The prevalence of nanoplastics in water has led to significant environmental and health concerns, yet effective and scalable strategies for mitigating this contamination remain limited. Here, we report a straightforward, efficient, and scalable approach to degrade nanoplastics in water using enzyme-loaded hydrogel granules with an interconnected porous structure and adjustable properties. These porous hydrogels were synthesized via a polymerization-induced phase separation method, allowing easy scaling-up. Our results show that enzyme-functionalized porous hydrogels slightly outperform free cutinase in nanoplastic degradation. Furthermore, immobilized enzymes exhibited enhanced stability under harsh conditions, achieving a 104.1 % higher PET removal rate at pH 5 than free cutinase. Notably, the immobilized enzyme retained 39.9 % of its initial degradation activity after five cycles, demonstrating good reuse stability. This method offers a promising and practical solution for using enzymes to address nanoplastic pollution in aquatic environments.
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http://dx.doi.org/10.1016/j.jhazmat.2025.137196 | DOI Listing |
J Hazard Mater
January 2025
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, 30 Puzhu South Road, Nanjing 211816, China. Electronic address:
The prevalence of nanoplastics in water has led to significant environmental and health concerns, yet effective and scalable strategies for mitigating this contamination remain limited. Here, we report a straightforward, efficient, and scalable approach to degrade nanoplastics in water using enzyme-loaded hydrogel granules with an interconnected porous structure and adjustable properties. These porous hydrogels were synthesized via a polymerization-induced phase separation method, allowing easy scaling-up.
View Article and Find Full Text PDFCurr Drug Deliv
January 2025
Faculty of Pharmacy, The National University of Malaysia (UKM), Jalan Raja Muda Abdul Aziz, 50300, Kuala Lumpur, Malaysia.
Introduction: Poly(methyl vinyl ether co-maleic acid) (PMVE/MA) hydrogel microneedles (HMN) are investigated for transdermal delivery of macromolecular drugs owing to their biocompatibility and super-swelling properties. However, the drug delivery efficacy reduces with increasing molecular weight due to the entrapment within the HMN matrices. Furthermore, integrating external drug reservoirs extends the drug diffusion path and reduces the efficiency of drug permeation.
View Article and Find Full Text PDFRSC Adv
January 2025
School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Shandong Key Laboratory of Oral Tissue Regeneration, Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneratioon, Shandong Provincial Clinical Research Center for Oral Diseases Ji'nan 250012 China
Bone defects represent a significant challenge in clinical practice, driving the need for innovative solutions that effectively support bone regeneration. Barrier membranes, due to playing a critical role in creating an environment conducive to bone regeneration by preventing the infiltration of non-osteogenic tissues, are widely applied to bone repair. However, inadequate spatial stability and osteogenesis-promoting ability often limit current barrier membranes.
View Article and Find Full Text PDFSoft Matter
January 2025
Department of Mechanical Engineering and Materials Science, Yale University, New Haven, CT 06510, USA.
Hydrogels are popular platforms for cell encapsulation in biomedicine and tissue engineering due to their soft, porous structures, high water content, and excellent tunability. Recent studies highlight that the timing of network formation can be just as important as mechanical properties in influencing cell morphologies. Conventionally, time-dependent properties can be achieved through multi-step processes.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Tianjin Key Laboratory of Pulp and Paper, Tianjin University of Science & Technology, No. 29, 13th Avenue, Tianjin Economic and Technological Development Area, Tianjin 300457, China. Electronic address:
In this study, we innovatively prepared a multifunctional lignin crosslinked polyacrylamide (L-cPAM) hydrogel by a sequential two-step strategy of crosslinking of lignin and crosslinked polyacrylamide (cPAM) followed by the polymerization of cPAM. The hydrogen bonding and crosslinking between the molecular chains of lignin and PAM established a rigid and porous network structure, which provided the L-cPAM hydrogel with excellent mechanical strength, thermal stability, and salinity resistance. A series of lignin dosages (0 to 30 %) were investigated during the crosslinking of lignin and PAM.
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