Nitric Oxide Encapsulation in Metal‐Organic Cages via Physical Confinement

Author:

Zhou Chuang‐Wei1,Liu Yi‐Tong1,Wang Xue‐Zhi2,Hao De‐Bo1,Pang Jie3,Lian Zhao‐Xia1,Huang Yong‐Liang4,Wu Yan5,Li Yan Yan6,Li Xue7,Zhou Xiao‐Ping1,Li Dan1

Affiliation:

1. College of Chemistry and Materials Science, and Guangdong Provincial Key Laboratory of Supramolecular Coordination Chemistry Jinan University Guangzhou Guangdong 510632 China

2. Department of Ultrasound, Institute of Ultrasound in Musculoskeletal Sports Medicine, The Affiliated Guangdong Second Provincial General Hospital Jinan University Guangzhou Guangzhou Guangdong 510317 China

3. Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering Jinan University Guangzhou Guangdong 510632 China

4. Department of Chemistry Shantou University Medical College Shantou Guangdong 515041 China

5. Department of Anesthesiology The First Affiliated Hospital of Sun Yat‐Sen University Guangzhou Guangdong 510080 China

6. Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Engineering Technology Research Center of Drug Carrier of Guangdong, Department of Biomedical Engineering Jinan University Guangzhou Guangzhou 510632 China

7. Institute of Mass Spectrometry and Atmospheric Environment; Guangdong Provincial Key Laboratory of Speed Capability Research Jinan University Guangzhou Guangzhou 510632 China

Abstract

Comprehensive SummaryThe stabilization of active molecules is significantly important for chemistry, especially for the bioactive molecules. In this work, we report the synthesis and characterization of three tetrahedral Fe4L6 cages, which are water‐soluble and functionalized with or without PEG chains. All cages can physically trap NO molecules in their cavities to prevent a reaction with O2. Single‐crystal X‐ray diffraction (SCXRD), Griess assay, electron paramagnetic resonance (EPR) spectroscopy, and fluorescence assay demonstrate that NO molecules were encapsulated and stabilized by these cage molecules through the formation of host‐guest supramolecules. These NO‐loaded cages show high antibacterial activities for inhibiting Staphylococcus aureus and Escherichia coli, providing a convenient method for making antibiotic agents. Moreover, these PEG‐functionalized cages exhibit excellent biocompatibility, providing a new strategy for developing materials for NO delivery in biomedical applications

Funder

Natural Science Foundation of Guangdong Province

National Natural Science Foundation of China

Publisher

Wiley

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