4.8 Article

Metal-Organic Framework Traps with Record-High Bilirubin Removal Capacity for Hemoperfusion Therapy

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 23, Pages 25546-25556

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c03859

Keywords

metal-organic frameworks; PCN-333; MOF-808; bilirubin capture; hemoperfusion

Funding

  1. National Natural Science Foundation of China [21621004, 21961132005, 21908160, 21422605]
  2. Qingdao National Laboratory for Marine Science and Technology [QNLM2016ORP0407]
  3. Tianjin Natural Science Foundation [18JCYBJC29500]
  4. China Postdoctoral Science Foundation [2019M651041]

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Adsorption-based hemoperfusion has been widely used to remove toxins from the blood of patients suffering acute liver failure (ALF). However, its detoxification effect has been severely hampered by the unsatisfactory adsorption performance of clinically used porous adsorbents, such as activated carbon (AC) and adsorption resin. Herein, two cage-based metal-organic frameworks (MOFs), PCN-333 (constructed from 4,4,4-s-triazine-2,4,6-triyl-tribenzoic acid (H(3)TATB) ligands and Al-3 metal clusters) and MOF-808 (constructed from 1,3,5-benzenetricarboxylic acid (H3BTC) ligands and Zr-6 metal clusters), are introduced for highly efficient hemoperfusion. They possess negligible hemolytic activity and can act as bilirubin traps to achieve outstanding adsorption performance toward bilirubin, a typical toxin related to ALF. Notably, PCN-333 shows a record-high adsorption capacity (similar to 1003.8 mg g(-1)) among various bilirubin adsorbents previously reported. More importantly, they can efficiently adsorb bilirubin in bovine serum albumin (BSA) solution or even in 100% fetal bovine serum (FBS) due to their high selectivity. Strikingly, the adsorption rate and capacity of PCN-333 in biological solutions are approximately four times faster and 69 times higher than those of clinical AC, respectively. Findings in this work pave a new avenue to overcome the challenge of low adsorption efficiency and capacity in hemoperfusion therapy.

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