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1.
PLoS One ; 19(6): e0303933, 2024.
Article in English | MEDLINE | ID: mdl-38848431

ABSTRACT

Lithium batteries, as an important energy storage device, are widely used in the fields of renewable vehicles and renewable energy. The related lithium battery recycling industry has also ushered in a golden period of development. However, the high cost of lithium battery recycling makes it difficult to accurately evaluate its recycling value, which seriously restricts the development of the industry. To address the above issues, machine learning will be applied in the field of economic benefit analysis for lithium battery recycling, and backpropagation neural networks will be combined with stepwise regression. On the basis of considering social and commercial values, a lithium battery recycling and utilization economic benefit analysis model based on stepwise regression backpropagation neural network was designed. The experimental results show that the mean square error of the model converges between 10-6 and 10-7, and the convergence speed is improved by 33%. In addition, in practical experiments, the model predicted the actual economic benefits of recycling a batch of lithium batteries. The results show that the predictions are basically in line with the true values. Therefore, the economic benefit analysis and prediction model for lithium battery recycling proposed in the study has the advantages of high accuracy and fast operation speed, providing new ideas and tools for promoting innovation in the field of economic benefit analysis. It has certain application potential in the evaluation of the benefits of lithium battery recycling.


Subject(s)
Electric Power Supplies , Lithium , Machine Learning , Recycling , Lithium/economics , Recycling/economics , Recycling/methods , Electric Power Supplies/economics , Algorithms , Neural Networks, Computer , Cost-Benefit Analysis
2.
J Environ Manage ; 363: 121314, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38843731

ABSTRACT

Pretreatment, the initial step in recycling spent lithium-ion batteries (LIBs), efficiently separates cathode and anode materials to facilitate key element recovery. Despite brief introductions in existing research, a comprehensive evaluation and comparison of processing methods is lacking. This study reviews 346 references on LIBs recycling, analyzing pretreatment stages, treatment conditions, and method effects. Our analysis highlights insufficient attention to discharge voltage safety and environmental impact. Mechanical disassembly, while suitable for industrial production, overlooks electrolyte recovery and complicates LIBs separation. High temperature pyrolysis flotation offers efficient separation of mixed electrode materials, enhancing mineral recovery. We propose four primary pretreatment processes: discharge, electrolyte recovery, crushing and separation, and electrode material recovery, offering simplified, efficient, green, low-cost, and high-purity raw materials for subsequent recovery processes.


Subject(s)
Electric Power Supplies , Lithium , Recycling , Lithium/chemistry , Recycling/methods , Electrodes , Ions
3.
Biosens Bioelectron ; 260: 116462, 2024 Sep 15.
Article in English | MEDLINE | ID: mdl-38833834

ABSTRACT

Design and intelligent use renewable natural bioenergy is an important challenge. Electric microorganism-based materials are being serve as an important part of bioenergy devices for energy release and collection, calling for suitable skeleton materials to anchor live microbes. Herein we verified the feasibility of constructing bio-abiotic hybrid living materials based on the combination of gelatin, Li-ions and exoelectrogenic bacteria Shewanella oneidensis manganese-reducing-1 (MR-1). The gelatin-based mesh contains abundant pores, allowing microbes to dock and small molecules to diffuse. The hybrid materials hold plentiful electronegative groups, which effectively anchor Li-ions and facilitate their transition. Moreover, the electrochemical characteristics of the materials can be modulated through changing the ratios of gelatin, bacteria and Li-ions. Based on the gelatin-Li-ion-microorganism hybrid materials, a bifunctional device was fabricated, which could play dual roles alternatively, generation of electricity as a microbial fuel cell and energy storage as a pseudocapacitor. The capacitance and the maximum voltage output of the device reaches 68 F g-1 and 0.67 V, respectively. This system is a new platform and fresh start to fabricate bio-abiotic living materials for microbial electron storage and transfer. We expect the setup will extend to other living systems and devices for synthetic biological energy conversion.


Subject(s)
Bioelectric Energy Sources , Biosensing Techniques , Hydrogels , Shewanella , Bioelectric Energy Sources/microbiology , Shewanella/chemistry , Shewanella/metabolism , Hydrogels/chemistry , Biosensing Techniques/methods , Gelatin/chemistry , Lithium/chemistry , Electrochemical Techniques/methods , Equipment Design , Electric Capacitance
4.
Brain Behav ; 14(6): e3595, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38874089

ABSTRACT

INTRODUCTION: Traumatic brain injury (TBI) refers to damage to brain tissue by mechanical or blunt force via trauma. TBI is often associated with impaired cognitive abilities, like difficulties in memory, learning, attention, and other higher brain functions, that typically remain for years after the injury. Lithium is an elementary light metal that is only utilized in salt form due to its high intrinsic reactivity. This current review discusses the molecular mechanisms and therapeutic and neuroprotective effects of lithium in TBI. METHOD: The "Boolean logic" was used to search for articles on the subject matter in PubMed and PubMed Central, as well as Google Scholar. RESULTS: Lithium's therapeutic action is extremely complex, involving multiple effects on gene secretion, neurotransmitter or receptor-mediated signaling, signal transduction processes, circadian modulation, as well as ion transport. Lithium is able to normalize multiple short- as well as long-term modifications in neuronal circuits that ultimately result in disparity in cortical excitation and inhibition activated by TBI. Also, lithium levels are more distinct in the hippocampus, thalamus, neo-cortex, olfactory bulb, amygdala as well as the gray matter of the cerebellum following treatment of TBI. CONCLUSION: Lithium attenuates neuroinflammation and neuronal toxicity as well as protects the brain from edema, hippocampal neurodegeneration, loss of hemispheric tissues, and enhanced memory as well as spatial learning after TBI.


Subject(s)
Brain Injuries, Traumatic , Neuroprotective Agents , Brain Injuries, Traumatic/drug therapy , Brain Injuries, Traumatic/metabolism , Humans , Neuroprotective Agents/pharmacology , Neuroprotective Agents/administration & dosage , Animals , Lithium/pharmacology , Lithium/therapeutic use , Brain/drug effects , Brain/metabolism , Lithium Compounds/pharmacology
5.
Waste Manag ; 183: 209-219, 2024 Jun 30.
Article in English | MEDLINE | ID: mdl-38761485

ABSTRACT

Lithium iron phosphate batteries, known for their durability, safety, and cost-efficiency, have become essential in new energy applications. However, their widespread use has highlighted the urgency of battery recycling. Inadequate management could lead to resource waste and environmental harm. Traditional recycling methods, like hydrometallurgy and pyrometallurgy, are complex and energy-intensive, resulting in high costs. To address these challenges, this study introduces a novel low-temperature liquid-phase method for regenerating lithium iron phosphate positive electrode materials. By using N2H4·H2O as a reducing agent, missing Li+ ions are replenished, and anti-site defects are reduced through annealing. This process restores nearly all missing Li+ ions at 80 °C/6h. After high-temperature sintering at 700 °C/2h, the regenerated LiFePO4 matches commercial LiFePO4 in terms of anti-site defects and exhibits excellent performance with a 97 % capacity retention rate after 100 cycles at 1C. Compared to high-temperature techniques, this low-temperature liquid-phase method is simpler, safer, and more energy-efficient, offering a blueprint for reclaiming discarded LiFePO4 and similar materials.


Subject(s)
Electric Power Supplies , Lithium , Phosphates , Recycling , Recycling/methods , Lithium/chemistry , Phosphates/chemistry , Temperature , Electrodes , Ferric Compounds , Iron
6.
Waste Manag ; 183: 199-208, 2024 Jun 30.
Article in English | MEDLINE | ID: mdl-38761484

ABSTRACT

Recovering valuable resources from spent cathodes while minimizing secondary waste generation is emerging as an important objective for the future recycling of spent lithium-ion batteries, including lithium iron phosphate (LFP) batteries. This study proposes the use of oxalic acid leaching followed by ferrioxalate photolysis to separate and recover cathode active material elements from spent LFP batteries. The cathode active material can be rapidly dissolved at room temperature using appropriate quantities of oxalic acid and hydrogen peroxide, as determined through thermodynamic calculations. The dissolved ferrioxalate complex ion (Fe(C2O4)33-) is selectively precipitated through subsequent photolysis at room temperature. Depending on the initial concentration, the decomposition ratio can exceed 95 % within 1-4 h. Molecular mechanism analysis reveals that the decomposition of the Fe(C2O4)33- complex ion into water-insoluble FeC2O4·2H2O results in the precipitation of iron and the separation of metal elements. Lithium can be recovered as dihydrogen phosphates through filtration and water evaporation. No additional precipitant is needed and no other side products are generated during the process. Oxalic acid leaching followed by photolysis offers an environmentally friendly and efficient method for metal recovery from spent LFP cathodes. The photochemical process is a promising approach for reducing secondary waste generation in battery recycling.


Subject(s)
Electric Power Supplies , Ferric Compounds , Lithium , Phosphates , Photolysis , Recycling , Recycling/methods , Lithium/chemistry , Phosphates/chemistry , Ferric Compounds/chemistry , Oxalates/chemistry , Electrodes , Oxalic Acid/chemistry , Iron/chemistry , Hydrogen Peroxide/chemistry
7.
Waste Manag ; 184: 120-131, 2024 Jul 15.
Article in English | MEDLINE | ID: mdl-38815286

ABSTRACT

The recycling of spent lithium-ion batteries (LIBs) can not only reduce the potential harm caused by solid waste piles to the local environment but also provide raw materials for manufacturing new batteries. Flotation is an alternative approach to achieve the selective separation of cathode and anode active materials from spent LIBs. However, the presence of organic binder on the surface of hydrophilic lithium transition-metal oxides results in losses of cathode materials in the froth phase. In this study, plasma treatment was utilized to remove organic layers from cathode and anode active materials. Firstly, the correlations between plasma treatment parameters (e.g., input power, air flowrate, and treatment time) were explored and the contact angles of cathode and anode active materials were investigated by the response surface methodology. Secondly, differences in the flotation recoveries of cathode and anode active materials were enhanced with plasma modification prior to flotation, which is consistent with the contact angle measurement. Finally, the plasma-modification mechanisms of hydrophobicity of cathode and anode active materials were discussed according to Fourier Transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) analyses. The proposed method could be a promising tool to enhance the flotation separation efficiency of cathode and anode active materials for the recycling of spent LIBs.


Subject(s)
Electric Power Supplies , Electrodes , Hydrophobic and Hydrophilic Interactions , Lithium , Recycling , Lithium/chemistry , Recycling/methods , Photoelectron Spectroscopy , Spectroscopy, Fourier Transform Infrared , Electronic Waste
8.
Chemosphere ; 360: 142325, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38754489

ABSTRACT

Enhancing the kinetic performance of thick electrodes is essential for improving the efficiency of lithium extraction processes. Biochar, known for its affordability and unique three-dimensional (3D) structure, is utilized across various applications. In this study, we developed a biochar-based, 3D-conductive network thick electrode (∼20 mg cm-2) by in-situ deposition of LiFePO4 (LFP) onto watermelon peel biomass (WB). Utilizing Density Functional Theory (DFT) calculations complemented by experimental data, we confirmed that this The thick electrode exhibits outstanding kinetic properties and a high capacity for lithium intercalation in brines, even in environments where the Magnesia-lithium ratios are significantly high. The electrode showed an impressive intercalation capacity of 30.67 mg g-1 within 10 min in a pure lithium solution. It also maintained high intercalation performance (31.17 mg g-1) in simulated brines with high Magnesia-lithium ratios. Moreover, in actual brine, it demonstrated a significant extraction capacity (23.87 mg g-1), effectively lowering the Magnesia-lithium ratio from 65 to 0.50. This breakthrough in high-conductivity thick electrode design offers new perspectives for lithium extraction technologies.


Subject(s)
Charcoal , Electrodes , Lithium , Lithium/chemistry , Lithium/isolation & purification , Charcoal/chemistry , Lakes/chemistry , Magnesium/chemistry , Citrullus/chemistry , Salts/chemistry , Water Pollutants, Chemical/chemistry , Water Pollutants, Chemical/analysis , Kinetics , Iron , Phosphates
9.
J Environ Manage ; 359: 120963, 2024 May.
Article in English | MEDLINE | ID: mdl-38728980

ABSTRACT

An efficient recycling process is developed to recover valuable materials from overhaul slag and reduce its harm to the ecological environment. The high temperature sulfuric acid roasting - water leaching technology is innovatively proposed to prepare Li2CO3 from overhaul slag. Under roasting conditions, fluorine volatilizes into the flue gas with HF, lithium is transformed into NaLi(SO4), aluminum is firstly transformed into NaAl(SO4)2, and then decomposed into Al2O3, so as to selective extraction of lithium. Under the optimal roasting - leaching conditions, the leaching rate of lithium and aluminum are 95.6% and 0.9%, respectively. Then the processes of impurity removal, and settling lithium are carried out. The Li2CO3 with recovery rate of 72.6% and purity of 98.6% could be obtained under the best settling lithium conditions. Compared with the traditional process, this work has short flow, high controllability, remarkable technical, economic, and environmental benefits. This comprehensive recycling technology is suitable for overhaul slag, and has great practical application potential for the disposal of other hazardous wastes in electrolytic aluminum industry.


Subject(s)
Lithium Carbonate , Recycling , Sulfuric Acids , Sulfuric Acids/chemistry , Recycling/methods , Lithium Carbonate/chemistry , Aluminum/chemistry , Lithium/chemistry , Water/chemistry
10.
EBioMedicine ; 104: 105161, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38772282

ABSTRACT

BACKGROUND: Bipolar disorder (BD) is a multifactorial psychiatric illness affecting ∼1% of the global adult population. Lithium (Li), is the most effective mood stabilizer for BD but works only for a subset of patients and its mechanism of action remains largely elusive. METHODS: In the present study, we used iPSC-derived neurons from patients with BD who are responsive (LR) or not (LNR) to lithium. Combined electrophysiology, calcium imaging, biochemistry, transcriptomics, and phosphoproteomics were employed to provide mechanistic insights into neuronal hyperactivity in BD, investigate Li's mode of action, and identify alternative treatment strategies. FINDINGS: We show a selective rescue of the neuronal hyperactivity phenotype by Li in LR neurons, correlated with changes to Na+ conductance. Whole transcriptome sequencing in BD neurons revealed altered gene expression pathways related to glutamate transmission, alterations in cell signalling and ion transport/channel activity. We found altered Akt signalling as a potential therapeutic effect of Li in LR neurons from patients with BD, and that Akt activation mimics Li effect in LR neurons. Furthermore, the increased neural network activity observed in both LR & LNR neurons from patients with BD were reversed by AMP-activated protein kinase (AMPK) activation. INTERPRETATION: These results suggest potential for new treatment strategies in BD, such as Akt activators in LR cases, and the use of AMPK activators for LNR patients with BD. FUNDING: Supported by funding from ERA PerMed, Bell Brain Canada Mental Research Program and Brain & Behavior Research Foundation.


Subject(s)
AMP-Activated Protein Kinases , Bipolar Disorder , Induced Pluripotent Stem Cells , Neurons , Proto-Oncogene Proteins c-akt , Bipolar Disorder/metabolism , Bipolar Disorder/drug therapy , Humans , Neurons/metabolism , AMP-Activated Protein Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Induced Pluripotent Stem Cells/metabolism , Induced Pluripotent Stem Cells/cytology , Lithium/pharmacology , Lithium/therapeutic use , Signal Transduction , Gene Expression Profiling , Transcriptome
11.
Talanta ; 276: 126177, 2024 Aug 15.
Article in English | MEDLINE | ID: mdl-38718643

ABSTRACT

A novel sample double dilution calibration method (SDDCM) and an automatic flow system with in-syringe reaction and spectrophotometric detection were developed for determining lithium in biological samples. The method is based on the reaction of lithium with Thorin in an alkaline medium and the signal was measured at 480 nm. The reaction was performed simultaneously for both standards and samples in three syringes of the automatic flow system. The method was validated and successfully applied to the determination of lithium in synthetic and pharmaceutical samples, with results consistent with the ICP OES method. The novel calibration method, developed for the determination of lithium in biological samples, uses a sample with two dilution degrees. Using the method, the concentration of the analyte is determined by relating the signal for a less diluted sample to the calibration plot for a more diluted sample and vice versa. The implementation of the calibration method was facilitated by preparing solutions directly in the flow system. The use of two sample dilutions makes it possible to determine the analyte in the sample without preliminary preparation. Moreover, obtaining two results based on signals for a sample diluted to different degrees allows them to be verified for accuracy. The proposed approach was successfully verified by the determination of lithium in certified reference materials of blood serum and urine. Using the developed method lithium was determined within the concentration range of 0.06-1.5 mg L-1, with precision (CV, %) less than 6.7, and accuracy (RE, %) better than 6.9. The detection limit was 0.03 mg L-1.


Subject(s)
Lithium , Syringes , Calibration , Lithium/blood , Lithium/chemistry , Humans , Automation , Spectrophotometry/methods , Limit of Detection
12.
Biomed Phys Eng Express ; 10(4)2024 May 22.
Article in English | MEDLINE | ID: mdl-38744248

ABSTRACT

Evaluating neutron output is important to ensure proper dose delivery for patients in boron neutron capture therapy (BNCT). It requires efficient quality assurance (QA) and quality control (QC) while maintaining measurement accuracy. This study investigated the optimal measurement conditions for QA/QC of activation measurements using a high-purity germanium (HP-Ge) detector in an accelerator-based boron neutron capture therapy (AB-BNCT) system employing a lithium target. The QA/QC uncertainty of the activation measurement was evaluated based on counts, reproducibility, and standard radiation source uncertainties. Measurements in a polymethyl methacrylate (PMMA) cylindrical phantom using aluminum-manganese (Al-Mn) foils and aluminum-gold (Al-Au) foils and measurements in a water phantom using gold wire with and without cadmium cover were performed to determine the optimal measurement conditions. The QA/QC uncertainties of the activation measurements were 4.5% for Au and 4.6% for Mn. The optimum irradiation proton charge and measurement time were determined to be 36 C and 900 s for measurements in a PMMA cylindrical phantom, 7.0 C and 900 s for gold wire measurements in a water phantom, and 54 C and 900 s at 0-2.2 cm depth and 3,600 s at deeper depths for gold wire measurements with cadmium cover. Our results serve as a reference for determining measurement conditions when performing QA/QC of activation measurements using HP-Ge detectors at an AB-BNCT employing a lithium target.


Subject(s)
Boron Neutron Capture Therapy , Lithium , Particle Accelerators , Phantoms, Imaging , Quality Control , Lithium/chemistry , Boron Neutron Capture Therapy/methods , Humans , Particle Accelerators/instrumentation , Reproducibility of Results , Polymethyl Methacrylate/chemistry , Neutrons , Gold/chemistry , Aluminum/chemistry , Water/chemistry , Radiometry/methods , Radiometry/instrumentation , Radiotherapy Dosage
14.
Ther Drug Monit ; 46(3): 281-284, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38723114

ABSTRACT

ABSTRACT: This is a case description of a patient with bipolar disorder undergoing lithium therapy who received plasmapheresis for neuromyelitis optica spectrum disorder. Plasmapheresis resulted in lower and subtherapeutic serum lithium levels. Using therapeutic drug monitoring, a dose escalation of 80% was necessary to maintain therapeutic serum lithium levels. This underscores the importance of individualized therapy through therapeutic drug monitoring.


Subject(s)
Bipolar Disorder , Drug Monitoring , Neuromyelitis Optica , Plasmapheresis , Humans , Plasmapheresis/methods , Bipolar Disorder/therapy , Bipolar Disorder/blood , Neuromyelitis Optica/therapy , Neuromyelitis Optica/blood , Drug Monitoring/methods , Female , Lithium/blood , Lithium/therapeutic use , Intensive Care Units , Antimanic Agents/therapeutic use , Antimanic Agents/blood , Adult , Middle Aged
15.
Gen Physiol Biophys ; 43(3): 263-271, 2024 May.
Article in English | MEDLINE | ID: mdl-38774925

ABSTRACT

Lithium (Li) is a mood-stabilizing drug. Although one of the potential mechanisms underlying the neuroprotective effects of lithium is related to its antioxidative effect, its mechanisms of action are not fully understood. Herein we aimed to investigate the impact of varied dosages of long-term lithium therapy on oxidative stress parameters in the brains of healthy rats, and on anxiety-like behaviors, and whether any changes in behavior can be attributed to modifications in oxidative stress levels within the brain. Thirty-two adult Wistar albino male rats were randomly assigned to four treatment groups. While the control (C) group was fed with a standard diet, low Li (1.4 g/kg/diet), moderate Li (1.8 g/kg/diet), and high Li (2.2 g/kg/diet) groups were fed with lithium bicarbonate (Li2CO3) for 30 days. Malondialdehyde increased, while superoxide dismutase and catalase levels decreased in the brains of the high Li group animals. In addition, anxiety-like behaviors of animals increased in the high Li group considering fewer entries to and less time spent in the open arms of the elevated plus maze test. Our findings underscore the potential adverse effects of prolonged lithium treatment, especially at doses approaching the upper therapeutic range. The induction of toxicity, manifested through heightened oxidative stress, appears to be a key mechanism contributing to the observed increase in anxiety-like behaviors. Consequently, caution is warranted when considering extended lithium therapy at higher doses, emphasizing the need for further research to delineate the precise mechanisms underlying these effects and to inform safer therapeutic practices.


Subject(s)
Anxiety , Brain , Dose-Response Relationship, Drug , Oxidative Stress , Rats, Wistar , Animals , Oxidative Stress/drug effects , Male , Rats , Anxiety/chemically induced , Anxiety/drug therapy , Brain/drug effects , Brain/metabolism , Lithium/pharmacology , Lithium/administration & dosage , Behavior, Animal/drug effects , Drug Administration Schedule , Lithium Compounds/pharmacology , Lithium Compounds/administration & dosage
16.
Epidemiol Psychiatr Sci ; 33: e31, 2024 May 23.
Article in English | MEDLINE | ID: mdl-38779809

ABSTRACT

AIMS: Accumulating studies have assessed mortality risk associated with mood-stabilizers, the mainstay treatment for bipolar disorder (BD). However, existing data were mostly restricted to suicide risk, focused on lithium and valproate and rarely adequately adjusted for potential confounders. This study aimed to assess comparative mortality risk with all, natural and unnatural causes between lithium, valproate and three frequently prescribed second-generation antipsychotics (SGA), with adjustment for important confounders. METHODS: This population-based cohort study identified 8137 patients with first-diagnosed BD, who had exposed to lithium (n = 1028), valproate (n = 3580), olanzapine (n = 797), quetiapine (n = 1975) or risperidone (n = 757) between 2002 and 2018. Data were retrieved from territory-wide medical-record database of public healthcare services in Hong Kong. Propensity-score (PS)-weighting method was applied to optimize control for potential confounders including pre-existing chronic physical diseases, substance/alcohol use disorders and other psychotropic medications. PS-weighted Cox proportional-hazards regression was conducted to assess risk of all-, natural- and unnatural-cause mortality related to each mood-stabilizer, compared to lithium. Three sets of sensitivity analyses were conducted by restricting to patients with (i) length of cumulative exposure to specified mood-stabilizer ≥90 days and its medication possession ratio (MPR) ≥90%, (ii) MPR of specified mood-stabilizer ≥80% and MPR of other studied mood-stabilizers <20% and (iii) monotherapy. RESULTS: Incidence rates of all-cause mortality per 1000 person-years were 5.9 (95% confidence interval [CI]: 4.5-7.6), 8.4 (7.4-9.5), 11.1 (8.3-14.9), 7.4 (6.0-9.2) and 12.0 (9.3-15.6) for lithium-, valproate-, olanzapine-, quetiapine- and risperidone-treated groups, respectively. BD patients treated with olanzapine (PS-weighted hazard ratio = 2.07 [95% CI: 1.33-3.22]) and risperidone (1.66 [1.08-2.55]) had significantly higher all-cause mortality rate than lithium-treated group. Olanzapine was associated with increased risk of natural-cause mortality (3.04 [1.54-6.00]) and risperidone was related to elevated risk of unnatural-cause mortality (3.33 [1.62-6.86]), relative to lithium. The association between olanzapine and increased natural-cause mortality rate was consistently affirmed in sensitivity analyses. Relationship between risperidone and elevated unnatural-cause mortality became non-significant in sensitivity analyses restricted to low MPR in other mood-stabilizers and monotherapy. Valproate- and lithium-treated groups did not show significant differences in all-, natural- or unnatural-cause mortality risk. CONCLUSION: Our data showed that olanzapine and risperidone were associated with higher mortality risk than lithium, and further supported the clinical guidelines recommending lithium as the first-line mood-stabilizer for BD. Future research is required to further clarify comparative mortality risk associated with individual SGA agents to facilitate risk-benefit evaluation of alternative mood-stabilizers to minimize avoidable premature mortality in BD.


Subject(s)
Antimanic Agents , Antipsychotic Agents , Bipolar Disorder , Propensity Score , Quetiapine Fumarate , Valproic Acid , Humans , Bipolar Disorder/drug therapy , Bipolar Disorder/mortality , Antipsychotic Agents/therapeutic use , Antipsychotic Agents/adverse effects , Female , Male , Adult , Middle Aged , Valproic Acid/therapeutic use , Antimanic Agents/therapeutic use , Cohort Studies , Quetiapine Fumarate/therapeutic use , Quetiapine Fumarate/adverse effects , Olanzapine/therapeutic use , Hong Kong/epidemiology , Risperidone/therapeutic use , Risperidone/adverse effects , Lithium/therapeutic use , Cause of Death
17.
Sci Rep ; 14(1): 11253, 2024 05 16.
Article in English | MEDLINE | ID: mdl-38755333

ABSTRACT

Accelerator-based boron neutron capture therapy (BNCT) systems employing a solid-state lithium target indicated the reduction of neutron flux over the lifetime of a target, and its reduction could represent the neutron flux model. This study proposes a novel compensatory approach for delivering the required neutron fluence and validates its clinical applicability. The proposed approach relies on the neutron flux model and the cumulative sum of real-time measurements of proton charges. The accuracy of delivering the required neutron fluence for BNCT using the proposed approach was examined in five Li targets. With the proposed approach, the required neutron fluence could be delivered within 3.0%, and within 1.0% in most cases. However, those without using the proposed approach exceeded 3.0% in some cases. The proposed approach can consider the neutron flux reduction adequately and decrease the effect of uncertainty in neutron measurements. Therefore, the proposed approach can improve the accuracy of delivering the required fluence for BNCT even if a neutron flux reduction is expected during treatment and over the lifetime of the Li target. Additionally, by adequately revising the approach, it may apply to other type of BNCT systems employing a Li target, furthering research in this direction.


Subject(s)
Boron Neutron Capture Therapy , Lithium , Neutrons , Boron Neutron Capture Therapy/methods , Lithium/chemistry , Humans , Particle Accelerators , Radiotherapy Dosage
18.
J Cell Mol Med ; 28(10): e18385, 2024 May.
Article in English | MEDLINE | ID: mdl-38801405

ABSTRACT

Autophagy may play an important role in the occurrence and development of glucocorticoid-induced osteonecrosis of the femoral head (GC-ONFH). Lithium is a classical autophagy regulator, and lithium can also activate osteogenic pathways, making it a highly promising therapeutic agent for GC-ONFH. We aimed to evaluate the potential therapeutic effect of lithium on GC-ONFH. For in vitro experiments, primary osteoblasts of rats were used for investigating the underlying mechanism of lithium's protective effect on GC-induced autophagy levels and osteogenic activity dysfunction. For in vivo experiments, a rat model of GC-ONFH was used for evaluating the therapeutic effect of oral lithium on GC-ONFH and underlying mechanism. Findings demonstrated that GC over-activated the autophagy of osteoblasts and reduced their osteogenic activity. Lithium reduced the over-activated autophagy of GC-treated osteoblasts through PI3K/AKT/mTOR signalling pathway and increased their osteogenic activity. Oral lithium reduced the osteonecrosis rates in a rat model of GC-ONFH, and restrained the increased expression of autophagy related proteins in bone tissues through PI3K/AKT/mTOR signalling pathway. In conclusion, lithium can restrain over-activated autophagy by activating PI3K/AKT/mTOR signalling pathway and up-regulate the expression of genes for bone formation both in GC induced osteoblasts and in a rat model of GC-ONFH. Lithium may be a promising therapeutic agent for GC-ONFH. However, the role of autophagy in the pathogenesis of GC-ONFH remains controversial. Studies are still needed to further explore the role of autophagy in the pathogenesis of GC-ONFH, and the efficacy of lithium in the treatment of GC-ONFH and its underlying mechanisms.


Subject(s)
Autophagy , Femur Head Necrosis , Glucocorticoids , Lithium , Osteoblasts , Signal Transduction , TOR Serine-Threonine Kinases , Animals , Autophagy/drug effects , Glucocorticoids/pharmacology , Glucocorticoids/adverse effects , Rats , Femur Head Necrosis/chemically induced , Femur Head Necrosis/pathology , Femur Head Necrosis/drug therapy , Femur Head Necrosis/metabolism , TOR Serine-Threonine Kinases/metabolism , Signal Transduction/drug effects , Lithium/pharmacology , Osteoblasts/drug effects , Osteoblasts/metabolism , Male , Osteogenesis/drug effects , Rats, Sprague-Dawley , Proto-Oncogene Proteins c-akt/metabolism , Disease Models, Animal , Phosphatidylinositol 3-Kinases/metabolism , Femur Head/pathology , Femur Head/drug effects , Femur Head/metabolism , Osteonecrosis/chemically induced , Osteonecrosis/pathology , Osteonecrosis/drug therapy , Osteonecrosis/metabolism , Osteonecrosis/prevention & control
19.
Environ Sci Pollut Res Int ; 31(23): 34249-34257, 2024 May.
Article in English | MEDLINE | ID: mdl-38700765

ABSTRACT

In view of the importance of environmental protection and resource recovery, recycling of spent lithium ion batteries (LIBs) is quite necessary. In the present study, lithium and copper are recycled to lithium carbonate and copper oxide from anode electrode material of the spent LIBs. The anode electrode material is firstly treated with hydrochloric acid to leach lithium (96.6%) and then with nitric acid to leach copper (97.6%). Furthermore, lithium and copper are recovered as lithium carbonate and copper oxide from their respective solutions using precipitation and calcinations. These synthesized products are further characterized using XRD, FE-SEM, and EDX analysis. Finally, a simple process is proposed for the recovery of lithium and copper from anode electrode material of spent LIBs.


Subject(s)
Copper , Electrodes , Lithium , Lithium/chemistry , Copper/chemistry , Recycling , Electric Power Supplies
20.
J Affect Disord ; 358: 416-421, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38735581

ABSTRACT

BACKGROUND: The therapeutic response to lithium in patients with bipolar disorder is highly variable and has a polygenic basis. Genome-wide association studies investigating lithium response have identified several relevant loci, though the precise mechanisms driving these associations are poorly understood. We aimed to prioritise the most likely effector gene and determine the mechanisms underlying an intergenic lithium response locus on chromosome 21 identified by the International Consortium on Lithium Genetics (ConLi+Gen). METHODS: We conducted in-silico functional analyses by integrating and synthesising information from several publicly available functional genetic datasets and databases including the Genotype-Tissue Expression (GTEx) project and HaploReg. RESULTS: The findings from this study highlighted TMPRSS15 as the most likely effector gene at the ConLi+Gen lithium response locus. TMPRSS15 encodes enterokinase, a gastrointestinal enzyme responsible for converting trypsinogen into trypsin and thus aiding digestion. Convergent findings from gene-based lookups in human and mouse databases as well as co-expression network analyses of small intestinal RNA-seq data (GTEx) implicated TMPRSS15 in the regulation of intestinal nutrient absorption, including ions like sodium and potassium, which may extend to lithium. LIMITATIONS: Although the findings from this study indicated that TMPRSS15 was the most likely effector gene at the ConLi+Gen lithium response locus, the evidence was circumstantial. Thus, the conclusions from this study need to be validated in appropriately designed wet-lab studies. CONCLUSIONS: The findings from this study are consistent with a model whereby TMPRSS15 impacts the efficacy of lithium treatment in patients with bipolar disorder by modulating intestinal lithium absorption.


Subject(s)
Bipolar Disorder , Computer Simulation , Intestinal Absorption , Serine Endopeptidases , Bipolar Disorder/drug therapy , Bipolar Disorder/genetics , Bipolar Disorder/metabolism , Humans , Intestinal Absorption/drug effects , Serine Endopeptidases/genetics , Serine Endopeptidases/metabolism , Mice , Animals , Membrane Proteins/genetics , Membrane Proteins/metabolism , Lithium/therapeutic use , Lithium/pharmacology , Antimanic Agents/pharmacology , Antimanic Agents/therapeutic use , Genome-Wide Association Study , Lithium Compounds/pharmacology , Lithium Compounds/therapeutic use , Lithium Compounds/pharmacokinetics
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