DIRECTLY COMPRESSIBLE LACTITOL AND METHOD THEREOF

PURPOSE: A lactitol offers an aqueous solubility which is similar to sucrose which contributes to its ability to provide a smooth, non-chalky mouth feel and suitable release of active ingredients. CONSTITUTION: A directly compressible non-carcinogenic free-flowing lactitol granulate comprises milled...

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Hauptverfasser:	OLINGER PHILIP M, PEARSON JULITA
Format:	Patent
Sprache:	eng
Schlagworte:	BABY COMFORTERS CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICALPURPOSES DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY DEVICES FOR RECEIVING SPITTLE DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGINGPHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL ORADMINISTERING FORMS FOODS OR FOODSTUFFS FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BYSUBCLASSES A23B - A23J HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OFNUTRITIVE QUALITIES, PHYSICAL TREATMENT THEIR TREATMENT, NOT COVERED BY OTHER CLASSES
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Beschreibung
Zusammenfassung:	PURPOSE: A lactitol offers an aqueous solubility which is similar to sucrose which contributes to its ability to provide a smooth, non-chalky mouth feel and suitable release of active ingredients. CONSTITUTION: A directly compressible non-carcinogenic free-flowing lactitol granulate comprises milled lactitol and a physiologically acceptable, binder taken from the group consisting of sugar alcohols, polymerized reducing sugars, alkali carboxy methyl cellulose, hydrogenated starch hydrolysate, hydroxypropyl cellulose, physiologically acceptable cellulose derivatives, polyvinylpyrrolidone, gum arabic, and other physiologically acceptable gums. The granulate is directly compressible, and manifests the taste profile, metabolic, and non-carcinogenic properties of lactitol. The milled lactitol is present in the granulate in the range of about 70% to about 98% by dry weight and the physiologically acceptable, non-carcinogenic binder is present in the granulate in the range of about 2% to about 30% by dry weight. The granulate consists of 70-98% milled lactitol and 2-30% of a lactitol binder.