Molecularly Imprinted Porous‐Organic Framework with pH‐Responsive Adsorption Sites for the Selective Adsorption of Iron

Author:

Yang Yajie1,Cai Fuli2,Zhang Cheng2,Gao Nan2,Zhang Suming3,Wang Guangtong4,Yuan Ye2

Affiliation:

1. Key Laboratory of Automobile Materials of Ministry of Education & School of Materials Science and Engineering Jilin University Changchun Jilin 130022 China

2. Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education Northeast Normal University Changchun Jilin 130012 China

3. Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry Beijing Normal University Beijing 100875 China

4. School of Medicine and Health, Harbin Institute of Technology Harbin Heilongjiang 150080 China

Abstract

Comprehensive SummaryRegulating brain iron metabolism and reducing neuronal ferroptosis is proven to be a potential method for treating Alzheimer's disease (AD). However, gastric juice has a pH of 1.1—2.2 where a large number of interfering ions are dissociated from the food, which in turn causes traditional oral iron chelators to be saturated and inactivated. Herein, poly(4‐vinylbenzoic acid) polymer chains were introduced as guided by Fe3+ ion template into the porous network (TpPa‐1) via molecularly imprinted technology to obtain porous iron chelators, COOH@TpPa‐1. The COOH@TpPa‐1 maintains a multiple hydrogen bonding structure to block the channels in the stomach (pH ~1.1—2.2) with a strongly acidic environment, so just a small amount of active sites have been occupied. As COOH@TpPa‐1 enters the colon, the alkaline environment disrupts the original hydrogen‐bonded structure and forms anionic fragments, the bonding affinity for Fe3+ ions was ~4.0 times that in the stomach, and also gave a high selective coefficient 4.2 times higher than that of conventional iron chelators. These designable "on" and "off" states promote the effective enrichment of iron ions within the colon by the porous chelator and produce a favorable therapeutic effect on Alzheimer's symptoms caused by ferroptosis in mice.

Funder

National Key Research and Development Program of China

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Wiley

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