0000000000040104

AUTHOR

C. Andrès

showing 14 related works from this author

Structural properties of magnesium stearate pseudopolymorphs: effect of temperature.

2003

A thorough review of the relevant literature reveals that the interaction between water vapour and magnesium stearate, in contrast to many other metal soaps, is not properly understood. The structural modifications associated with the up-take or loss of water of vegetable-derived commercial magnesium stearate powders exposed to humid air or vacuum at room temperature are investigated using standard powder X-ray diffractometry. It is found that in such conditions magnesium stearate reacts reversibly with the vapour phase with structural consequences very similar to the high temperature transition between the crystalline and rotator phases of other anhydrous metal soaps. When temperature is i…

DiffractionChemical PhenomenaChemistry PhysicalAnalytical chemistryPharmaceutical ScienceWaterMetalHeatingCrystallographychemistry.chemical_compoundLattice constantchemistryDrug StabilityX-Ray Diffractionvisual_artX-ray crystallographyAnhydrousvisual_art.visual_art_mediumTechnology PharmaceuticalMagnesium stearateHydratePowder diffractionStearic AcidsInternational journal of pharmaceutics
researchProduct

On the difficulty of assessing the specific surface area of magnesium stearate

2001

Abstract The water content of as-received commercial magnesium stearate batches from animal and vegetable sources have been modified by ageing in humid air at room temperature or by vacuum treatment. The complete adsorption–desorption isotherms of nitrogen and krypton vapours by samples of these as received and modified materials have been measured at liquid nitrogen temperature after standardised vacuum degassing. They are greatly affected by the initial water content of the material. In particular: (a) the BET surface area values computed from the adsorption branch vary widely and is increasing with increasing water content; (b) anomalous hysteresis of varying amplitude is observed in all…

NitrogenChemistry PharmaceuticalKryptonKryptonAnalytical chemistryWaterPharmaceutical Sciencechemistry.chemical_elementMineralogyLiquid nitrogenExcipientschemistry.chemical_compoundAdsorptionchemistrySpecific surface areaDesorptionAdsorptionMagnesium stearateWater contentStearic AcidsBET theoryInternational Journal of Pharmaceutics
researchProduct

Comparative study of the lubricant performance of Compritol® HD5 ATO and Compritol® 888 ATO: effect of polyethylene glycol behenate on lubricant capa…

2003

The aim of this paper is to study the lubricant capacity of Compritol HD5 ATO, a glyceryl and polyethylene glycol dibehenate, obtained by atomization. This material is compared to Compritol 888 ATO, constituted only by glyceryl dibehenate. First, this study verifies that Compritol HD5 ATO and Compritol 888 ATO present the same granular characteristics and that their mixes with Lactopress present no structural differences. Secondly, in term of compressibility and cohesiveness, the use of Compritol 888 ATO or Compritol HD5 ATO with Lactopress does not involve any significant modification. Finally, the minor difference of lubricant capacity between Compritol HD5 ATO and Compritol 888 ATO has n…

GlycerolMaterials scienceCompressive StrengthChemistry PharmaceuticalPharmaceutical ScienceExcipientLactosePolyethylene glycolCompritol HD5 ATODosage formCompritol 888Polyethylene Glycolschemistry.chemical_compoundPharmaceutical technologyTensile StrengthLubricationmedicineOrganic chemistryParticle SizeLubricantGLYCERYL DIBEHENATEFatty AcidschemistryChemical engineeringMicroscopy Electron ScanningTabletsmedicine.drugInternational Journal of Pharmaceutics
researchProduct

Thermal analyses of commercial magnesium stearate pseudopolymorphs

2005

Abstract Two commercial magnesium stearate powders in two well-characterised structural states are investigated using DSC and coupled TGA–DTA under dry nitrogen flow. They consist of either a mixture of crystalline hydrates or a poorly crystallised so-called anhydrate. Following the degassing of unbound water, 1 or 3 weight-loss peaks are observed below about 100 °C, each associated with one heat loss peak at the same temperature. The present results and a review of graphical data from literature show that the so-called anhydrate always contains a significant amount of water. At the beginning of the dehydration process, the heat loss is the same as the standard heat of vaporisation of water…

ChemistryMineralogyCondensed Matter Physicsmedicine.diseaseThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryChemical engineeringPolymorphism (materials science)medicineGravimetric analysisDehydrationMagnesium stearatePhysical and Theoretical ChemistryThermal analysisHydrateInstrumentationThermochimica Acta
researchProduct

Comparative study of the lubricant performance of Compritol 888 ATO either used by blending or by hot melt coating.

2003

Compritol 888 ATO is used as a lubricant in oral solid dosage formulations. It can also be used as a hot melt coating agent sprayed onto a powder. In this study, we compare the lubricant performance of Compritol 888 ATO either used by classical blending or by hot melt coating onto Lactopress by compression tests. In physical mix, the Compritol concentration does not affect the compressibility. The same compressibility is obtained with lactose coated by 0.5 or 1% of Compritol, but a higher compressibility can be observed with 2 and 3%. Cohesiveness of lactose depends on the process: hot melt coating induces a decrease of tablet tensile strength. In terms of forces transmission during compres…

Materials scienceCompressive StrengthChemistry PharmaceuticalDrug CompoundingFatty AcidsMixing (process engineering)Pharmaceutical ScienceAdministration OralLactoseengineering.materialExcipientsHeatingCompressive strengthCoatingUltimate tensile strengthLubricationLubricationCompressibilityengineeringHot melt coatingLubricantComposite materialPowdersTabletsInternational journal of pharmaceutics
researchProduct

New binary solid dispersion of indomethacin with surfactant polymer: From physical characterization to in vitro dissolution enhancement

2009

This article investigated preparation of solid dispersions containing a poor water-soluble drug, indomethacin (IND), and a new surfactant polymer, polyoxyethylene 32 distearate (POED). Solid dispersions were prepared by the melting method and characterized by DSC, hot-stage microscopy (HSM), X-ray diffraction (XRD) and scanning electron microscopy (SEM). DSC and HSM analyses performed on IND/POED physical mixtures indicated that IND could dissolve in liquid POED. The materials showed complete miscibility at liquid state. Combination of DSC, XRD, and SEM revealed that these materials had limited miscibility at the solid state. Up to 20% w/w IND in POED, we did not detect significant modifica…

Drug CarriersRecrystallization (geology)PolymersChemistryDrug CompoundingDrug StorageIndomethacinPharmaceutical ScienceMiscibilityPolyethylene GlycolsSurface-Active AgentsDifferential scanning calorimetryDrug StabilitySolubilityPulmonary surfactantChemical engineeringOrganic chemistryCrystalliteSolubilityCrystallizationDissolutionSolid solutionJournal of Pharmaceutical Sciences
researchProduct

Study of Morphology of Reactive Dissolution Interface Using Fractal Geometry

1996

J. Pharm. Sci. ISI Document Delivery No.: VF662 Times Cited: 7 Cited Reference Count: 15 Tromelin, A Gnanou, JC Andres, C Pourcelot, Y Chaillot, B; International audience; The determination of reactive fractal dimension was carried out using two forms of the Noyes-Whitney equation, -dQ/dt = K(Q/Q(0))(DR/3) and -d Q/dt = K' R(DR-3) using the Richardson plot on the basis of previous data obtained by dissolution of an orthoboric acid powder. The correlation of the results provided by the two ways of calculation allows proposal of the hypothesis that dissolution begins on a specific population of reactive sites and probably promotes the formation of microporous volumes or cracks.

Materials scienceMorphology (linguistics)Pharmaceutical ScienceThermodynamics02 engineering and technology030226 pharmacology & pharmacyFractal dimension03 medical and health sciences0302 clinical medicineFractalfractaldimension[CHIM.ANAL]Chemical Sciences/Analytical chemistrysurface morphologysurfaceParticle SizeSolubilitydissolution rateDissolutionMicroporous material021001 nanoscience & nanotechnology[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[SDV.SP.PG]Life Sciences [q-bio]/Pharmaceutical sciences/Galenic pharmacologySolubilityMicroscopy Electron ScanningParticle size0210 nano-technologySpecific populationJournal of Pharmaceutical Sciences
researchProduct

Assessing the particle size of a broadly dispersed powder by complementary techniques

1998

The experimental determination of reliable particle size distribution curves and statistical parameters of broad distributions is known to be a difficult task. This problem is addressed here in an attempt to characterize the granularity of three distinct batches of a pharmaceutical powder (fenofibrate from Fournier Laboratories). The methodology consists in comparing the results, expressed in terms of surface based mean diameter, as obtained by three complementary techniques, namely optical microscopy image analysis, laser light low angle diffraction and surface area measurement by krypton physisorption. These techniques are applied in parallel to the material of interest and to a certified…

Diffractionbusiness.industryKryptonStatistical parameterPharmaceutical Sciencechemistry.chemical_elementlaw.inventionCertified reference materialsOpticschemistryOptical microscopelawParticle-size distributionParticle sizeGranularityBiological systembusinessInternational Journal of Pharmaceutics
researchProduct

Influence of the parameters molecular structure and granularity on the compactibility of a powder

1995

Drug Dev. Ind. Pharm. ISI Document Delivery No.: RP128 Times Cited: 3 Cited Reference Count: 14 Andres, c ndiaye, a thomas, c tromelin, a chaillot, b pourcelot, y; International audience; The aim of this study was to determine whether it is possible to obtain better characterization of materials in order to find out if these one are suitable in Quality Assurance for direct tableting. We tried to show that a methodological approach combining chemical, physical and technological aspects could control the direct compression process. We chose orthoboric acid as a study model for the direct compression. From a chemical point of view, our findings show only one crystalline molecular structure (RX…

Materials sciencePharmaceutical Sciencemolecular structure02 engineering and technologypowdergranularity030226 pharmacology & pharmacy03 medical and health sciencesTableting0302 clinical medicineRheology[CHIM.ANAL]Chemical Sciences/Analytical chemistryDrug DiscoveryMoleculePharmacologyOrganic Chemistry021001 nanoscience & nanotechnologyCompression (physics)Characterization (materials science)[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallography[SDV.SP.PG]Life Sciences [q-bio]/Pharmaceutical sciences/Galenic pharmacologyGas pycnometerHomogeneouscompactibilityGranularity0210 nano-technologyBiological system
researchProduct

Preformulation: Effect of Moisture Content on Microcrystalline Cellulose (Avicel PH-302) and Its Consequences on Packing Performances

1999

This study evaluates the influence of moisture content on the packing performances of a new grade of microcrystalline cellulose (MCC) (Avicel PH-302) either by classical method or by an unconventional compression technique (constant volume reduction of powder bed). An increase in moisture content decreases the apparent density of the powder bed, resulting from interparticulate friction enhancement. This modification of apparent density seems to be the main effect caused by the presence of humidity, which explains the variations of compression properties, like an increase of powder plasticity generally observed in the experimental conditions.

Materials scienceChemistry PharmaceuticalPharmaceutical SciencePlasticityDosage formExcipientschemistry.chemical_compoundDrug DiscoveryCelluloseCelluloseWater contentPharmacologyChromatographyOrganic ChemistryWaterHumidityCompression (physics)Microcrystalline celluloseKineticschemistryChemical engineeringStress MechanicalParticle sizePowdersRheologyPlasticsTabletsDrug Development and Industrial Pharmacy
researchProduct

Affinity scale between a carrier and a drug in DPI studied by atomic force microscopy.

2002

The dry powder inhalers (DPIs) consist, in the most cases, of ordered mixture where the particles adhesion results of interactions between the drug and the carrier. Generally, one step of production process is the micronization of the drug particles in order to reduce the size for ordered mixing optimization. But this operation is known to partially create an amorphous surface. In this case, surrounding storage conditions, like relative humidity (RH), are able to modify the percentage of amorphous drug surface. The aim of this study was to investigate surface reactivity, surface energy and direct force measurements by atomic force microscopy (AFM) between lactose (carrier) and zanamivir (dr…

In situDrug CarriersChemistryNebulizers and VaporizersPharmaceutical ScienceNanotechnologyOne-StepAdhesionMicroscopy Atomic ForceGuanidinesSurface energyAmorphous solidCrystalChemical engineeringSialic AcidsRelative humidityZanamivirMicronizationPowdersPyransInternational journal of pharmaceutics
researchProduct

Functional characterisation of powders consisting of mixtures of glyceryl behenate and a non-ionic surfactant applied by hot-melt coating: lubricant …

2013

Solid-phase lubricants are routinely used in tablet manufacturing to reduce friction during the densification and ejection phases. However, two main challenges are commonly observed: a) poor blending of the lubricant with the other components; b) increased hydrophobicity of the mix. Hot-melt coating, wherein the substrate is coated with a composite lubricant consisting of glyceryl behenate and a non-ionic surfactant (polyethylene glycol behenate), offers a solution to these challenges. Comparative studies were undertaken using the composite lubricant in a hot-melt coating process and in a ‘standard’ physical blending method. This study shows that the addition of a surfactant to glyceryl beh…

Materials scienceComposite numberPharmaceutical ScienceExcipientPolyethylene glycolengineering.materialchemistry.chemical_compoundchemistryPulmonary surfactantCoatingmedicineengineeringHot melt coatingGlyceryl behenateLubricantComposite materialmedicine.drugJournal of Drug Delivery Science and Technology
researchProduct

Relationship between particle size and dissolution rate of bulk powders and sieving characterized fractions of two qualities of orthoboric acid

1996

Drug Dev. Ind. Pharm. ISI Document Delivery No.: VN279 Times Cited: 1 Cited Reference Count: 22 Tromelin, A Habillon, S Andres, C Pourcelot, Y Chaillot, B; International audience; We have carried out a study of the particle size distribution and aqueous dissolution rate of two commercially available qualities of orthoboric acid, labeled ''crystal'' (ABC) and ''powder'' (ABP). In a previous work, we have shown that the two commercial qualities of orthoboric acid chosen as model compound (''powder'' and ''crystal'') are related to the same crystal network in spite of their different names. However, these two qualities have very different size particle distributions, as previously determined b…

Analytical chemistryPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyrelease03 medical and health sciences0302 clinical medicine[CHIM.ANAL]Chemical Sciences/Analytical chemistryDrug DiscoverymorphologySize fractionsDissolution testingdissolution rateDissolutionfractal geometryPharmacologyAqueous solutionChemistryOrganic Chemistryparticle size021001 nanoscience & nanotechnologyLaser light scattering[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallography[SDV.SP.PG]Life Sciences [q-bio]/Pharmaceutical sciences/Galenic pharmacologyParticle-size distributionParticle size0210 nano-technology
researchProduct

LIM Kinases: new anticancer therapeutic targets

2017

International audience

[SDV] Life Sciences [q-bio][SDV]Life Sciences [q-bio]ComputingMilieux_MISCELLANEOUS
researchProduct