Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Structural and sorption characteristics of an aerogel composite material loaded with flufenamic acid: insights from MAS NMR and high-pressure NOESY studies. / Sobornova, V.V.; Mulloyarova, V.V.; Belov, K.V.; Dyshin, A.A.; Tolstoy, P.M.; Kiselev, M.G.; Khodov, I.A.
в: Physical Chemistry Chemical Physics, Том 26, 2024, стр. 27301-27313.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Structural and sorption characteristics of an aerogel composite material loaded with flufenamic acid: insights from MAS NMR and high-pressure NOESY studies
AU - Sobornova, V.V.
AU - Mulloyarova, V.V.
AU - Belov, K.V.
AU - Dyshin, A.A.
AU - Tolstoy, P.M.
AU - Kiselev, M.G.
AU - Khodov, I.A.
N1 - Export Date: 4 November 2024 CODEN: PPCPF Сведения о финансировании: Russian Science Foundation, RSF, 22-13-00257 Сведения о финансировании: Russian Science Foundation, RSF Текст о финансировании 1: This research was funded by the grant of the Russian Science Foundation (project no. 22-13-00257).
PY - 2024
Y1 - 2024
N2 - The structural and sorption characteristics of a composite material consisting of a silica aerogel loaded with flufenamic acid were investigated using a variety of nuclear magnetic resonance techniques. The composite structure was analyzed using magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy, which revealed significant interactions between the aerogel matrix and the FFA molecules. Solid-state 29Si NMR provided insights into the aerogel's stability, while 1H and 13C NMR confirmed the presence of FFA in the matrix, with signals from FFA molecules observed alongside tetraethoxysilane (TEOS) groups. Ethanol-induced desorption of FFA led to narrowed spectral lines, suggesting the breaking of intermolecular hydrogen bonds. 19F MAS NMR spectra indicated changes in FFA local environments upon loading into AG pores. Evaluation of CO2 sorption characteristics using 13C NMR demonstrated a slower sorption rate for AG + FFA than that for pure AG, attributed to decreased pore volume. Furthermore, nuclear Overhauser effect spectroscopy (NOESY) was employed to explore the conformational behavior of FFA within the aerogel matrix. The results indicated a shift in conformer populations, particularly those related to the rotation of one cyclic fragment relative to the other. These findings provide insights into the structural and sorption characteristics of the AG + FFA composite, which are valuable for developing novel drug solid forms. © 2024 The Royal Society of Chemistry.
AB - The structural and sorption characteristics of a composite material consisting of a silica aerogel loaded with flufenamic acid were investigated using a variety of nuclear magnetic resonance techniques. The composite structure was analyzed using magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy, which revealed significant interactions between the aerogel matrix and the FFA molecules. Solid-state 29Si NMR provided insights into the aerogel's stability, while 1H and 13C NMR confirmed the presence of FFA in the matrix, with signals from FFA molecules observed alongside tetraethoxysilane (TEOS) groups. Ethanol-induced desorption of FFA led to narrowed spectral lines, suggesting the breaking of intermolecular hydrogen bonds. 19F MAS NMR spectra indicated changes in FFA local environments upon loading into AG pores. Evaluation of CO2 sorption characteristics using 13C NMR demonstrated a slower sorption rate for AG + FFA than that for pure AG, attributed to decreased pore volume. Furthermore, nuclear Overhauser effect spectroscopy (NOESY) was employed to explore the conformational behavior of FFA within the aerogel matrix. The results indicated a shift in conformer populations, particularly those related to the rotation of one cyclic fragment relative to the other. These findings provide insights into the structural and sorption characteristics of the AG + FFA composite, which are valuable for developing novel drug solid forms. © 2024 The Royal Society of Chemistry.
KW - Atomic emission spectroscopy
KW - Fourier transform infrared spectroscopy
KW - Hydrogen bonds
KW - Nuclear magnetic resonance spectroscopy
KW - Silicones
KW - Composites material
KW - Flufenamic acid
KW - High pressure
KW - Magic angle spinning nuclear magnetic resonance
KW - Material loaded
KW - matrix
KW - Nuclear overhauser effect spectroscopy
KW - Silica aerogels
KW - Sorption characteristics
KW - Structural characteristics
KW - Magic angle spinning
UR - https://www.mendeley.com/catalogue/5aa46590-e945-3c10-9ef7-2b40a46b93fb/
U2 - 10.1039/d4cp03217a
DO - 10.1039/d4cp03217a
M3 - статья
VL - 26
SP - 27301
EP - 27313
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
SN - 1463-9076
ER -
ID: 126740126