Super Disintegrants
EFFECT OF SUPER DISINTEGRANTS ON SOLUBILITY AND DISSOLUTION RATE OF LAFUTIDINE
... The super disintegrants acts as hydrophilic carrier for poorly water insoluble ...the super disintegrants sodium starch glycolate, Crosscarmellose, and ...
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COMPARATIVE STUDY OF NATURAL SUPER DISINTEGRANTS ON THE FORMULATION DEVELOPMENT OF OROMELTS CONTAINING BROMHEXINE HYDROCHLORIDE
... The tablet formulations of oromelts of Bromhexine hydrochloride were prepared by direct compression technique. Totally nine formulations (H-I to H-III, G-I to G-III & P-I to P-III) of oromelts of bromhexine ...
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FORMULATION AND IN VITRO EVALUATION OF FAST DISSOLVING TABLETS OF LACOSAMIDE USING NATURAL SUPER DISINTEGRANTS
... Formulation of Lacosamide Fast Dissolving Tablets: Fast dissolving tablets containing Lacosamide were prepared by direct compression method using varying concentrations of natural super-disintegrants like ...
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Formulation And Evaluation Of Mouth Dissolving Tablets Of Flunarizine Dihydrochloride By Using Super Disintegrants
... Twelve formulations of flunarizine dihydrochloride were prepared by direct compression method with varying concentration of three super disintegrants sodium starch glycolate, cross povidone, cross ...
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Formulation and Evaluation of Atorvastatin Calcium Immediate Release Tablets Using Super Disintegrants.
... Metoprololtartarate as Sustained release (SR) formulation for Hypertension and Atherosclerosis. The Inlay tablet was prepared by Wet granulation method. The Compatibility of the drug with various excipients was studied ...
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PHARMACEUTICAL EVALUATION OF DIFFERENT SUPER DISINTEGRANTS IN DESIGN OF METOPROLOL TARTRATE ORODISPERSIBLE TABLETS
... In-vitro drug release studies of prepared tablets F1 to F9using different super disintegrating agents by differentconcentrations. The maximum drug release for theformulation F4 containing crospovidone 3% is 96% ...
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NIFEDIPINE SUBLINGUAL TABLETS: FABRICATION USING SUPER DISINTEGRANTS AND THEIR EVALUATION
... Post-compression studies of the prepared tablets were subjected to different evaluation parameters such as hardness, friability, and weight variation, drug content[r] ...
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FORMULATION AND EVALUATION OF PANTOPRAZOLE SODIUM ENTERIC COATED TABLETS USING DIFFERENT SUPER DISINTEGRANTS
... In vitro Evaluvation of Dissolution Behaviour of Time and pH Dependent Colon Specific Drug Delivery for Aceclofenac Coated Tablets. Development of Time and pH Depende[r] ...
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FORMULATION AND OPTIMIZATION OF KETOROLAC TROMETHAMINE HCl FAST DISINTEGRATING TABLETS BY EXPERIMENTAL DESIGN
... ingredients were passed through mesh no. 60 separately and collected. The drug, mannitol and microcrystalline cellulose were mixed uniformly with geometric mixing to get a uniform mixture. Required quantity of ...
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Formulation and Evaluation of Mouth Dissolving Tablets of Ondansetron Hydrochloride
... three super disintegrants, ...containing super disintegrating agent crospovidone with solid dispersions (melt method) formulation F9 were optimized due to its fast in vitro dispersion when compare to ...
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Formulation and Evaluation of Oro Dispersible Tablets of Clonazepam by Direct Compression Method
... three super disintegrants, croscarmellose sodium, crospovidone and sodium starch glycolate at different ...three super disintegrants, effect on the in vitro dispersion time, in vitro drug ...
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DISPERSIBLE FORMULATION MAKEUPS FOR PEDIATRIC USE: A REVIEW
... of super- disintegrants (X1) and SLS (X2) which were selected as independent variables, and friability, disintegration time and % CDR was selected as the dependent ...
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Development of Aceclofenac Mouth Dissolving Tablets using Solid Dispersion Technique: In-vitro Evaluation
... of super-disintegrants on the dissolution of aceclofenac from tablets is shown in ...of super-disintegrants ...in super-disintegrant ...
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COMPATIBILITY STUDIES OF ATORVASTATIN CALCIUM WITH SELECTED EXCIPIENTS BY MEANS OF THERMAL AND FT-IR SPECTROSCOPIC METHODS FOR THE DEVELOPMENT OF IMMEDIATE RELEASE TABLET
... two super disintegrants have shown the disintegration time less than 25 sec and better dissolution than all other formulations releasing more than 80% of the drug after 20 ...two super ...
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Formulation and evaluation of salbutamol sulphate sublingual tablets
... natural super disintegrants like karaya gum, locust bean gum, gellan gum by direct compression ...natural super disintegrant, may be due to swelling at faster rate upon contact with water and ...
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FORMULATION AND INVITRO CHARACTERISATION OF VILDAGLIPTIN FAST DISINTIGRATING TABLETS
... Vildagliptin, a type-II antidiabetic drug, enhances islet cell insulin secretion via augmented incretin effect. It possesses more affinity for dipeptidyl-peptidase-4 (DPP-4) inhibitor that increases glycaemic control. ...
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DEVELOPMENT AND EVALUATION OF PAROXETINE HYDROCHLORIDE FAST DISSOLVING TABLETSRLC Sasidhar*, S.Vidyadhara, T.Balakrishna, K.Vijetha and V. KasaiahDOWNLOAD/VIEW
... a super disintegrants into the formulation the use or ...of super disintegrants like cross linked Croscarmellose Sodium, Polyvinyl Pyrrolidone K30, Microcrystalline Cellulose, Crospovidone ...
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“Design and Characterization of Fast Release Sublingual Tablets of Atenolol” by Gottumukkula Srilalitha, Naga Raju Potnuri, K.Shivabindu, India.
... using super disintegrants like cross Carmellose sodium, cross povidone, and sodium starch glycolate by direct compression ...and super disintegration ratios is present ...
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Formulation and evaluation of bilayer floating tablets of simvastatin and lovastatin
... and super disintegrants like sodium alginate, sodium starch glycolate, croscarmellose sodium, L-HPC and polyox WSR 303 which offers a suitable and practical approach in management of ...
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Journal of Applied Pharmaceutical Science
... Amlodipine besylate is a long‐acting calcium channel blocker used to treat chronic stable angina, vasospastic angina and hypertension. Amlodipine is a sparingly soluble orally administered drug and the rate of absorption ...
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