Hydrates of active pharmaceutical ingredients: A 35Cl and 2H solid-state NMR and DFT study

被引:10
|
作者
Holmes, Sean T. [1 ,2 ]
Vojvodin, Cameron S. [1 ,2 ]
Veinberg, Natan [3 ]
Iacobelli, Emilia M. [3 ]
Hirsh, David A. [3 ]
Schurko, Robert W. [1 ,2 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
[2] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[3] Univ Windsor, Dept Chem & Biochem, Windsor, ON N9B 3P4, Canada
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
NUCLEAR-MAGNETIC-RESONANCE; AMPLITUDE CROSS-POLARIZATION; ELECTRIC-FIELD GRADIENT; X-RAY-DIFFRACTION; QUADRUPOLAR NUCLEI; CRYSTAL-STRUCTURES; DEHYDRATION BEHAVIOR; HYDROCHLORIDE SALTS; INTERACTION TENSORS; ADIABATIC PULSES;
D O I
10.1016/j.ssnmr.2022.101837
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study uses Cl-35 and H-2 solid-state NMR (SSNMR) spectroscopy and dispersion-corrected plane-wave density functional theory (DFT) calculations to characterize the molecular-level structures and dynamics of hydrates of active pharmaceutical ingredients (APIs). We use Cl-35 SSNMR to measure the EFG tensors of the chloride ions to characterize hydrated forms of hydrochloride salts of APIs, along with two corresponding anhydrous forms. DFT calculations are used to refine the crystal structures of the APIs and determine relationships between the Cl-35 EFG tensors and the spatial arrangements of proximate hydrogen bonds, which are particularly influenced by interactions with water molecules. We find that the relationship between Cl-35 EFG tensors and local hydrogen bonding geometries is complex, but meaningful structure/property relationships can be garnered through use of DFT calculations. Specifically, for every case in which such a comparison could be made, we find that the hydrate has a smaller magnitude of CQ than the corresponding anhydrous form, indicating a chloride ion environment with a ground-state electron density of higher spherical symmetry in the former. Finally, variable-temperature Cl-35 and H-2 SSNMR experiments on a deuterium-exchanged sample of the API cimetidine hydrochloride monohydrate are used to monitor temperature-dependent influences on the spectra that may arise from motional influences on the Cl-35 and H-2 EFG tensors. From the H-2 SSNMR spectra, we determine that the motions of water molecules are characterized by jump-like motions about their C2 rotational axes that occur on timescales that are unlikely to influence the Cl-35 central-transition (+1/2 ? -1/2) powder patterns (this is confirmed by Cl-35 SSNMR). Together, these methods show great promise for the future study of APIs in their bulk and dosage forms, especially variable hydrates in which crystallographic water content varies with external conditions such as humidity.
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页数:13
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