Roquette® Mannitol is a white crystalline powder with a very light sweet flavour. It is non-cariogenic, and has good thermal stability and low hygroscop. PEARLITOL®. Mannitol. Roquette. Obtained industrially by hydrogenation of fructose, it’s main uses in the food industry are in chewing gums, chewy sweets and. Mannitol is widely used in pharmaceutical formulations and food products. Mannitol may be used in direct-compression tablet applica- . Roquette Fre`res).
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With an array of wheat, corn, potato, and pea starches and starch derivatives, its lineup of high quality ingredients deliver solutions for various product needs such as acidity regulation, anticrystallisation, binding, calorie and fat reduction, colouring, emulsification, and fibre enrichment.
Maltitol liquids are widely used in various pharma oral mannitool and nutraceutical applications including manniitol a vehicle for losenges; medicated confectionary; syrups, suspensions, liquids. Federated States of Micronesia. The password field is required and must matches with: These are in particular used as excipients in dry forms represented, for example, by powders for filling hard gelatin capsules, sachet powders to be extemporaneously dispersed or dissolved in water, oral solid forms and tablets.
Description Documents Request a quote Make an enquiry Order sample. The value retained for this test is the average of these fifteen disintegration times thus measured. The tableting capacity of lactose remains insufficient but it has been possible to improve it by adding to the lactose a binding or diluting excipient having a better tableting capacity, such as a microcrystalline cellulose.
The behavior of the mannitol coagglomerates according to the invention is entirely satisfactory in terms of disintegration time in the mouth. Please agree to our terms before we can reply to your question see Data Protection page Please agree to our terms before we can reply to your question see Data Protection page. View Cosmetics products View market information. View BioPharma products View market information. The coagglomerates in accordance with the invention The coagglomerates in accordance with the invention having the characteristics mentioned above can be obtained most particularly according to a method which comprises a step of spray-drying a suspension of mannitol crystals and of starch.
The particle size distribution curve also makes it possible to determine the value of the mean volume diameter arithmetic average D4,3. Your success is our greatest priority and together we can write a new chapter for Beauty!
The invention will be understood more clearly from the examples which follow, which are intended to illustrate the invention in a nonlimiting manner. In the method in accordance with the invention, it is particularly advantageous to have a high content of mannitol crystals in the suspension of mannitol and of starch.
Amylomaize and Waxy Maize Starch provide excipient benefits as a disintegrant and filler or binder, as well as nutrient benefits as a carbohydrate source. However, UL assumes no responsibility or liability for the accuracy of the information contained on this website and strongly encourages that upon final product or material selection information is validated with the manufacturer.
Mannitol is, among the soluble excipients, the one which confers the greatest stability on solid medicament forms, by virtue of its very high chemical inertia with respect to the active ingredients and its lack of water absorption. On the other hand, because of the small size of its particles and its low density, it has the drawback of not flowing. The method as claimed in claim 8, characterized in that it comprises the following steps: It is therefore impossible for them to fill the die, which is the first step in obtaining a tablet on a tableting press.
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Are you a distributor who is interested in being listed here? These are sorbitol and xylitol, but especially mannitol. The composition of each tablet roqutete described in the following table 8. The coagglomerates according to the invention make it possible to prepare tablets which disintegrate in the mouth, according to a test D, in less than 60 seconds, preferably in less than 40 seconds.
A SumoBrain Solutions Company. Be inspired by Roquette’s unique product range to meet your specific needs. The tablet is then placed in a hollow receptacle with an internal diameter of 24 mm. The password field is required and must matches with: Add to basket Order now.
Pharma and Nutraceuticals Coprocessed Mannitol starch Print: To facilitate your successful biopharmaceutical formulation, Roquette offers expertise and innovation to all stages of development, backed by uncompromised quality standards and a secure supply chain. Our ingredients help you address the needs of consumers who are looking for cleaner and safer material consumption.
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Roquette helps save and sustain lives as a trusted supplier of excipients and active pharmaceutical ingredients. Modified waxy maize starch provides excipient benefits as a suspending agent and viscosifier. Registrations may vary depending on local regulations.
These modifications are, however, introduced mainly by adding multiple ingredients: Native starches are well known as disintegrants, fillers and binders once cooked in nutraceutical and pharmaceutical dosage forms. As will be exemplified hereinafter, the applicant company recommends using a MSD 20 type spray-drier sold by the company Niro.
Please mannotol the usage country to continue. Each individual drinks a glass of water of at least ml and then waits 30 seconds before placing a tablet on the tongue. Roquette can help you give consumers the food they want and can feel good about: View Cosmetics products View market information.
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The test C consists in measuring the compression force required to produce tablets with a hardness of between N and N. The lubricant is added to this mixture. The following table 7 gives the results obtained. We provide expertise and innovation to all stages of pharmaceutical development, backed by uncompromised quality standards and a secure supply chain, instilling confidence to create a robust formulation.
The applicant company has, for its part, proposed, in its patent EP 1. The coagglomerates as claimed in claim 1, characterized in that they give, according to a test C, tablets with a hardness of between N and N at a compression force of less than 40 kN.