Containing Metformin Hydrochloride

... In vitro dissolution studies of all the formulations of sustained release tablets of Metformin HCL were carried out in pH 6.8 phosphate buffers for 16 hours. All the tablet formulations showed ...

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FORMULATION AND EVALUATION OF NATEGLINIDE SUSTAINED RELEASE TABLETS

FORMULATION AND EVALUATION OF NATEGLINIDE SUSTAINED RELEASE TABLETS

... Int. J. Pharm. Sci. Drug Res. January-February, 2016, Vol 8, Issue 1 (07-12) to the achievement of a 12 to 24 hours oral prolonged release dosage form. Some of the characteristics militating against success are ...

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Formulation and Evaluation of Nicardipine Sustained Release Tablets

Formulation and Evaluation of Nicardipine Sustained Release Tablets

... The pharmaceutical development studies have to be carried out with the purpose of selecting right dosage form and a stable formulation. These studies give detailed description of all the steps involved in the ...

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Formulation and evaluation of magnesium sustained release tablets

Formulation and evaluation of magnesium sustained release tablets

... Formulation Development The pharmaceutical development studies have be carried out with the purpose of selecting right dosage form and stable ...process development of Sustained release ...

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Formulation, Development and Evaluation of Sustained Release Matrix Tablets Containing Salbutamol Sulphate

Formulation, Development and Evaluation of Sustained Release Matrix Tablets Containing Salbutamol Sulphate

... of sustained release tablets of salbutamol sulphate were carried out in pH ...drug release from ...drug release from the ...drug release profile, ...

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Development and Evaluation of Sustained Release Bilayer Tablets of Carvedilol.

Development and Evaluation of Sustained Release Bilayer Tablets of Carvedilol.

... vitro release study, it was observed that the release of Carvedilol from the prepared formulations was analyzed by plotting the cumulative percent drug released ...drug release can be attributed the ...

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FORMULATION AND DEVELOPMENT OF SUSTAINED RELEASE MATRIX TABLETS OF METFORMIN HYDROCHLORIDE

FORMULATION AND DEVELOPMENT OF SUSTAINED RELEASE MATRIX TABLETS OF METFORMIN HYDROCHLORIDE

... different release mechanisms are operative, either of which is zero-order erosion and decreasing surface area, and dissolution of coated particles, but the overall tablet release profile comprising the two ...

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Formulation Development and Evaluation of Bilayer Tablets of Lisinopril for Immediate Release and Glipizide for Sustained Release

Formulation Development and Evaluation of Bilayer Tablets of Lisinopril for Immediate Release and Glipizide for Sustained Release

... and release follows first order ...in sustained release layer and Atorvastatin Calcium in immediate release ...Bilayer tablets were prepared by wet granulation ...burst release ...

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Development and Charecterisation of Ramipril as Immediate Release and Metformin Hydrochloride as 
     Sustained Release  Bilayered Tablets

Development and Charecterisation of Ramipril as Immediate Release and Metformin Hydrochloride as Sustained Release Bilayered Tablets

... of tablets. The bilayer tablets were prepared by direct compression technique in which Metformin HCl was compressed as sustained release layer with the help of different controlled ...

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Formulation, Development and Evaluation of Timolol Maleate Sustained Release Matrix Tablets

Formulation, Development and Evaluation of Timolol Maleate Sustained Release Matrix Tablets

... The tablets were taken out after completion of the respected stipulated time span as mentioned above and weighed after the excess of water at the surface had been removed with filter ...

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