دورية أكاديمية

Core–Shell Structured Nanozyme with PDA-Mediated Enhanced Antioxidant Efficiency to Treat Early Intervertebral Disc Degeneration

التفاصيل البيبلوغرافية
العنوان: Core–Shell Structured Nanozyme with PDA-Mediated Enhanced Antioxidant Efficiency to Treat Early Intervertebral Disc Degeneration
المؤلفون: Jing Wang, Ruibang Wu, Zheng Liu, Lin Qi, Huilun Xu, Hao Yang, Yubao Li, Limin Liu, Ganjun Feng, Li Zhang
سنة النشر: 2024
مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, suggesting great potential, multiple antioxidative enzyme, local injection experiments, intervertebral disc degeneration, high oxidative stress, doped nio nanoparticle, desirable therapeutic effects, coupled electron transfer, • oh efficiently, rat idd model, protect np cells, 2 +, 2 , scavenge •, vivo <, vitro <, vital role, thus endowing, thereby reconstructing, stagnant proliferation, results indicated, regenerative process, redox couples, prohibiting idd, pathological environment
الوصف: Early intervention during intervertebral disc degeneration (IDD) plays a vital role in inhibiting its deterioration and activating the regenerative process. Aiming at the high oxidative stress (OS) in the IDD microenvironment, a core–shell structured nanozyme composed of Co-doped NiO nanoparticle (CNO) as the core encapsulated with a polydopamine (PDA) shell, named PDA@CNO, was constructed, hoping to regulate the pathological environment. The results indicated that the coexistence of abundant Ni 3+ /Ni 2+ and Co 3+ /Co 2+ redox couples in CNO provided rich catalytic sites; meanwhile, the quinone and catechol groups in the PDA shell could enable the proton-coupled electron transfer, thus endowing the PDA@CNO nanozyme with multiple antioxidative enzyme-like activities to scavenge •O 2 – , H 2 O 2 , and •OH efficiently. Under OS conditions in vitro , PDA@CNO could effectively reduce the intracellular ROS in nucleus pulposus (NP) into friendly H 2 O and O 2 , to protect NP cells from stagnant proliferation, abnormal metabolism (senescence, mitochondria dysfunction, and impaired redox homeostasis), and inflammation, thereby reconstructing the extracellular matrix (ECM) homeostasis. The in vivo local injection experiments further proved the desirable therapeutic effects of the PDA@CNO nanozyme in a rat IDD model, suggesting great potential in prohibiting IDD from deterioration.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: https://figshare.com/articles/journal_contribution/Core_Shell_Structured_Nanozyme_with_PDA-Mediated_Enhanced_Antioxidant_Efficiency_to_Treat_Early_Intervertebral_Disc_Degeneration/25017024Test
DOI: 10.1021/acsami.3c15938.s001
الإتاحة: https://doi.org/10.1021/acsami.3c15938.s001Test
https://figshare.com/articles/journal_contribution/Core_Shell_Structured_Nanozyme_with_PDA-Mediated_Enhanced_Antioxidant_Efficiency_to_Treat_Early_Intervertebral_Disc_Degeneration/25017024Test
حقوق: CC BY-NC 4.0
رقم الانضمام: edsbas.4F1139D2
قاعدة البيانات: BASE