Preparation of Co-ground Mixture of Erythritol and Micronized Crospovidone Using a Ball Mill for Orally Disintegrating Tablets
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چکیده
منابع مشابه
Formulation and Preparation of Orally Disintegrating Tablets Using Innovative Binder
The present study investigates the use of glyceryl palmitostearate (Precirol ATO 5 – coded PATO) as binder in orally disintegrating tablets (ODT), prepared by melt granulation. PATO has been mentioned in literature for its lipophilic nature and fine powder properties, providing excelent coating and slow release of active drugs, but it can also be used for taste masking purposes, with possible a...
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We attempted the development of rapid oral disintegration tablets by direct compression using co-ground mixture of D-mannitol and crospovidone. The co-ground mixture was prepared with a vibration rod mill. The tablets were formed by compression using a single punch-tableting machine after addition of the co-ground mixture to non-ground D-mannitol, crospovidone and magnesium stearate. Regarding ...
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Pramipexole is the mostly prescribed drug in patients with Parkinson disease. The incidence of Parkinson disease is related to aging and mostly developed in elderly people with difficulty in swallowing or dysphagia. In the current study we aimed to develop an orally fast disintegrating tablet (ODT) of pramipexole as a preferable alternative in geriatric patients. Hence, the fast disintegration ...
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متن کاملPreparation and Characterization of Orally Disintegrating Loratadine Tablets Manufactured with Co-processed Mixtures.
The aim of this study was to develop orally disintegrated tablets (ODT) with loratadine using Parteck ODT and Ludiflash--new commercially available tableting excipients based on co-processed mannitol. ODT containing loratadine were prepared with 3% addition of various superdisintegrants (AcDiSol, Kollidon CL-F and Kollidon CL-SF) by direct compression method. Obtained tablets were characterized...
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ژورنال
عنوان ژورنال: Journal of the Society of Powder Technology, Japan
سال: 2014
ISSN: 0386-6157,1883-7239
DOI: 10.4164/sptj.51.16