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Littérature scientifique sur le sujet « Fast dispersing tablet »

Auteur : Grafiati

Publié le 7 juin 2025

Mis à jour le 2 août 2025

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Articles de revues sur le sujet "Fast dispersing tablet"

Kumar Bhasin, Rakesh, Nirika Bhasin, and Pradip Kumar Ghosh. "Advances in Formulation of Orally Disintegrating Dosage Forms: A Review Article." Indo Global Journal of Pharmaceutical Sciences 01, no. 04 (2011): 328–53. http://dx.doi.org/10.35652/igjps.2011.33.

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Oral disintegrating tablets are solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue The products are designed to disintegrate or dissolve rapidly on contact with saliva, thus eliminating the need for chewing the tablet, swallowing an intact tablet, or taking the tablet with water. ODT is general form of nomenclature for tablets that disintegrate rapidly or instantly in the oral cavity. Other alias are Quick Dissolve, Rapid Dissolve, Rapid Disintegrating, Fast Disintegrating, Fast Melt, Flash Melt and Mou

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Jayaramu, Rajamma Abburu, Sateesha Shivally Boregowda, Addanki Rahul Deva Varma, and Chandan Kalegowda. "Development of fast dispersing tablets of nebivolol: experimental and computational approaches to study formulation characteristics." Brazilian Journal of Pharmaceutical Sciences 50, no. 4 (2014): 956–63. http://dx.doi.org/10.1590/s1984-82502014000400031.

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Formulation of FDT (fast dispersing tablets) of nebivolol was optimized and evaluated using simplex lattice design (SLD). The influence of type and concentration of three disintegrants viz.,Ac-Di-Sol, Primojel and Polyplasdone XL on hardness, friability and disintegration time of tablet was studied. Response surface plot and the polynomial equations were used to evaluate influence of polymer on the tablet properties. Results were statistically analyzed using ANOVA, and a p < 0.05 was considered statistically significant. Results reveal that fibrous integrity and optimal degree of substituti

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Abdul Qadir, Bhavana Singh, Deepika Joshi, and Nidhi Semwal. "Fast dissolving tablet: An updated review." World Journal of Biology Pharmacy and Health Sciences 11, no. 3 (2022): 052–59. http://dx.doi.org/10.30574/wjbphs.2022.11.3.0135.

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Improved patient management and patient tracking are essential to the development of an oral drug delivery system that remains a popular drug delivery route despite various maladies. Fast-dispersing pills (FDTs) have found growing demand over the past decade, and the field has become a fast-growing area in the pharmaceutical industry. The popularity and usefulness of the construction has led to the development of many FDT technologies. These are ways to make the tablet dissolve faster and spill in the mouth for five seconds without chewing and the need for beneficial water especially for child

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Abdul, Qadir, Singh Bhavana, Joshi Deepika, and Semwal Nidhi. "Fast dissolving tablet: An updated review." World Journal of Biology Pharmacy and Health Sciences 11, no. 3 (2022): 052–59. https://doi.org/10.5281/zenodo.7181372.

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Jain, P., A. Mishra, and A. Pathak. "PREPARATION & EVALUATION OF ORODISPERSIBLE TABLET CONTAINING ASPIRIN BY SUBLIMATION METHOD." INDIAN DRUGS 52, no. 12 (2015): 60–62. http://dx.doi.org/10.53879/id.52.12.10465.

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Orodispersible tablets are uncoated tablets which when taken into the mouth, get easily dispersed within 3 min before swallowing. they are also known as orally disintegrating tablets, mouth-dissolving tablets, rapid dissolving tablets fast-disintegrating tablets, fast-dissolving tablets. In this work, sublimation process was used to prepare orodispersible tablets of aspirin by formulating various batches using different concentration of sodium starch glycolate, camphor and cross povidone. An effort was made by using two modes, first, to increase water uptake for the fast dispersion by creating

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Philip, Christine, Shahnaz Usman, Muhammad Akram, and Quamrul Islam. "Formulation development, optimization, and evaluation of fast-dispersing tablets of cefixime trihydrate for pediatric use." Pharmacia 72 (May 7, 2025): 1–16. https://doi.org/10.3897/pharmacia.72.e144228.

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The proposed study aimed to formulate and optimize the design of a fast-dispersing tablet (FDT) of cefixime trihydrate (dispersed in a teaspoon of water) tailored for pediatric patients (0–12 years). To assess the percentage concentration of the cefixime in the formulated tablets, the HPLC method was validated and established linearity, r² = 0.9998 in the range of 20–0.078 µg/mL. The preformulation study was carried out. Crospovidone (X1), croscarmellose sodium (X2), and sodium starch glycolate (X3) were selected as key independent variables, and their impact was executed on friability and dis

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Pabari, Ritesh M., Claire McDermott, James Barlow, and Zebunnissa Ramtoola. "Stability of an Alternative Extemporaneous Captopril Fast-Dispersing Tablet Formulation Versus an Extemporaneous Oral Liquid Formulation." Clinical Therapeutics 34, no. 11 (2012): 2221–29. http://dx.doi.org/10.1016/j.clinthera.2012.10.005.

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Bhide, Prashant, and Reeshwa Nachinolkar. "FORMULATION DEVELOPMENT AND CHARACTERISATION OF MECLIZINE HYDROCHLORIDE FAST DISSOLVING TABLETS USING SOLID DISPERSION TECHNIQUE." International Journal of Applied Pharmaceutics 10, no. 4 (2018): 141. http://dx.doi.org/10.22159/ijap.2018v10i4.26493.

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Objective: The aim of the present investigation was to design and evaluate fast dissolving tablet (FDT) for the oral delivery containing solid dispersion of meclizine (MCZ) hydrochloride, an antiemetic drug.Methods: The solubility of meclizine was increased by preparing solid dispersions using mannitol as a carrier by fusion method. The prepared solid dispersion, was subjected for in vitro drug release, percent practical yield, drug content, infrared spectroscopy (IR), differential scanning calorimetry (DSC), scanning electron microscopy (SEM). Optimized solid dispersion was incorporated to pr

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Dr., G. Nagaraju, Sirisha V., Ramakrishna Kavati, and Hareesh Dara Dr. "FORMULATION AND EVALUATION OF DEXIBUPROFEN FAST DISINTEGRATING TABLETS WITH NATURAL SUPER DISINTEGRANTS." Journal of Pharma Research 8, no. 12 (2019): 744–50. https://doi.org/10.5281/zenodo.14233228.

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<strong>Abstract</strong> <strong>I</strong>n this present research work, an attempt was made to develop solid dispersions for the enhancement of solubility, dissolution and bioavailability of Dexibuprofen and also to find the effect of natural super disintegrants in the development of quickly disintegrating tablets.Solid dispersions were prepared by solvent evaporation method using PEG 20,000as carrier in different ratios. The optimized solid dispersions were prepared in the form of quick disintegrating tablets using different natural super disintegrants in different concentrations. The prepa

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Chapitres de livres sur le sujet "Fast dispersing tablet"

Devi, V. Rupa Sree, M. Sukanya, K. Ravi Shankar, G. Ramana Reddy, and KNV Chenchu Lakshmi. "Formulation, Preparation, and Evaluation of Nebivolol Fast-Dissolving Tablets by Using 32 Factorial Design." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00510.

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Nebivolol comes under BCS Class II Classification, so there is a need to improve the dissolution rate. The motive of the current work is to formulate the fast-dissolving tablets of Nebivolol from optimised solid dispersion by allowing complexation using solid dispersions of PEG 4000, Starch 1500, Poloxamer 188, and β-cyclodextrin (β CD). Nebivolol tablets with fast dissolution characteristics employing βCD were prepared using a 32 factorial study employing by direct compression technique. Dissolution of Nebivolol from the β-CD complexes was rapid and higher when seen with that of Pure Nebivolo

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Sukanya, M., V. Rupa Sree Devi, K. Ravi Shankar, G. Ramana Reddy, and R. Anusha. "Optimization of Telmisartan Fast Dissolving Tablets by 32 Factorial Design." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00533.

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Telmisartan belongs to BCS Class II drug and needs enhancement in dissolution rate. The main objective of the study is to produce rapid dissolving tablets of telmisartan by complexation with β-cyclodextrin(βCD) and by using solid dispersions of MCC, Starch 1500, PEG 4000, Primojel and Mannitol. Telmisartan tablets with fast dissolution characteristics employing βCD were prepared using 32 factorial design and were prepared by direct compression method. Dissolution of Telmisartan from the βCD complexes was rapid and higher when compared to Telmisartan pure drug and with different carriers. Hence

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Noothi, Sadhana, Narender Malothu, and P. Vishnu. "Formulation and Characterization of Bilastine Oral Disintegrated Tablets Using Natural and Synthetic Super Disintegrants." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00361.

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Bilastine (BLS) is a second-generation H1- antihistamine that is approved recently for the symptomatic treatment of chronic urticaria. The present investigation was to develop oral disintegrating tablets of BLS to produce a fast onset of action. In this study, an attempt was made to compare the effect of different natural and synthetic super disintegrants on the release profile of the formulation. The formulations (BF1-BF15) of BLS oral disintegrating tablets were prepared by direct compression technique using synthetic and natural super disintegrants (Chitosan, Fenugreek mucilage, Sodium star

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Brun-Trigaud, Guylaine, and Philippe Del Giudice. "Du Babau au Mammouth : étude géolinguistique sur les personnages fantastiques occitans." In Péri-fééries : les êtres fantastiques et la triple expérience des limites. Éditions du Comité des travaux historiques et scientifiques, 2024. http://dx.doi.org/10.4000/12cdy.

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Dans le prolongement des principales analyses offertes par l’ethnologie, cet article propose un regard complémentaire sur la dénomination des êtres fantastiques dans le Midi de la France. Complémentaire, car des sources jusqu’alors non exploitées, c’est-à-dire les atlas linguistiques de la France par régions, ont fourni l’essentiel des données étudiées ici, que l’on a confrontées aux résultats – bien connus – qui avaient été obtenus par d’autres moyens. Le tout a donné lieu à une cartographie inédite qui offre au lecteur une vision géolinguistique de la répartition des appellations, des êtres

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