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High mobility group box proterin-1 (HMGB-1) is a multifunctional protein that can be released by various programmed cell deaths (PCDs), such as necroptosis and ferroptosis. PCDs play a critical role in the pathogenesis of systemic lupus erythematosus (SLE). However, the role of HMGB-1 in the process of SLE remains unclear. This study aims to demonstrate the potential diagnosing role of serum HMGB-1 in SLE that released by necroptosis and ferroptosis. We found that the serum levels of HMGB-1, receptor-interacting protein kinase 3 (RIPK3) /mixed lineage kinase domain-like protein (MLKL) related with necroptosis, and metabolites associated with ferroptosis were significantly upregulated in SLE patients compared to HC individuals. These serum levels were positively correlated with SLE disease activity. Additionally, the serum level of HMGB-1 showed a strong positive correlated with the levels of RIPK3/MLKL and ferroptosis metabolites. Moreover, the serum level of HMGB-1 was correlated with renal involvement and high-antinuclear antibodies (ANA) titer. After SLE serum and interferon γ (IFN-γ) treatment in vitro, the level of necroptosis and ferroptosis markers were activated and HMGB1 was released both in HEK293 and HK2 cells. Clinically, HMGB-1 was considered as a significant independent risk factor in SLE serum by binary logistic assay. Notably, HMGB-1 exhibited outstanding diagnostic ability for SLE by the area under the curve (AUC) in receiver operating characteristic (ROC) curve analysis. Taken together, our study indicates that the serum level of HMGB-1 is a promising biomarker for the diagnosis and monitoring of SLE., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

The conversion of biomass into high-performance carbon-based materials provides an opportunity to valorize biomass for advanced applications. Achieving this necessitates requires dedicated efforts and innovations in biocarbon synthesis, design, and applications. This study proposes the controllable conversion of biomass-derived cellulose into well-distributed carbon nanotubes (CNTs) by tuning the precipitation of cellulose pyrolysis generated vapors with in-situ formed ferric metal nanoparticles. The obtained CNTs exhibited lawn-like 3D architecture with similar length, uniform alignment, and dense distribution. The combined use of ferric chloride and dicyandiamide as the reagents with a mass ration of 0.162:1.05, demonstrated optimal performance in controlling the morphology of CNTs, enhancing the graphitization, and increasing the content of graphitic-N and pyridine-N. This multi-dimensional modification enhanced the electrocatalytic performance of the obtained CNTs, achieving an onset potential of 0.875 V vs. relative hydrogen electrode (RHE), a half-wave potential of 0.703 V vs. RHE, and a current density of -4.95 mA cm -2 during the oxygen reduction reaction. Following microbial fuel cells (MFCs) tests achieved an output voltage of 0.537 V and an output power density of 412.85 mW m -2 , comparable to MFC with Pt/C as the cathode catalyst. This biomass-derived catalyst is recommended as a high-quality, non-noble metal alternative to traditional noble-metal catalysts., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Valorization of lignocellulosic biomass via anaerobic digestion (AD) is limited by its reluctant structure, leading to a substantial energy remaining in the solid digestate. To mitigate this effect, the integration of AD and pyrolysis has attracted attention in recent years. However, the energy recovery efficiency of this cascading system is still unclear, especially the time node. Herein, a comprehensive evaluation of this integration, using varied AD periods, was conducted, to produce biogas, bio-oil and biochar, and to enhance the energy recovery, from the perspective of energy flow. The result indicated that the accumulative CH 4 yields increased from 33.23 to 249.20 mL/g VS as the AD time increased from 3 to 15 days. Pyrolysis of the obtained solid digestate obtained biochar from 28.81 to 35.96 %, while the bio-oil and pyrolysis gas slowly decreased. The highest energy efficiency of 71.9 % with a net energy gain of 2.0 MJ/kg wet biomass was achieved by the coupled system optimization at an AD time of 12 days as suggested by the energy flow analysis. This study provides new insight for the maximal conversion of biomass waste into energy products and provides a new way of recycling it., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)