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

被引:9
|
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.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] 35Cl dynamic nuclear polarization solid-state NMR of active pharmaceutical ingredients
    Hirsh, David A.
    Rossini, Aaron J.
    Emsley, Lyndon
    Schurko, Robert W.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2016, 18 (37) : 25893 - 25904
  • [2] Synthesis and Characterization of Xylazine Hydrochloride Polymorphs, Hydrates, and Cocrystals: A 35Cl Solid-State NMR and DFT Study
    Abdulla, Louae M.
    Peach, Austin A.
    Holmes, Sean T.
    Dowdell, Zachary T.
    Watanabe, Lara K.
    Iacobelli, Emilia M.
    Hirsh, David A.
    Rawson, Jeremy M.
    Schurko, Robert W.
    CRYSTAL GROWTH & DESIGN, 2023, 23 (05) : 3412 - 3426
  • [3] Quantifying Disproportionation in Pharmaceutical Formulations with 35Cl Solid-State NMR
    Hirsh, David A.
    Su, Yongchao
    Nie, Haichen
    Xu, Wei
    Stueber, Dirk
    Variankaval, Narayan
    Schurko, Robert W.
    MOLECULAR PHARMACEUTICS, 2018, 15 (09) : 4038 - 4048
  • [4] 35Cl solid-state NMR of HCl salts of active pharmaceutical ingredients: structural prediction, spectral fingerprinting and polymorph recognition
    Hildebrand, Marcel
    Hamaed, Hiyam
    Namespetra, Andrew M.
    Donohue, John M.
    Fu, Riqiang
    Hung, Ivan
    Gan, Zhehong
    Schurko, Robert W.
    CRYSTENGCOMM, 2014, 16 (31): : 7334 - 7356
  • [5] Ab initio 35Cl solid state NMR-based crystallography of active pharmaceutical ingredients.
    Pulido, Angeles
    Hirsh, David A.
    Schurko, Robert W.
    Day, Graeme M.
    ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2016, 72 : S117 - S117
  • [6] Nutraceuticals in Bulk and Dosage Forms: Analysis by 35Cl and 14N Solid-State NMR and DFT Calculations
    Holmes, Sean T.
    Hook, James M.
    Schurko, Robert W.
    MOLECULAR PHARMACEUTICS, 2022, 19 (02) : 440 - 455
  • [7] Mechanochemical syntheses and 35Cl solid-state NMR characterization of fluoxetine HCl cocrystals
    Peach, Austin A.
    Hirsh, David A.
    Holmes, Sean T.
    Schurko, Robert W.
    CRYSTENGCOMM, 2018, 20 (20): : 2780 - 2792
  • [8] Application of solid-state 35Cl NMR to the structural characterization of hydrochloride pharmaceuticals and their polymorphs
    Hamaed, Hiyam
    Pawlowski, Jenna M.
    Cooper, Benjamin F. T.
    Fu, Riqiang
    Eichhorn, S. Holger
    Schurko, Robert W.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (33) : 11056 - 11065
  • [9] Chloride ion sites in silicate and aluminosilicate glasses:: A preliminary study by 35Cl solid-state NMR
    Stebbins, JF
    Du, LS
    AMERICAN MINERALOGIST, 2002, 87 (2-3) : 359 - 363
  • [10] DNP-enhanced solid-state NMR spectroscopy of active pharmaceutical ingredients
    Zhao, Li
    Pinon, Arthur C.
    Emsley, Lyndon
    Rossini, Aaron J.
    MAGNETIC RESONANCE IN CHEMISTRY, 2018, 56 (07) : 583 - 609