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Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks

Novel and highly selective molecularly imprinted polymers based on the surface of metal–organic frameworks, NH(2)-MIL-101(Cr) (MIL@MIP(S)), were successfully fabricated to capture neuronal nitric oxide synthase–postsynaptic density protein-95 (nNOS–PSD-95) uncouplers from Sanhuang Xiexin Decoction (...

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Detalles Bibliográficos
Autores principales: Pan, Linli, Ding, Yingying, Ni, Xiaoting, Wang, Chong-Zhi, Jiang, Bo, Zhang, Yu, Jiang, Nan, Tang, Yulin, Chen, Lina, Yuan, Chun-Su
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049783/
https://www.ncbi.nlm.nih.gov/pubmed/35492204
http://dx.doi.org/10.1039/c9ra10537a
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author Pan, Linli
Ding, Yingying
Ni, Xiaoting
Wang, Chong-Zhi
Jiang, Bo
Zhang, Yu
Jiang, Nan
Tang, Yulin
Chen, Lina
Yuan, Chun-Su
author_facet Pan, Linli
Ding, Yingying
Ni, Xiaoting
Wang, Chong-Zhi
Jiang, Bo
Zhang, Yu
Jiang, Nan
Tang, Yulin
Chen, Lina
Yuan, Chun-Su
author_sort Pan, Linli
collection PubMed
description Novel and highly selective molecularly imprinted polymers based on the surface of metal–organic frameworks, NH(2)-MIL-101(Cr) (MIL@MIP(S)), were successfully fabricated to capture neuronal nitric oxide synthase–postsynaptic density protein-95 (nNOS–PSD-95) uncouplers from Sanhuang Xiexin Decoction (SXD) for stroke treatment. The resultant polymers were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and X-ray diffraction. The performance tests revealed that MIL@MIPs had a large binding capacity, fast kinetics, and excellent selectivity. Then the obtained polymers were satisfactorily applied to solid-phase extraction coupled with high-performance liquid chromatography to selectively capture nNOS–PSD-95 uncouplers from SXD. Furthermore, the biological activities of components obtained from SXD were evaluated in vivo and in vitro. As a consequence, the components showed a potent neuroprotective effect from the MTS assay and uncoupling activity from the co-immunoprecipitation experiment. In addition, the anti-ischemic stroke assay in vivo was further investigated to determine the effect of reducing infarct size and ameliorating neurological deficit by the active components. Therefore, this present study contributes a valuable new method and new tendency to selectively capture active components for stroke treatment from SXD and other natural medicines.
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spelling pubmed-90497832022-04-29 Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks Pan, Linli Ding, Yingying Ni, Xiaoting Wang, Chong-Zhi Jiang, Bo Zhang, Yu Jiang, Nan Tang, Yulin Chen, Lina Yuan, Chun-Su RSC Adv Chemistry Novel and highly selective molecularly imprinted polymers based on the surface of metal–organic frameworks, NH(2)-MIL-101(Cr) (MIL@MIP(S)), were successfully fabricated to capture neuronal nitric oxide synthase–postsynaptic density protein-95 (nNOS–PSD-95) uncouplers from Sanhuang Xiexin Decoction (SXD) for stroke treatment. The resultant polymers were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and X-ray diffraction. The performance tests revealed that MIL@MIPs had a large binding capacity, fast kinetics, and excellent selectivity. Then the obtained polymers were satisfactorily applied to solid-phase extraction coupled with high-performance liquid chromatography to selectively capture nNOS–PSD-95 uncouplers from SXD. Furthermore, the biological activities of components obtained from SXD were evaluated in vivo and in vitro. As a consequence, the components showed a potent neuroprotective effect from the MTS assay and uncoupling activity from the co-immunoprecipitation experiment. In addition, the anti-ischemic stroke assay in vivo was further investigated to determine the effect of reducing infarct size and ameliorating neurological deficit by the active components. Therefore, this present study contributes a valuable new method and new tendency to selectively capture active components for stroke treatment from SXD and other natural medicines. The Royal Society of Chemistry 2020-02-21 /pmc/articles/PMC9049783/ /pubmed/35492204 http://dx.doi.org/10.1039/c9ra10537a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Pan, Linli
Ding, Yingying
Ni, Xiaoting
Wang, Chong-Zhi
Jiang, Bo
Zhang, Yu
Jiang, Nan
Tang, Yulin
Chen, Lina
Yuan, Chun-Su
Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title_full Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title_fullStr Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title_full_unstemmed Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title_short Modeling rapid and selective capture of nNOS–PSD-95 uncouplers from Sanhuang Xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
title_sort modeling rapid and selective capture of nnos–psd-95 uncouplers from sanhuang xiexin decoction by novel molecularly imprinted polymers based on metal–organic frameworks
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049783/
https://www.ncbi.nlm.nih.gov/pubmed/35492204
http://dx.doi.org/10.1039/c9ra10537a
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