Theophylline is known to undergo vapor phase induced hydrate-anhydrate pseudopolymorphic transformations, which can affect its bioavailability. In this work, the kinetics of the pseudopolymorphic transitions of theophylline crystals in different storage conditions is studied using a vibrational spectroscopic technique. While the hydration is a single-step process with a half-life time of ca. 5 h, the dehydration occurs through a two-step mechanism. In addition, the phase stability of hydrate-anhydrate systems in different relative humidity (RH) conditions was probed. The critical RH for anhydrous teophylline was found to be at ca. 79%, while the critical RH for dehydration is ca. 30%.
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Chem Pharm Bull (Tokyo)
July 2024
Laboratory of Pharmaceutical Technology, School of Pharmacy and Pharmaceutical Sciences, University of Toyama.
The purpose of this study was to continuously monitor the pseudopolymorphic transition from anhydrate to monohydrate by measuring the NMR relaxation using time-domain NMR (TD-NMR). Taking advantage of the simplicity of the low-field NMR instrument configuration, which is an advantage of TD-NMR, the NMR instrument was connected to a humidity controller to monitor the pseudopolymorphic transition. First, ezetimibe (EZT) monohydrate was prepared from its anhydrate using a saturated salt solution method, and T relaxation of EZT monohydrate and anhydrate was measured without a humidity controller.
View Article and Find Full Text PDFPharmaceutics
December 2022
Food and Drug Department, University of Parma, 43121 Parma, Italy.
Rifaximin is a locally acting antibiotic practically insoluble in water. It presents several crystal phases characterized by different degrees of hydration. The aim of this work is to investigate the dissolution behaviour of rifaximin α, β, and amorphous forms in relation to their relative thermodynamic stability to contribute to clarifying possible solvent- or humidity-mediated conversion patterns.
View Article and Find Full Text PDFChem Sci
December 2022
Department of Chemistry "Ugo Schiff" & INSTM RU, University of Florence Via della Lastruccia 3 50019 Sesto Fiorentino Italy
We report here the synthesis of a new - (-) singly linked vanadyl-porphyrin dimer that crystallizes in two different pseudo-polymorphs. The single crystal continuous-wave electron paramagnetic resonance investigation evidences a small but crucial isotropic exchange interaction, , between the two tilted, and thus distinguishable, spin centers of the order of 10 cm. The experimental and DFT studies evidence a correlation between values and porphyrin plane tilting angle and distortion.
View Article and Find Full Text PDFInorg Chem
December 2022
Departamento de Química-Centro de Síntesis Química de La Rioja (CISQ), Universidad de La Rioja, 26006 Logroño, Spain.
New cyclometalated Pt complexes with 2-phenylbenzothiazole (pbt) and two different picolinate ligands [Pt(pbt)(R-pic-κ)] (R = H (), OH ()) were prepared. In contrast to , the OH substituent group on allows modulation of the packing in the solid state through donor-acceptor H-bonding interactions with the CHCl solvent. Thus, three pseudopolymorphs of with different aggregation degrees were isolated, including yellow , orange-red () and black () with emissions at 540, 656, and 740 nm, respectively, in the solid state at 298 K.
View Article and Find Full Text PDFBiomicrofluidics
December 2021
Complex Fluid Processing, Process & Energy Department, Delft University of Technology, Leeghwaterstraat 39, 2628 CB Delft, The Netherlands.
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