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[PDF] Top 20 FORMULATION AND EVALUATION OF MEFENAMIC ACID TABLETS BY USING MODIFIED STARCH

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FORMULATION AND EVALUATION OF MEFENAMIC ACID TABLETS BY USING MODIFIED STARCH

FORMULATION AND EVALUATION OF MEFENAMIC ACID TABLETS BY USING MODIFIED STARCH

... the starch citrate was prepared by reacting the citric acid with starch at elevated ...Prepared starch citrate was found to be insoluble in water, organic solvents, acidic and alkaline ...pH. ... See full document

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FORMULATION AND EVALUATION OF CAPTOPRIL FLOATING TABLETS EMPLOYING A NEW MODIFIED STARCH – OPTIMIZATION BY 23 FACTORIAL DESIGN

FORMULATION AND EVALUATION OF CAPTOPRIL FLOATING TABLETS EMPLOYING A NEW MODIFIED STARCH – OPTIMIZATION BY 23 FACTORIAL DESIGN

... uncertain. Formulation of floating drug delivery systems is a useful approach to avoid this variability with increased gastric retention time of the drug delivery ... See full document

13

ENHANCEMENT OF DISSOLUTION RATE AND FORMULATION DEVELOPMENT OF RITONAVIR TABLETS EMPLOYING STARCH PHOSPHATE  A NEW MODIFIED STARCH

ENHANCEMENT OF DISSOLUTION RATE AND FORMULATION DEVELOPMENT OF RITONAVIR TABLETS EMPLOYING STARCH PHOSPHATE A NEW MODIFIED STARCH

... C. Starch phosphate prepared was insoluble in water, aqueous fluids of acidic and alkaline pH and several organic solvents ...with starch phosphate when its aqueous dispersion was heated at 100 0 C for 30 ... See full document

6

PHYSICOCHEMICAL CHARACTERIZATION OF ACID MODIFIED DIOSCOREA STARCH AND ITS EVALUATION AS DIRECTLY COMPRESSIBLE EXCIPIENT IN TABLET FORMULATION

PHYSICOCHEMICAL CHARACTERIZATION OF ACID MODIFIED DIOSCOREA STARCH AND ITS EVALUATION AS DIRECTLY COMPRESSIBLE EXCIPIENT IN TABLET FORMULATION

... the starch, corresponding to the weakening of the hydrogen bonds (Osunsam et ...of acid modified starch with increasing temperature may be due to the loss of granular structure and release of ... See full document

8

Formulation and evaluation of fast dissolving oral film of mefenamic acid

Formulation and evaluation of fast dissolving oral film of mefenamic acid

... The oral route of administration still continues to be widely used accepted route, contributing to 50-60% of total drug formulations because of ease of administration, self- medicament, and pain avoidance as compared to ... See full document

9

Design and Optimization of Mefenamic acid Fast Dissolving Tablets Employing Modified Starch by 23 Factorial Design

Design and Optimization of Mefenamic acid Fast Dissolving Tablets Employing Modified Starch by 23 Factorial Design

... dissolving tablets each containing 200 mg of mefenamic acid could be prepared by employing modified starch and other known superdisintegrants, croscarmellose sodium and crospovidone by ... See full document

12

Formulation and Evaluation of Mefenamic Acid Solid Dispersions Employing Starch Citrate-A New Solubility Enhancer

Formulation and Evaluation of Mefenamic Acid Solid Dispersions Employing Starch Citrate-A New Solubility Enhancer

... The starch citrate prepared was found to be white amorphous free-flowing ...the starch citrate are given in table ...7.72. Starch citrate exhibited good swelling in ...of tablets. The density ... See full document

5

FORMULATION AND EVALUATION OF MEFENAMIC ACID EXTENDED RELEASE LIQUISOLID TABLETS

FORMULATION AND EVALUATION OF MEFENAMIC ACID EXTENDED RELEASE LIQUISOLID TABLETS

... Mefenamic acid. Liquisolid extended release formulations were prepared by using HPMC K100M as adjuvant for extended ...prepared using a mathematical model to calculate the required quantities ... See full document

17

ENHANCEMENT SOLUBILITY AND DISSOLUTION OF MEFENAMIC ACID BY MODIFIED STARCH

ENHANCEMENT SOLUBILITY AND DISSOLUTION OF MEFENAMIC ACID BY MODIFIED STARCH

... pharmaceutical formulation technologies are being developed for the solubility and dissolution rate of poorly water soluble drugs such as micronization, nano suspension, supercritical fluid process, solid ... See full document

8

FORMULATION AND INVITRO EVALUATION OF HYDROGEL MATRICES OF GLICLAZIDE MODIFIED RELEASE TABLETS

FORMULATION AND INVITRO EVALUATION OF HYDROGEL MATRICES OF GLICLAZIDE MODIFIED RELEASE TABLETS

... formulate modified release tablets, each class demonstrating a different approach to the modified release ...Stearic acid, Polyethylene glycol, Castor wax, Polyethylene glycol monostearate, ... See full document

7

Formulation and Evaluation of Simvastatin Floating Tablets

Formulation and Evaluation of Simvastatin Floating Tablets

... Four for mulations containing varying properties of polymers like HPMC K4M and Ethyl cellulose and fixed amount of gas generating agent i.e. Sodium bicarbonate and hydrophobic meltable material like Bee wax were prepared ... See full document

6

FORMULATION AND IN VITRO EVALUATION OF DRY EMULSION OF MEFENAMIC ACID IN HARD VEGETARIAN CAPSULES

FORMULATION AND IN VITRO EVALUATION OF DRY EMULSION OF MEFENAMIC ACID IN HARD VEGETARIAN CAPSULES

... Solubility studies were carried by placing an excess amount of mefenamic acid in vials containing 1 g of excipients (oil, surfactants and co-surfactants). The rest of the solubilizing procedure was same as ... See full document

8

DEVELOPMENT AND EVALUATION OF FAST DISINTEGRANT TABLETS (FDTs) OF TERBUTALINE SULPHATE

DEVELOPMENT AND EVALUATION OF FAST DISINTEGRANT TABLETS (FDTs) OF TERBUTALINE SULPHATE

... disintegrants tablets could be prepared by direct compression method using different superdisintegrants that enhanced dissolution will lead to improved ...disintegrants tablets formulation ... See full document

17

FORMULATION AND EVALUATION OF FAST MOUTH DISSOLVING TABLETS OF FLUPIRITIN BY USING CASSAVA STARCH AS BINDING AGENT

FORMULATION AND EVALUATION OF FAST MOUTH DISSOLVING TABLETS OF FLUPIRITIN BY USING CASSAVA STARCH AS BINDING AGENT

... For the determination of drug content total 10 FDTs were weighed and powdered, powder equivalent to 100 mg of Flupiritin was weighed and dissolved in 6.8 buffer solution and filtered the solution through the whattman ... See full document

11

FORMULATION AND EVALUATION OF DOLUTEGRAVIR SODIUM SOLID DISPERSIONS AND FAST DISSOLVING TABLETS USING POLOXAMER 188 AND JACK FRUIT SEED STARCH AS EXCIPIENTS

FORMULATION AND EVALUATION OF DOLUTEGRAVIR SODIUM SOLID DISPERSIONS AND FAST DISSOLVING TABLETS USING POLOXAMER 188 AND JACK FRUIT SEED STARCH AS EXCIPIENTS

... Solubility is an important physicochemical factor affecting the absorption of the drug and its therapeutic effectiveness. Nowadays, scientists are focusing on the development of oral dosage forms of poor aqueous ... See full document

10

FORMULATION AND EVALUATION OF SUSTAINED    RELEASE TABLETS OF VILDAGLIPTIN

FORMULATION AND EVALUATION OF SUSTAINED RELEASE TABLETS OF VILDAGLIPTIN

... The tablets of different formulations were subjected to various evaluation tests, such as thickness, diameter, weight variation, drug content, hardness, friability, and in vitro ...the tablets ranged ... See full document

7

“Formulation and Evaluation of Immediate Release Tablets of Topiramate Using Croscarmelose Sodium” by Kanhu Charan Panda, Chinmaya Keshari Sahoo, Jimidi Bhaskar, Ch.Swati, T.Madhuri, D. Venkata Ramana, India.

“Formulation and Evaluation of Immediate Release Tablets of Topiramate Using Croscarmelose Sodium” by Kanhu Charan Panda, Chinmaya Keshari Sahoo, Jimidi Bhaskar, Ch.Swati, T.Madhuri, D. Venkata Ramana, India.

... The tablets are still the most commonly used dosage forms due to its continuous development and implementation of innovative ideas to overcome the basic shortcomings of the existing ...solution.IRT tablets ... See full document

5

OPTIMIZATION OF VALSARTAN TABLET FORMULATION BY  23 FACTORIAL DESIGN

OPTIMIZATION OF VALSARTAN TABLET FORMULATION BY 23 FACTORIAL DESIGN

... tablet formulation significantly influence dissolution rate and consequently bioavailability of the drug requiring a rational selection of diluents, binder and disintegrant ...tablet formulation by 2 3 ... See full document

6

“Formulation and Evaluation of Theophylline Controlled Release Matrix Tablets by Using Natural Gums” by Pinnamraju Durga Nithya, Sajja Brahmani, Alapati Sriram, Nutalapati Prasanna Jaya Krishna, Poluri Koteswari, Puttagunta Srinivasa Babu, India.

“Formulation and Evaluation of Theophylline Controlled Release Matrix Tablets by Using Natural Gums” by Pinnamraju Durga Nithya, Sajja Brahmani, Alapati Sriram, Nutalapati Prasanna Jaya Krishna, Poluri Koteswari, Puttagunta Srinivasa Babu, India.

... fashion using polybags blending ...into tablets using 12mm round flat faced punches in a rotary tablet press (ELITE multi station tablet compression ... See full document

5

Formulation and evaluation of simvastatin buccal adhesive tablets

Formulation and evaluation of simvastatin buccal adhesive tablets

... Extraction of Aloe mucilage: The fresh leaves of Aloe barbadensis Miller were collected and washed with water to remove dirt and debris. Incisions were made on the leaves and left overnight. The leaves were crushed and ... See full document

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