Sulfonated Azocalix[4]arene-Modified Metal–Organic Framework Nanosheets for Doxorubicin Removal from Serum

Author:

Cao Xiao-Min1,Cheng Yuan-Qiu12,Chen Meng-Meng12,Yao Shun-Yu12,Ying An-Kang12,Wang Xiu-Zhen1,Guo Dong-Sheng123,Li Yue14

Affiliation:

1. College of Chemistry, Nankai University, Tianjin 300071, China

2. State Key Laboratory of Elemento-Organic Chemistry, Key Laboratory of Functional Polymer Materials (Ministry of Education), Frontiers Science Center for New Organic Matter, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071, China

3. Xinjiang Key Laboratory of Novel Functional Materials Chemistry, College of Chemistry, and Environmental Sciences, Kashi University, Kashi 844000, China

4. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China

Abstract

Chemotherapy is one of the most commonly used methods for treating cancer, but its side effects severely limit its application and impair treatment effectiveness. Removing off-target chemotherapy drugs from the serum promptly through adsorption is the most direct approach to minimize their side effects. In this study, we synthesized a series of adsorption materials to remove the chemotherapy drug doxorubicin by modifying MOF nanosheets with sulfonated azocalix[4]arenes. The strong affinity of sulfonated azocalix[4]arenes for doxorubicin results in high adsorption strength (Langmuir adsorption constant = 2.45–5.73 L mg−1) and more complete removal of the drug. The extensive external surface area of the 2D nanosheets facilitates the exposure of a large number of accessible adsorption sites, which capture DOX molecules without internal diffusion, leading to a high adsorption rate (pseudo-second-order rate constant = 0.0058–0.0065 g mg−1 min−1). These adsorbents perform effectively in physiological environments and exhibit low cytotoxicity and good hemocompatibility. These features make them suitable for removing doxorubicin from serum during “drug capture” procedures. The optimal adsorbent can remove 91% of the clinical concentration of doxorubicin within 5 min.

Funder

NSFC

Publisher

MDPI AG

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