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Immobilized Urease Vector System Based on the Dynamic Defect Regeneration Strategy for Efficient Urea Removal. | LitMetric

AI Article Synopsis

  • - The study focuses on improving the removal of urea, which can lead to renal diseases if it accumulates excessively, by developing a composite system called MCC@UiO/U that combines urease and a metal-organic framework.
  • - MCC@UiO/U achieves impressive urea removal efficiency, reaching a clearance rate of over 80% and effectively clearing urea from renal patients' peritoneal dialyzate within 2 hours, with a capacity of up to 1500 mg/g.
  • - The new composite shows excellent bioactivity, maintaining its performance even after 5 usage cycles, indicating strong stability and biocompatibility, which could lead to innovative clinical applications for kidney disease treatment.

Article Abstract

The clearance of urea poses a formidable challenge, and its excessive accumulation can cause various renal diseases. Urease demonstrates remarkable efficacy in eliminating urea, but cannot be reused. This study aimed to develop a composite vector system comprising microcrystalline cellulose (MCC) immobilized with urease and metal-organic framework (MOF) UiO-66-NH, denoted as MCC@UiO/U, through the dynamic defect generation strategy. By utilizing competitive coordination, effective immobilization of urease into MCC@UiO was achieved for efficient urea removal. Within 2 h, the urea removal efficiency could reach up to 1500 mg/g, surpassing an 80% clearance rate. Furthermore, an 80% clearance rate can also be attained in peritoneal dialyzate from patients. MCC@UiO/U also exhibits an exceptional bioactivity even after undergoing 5 cycles of perfusion, demonstrating remarkable stability and biocompatibility. This innovative approach and methodology provide a novel avenue and a wide range of immobilized enzyme vectors for clinical urea removal and treatment of kidney diseases, presenting immense potential for future clinical applications.

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Source
http://dx.doi.org/10.1021/acsami.4c08323DOI Listing

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