11 results on '"Carrière, Frédéric"'
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2. Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations. 5. Lipolysis of Representative Formulations by Gastric Lipase.
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Bakala-N'Goma, Jean-Claude, Williams, Hywel, Sassene, Philip, Kleberg, Karen, Calderone, Marilyn, Jannin, Vincent, Igonin, Annabel, Partheil, Anette, Marchaud, Delphine, Jule, Eduardo, Vertommen, Jan, Maio, Mario, Blundell, Ross, Benameur, Hassan, Müllertz, Anette, Pouton, Colin, Porter, Christopher, and Carrière, Frédéric
- Subjects
IN vitro studies ,EXCIPIENTS ,LIPIDS ,LIPOLYSIS ,GASTRIC enzymes ,LIPASES - Abstract
Purpose: Lipid-based formulations (LBF) are substrates for digestive lipases and digestion can significantly alter their properties and potential to support drug absorption. LBFs have been widely examined for their behaviour in the presence of pancreatic enzymes. Here, the impact of gastric lipase on the digestion of representative formulations from the Lipid Formulation Classification System has been investigated. Methods: The pHstat technique was used to measure the lipolysis by recombinant dog gastric lipase (rDGL) of eight LBFs containing either medium (MC) or long (LC) chain triglycerides and a range of surfactants, at various pH values [1.5 to 7] representative of gastric and small intestine contents under both fasting and fed conditions. Results: All LBFs were hydrolyzed by rDGL. The highest specific activities were measured at pH 4 with the type II and IIIA MC formulations that contained Tween®85 or Cremophor EL respectively. The maximum activity on LC formulations was recorded at pH 5 for the type IIIA-LC formulation. Direct measurement of LBF lipolysis using the pHstat, however, was limited by poor LC fatty acid ionization at low pH. Conclusions: Since gastric lipase initiates lipid digestion in the stomach, remains active in the intestine and acts on all representative LBFs, its implementation in future standardized in vitro assays may be beneficial. At this stage, however, routine use remains technically challenging. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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3. Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 6: Effects of Varying Pancreatin and Calcium Levels.
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Sassene, Philip, Kleberg, Karen, Williams, Hywel, Bakala-N'Goma, Jean-Claude, Carrière, Frédéric, Calderone, Marilyn, Jannin, Vincent, Igonin, Annabel, Partheil, Anette, Marchaud, Delphine, Jule, Eduardo, Vertommen, Jan, Maio, Mario, Blundell, Ross, Benameur, Hassan, Porter, Christopher, Pouton, Colin, and Müllertz, Anette
- Abstract
The impact of pancreatin and calcium addition on a wide array of lipid-based formulations (LBFs) during in vitro lipolysis, with regard to digestion rates and distribution of the model drug danazol, was investigated. Pancreatin primarily affected the extent of digestion, leaving drug distribution somewhat unaffected. Calcium only affected the extent of digestion slightly but had a major influence on drug distribution, with more drug precipitating at higher calcium levels. This is likely to be caused by a combination of removal of lipolysis products from solution by the formation of calcium soaps and calcium precipitating with bile acids, events known to reduce the solubilizing capacity of LBFs dispersed in biorelevant media. Further, during the digestion of hydrophilic LBFs, like IIIA-LC, the un-ionized-ionized ratio of free fatty acids (FFA) remained unchanged at physiological calcium levels. This makes the titration curves at pH 6.5 representable for digestion. However, caution should be taken when interpreting lipolysis curves of lipophilic LBFs, like I-LC, at pH 6.5, at physiological levels of calcium (1.4 mM); un-ionized-ionized ratio of FFA might change during digestion, rendering the lipolysis curve at pH 6.5 non-representable for the total digestion. The ratio of un-ionized-ionized FFAs can be maintained during digestion by applying non-physiological levels of calcium, resulting in a modified drug distribution with increased drug precipitation. However, as the main objective of the in vitro digestion model is to evaluate drug distribution, which is believed to have an impact on bioavailability in vivo, a physiological level (1.4 mM) of calcium is preferred. [ABSTRACT FROM AUTHOR]
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- 2014
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4. In Vitro Digestion of the Self-Emulsifying Lipid Excipient Labrasol® by Gastrointestinal Lipases and Influence of its Colloidal Structure on Lipolysis Rate.
- Author
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Fernandez, Sylvie, Jannin, Vincent, Chevrier, Stéphanie, Chavant, Yann, Demarne, Frédéric, and Carrière, Frédéric
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IN vitro studies ,EXCIPIENTS ,LIPASES ,ACINETOBACTER ,DRUG bioavailability ,LIPOLYSIS ,GLYCERIN ,BIOCHEMICAL substrates - Abstract
Purpose: Labrasol
® is a self-emulsifying excipient used to improve the oral bioavailability of poorly water-soluble drugs. It is a mixture of acylglycerols and PEG esters, these compounds being substrates for digestive lipases. The characterization of Labrasol® gastrointestinal lipolysis is essential for understanding its mode of action. Methods: Labrasol® lipolysis was investigated using either individual enzymes (gastric lipase, pancreatic lipase-related protein 2, pancreatic carboxyl ester hydrolase) or a combination of enzymes under in vitro conditions mimicking first the gastric phase of lipolysis and second the duodenal one. Specific methods for quantifying lipolysis products were established in order to determine which compounds in Labrasol® were preferentially hydrolyzed. Results: Gastric lipase showed a preference for di- and triacylglycerols and the main acylglycerols remaining after gastric lipolysis were monoacylglycerols. PEG-8 diesters were also hydrolyzed to a large extent by gastric lipase. Most of the compounds initially present in Labrasol® were found to be totally hydrolyzed after the duodenal phase of lipolysis. The rate of Labrasol® hydrolysis by individual lipases was found to vary significantly with the dilution of the excipient in water and the resulting colloidal structures (translucent dispersion; opaque emulsion; transparent microemulsion), each lipase displaying a distinct pattern depending on the particle size. Conclusions: The lipases with distinct substrate specificities used in this study were found to be sensitive probes of phase transitions occurring upon Labrasol® dilution. In addition to their use for developing in vitro digestion models, these enzymes are interesting tools for the characterization of self-emulsifying lipid-based formulations. [ABSTRACT FROM AUTHOR]- Published
- 2013
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5. Immunological Characterization of Digestive Lipases.
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Walker, John M., Doolittle, Mark, Reue, Karen, Caro, Alain De, Bezzine, Sofiane, Lopez, Véronique, Aoubala, Mustapha, Daniel, Cécile, Verger, Robert, and Carrière, Frédéric
- Abstract
In humans, the digestion of dietary triacylglycerols is mediated by two main enzymes, a gastric lipase which is secreted by the chief cells of the fundic mucosa and which acts in the stomach as well as the intestine, and a pancreatic lipase which contributes to the lipid digestion only in the duodenum (1-3). In order to overcome the inhibitory effect of bile-salts present in the intestinal lumen, pancreatic lipase specifically requires the presence of a small pancreatic cofactor (colipase) which acts as an anchor for pancreatic lipase (4). Gastric and pancreatic lipases belong to two distinct structural families and display very different biochemical and kinetic properties. The pancreatic lipase family also includes lipoprotein lipase and hepatic lipase (5-7). The gastric lipase family, defined also as the acidic lipase family (8-10), includes lingual, pharyngeal and lysosomal lipases. These lipases share no sequence homology with the pancreatic lipase family. [ABSTRACT FROM AUTHOR]
- Published
- 1999
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6. One-Step Purification and Biochemical Characterization of Recombinant Pancreatic Lipases Expressed in Insect Cells.
- Author
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Walker, John M., Doolittle, Mark, Reue, Karen, Bezzine, Sofiane, Ferrato, Francine, Lopez, Véronique, de Caro, Alain, Verger, Robert, and Carrière, Frédéric
- Abstract
The baculovirus expression system is very convenient to produce recombinant pancreatic lipases and mutants thereof, in substantial amounts (10-50 mg of enzyme per liter of culture) for structure-function studies (see also Chapters 17, 18, and 20 in this volume). Using the naturally occurring leader sequence, recombinant enzymes are secreted by insect cells and are easy to purify in a one-step procedure when insect cells are grown in a serum-free medium. [ABSTRACT FROM AUTHOR]
- Published
- 1999
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7. In Vitro Gastrointestinal Lipolysis: Replacement of Human Digestive Lipases by a Combination of Rabbit Gastric and Porcine Pancreatic Extracts.
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Capolino, Perrine, Guérin, Clémence, Paume, Julie, Giallo, Jacqueline, Ballester, Jean-Michel, Cavalier, Jean-François, and Carrière, Frédéric
- Abstract
Various combinations of digestive lipases were tested in vitro under conditions simulating the earlier phases of gastrointestinal lipolysis in the stomach and the duodenum. A solid/liquid test meal was mixed first with either human gastric juice or a solution containing gastric lipase, followed by either the addition of human pancreatic juice and bile or the addition of a solution containing pancreatic lipase, colipase, and bile salts. The rate of lipolysis and the composition of the lipolysis products were assessed as a function of time after lipid extraction and analysis by thin-layer chromatography coupled to flame ionization detection. The lipolytic potential of a crude rabbit gastric extract (RGE) associated with porcine pancreatic extract (PPE) was assessed and compared with the rates of lipolysis of the meal triacylglycerols by human digestive lipases recorded under the same in vitro conditions. RGE combined with PPE appeared to be a good substitute for human gastric and pancreatic lipases. RGE and PPE could therefore be used to simulate the gastrointestinal lipolysis of various foods and emulsions in vitro, as well as that of pharmaceutical lipid formulations. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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8. Effects of Surfactants on Lipase Structure, Activity, and Inhibition.
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Delorme, Vincent, Dhouib, Rabeb, Canaan, Stéphane, Fotiadu, Frédéric, Carrière, Frédéric, and Cavalier, Jean-François
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SURFACE active agents ,LIPASE inhibitors ,MOLECULAR structure ,ENZYME activation ,WEIGHT loss ,LIPOLYSIS ,ADSORPTION (Biology) ,SOLUTIONS (Pharmacy) ,HYDROPHOBIC surfaces - Abstract
Lipase inhibitors are the main anti-obesity drugs prescribed these days, but the complexity of their mechanism of action is making it difficult to develop new molecules for this purpose. The efficacy of these drugs is known to depend closely on the physico-chemistry of the lipid-water interfaces involved and on the unconventional behavior of the lipases which are their target enzymes. The lipolysis reaction which occurs at an oil-water interface involves complex equilibria between adsorption-desorption processes, conformational changes and catalytic mechanisms. In this context, surfactants can induce significant changes in the partitioning of the enzyme and the inhibitor between the water phase and lipid-water interfaces. Surfactants can be found at the oil-water interface where they compete with lipases for adsorption, but also in solution in the form of micellar aggregates and monomers that may interact with hydrophobic parts of lipases in solution. These various interactions, combined with the emulsification and dispersion of insoluble substrates and inhibitors, can either promote or decrease the activity and the inhibition of lipases. Here, we review some examples of the various effects of surfactants on lipase structure, activity and inhibition, which show how complex the various equilibria involved in the lipolysis reaction tend to be. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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9. Quantitative study of lipase secretion, extracellular lipolysis, and lipid storage in the yeast Yarrowia lipolytica grown in the presence of olive oil: analogies with lipolysis in humans.
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Najjar, Amal, Robert, Sylvie, Guérin, Clémence, Violet-Asther, Michèle, and Carrière, Frédéric
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YEAST ,QUANTITATIVE research ,LIPASES ,LIPOLYSIS ,LIPIDS - Abstract
Lipase secretion, extracellular lipolysis, and fatty acid uptake were quantified in the yeast Yarrowia lipolytica grown in the presence of olive oil and/or glucose. Specific lipase assays, Western blot analysis, and ELISA indicated that most of the lipase activity measured in Y. lipolytica cultures resulted from the YLLIP2 lipase. Lipase production was triggered by olive oil and, during the first hours of culture, most of the lipase activity and YLLIP2 immunodetection remained associated with the yeast cells. YLLIP2 was then released in the culture medium before it was totally degraded by proteases. Olive oil triglycerides were largely degraded when the lipase was still attached to the cell wall. The fate of lipolysis products in the culture medium and inside the yeast cell, as well as lipid storage, was investigated simultaneously by quantitative TLC-FID and GC analysis. The intracellular levels of free fatty acids (FFA) and triglycerides increased transiently and were dependent on the carbon sources. A maximum fat storage of 37.8% w/ w of yeast dry mass was observed with olive oil alone. A transient accumulation of saturated FFA was observed whereas intracellular triglycerides became enriched in unsaturated fatty acids. So far, yeasts have been mainly used for studying the intracellular synthesis, storage, and mobilization of neutral lipids. The present study shows that yeasts are also interesting models for studying extracellular lipolysis and fat uptake by the cell. The quantitative data obtained here allow for the first time to establish interesting analogies with gastrointestinal and vascular lipolysis in humans. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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10. Carica papaya Lipase: A Naturally Immobilized Enzyme with Interesting Biochemical Properties.
- Author
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Abdelkafi, Slim, Barouh, Nathalie, Fouquet, Benjamin, Fendri, Imen, Pina, Michel, Scheirlinckx, Frantz, Villeneuve, Pierre, and Carrière, Frédéric
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PAPAYA ,PLANT exudates ,IMMOBILIZED proteins ,LIPASES ,IMMOBILIZED enzymes ,DIGESTIVE enzymes ,PROTEOLYTIC enzymes - Abstract
Triacylglycerol (TAG) lipases have been thoroughly characterized in mammals and microorganisms, whereas very little is known about plant TAG lipases. The lipolytic activity occurring in all the laticies is known to be associated with sedimentable particles, and all attempts to solubilize the lipolytic activity of Carica papaya latex have been unsuccessful so far. However, some of the biochemical properties of the lipase from Carica papaya latex (CPL) were determined from the insoluble fraction of the latex. The activity was optimum at a temperature of 37°C and a pH of 9.0, and the specific activities of CPL were found to be 2,000 ± 185 and 256 ± 8 U/g when tributyrin and olive oil were used as substrates, respectively. CPL was found to be active in the absence of any detergent, whereas many lipases require detergent to prevent the occurrence of interfacial denaturation. CPL was inactive in the presence of micellar concentrations of Triton X-100, sodium dodecyl sulfate (SDS) and tetradecyl trimethylammonium bromide (TTAB), and still showed high levels of activity in the presence of sodium taurodeoxycholate (NaTDC) and the zwitterionic Chaps detergent. The effects of various proteases on the lipolytic activity of CPL were studied, and CPL was found to be resistant to treatment with various enzymes, except in the presence of trypsin. All these properties suggest that CPL may be a good candidate for various biotechnological applications. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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11. Lipids in the Stomach – Implications for the Evaluation of Food Effects on Oral Drug Absorption.
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Koziolek, Mirko, Carrière, Frédéric, and Porter, Christopher J. H.
- Published
- 2018
- Full Text
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