0000000000535642

AUTHOR

Korbinian Löbmann

0000-0002-8710-6347

showing 4 related works from this author

Preparation and recrystallization behavior of spray-dried co-amorphous naproxen–indomethacin

2016

To improve the dissolution properties and the physical stability of amorphous active pharmaceutical ingredients, small molecule stabilizing agents may be added to prepare co-amorphous systems. The objective of the study was to investigate if spray-drying allows the preparation of co-amorphous drug-drug systems such as naproxen-indomethacin and to examine the influence of the process conditions on the resulting initial sample crystallinity and the recrystallization behavior of the drug(s). For this purpose, the process parameters inlet temperature and pump feed rate were varied according to a 2(2) factorial design and the obtained samples were analyzed with X-ray powder diffractometry and Fo…

NaproxenRecrystallization (geology)Materials scienceIndomethacinPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacylaw.invention03 medical and health sciencesCrystallinityNaproxen0302 clinical medicinelawmedicineCrystallizationDissolutionAnti-Inflammatory Agents Non-SteroidalGeneral MedicineFactorial experiment021001 nanoscience & nanotechnologyAmorphous solidCrystallographyChemical engineeringSpray dryingCrystallization0210 nano-technologyPowder DiffractionBiotechnologymedicine.drugEuropean Journal of Pharmaceutics and Biopharmaceutics
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Evaluation of drug-polymer solubility curves through formal statistical analysis: comparison of preparation techniques.

2014

ABSTRACT: In this study, the influence of the preparation technique (ball milling, spray drying, and film casting) of a supersaturated amorphous dispersion on the quality of solubility determinations of indomethacin in polyvinylpyrrolidone was investigated by means of statistical analysis. After annealing of the amorphous dispersions above the crystallization temperature for 2 h, the solubility curve was derived from the glass transition temperature of the demixed material using the Gordon–Taylor relationship and fitting with the Flory–Huggins model. The study showed that the predicted solubility from the ball-milled mixtures was not consistent with those from spray drying and film casting,…

Models MolecularMaterials scienceHot TemperatureChemistry PharmaceuticalDrug CompoundingIndomethacinAnalytical chemistryPharmaceutical SciencemedicinePharmaceutic AidsSolubilitySupersaturationReproducibilityPolyvinylpyrrolidoneCalorimetry Differential ScanningAnti-Inflammatory Agents Non-SteroidalPovidoneReproducibility of ResultsCastingAmorphous solidChemical engineeringSolubilitySpray dryingEmulsionsGlass transitionPowder Diffractionmedicine.drugJournal of pharmaceutical sciences
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Recent advances and potential applications of modulated differential scanning calorimetry (mDSC) in drug development.

2016

Differential scanning calorimetry (DSC) is frequently the thermal analysis technique of choice within preformulation and formulation sciences because of its ability to provide detailed information about both the physical and energetic properties of a substance and/or formulation. However, conventional DSC has shortcomings with respect to weak transitions and overlapping events, which could be solved by the use of the more sophisticated modulated DSC (mDSC). mDSC has multiple potential applications within the pharmaceutical field and the present review provides an up-to-date overview of these applications. It is aimed to serve as a broad introduction to newcomers, and also as a valuable refe…

Materials scienceCalorimetry Differential ScanningChemistry PharmaceuticalPharmaceutical ScienceNanotechnology02 engineering and technology021001 nanoscience & nanotechnology030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineDifferential scanning calorimetryDrug developmentPharmaceutical Preparations0210 nano-technologyEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
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Comparative Study of Different Methods for the Prediction of Drug–Polymer Solubility

2015

In this study, a comparison of different methods to predict drug-polymer solubility was carried out on binary systems consisting of five model drugs (paracetamol, chloramphenicol, celecoxib, indomethacin, and felodipine) and polyvinylpyrrolidone/vinyl acetate copolymers (PVP/VA) of different monomer weight ratios. The drug-polymer solubility at 25 °C was predicted using the Flory-Huggins model, from data obtained at elevated temperature using thermal analysis methods based on the recrystallization of a supersaturated amorphous solid dispersion and two variations of the melting point depression method. These predictions were compared with the solubility in the low molecular weight liquid ana…

Vinyl CompoundsRecrystallization (geology)PolymersChemistry PharmaceuticalIndomethacinAnalytical chemistryPharmaceutical ScienceFlory–Huggins solution theorychemistry.chemical_compoundDrug StabilityDrug DiscoveryVinyl acetatemedicineSolubilityThermal analysisAcetaminophenSupersaturationChromatographyCalorimetry Differential ScanningFelodipinePolyvinylpyrrolidonePovidonePyrrolidinonesChloramphenicolSolubilitychemistryCelecoxibThermodynamicsMolecular MedicineCrystallizationMelting-point depressionmedicine.drugMolecular Pharmaceutics
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