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Comparison of the Four Anhydrous Polymorphs of Carbamazepine and the Crystal Structure of Form I**Supplementary material: X‐ray crystallographic information file (CIF) of triclinic CBZ (form I) is available.
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings 1PII of original article: S0169-409X(96)00423-1. The article was originally published in Advanced Drug Delivery Reviews 23 (1997) 3–25. 1
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract1PII of original article: S0169-409X(96)00487-5. The article was originally published in Advanced Drug Delivery Reviews 25 (1997) 3–14.1
Water Properties in a Novel Thermoswelling Poly(vinyl alcohol) Derivative Hydrogel as Studied by Nuclear Magnetic Resonance and Fourier Transform Infrared Spectroscopy
Anomalous Role Change of Tertiary Amino and Ester Groups as Hydrogen Acceptors in Eudragit E Based Solid Dispersion Depending on the Concentration of Naproxen
The Effect of Excipients on the Molecular Mobility of Lyophilized Formulations, as Measured by Glass Transition Temperature and NMR Relaxation-Based Critical Mobility Temperature
A biopharmaceutical classification-based Right-First-Time formulation approach to reduce human pharmacokinetic variability and project cycle time from First-In-Human to clinical Proof-Of-Concept
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Elucidating structure and dynamics of crystalline α‐zirconium phosphates intercalated with water and methanol by multinuclear solid‐state MAS NMR: A comprehensive NMR approach
RETRACTED: Cocrystals of Curcumin-Isonicotinamide and Curcumin-Gallic Acid: Does the Weak Forces in Cocrystals Effect on Binding Profiles with BSA and Cell Cytotoxicity?
Effect of the molecular mobility of water adsorbed by disintegrants on storage-induced hydrolytic degradation of acetylsalicylic acid incorporated into tablets under humid conditions
Discrimination of crystal polymorphism in active pharmaceutical ingredients using time-domain 1H NMR relaxation combined with multivariate statistical process control
Quantitative evaluation of crystallinity of active pharmaceutical ingredients in amorphous solid dispersion using T2 relaxometry measured by time-domain NMR
Quantitation of Commercially Available API Solid Forms by Application of the NMR-qSRC Approach: An Optimization Strategy Based on In Silico Simulations
NMR Longitudinal Rotating Frame Relaxation Time (T1ρ) with a Weak Spin Locking Field as an Approach to Characterize Solid-State Active Pharmaceutical Ingredients: Proof of Concept
A Time-Domain NMR Study of the State of Water in Wet Granules with Different Fillers and Its Contribution to the Wet Granulation Process and to the Characteristics of Granules
Investigation of the Relationship between the Chemical Stability of Itraconazole Adsorbed on Silica during Humidification and NMR Relaxation Using Time-Domain NMR
Usefulness of Time-Domain NMR in Characterizing Pharmaceutical Properties
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