Gotowe bibliografie tematyczne / Oro dispersible tablets

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Gotowa bibliografia na temat „Oro dispersible tablets”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Oro dispersible tablets"

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Qureshi, Aminabi, Umaima Shaikh, Mehrunnisa Shaikh, Wafa Parkar, Maria Lal, and Mirza Salman Baig. "Solid Dispersion Incorporated Indomethacin Oro- Dispersible Tablet." International Journal of Pharmaceutical Sciences and Nanotechnology(IJPSN) 17, no. 5 (2024): 7580–88. https://doi.org/10.37285/ijpsn.2024.17.5.4.

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Aim: This study aimed to enhance the dissolution profile of indomethacin by formulating oro-dispersible tablets, using the Solid Dispersion technique and PEG 6000 and PVP K-30 as carriers. Method: Solid Dispersion (SD) of indomethacin were prepared using the kneading method. Pre-compression studies include evaluating granules' density and flow properties, while post-compression studies assessed tablet properties such as hardness, friability, wetting time, dissolution, drug content and material interactions. Result: All pre- and post-compressional parameters were found within pre-determined lim
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Pokhrel, Gopal, Ganga Kunwar, Jun Devi Rai, Sheela Thapa, Sudip Dhakal, and Prashant Basnet. "Formulation and in-vitro Evaluation of Oro-dispersible tablets of Indomethacin." Nepal Journal of Health Sciences 2, no. 1 (2022): 90–97. http://dx.doi.org/10.3126/njhs.v2i1.47172.

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Introduction: Oro-dispersible tablets are rapidly dissolved in saliva without the need for water and are beneficial for renal impaired, bedridden and psychiatric patients. Objective: The study aimed to formulate oro-dispersible tablets of indomethacin with reduced adverse effects, better patient compliance, faster action, and convenience for patients. Methods: Oro-dispersible tablets of indomethacin were prepared using three different super disintegrants; crospovidone, croscarmellose sodium and sodium starch glycolate with three different concentrations (2.5%, 5.2%, and 7.7%) by direct compres
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Khobragde, Deepak, Arun Kotha, K. Ravalika, Richa Gupta, and P. Vasu Kumar. "Oro-Dispersible Tablets of Ayurvedic Powder For improving Taste, Compliance, Ease and Accuracy of administration." International Journal of Advances in Scientific Research 2, no. 6 (2016): 131. http://dx.doi.org/10.7439/ijasr.v2i6.3458.

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Most of the ayurvedic medicines are in the form of powder. Being in powder form the administration of accurate dose with ease is a problem. They may have some kind of unacceptable bitter taste. Furthermore it needs water or honey for administration and chances of spoilage and waste are more. Oro-dispersible tablet which rapidly disintegrating in mouth will be the best remedy for efficient use of ayurvedic powders. The aim of this study was to formulate oro-dispersible tablets of ayurvedic polyherbal powder Talisadi. Talisadi is a traditional Ayurvedic powder preparation well known and effectiv
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Kumar, Voleti Vijaya, Nandhini M, Sreelekhaa T, et al. "Comprehensive Review of Oro Dispersible Tablets and Co Processed Super disintegrants." Future Journal of Pharmaceuticals and Health Sciences 4, no. 1 (2024): 1–13. http://dx.doi.org/10.26452/fjphs.v4i1.548.

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Due to their ease of administration, self-administration, and improved patient compliance, solid dosage forms are most popular. The most normally utilized strong dose structures are tablets and capsules, which is challenging for pediatric and geriatric patients. Considering these prerequisites endeavors have been made to foster rapid dissolving Tablets. The solid dosage form of a medicine that dissolves in a matter of seconds when swallowed is known as orodispersible tablet. The utilization of Superdisintegrants improves the crumbling season of the tablet. Fast Dissolving Tablets are generally
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V, Vijaya Kumar. "Comprehensive Review of Oro Dispersible Tablets and Co Processed Super disintegrants." Comprehensive Review of Oro Dispersible Tablets and Co Processed Super disintegrants 4, no. 1 (2024): 1–13. https://doi.org/10.5281/zenodo.14649969.

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Due to their ease of administration, self-administration, and improved patient compliance, solid dosage forms are most popular. The most normally utilized strong dose structures are tablets and capsules, which is challenging for pediatric and geriatric patients. Considering these prerequisites endeavors have been made to foster rapid dissolving Tablets. The solid dosage form of a medicine that dissolves in a matter of seconds when swallowed is known as orodispersible tablet. The utilization of Superdisintegrants improves the crumbling season of the tablet. Fast Dissolving Tablets are generally
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Akshay Kumar S, Gowda D V, Sharadha M, and Akhila A R. "The insights on Oro-dispersible tablet." International Journal of Research in Pharmaceutical Sciences 11, no. 1 (2020): 260–73. http://dx.doi.org/10.26452/ijrps.v11i1.1815.

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Orodispersible tablets (ODTs) were the conventional product that disintegrates or dissolves into the buccal mucosa in less than 1mins in the absence of water and without chewing. They were first acquainted with the market during the 1980s, and end up one of the quickest developing subdivisions of the oral medication conveyance industry and their items are creating at an extraordinary rate. New orodispersible tablet innovations address numerous pharmaceutical and need of patients, extending from upgraded life-cycle the executives for reasonable medicating for pediatric, aged, and mental patient
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R, Yogaraj, Surinder Kaur, and Padmaa M. Paarakh. "A Brief Introduction on Oro Dispersible Tablets." April-May 2023, no. 33 (April 10, 2023): 9–16. http://dx.doi.org/10.55529/jcpp.33.9.16.

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Oro dispersible tablets (ODTs), which have improved solubility and stability over the past three decades, have drawn a lot of interest as a superior alternative to traditional tablets and capsules. ODTs—solid dosage forms with medications that dissolve on the tongue fast, usually in a few seconds. New ODT technologies answer a wide range of pharmaceutical preparations and patient needs, to enhance the lifecycle management to straightforward dosage regimen for dysphagic, children, old, and mentally imbalanced patients. Methods for administering orally dispersible drugs are frequently used to im
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Bommana, Anusha* Girija Karike Koppula Maheshwari Ramya Sri Sura. "FORMULATION AND IN VITRO EVALUATION OF ORO DISPERSIBLE TABLETS OF LORAZEPAM." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 05 (2018): 3945–53. https://doi.org/10.5281/zenodo.1249808.

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<em>The present investigation was done on lorazepam orodispersible tablets using super disintegrants. The prepared powder blend for all formulations was found to be within limits. Tablets were compressed using rotary tablet compression machine. Post compression studies like weight variation, hardness, thickness, friability, drug content, in vitro disintegration time were carried out which were found to be within limits. In vitro drug release studies revealed that Among all formulations F4 formulation were shown maximum drug release(99.99%) at 45 min. Among these three formulations F4 was consi
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Khan, MD Abdul Aali, M. S. Sudheesh, and Rajesh Singh Pawar. "Formulation Development and Evaluation of Oro-Dispersible Tablets Based On Solid Dispersion of Cimetidine." Journal of Drug Delivery and Therapeutics 12, no. 6-S (2022): 42–46. http://dx.doi.org/10.22270/jddt.v12i6-s.5696.

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The most common problem about conventional dosage form is dysphagia (difficulty in swallowing). So, we design a new approach in a conventional dosage form which is oral dispersible tablet. Oral dispersible tablet is also called as mouth dissolving tablet, fast dissolving tablet, or oral disintegrating tablet. Oral dispersible tablet has advantage as it quickly disintegrates into saliva when it is put on the tongue. The faster the drug disintegrates or is dissolved, the faster the absorption and the quicker the therapeutic effect of drug will be attained. The objective of present study was to f
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Desai, Sushma, Chandrasekhara Rao Baru, Darupally Madhuri, et al. "Formulation and evaluation of amoxicillin Oro-dispersible tablets." International Journal of Pharmacy and Pharmaceutical Science 7, no. 1 (2025): 121–24. https://doi.org/10.33545/26647222.2025.v7.i1b.159.

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Rozprawy doktorskie na temat "Oro dispersible tablets"

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Uslu, Sibel. "Formulation development and characterization of liquisolid tablets containing clozapine." Thèse, 2014. http://hdl.handle.net/1866/11571.

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L’objectif de ce projet était de développer une formulation liquisolide (LS) de clozapine ayant des propriétés de dissolution améliorées et évaluer sa stabilité et ainsi que sa robustesse à la modification d’excipients. Le propylène glycol (PG), la cellulose microcrystalline (MCC) et le glycolate d’amidon sodique (SSG) ont été utilisés respectivement en tant que véhicule liquide non volatile, agent de masse et agent désintégrant pour la préparation de comprimés LS. Le dioxyde de silicium colloïdal (CSD), le silicate de calcium (CS) et l'aluminométasilicate de magnésium (MAMS) ont été choisis c
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Książki na temat "Oro dispersible tablets"

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Appapurapu, Ashok kumar. Oro dispersible tablets: Effect of superdisintegrants. LAP Lambert Academic Publishing, 2015.

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Części książek na temat "Oro dispersible tablets"

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B., Raja Narender, and T. Gayathri. "Design and Evaluation of Oro-Dispersible Tablets of Tramadol Hydrochloride." In Advanced Concepts in Pharmaceutical Research Vol. 9. B P International, 2024. http://dx.doi.org/10.9734/bpi/acpr/v9/3764g.

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