Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Pharm Res ; 24(11): 2084-96, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17657595

ABSTRACT

PURPOSE: Food stimulates changes to gastrointestinal secretion and motility patterns, however, the effect of smaller quantities of lipid, such as that contained in a lipid-based drug formulation, has not been detailed. This study aimed to examine the effects of small quantities of lipid on gastric emptying and biliary secretion. METHODS: The influence of oral administration of three lipid-based formulations and a negative control formulation on gastric emptying and biliary secretion was evaluated in 16 healthy male subjects using gamma scintigraphy, ultrasonography and duodenal aspiration. RESULTS: Low quantities (2 g) of long chain lipid stimulated gall bladder contraction and elevated intestinal bile salt, phospholipid and cholesterol levels. Changes in gastric emptying were also evident, although these did not reach statistical significance. Administration of a similar quantity of medium chain lipid, however, had little effect on gastric emptying and gallbladder contraction and did not stimulate appreciable increases in intestinal concentrations of biliary-derived lipids. CONCLUSIONS: The quantities of long chain lipid that might be administered in a pharmaceutical formulation stimulate gallbladder contraction and elevate intestinal levels of bile salt and phospholipid. This effect is a likely contributor to the ability of lipid based formulations to enhance the absorption of poorly water-soluble drugs.


Subject(s)
Bile/metabolism , Gastric Emptying/drug effects , Lipids/administration & dosage , Chemistry, Pharmaceutical , Cross-Over Studies , Duodenum/metabolism , Gallbladder/physiology , Humans , Lipids/analysis , Male , Technetium Tc 99m Pentetate
2.
J Pharm Pharmacol ; 56(5): 605-10, 2004 May.
Article in English | MEDLINE | ID: mdl-15142337

ABSTRACT

To better predict food effects on the bioavailability/bioequivalence of drugs and drug products from in-vitro data, a dissolution medium that simulates the initial composition of the postprandial stomach was developed. First, the physical parameters of two homogenized standard breakfasts often administered to assess food effects in pharmacokinetic studies were measured. These included pH, buffer capacity, osmolality, surface tension and viscosity. Subsequently, the match of the physical parameters of several commercially available liquid meals, including long-life milk, Ensure and Ensure Plus to those of the breakfasts was evaluated. Of the three liquid meals studied, Ensure Plus had the closest physicochemical behaviour to that of homogenized standard breakfasts. By increasing the viscosity of Ensure Plus with 0.45% pectin, it was possible to obtain a medium that closely resembles the FDA standard breakfast.


Subject(s)
Food , Postprandial Period , Stomach/chemistry , Animals , Chemical Phenomena , Chemistry, Physical , Dietary Sucrose , Fasting , Food, Formulated , Food-Drug Interactions , Hydrogen-Ion Concentration , Milk/chemistry , Pectins/chemistry , Pharmacokinetics , Solubility , United States , United States Food and Drug Administration , Viscosity , Vitamin K/chemistry
SELECTION OF CITATIONS
SEARCH DETAIL
...