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Relevant bibliographies by topics / Sodium starch glycollate

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Journal articles

Academic literature on the topic 'Sodium starch glycollate'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Sodium starch glycollate"

1

Mohd, Abdul Hadi. "FORMULATION AND EVALUATION OF SUBLINGUAL TABLETS OF FELODIPINE FOR THE TREATMENT OF HYPERTENSION." Indo American Journal of Pharmaceutical Sciences 04, no. 12 (2017): 4781–90. https://doi.org/10.5281/zenodo.1091572.

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Sublingual administration of the drug means placement of the drug under the tongue and drug reaches directly in to the blood stream through the ventral surface of the tongue and floor of the mouth. The concept of formulating Sublingual tablets of Felodipine (antihypertensive drug) offer suitable and practical approach in serving the desired objective of faster disintegration and dissolution characteristic with increase bioavailability and to know the effects of two synthetic superdisintegrants (crospovidone and sodium starch glycollate) In the present work comparison between crospovidone and s

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2

Sepuri, Vijayalaxmi and N. Umasri. "FORMULATION DEVELOPMENT AND IN VITRO EVALUATION OF TENOFOVIR DISOPROXIL FUMARATE (TDF) IMMEDIATE RELEASE TABLETS." Indo Am. J. P. Sci, 2017 04, no. 05 (2017): 1229–41. https://doi.org/10.5281/zenodo.583712.

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In the present work, an attempt has been made to develop immediate release tablets of Tenofovir Disoproxil Fumarate (TDF). In the present work Sodium starch glycollate and Cross carmellose sodium were employed as super disintegrating agents for the selected drug molecule.. All the formulations were prepared by wet granulation method. The blend of all the formulations showed god flow properties such as angle of repose, bulk density, tapped density. The prepared tablets were shown good post compression parameters and they passed all the quality control evaluation parameters as per I.P limits. Am

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3

Singh, Sudarshan, S. S. Shyale, and G. Bhosale. "Formulation and Evaluation of Mouth Dissolving Tablets of Piroxicam." International Journal of Pharmaceutical Sciences and Nanotechnology 8, no. 3 (2015): 2941–46. http://dx.doi.org/10.37285/ijpsn.2015.8.3.8.

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Piroxicam, a non-steroidal anti-inflammatory agent, is widely used in rheumatoid arthritis, osteoarthritis, musculo-skeletal disorders, dysmenorrhoeal and post-operative pain. It has poor bioavailability due to its inherent properties. The objective of present study is to enhance water solubility of Piroxicam by solid dispersion technique and to develop novel method of preparing compressed tablets for Piroxicam with high porosity which dissolves rapidly in mouth, using camphor as sublimating agent and super disintegrants such as Crosscarmellose sodium and sodium starch glycollate. The tablets

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4

Shanmugam, S., Dr Senthil, and T. Ventrichelvan. "Formulation and evaluation of loratadine mouth dissolving tablet." Bangladesh Journal of Scientific and Industrial Research 48, no. 2 (2013): 137–42. http://dx.doi.org/10.3329/bjsir.v48i2.15745.

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Loratadine 10 mg mouth dissolving tablet (MDT) was prepared by using super disintegrant such as sodium starch glycollate, crosscarmellose sodium, crospovidone at various concentration, aspartame was used as sweetening agent. The excipients were used for this study was based on the compatibillity studies. All the formulation was prepared by direct compression method. Among all the formulations crospovidone at 10 mg/tab gives 99.1% drug release at end of 12th min. It was considered as optimized batch. The optimized batch was processed for all the evaluation parameter and stability studies. The f

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5

Maji, Subhajit, and Mrs Vasia. "Development Optimization and Evaluation of Fast Disintegrating Tablets of Antiepileptic Drug Carbamazepine." Journal of Drug Discovery and Therapeutics 11, no. 1 (2023): 19–27. http://dx.doi.org/10.32553/jddt.v11i1.452.

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Background: The main objective of present research work is to formulate the Carbamazepine as Fast Disintegrating tablets to give fast relief and an increase in the patient compliance. Carbamazepine, an antiepileptic, belongs to BCS Class-II and used to control some types of seizures in the treatment of epilepsy and Neuropathic Pain by blocking use-dependent sodium channels. Methods: The powdered materials were compressed by direct compression technique using super disintegrants like sodium starch glycollate, croscarmellose sodium and starch, Magnesium Stearate and Di Calcium Phosphate ar

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6

V., Rajesh Babu V. Mallikarjun Abdul Sayeed P. Rajasridhar Rao. "DESIGN AND EVALUATION OF MINI-TABLETS - PULSATILE DRUG DELIVERY SYSTEM OF RAMIPRIL." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 03 (2018): 1839–49. https://doi.org/10.5281/zenodo.1211347.

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The aim of present study was to design and evaluate mini-tablets: pulsatile delivery of Ramipril based on chronophamaceutical approach for the treatment of hypertension. In the present study the immediate release core mini tablets were prepared by direct compression by using different superdisintegrantslike sodium starch glycollate, croscaramellose sodium and crospovidone. The optimized core tablets were then coated with PH sensitive polymers like Eudragit -S100 and Eudragit- L100. To get the desired dissolution profile various parameters like coating time and coat thickness studied. The formu

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7

Jeet, Kamal, Kapil Kumar, Aparna Joshi, Ikram Ikram, and Vaishali Rajput. "Development and Evaluation of Solid Dispersion Formulations of Olanzepine." Journal of Drug Delivery and Therapeutics 13, no. 10 (2023): 109–16. http://dx.doi.org/10.22270/jddt.v13i10.5985.

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The purpose of present study was to enhance the aqueous solubility of olanzapine by using the Solid dispersion technique. Solid dispersions of olanzapine were prepared by the dispersion method using PGS and SSG as carriers. Drug-carrier ratios such as 1 : 1, 1 : 2, 1 : 4, 1 : 6, 1: 8 and 1 : 10 were tried for optimization. Characterization was done by phase solubility, in-vitro release, saturation solubility, permeation, wettability, XRD and FTIR analysis. Solid dispersions showed higher solubility and an improved drug release profile than the pure drug. Solid dispersion and physical mixture w

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8

Reddy, Dr D. RamaBrahma, Dr Ch N. V. S. Mastan Rao, K. John Abhi K. John Abhi, et al. "An Overview on Immediate Drug Release of Pravastatin Drug." International Journal of Pharmaceutical Research and Applications 10, no. 1 (2025): 847–50. https://doi.org/10.35629/4494-1001847850.

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The objective of this research was to formulate fast dissolving tablets of Pravastatin sodium that disintegrate in the oral cavity upon contact with saliva and there by improve therapeutic efficacy. Pravastatin sodium is used for the treatment of myocardial infarction. Fast dissolving tablets of pravastatin sodium were prepared by direct compression method using three different superdisintegrants-Sodium starch glycollate, Croscarmellose sodium and Crosspovidone (2%, 4% and 6%) and three different diluents (mannitol and spray dried lactose) in different concentrations. Eighteen formulations wer

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9

Yash, Paul, Tyagi Sarvan, and Singh Bhupinder. "Formulation and Evaluation of Oral Dispersible Tablets of Zidovudine with different Superdisintegrants." International Journal of Current Pharmaceutical Review and Research 2, no. 2 (2011): 82–91. https://doi.org/10.5281/zenodo.12698580.

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Oral dispersible tablets (ODTs) are patient friendly dosage form that rapidly disintegrate ordispersed in mouth without the need of water. In the present investigation eight ODTformulations of zidovudine, an antiretroviral drug, were prepared using differentsuperdisintegrants viz. Crospovidone (PPXL), Crosscarmellose sodium (Ac-di-sol) andsodium starch glycollate by direct compression method. The effects of disintegrants indifferent concentration on the release profile of zidovudine ODTs were studied. DevelopedODTs were studied for their physicochemical properties and in vitro drug release pro

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10

Singh Chundawat, Lokendra, and Vishal Sharma. "FORMULATION EVALUATION AND OPTIMIZATION OF ORODISPERSIBLE TABLETS OF PANTOPRAZOLE SODIUM BY THE USING OF DIFFERENT SUPERDISINTEGRANTS." Asian Journal of Pharmaceutical and Clinical Research 11, no. 5 (2018): 84. http://dx.doi.org/10.22159/ajpcr.2018.v11i5.24595.

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Objective: The objective of this study was to formulate and optimize an orodispersible formulation of pantoprazole sodium using a 32 factorial design for optimized the superdisintegrant concentration. Methods: Various concentrations (2%, 4%, and 6%) of superdisintegrants (sodium starch glycollate [SSG] and crospovidone [CP]) were added in the formulation, all processing steps are carried out at a temperature below 250c and relative humidity <35%. Procedure to manufacture orodispersible tablets by direct compression was established. Results: The results show that the presence of a superdisin

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