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crosscarmellose sodium and crospovidone

DEVELOPMENT AND IN VITRO EVALUATION OF FAST DISSOLVING TABLETS OF TIZANIDINE HYDROCHLORIDE BY DIRECT COMPRESSION METHOD

DEVELOPMENT AND IN VITRO EVALUATION OF FAST DISSOLVING TABLETS OF TIZANIDINE HYDROCHLORIDE BY DIRECT COMPRESSION METHOD

... In the present work, fast dissolving tablets (FDTs) have been prepared by direct compression method using tizanidine hydrochloride as a drug candidate. Tizanidine HCl is a centrally acting α-2 adrenergic agonist muscle ...

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Formulation and Assessment of Mouth Dissolving Tablets of Repaglinide-ß-Cyclodextrin Complex

Formulation and Assessment of Mouth Dissolving Tablets of Repaglinide-ß-Cyclodextrin Complex

... namely Crosscarmellose sodium, Crosspovidone and Sodium Starch ...having crospovidone as disintegrant showed ...Therefore crospovidone is considered best superdisintegrant among ...

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Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... using Crospovidone and Sodium starch glycolate exhibited quicker disintegration of tablets than compared to those of L-HPC and Crosscarmellose ...

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FORMULATION AND EVALUATION OF FAST DISSOLVING TABLET OF TOLVAPTAN

FORMULATION AND EVALUATION OF FAST DISSOLVING TABLET OF TOLVAPTAN

... Starch, Sodium Starch Glycolate/Croscarmellose Sodium/Crosspovidone were passed through sieve # 40 (Pore size 420µ) and then all are mixed in polybag for ...

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Formulation And  Evaluation Of Mouth Dissolving Tablet Of Prochlorperzine Maleate

Formulation And Evaluation Of Mouth Dissolving Tablet Of Prochlorperzine Maleate

... (Croscarmellose Sodium, Crospovidone and sodium starch glyco- late), Binder (Povidone K-30), Diluent (Starlac) along with sweetening agent (aspartame) were used in the formulation of tablets by ...

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FORMULATION AND EVALUATION OF DICOFENAC POTASSIUM ORALLY DISINTEGRATANT TABLETS (ODT) BY USING DIFFERENT SUPERDISINTEGRANTSR.PranithaDOWNLOAD/VIEW

FORMULATION AND EVALUATION OF DICOFENAC POTASSIUM ORALLY DISINTEGRATANT TABLETS (ODT) BY USING DIFFERENT SUPERDISINTEGRANTSR.PranithaDOWNLOAD/VIEW

... Diclofenac sodium is traditional non steroidal anti- inflammatory (NSAIDS) affords quick relief of pain and wound edema ...Diclofenac sodium and to formulate ODTs with good mouth feel so as to prepare a ...

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FORMULATION AND IN VITRO EVALUATION OF RAPIDLY DISINTEGRATING TABLETS OF LORATADINE

FORMULATION AND IN VITRO EVALUATION OF RAPIDLY DISINTEGRATING TABLETS OF LORATADINE

... RESULTS AND DISCUSSION: In the present study, Loratadine Rapidly Disintegrating Tablets were prepared by using Crosscarmellose sodium, Low substituted hydroxyl propyl cellulose, and Microcrystalline ...

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Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... Diclofenac fast dispersing tablets were prepared by direct compression method being the most simplest and economic technique. Mannitol was used as diluent to impart multidimensional benefits such as good aqueous ...

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Development of Aceclofenac Mouth Dissolving Tablets using Solid Dispersion Technique: In-vitro Evaluation

Development of Aceclofenac Mouth Dissolving Tablets using Solid Dispersion Technique: In-vitro Evaluation

... The prepared SD formulations were characterized by Fourier Transform Infra-Red (FTIR) spectroscopy, differential scanning calorimetry (DSC), and in vitro drug release. Mouth dissolving tablets of ACE were formulated ...

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DEVELOPMENT AND IN VITRO ASSESSMENT OF MELT IN MOUTH TABLETS OF LURASIDONE HYDROCHLORIDE

DEVELOPMENT AND IN VITRO ASSESSMENT OF MELT IN MOUTH TABLETS OF LURASIDONE HYDROCHLORIDE

... Superdisintegrants; Crospovidone, Croscarmellose sodium, Sodium starch glycolate and disintegrant Pregelatinized starch in three different concentrations of 3%, 4%, 5% respectively and combination of ...

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OPTIMISATION OF STARCH OXALATE AS A NOVEL SUPERDISINTEGRANT IN FAST DISSOLVING SYSTEMS OF POORLY SOLUBLE DRUGS

OPTIMISATION OF STARCH OXALATE AS A NOVEL SUPERDISINTEGRANT IN FAST DISSOLVING SYSTEMS OF POORLY SOLUBLE DRUGS

... (5%), sodium starch glycolate (5%) and crospovidone (5%) as super disintegrants exhibited less disintegration time and more dissolution efficiency in 5 ...

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Design, optimization and evaluation of ibuprofen fast dissolving tablets employing starch succinate: A new superdisintegrant

Design, optimization and evaluation of ibuprofen fast dissolving tablets employing starch succinate: A new superdisintegrant

... (A), crospovidone (B), croscarmellose sodium(C)} and 1 dependent variable (dissolution efficiency in 5 min) were ...(A), crospovidone (B) and croscarmellose sodium(C) and at the lower level ...

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Design, Development And Evaluation Of Pulsatile Tablets Of Flurbiprofen For The Chronotherapy Of Rheumatoid Arthritis

Design, Development And Evaluation Of Pulsatile Tablets Of Flurbiprofen For The Chronotherapy Of Rheumatoid Arthritis

... 0.1M sodium hydroxide and shaken for 5 minutes and the volume was made up to the mark with ...0.1M sodium hydroxide in a 100ml standard ...0.1M sodium hydroxide as blank using UV- Visible ...

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Oral disintegration tablets of stavudine for HIV management: A new technological approach

Oral disintegration tablets of stavudine for HIV management: A new technological approach

... Stavudine tablets (30 mg) were prepared using different ratios of superdisintegrants by direct compression. The superdisintegrants such as sodium starch glycolate and crospovidone were used in different ...

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DEVELOPMENT AND OPTIMIZATION OF ORODISPERSIBLE TABLETS OF SEROTONIN HYDROCHLORIDE

DEVELOPMENT AND OPTIMIZATION OF ORODISPERSIBLE TABLETS OF SEROTONIN HYDROCHLORIDE

... Croscarmellulose sodium, Crospovidone, Sodium starch glycolate and respectively were used along with the drug, the release of the drug from the F1 and F2 was showed satisfactory ...with ...

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DISPERSIBLE FORMULATION MAKEUPS FOR PEDIATRIC USE: A REVIEW

DISPERSIBLE FORMULATION MAKEUPS FOR PEDIATRIC USE: A REVIEW

... research was to formulate and evaluate taste masked dispersible tablets. Dispersible tablets of zidovudine were prepared using croscarmellose sodium (Ac-di-sol) as a disintegrant. Surelease Clear (E-7-19010) ...

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FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF TELMISARTAN

FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF TELMISARTAN

... Superdisintegrants– Crosscarmellose Sodium, Doshion ,Sodium Starch Glycolate, level of addition to increase the rate of drug release from dosage form to increase the dissolution rate and hence its ...

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Development of fast dispersible aceclofenac tablets: Effect of functionality of superdisintegrants

Development of fast dispersible aceclofenac tablets: Effect of functionality of superdisintegrants

... croscarmellose sodium, sodium starch glycolate and crospovidone) on wetting time, disintegration time, drug content, in vitro release and stability parameters has been ...of sodium starch ...

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FORMULATION AND IN-VITRO EVALUATION OF ZOLMITRIPTAN ORO-DISPERSIBLE TABLETSArigela Bharathi*,Vemugunta Ramakrishna,Baratam Anupama,Chukkapalli ManishaDOWNLOAD/VIEW

FORMULATION AND IN-VITRO EVALUATION OF ZOLMITRIPTAN ORO-DISPERSIBLE TABLETSArigela Bharathi*,Vemugunta Ramakrishna,Baratam Anupama,Chukkapalli ManishaDOWNLOAD/VIEW

... croscarmellose sodium and sodium starch glycolate with different concentrations of 2%, 3% 4% while microcrystalline cellulose, lactose aerosil magnesium stearate used as ...

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FORMULATION AND EVALUATION OF ORAL DISINTEGRATION TABLETS OF OMEPRAZOLEK. Rekha Rani* , Y. Navya Reddy, R. Mohana Priya, G.Anusha and T. SpurthiDOWNLOAD/VIEW

FORMULATION AND EVALUATION OF ORAL DISINTEGRATION TABLETS OF OMEPRAZOLEK. Rekha Rani* , Y. Navya Reddy, R. Mohana Priya, G.Anusha and T. SpurthiDOWNLOAD/VIEW

... like crospovidone, croscarmellose sodium and Sodium starch glycolate by direct ...croscarmellose sodium and sodium starch glycolate shown more disintegration time than ...

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