首页 > 最新文献

SLAS Technology最新文献

英文 中文
Construction of a nomogram prediction model for screening of serum markers for lower extremity vasculopathy secondary to type 2 diabetes mellitus 2型糖尿病继发下肢血管病变血清标志物Nomogram预测模型的建立
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-09-19 DOI: 10.1016/j.slast.2025.100352
Jingjing Yang , Jinyan Chen , Lanying Shen

Objective

To screen serum markers for secondary lower extremity angiopathy (LEAD) in patients with type 2 diabetes mellitus (T2DM) and construct a nomogram prediction model accordingly.

Methods

The clinical data of 200 T2DM patients admitted to the hospital from December 2022 to October 2024 were retrospectively collected. It was also divided into modeling group (n = 160) and internal validation group (n = 40) in a 4:1 ratio by using the leave-out method. As the external validation group, clinical data from 100 T2DM patients who were admitted to other hospitals within the same time period were also gathered. Combined with previous reports of collecting serum marker data related to LEAD secondary to T2DM, key serum markers were screened using LASSO regression. Moreover, multifactorial analysis helped to clarify independent risk factors, and a nomogram prediction model was built and tested for accuracy.

Results

The incidence of LEAD in 200 T2DM patients in the hospital was 21.00 % (42/200). A total of 14 variables were screened by LASSO regression analysis. After multifactorial analysis, it was found that disease duration, history of alcohol consumption, mean platelet volume, fasting blood glucose, fibrinogen, high-sensitivity C-reactive protein, insulin-like growth factor 1, nucleotide binding oligomerization domain like receptor protein 3 were independent risk factors for LEAD secondary to T2DM.The results of model validation showed AUCs of 0.971, 0.900, and 0.959 for the modeling cohort, internal validation cohort, and external validation cohort, respectively. The Hosmer-Lemeshow test was χ2=6.607, 7.962, and 6.585 (p > 0.05). Positive net benefits were obtained by intervening with patients using a nomogram model within the high-risk threshold of 0 to 0.9.

Conclusion

In this study, eight risk factors associated with LEAD secondary to T2DM are screened by LASSO regression and multifactorial analysis, and a nomogram prediction model is constructed.
目的:筛选2型糖尿病(T2DM)患者继发性下肢血管病变(LEAD)的血清标志物,并建立相应的nomogram预测模型。方法:回顾性收集2022年12月至2024年10月我院收治的200例T2DM患者的临床资料。采用省略法将其按4:1的比例分为建模组(n=160)和内部验证组(n=40)。作为外部验证组,收集同期在其他医院住院的100例T2DM患者的临床资料。结合以往报告收集的与T2DM继发铅相关的血清标志物数据,使用LASSO回归筛选关键血清标志物。此外,多因素分析有助于明确独立的危险因素,并建立了一个nomogram预测模型,并对其准确性进行了检验。结果:该院200例T2DM患者中铅的发生率为21.00%(42/200)。LASSO回归分析共筛选了14个变量。经多因素分析,发现病程、饮酒史、平均血小板体积、空腹血糖、纤维蛋白原、高敏c反应蛋白、胰岛素样生长因子1、核苷酸结合寡聚化结构域样受体蛋白3是T2DM继发铅的独立危险因素。模型验证结果显示,建模队列、内部验证队列和外部验证队列的auc分别为0.971、0.900和0.959。Hosmer-Lemeshow检验的χ2分别为6.607、7.962、6.585 (p < 0.05)。使用nomogram模型在0 - 0.9的高风险阈值范围内对患者进行干预,获得了正的净收益。结论:本研究通过LASSO回归和多因素分析筛选出8个与2型糖尿病继发铅相关的危险因素,并构建了nomogram预测模型。
{"title":"Construction of a nomogram prediction model for screening of serum markers for lower extremity vasculopathy secondary to type 2 diabetes mellitus","authors":"Jingjing Yang ,&nbsp;Jinyan Chen ,&nbsp;Lanying Shen","doi":"10.1016/j.slast.2025.100352","DOIUrl":"10.1016/j.slast.2025.100352","url":null,"abstract":"<div><h3>Objective</h3><div>To screen serum markers for secondary lower extremity angiopathy (LEAD) in patients with type 2 diabetes mellitus (T2DM) and construct a nomogram prediction model accordingly.</div></div><div><h3>Methods</h3><div>The clinical data of 200 T2DM patients admitted to the hospital from December 2022 to October 2024 were retrospectively collected. It was also divided into modeling group (<em>n</em> = 160) and internal validation group (<em>n</em> = 40) in a 4:1 ratio by using the leave-out method. As the external validation group, clinical data from 100 T2DM patients who were admitted to other hospitals within the same time period were also gathered. Combined with previous reports of collecting serum marker data related to LEAD secondary to T2DM, key serum markers were screened using LASSO regression. Moreover, multifactorial analysis helped to clarify independent risk factors, and a nomogram prediction model was built and tested for accuracy.</div></div><div><h3>Results</h3><div>The incidence of LEAD in 200 T2DM patients in the hospital was 21.00 % (42/200). A total of 14 variables were screened by LASSO regression analysis. After multifactorial analysis, it was found that disease duration, history of alcohol consumption, mean platelet volume, fasting blood glucose, fibrinogen, high-sensitivity C-reactive protein, insulin-like growth factor 1, nucleotide binding oligomerization domain like receptor protein 3 were independent risk factors for LEAD secondary to T2DM.The results of model validation showed AUCs of 0.971, 0.900, and 0.959 for the modeling cohort, internal validation cohort, and external validation cohort, respectively. The Hosmer-Lemeshow test was <em>χ<sup>2</sup></em>=6.607, 7.962, and 6.585 (<em>p</em> &gt; 0.05). Positive net benefits were obtained by intervening with patients using a nomogram model within the high-risk threshold of 0 to 0.9.</div></div><div><h3>Conclusion</h3><div>In this study, eight risk factors associated with LEAD secondary to T2DM are screened by LASSO regression and multifactorial analysis, and a nomogram prediction model is constructed.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100352"},"PeriodicalIF":3.7,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145115029","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Low code, high impact: Application of low-code platforms to enable and democratize the development of laboratory digitalization and automation applications 低代码,高影响:低代码平台的应用,使实验室数字化和自动化应用的发展民主化。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-09-19 DOI: 10.1016/j.slast.2025.100353
Jonas Austerjost , Elias Knöchelmann , Thomas Kruse , Janina Kilian , Bastian Quaas , Michael W. Olszowy
Conventionally, the initialization of new prototypes and concepts in laboratory automation and life science software applications has required close collaboration between hardware and software experts, as well as lab personnel such as biologists, chemists, biotechnologists, or process engineers. This setup - still common today - often means that the ideas and requests of lab personnel must be translated into software applications by software developers, which frequently results in long development times. Low-Code Development Platforms (LCDPs) seek to address this challenge by providing a way to accelerate application development by reducing dependence on traditional software development methods, empowering lab personnel to build applications without writing extensive amount of code. By offering a visual, drag-and-drop interface, lab personnel can actively participate in the software development process. This helps democratize application creation and can lead to the quick setup of software solutions tailored to laboratory needs.
This study demonstrates the implementation of four different use cases in a bioprocessing laboratory environment using an open-source LCDP and commercially available upstream and downstream equipment. The LCDP facilitated the integration and control of different device types with varying communication protocols also enabling dashboarding, monitoring and data processing capabilities. This methodology highlights the suitability of LCDPs for rapidly prototyping and evaluating laboratory and bioprocess automation pipelines, potentially expediting the development of biotechnological production processes and products. All developed components are made available through a publicly accessible repository, facilitating reuse and further development by the scientific community.
通常,在实验室自动化和生命科学软件应用中,新原型和概念的初始化需要硬件和软件专家之间的密切合作,以及生物学家、化学家、生物技术专家或过程工程师等实验室人员。这种设置——今天仍然很常见——通常意味着实验室人员的想法和要求必须由软件开发人员转化为软件应用程序,这经常导致较长的开发时间。低代码开发平台(LCDPs)通过提供一种方法来减少对传统软件开发方法的依赖,从而加速应用程序开发,使实验室人员无需编写大量代码即可构建应用程序,从而寻求解决这一挑战。通过提供可视化的拖放界面,实验室人员可以积极地参与软件开发过程。这有助于实现应用程序创建的民主化,并可以快速设置适合实验室需求的软件解决方案。本研究演示了在生物处理实验室环境中使用开源LCDP和商用上游和下游设备的四种不同用例的实现。通过不同的通信协议,LCDP促进了不同设备类型的集成和控制,还实现了仪表板、监控和数据处理功能。该方法强调了LCDPs用于快速原型设计和评估实验室和生物过程自动化管道的适用性,潜在地加快了生物技术生产过程和产品的开发。所有开发的组件都可以通过一个公开访问的存储库获得,从而促进科学界的重用和进一步开发。
{"title":"Low code, high impact: Application of low-code platforms to enable and democratize the development of laboratory digitalization and automation applications","authors":"Jonas Austerjost ,&nbsp;Elias Knöchelmann ,&nbsp;Thomas Kruse ,&nbsp;Janina Kilian ,&nbsp;Bastian Quaas ,&nbsp;Michael W. Olszowy","doi":"10.1016/j.slast.2025.100353","DOIUrl":"10.1016/j.slast.2025.100353","url":null,"abstract":"<div><div>Conventionally, the initialization of new prototypes and concepts in laboratory automation and life science software applications has required close collaboration between hardware and software experts, as well as lab personnel such as biologists, chemists, biotechnologists, or process engineers. This setup - still common today - often means that the ideas and requests of lab personnel must be translated into software applications by software developers, which frequently results in long development times. Low-Code Development Platforms (LCDPs) seek to address this challenge by providing a way to accelerate application development by reducing dependence on traditional software development methods, empowering lab personnel to build applications without writing extensive amount of code. By offering a visual, drag-and-drop interface, lab personnel can actively participate in the software development process. This helps democratize application creation and can lead to the quick setup of software solutions tailored to laboratory needs.</div><div>This study demonstrates the implementation of four different use cases in a bioprocessing laboratory environment using an open-source LCDP and commercially available upstream and downstream equipment. The LCDP facilitated the integration and control of different device types with varying communication protocols also enabling dashboarding, monitoring and data processing capabilities. This methodology highlights the suitability of LCDPs for rapidly prototyping and evaluating laboratory and bioprocess automation pipelines, potentially expediting the development of biotechnological production processes and products. All developed components are made available through a publicly accessible repository, facilitating reuse and further development by the scientific community.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100353"},"PeriodicalIF":3.7,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145114986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-step purification and formulation of antibody-drug conjugates using a miniaturized tangential flow filtration system 使用小型切向流过滤系统的抗体-药物偶联物单步纯化和配方
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-09-19 DOI: 10.1016/j.slast.2025.100351
Muhammad Sajed , Zahoor Khan , Muhammad Usman Ashraf , Hafsa Iftikhar , Talha Bin Rahat , Samia Falak , Salman Fozail , Quiterie Gue , Raul Pardo , Lance Ramsey , Muhammad Saqib Shahzad
Antibody-drug conjugates (ADCs) are a promising therapeutic modality that enables the delivery of cytotoxic drugs to the target cells that express the corresponding antigen. However, the purification of ADCs while ensuring product safety, homogeneity, and stability is a challenging task due to their complex and fragile structure. Size exclusion chromatography (SEC), the conventional method for ADC purification, is time-consuming as it requires multiple column washes and equilibration steps. Moreover, subsequent formulation of ADCs, typically using dead-end filtration (DEF), further complicates the production workflow. We compared SEC+DEF with the µPulse®, a miniaturized and automated tangential flow filtration system, for purification and formulation of ADCs. Quality analysis revealed that both approaches were equally gentle as comparable drug-to-antibody ratios (DARs) and monomer purities were observed in the purified samples. Most importantly, both methods exhibited equivalent cleanup efficiency with a 99.8% reduction in free linker-drug concentration. The endotoxin loads comprised 0.11 EU mg-1 for the µPulse and 0.07 EU mg-1 for SEC+DEF, ensuring validation of the safe application of purified ADCs in living systems. However, the µPulse performed purification and formulation of ADCs simultaneously as compared to SEC+DEF, which required multiple manual interventions. Our results indicate that the µPulse is a gentle, single-step, and walk-away approach for the purification of ADCs.
抗体-药物偶联物(adc)是一种很有前途的治疗方式,可以将细胞毒性药物传递到表达相应抗原的靶细胞。然而,由于adc结构复杂和脆弱,在保证产品安全性、均匀性和稳定性的同时进行纯化是一项具有挑战性的任务。粒径排除色谱法(SEC)是ADC的常规纯化方法,由于需要多次清洗柱和平衡步骤,因此非常耗时。此外,adc的后续配方通常使用终端过滤(DEF),这进一步复杂化了生产流程。我们将SEC+DEF与µPulse®进行了比较,µPulse®是一种小型化、自动化的切向流过滤系统,用于adc的纯化和配方。质量分析表明,这两种方法都同样温和,因为在纯化的样品中观察到类似的药物-抗体比率(dar)和单体纯度。最重要的是,两种方法的清除效率相当,游离连接剂浓度降低99.8%。µPulse的内毒素负荷为0.11 EU mg-1, SEC+DEF的内毒素负荷为0.07 EU mg-1,确保了纯化adc在生命系统中的安全应用。然而,与SEC+DEF相比,µPulse可以同时进行adc的纯化和配制,后者需要多次人工干预。我们的研究结果表明,µPulse是一种温和的、单步的、走开的adc纯化方法。
{"title":"Single-step purification and formulation of antibody-drug conjugates using a miniaturized tangential flow filtration system","authors":"Muhammad Sajed ,&nbsp;Zahoor Khan ,&nbsp;Muhammad Usman Ashraf ,&nbsp;Hafsa Iftikhar ,&nbsp;Talha Bin Rahat ,&nbsp;Samia Falak ,&nbsp;Salman Fozail ,&nbsp;Quiterie Gue ,&nbsp;Raul Pardo ,&nbsp;Lance Ramsey ,&nbsp;Muhammad Saqib Shahzad","doi":"10.1016/j.slast.2025.100351","DOIUrl":"10.1016/j.slast.2025.100351","url":null,"abstract":"<div><div>Antibody-drug conjugates (ADCs) are a promising therapeutic modality that enables the delivery of cytotoxic drugs to the target cells that express the corresponding antigen. However, the purification of ADCs while ensuring product safety, homogeneity, and stability is a challenging task due to their complex and fragile structure. Size exclusion chromatography (SEC), the conventional method for ADC purification, is time-consuming as it requires multiple column washes and equilibration steps. Moreover, subsequent formulation of ADCs, typically using dead-end filtration (DEF), further complicates the production workflow. We compared SEC+DEF with the µPulse®, a miniaturized and automated tangential flow filtration system, for purification and formulation of ADCs. Quality analysis revealed that both approaches were equally gentle as comparable drug-to-antibody ratios (DARs) and monomer purities were observed in the purified samples. Most importantly, both methods exhibited equivalent cleanup efficiency with a 99.8% reduction in free linker-drug concentration. The endotoxin loads comprised 0.11 EU mg<sup>-1</sup> for the µPulse and 0.07 EU mg<sup>-1</sup> for SEC+DEF, ensuring validation of the safe application of purified ADCs in living systems. However, the µPulse performed purification and formulation of ADCs simultaneously as compared to SEC+DEF, which required multiple manual interventions. Our results indicate that the µPulse is a gentle, single-step, and walk-away approach for the purification of ADCs.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100351"},"PeriodicalIF":3.7,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145098086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
IoT-based approach for diabetes patient monitoring using machine learning 基于物联网的糖尿病患者机器学习监测方法
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-09-13 DOI: 10.1016/j.slast.2025.100348
Sarra Ayouni , Muhammad Hamza Khan , Muhammad Ibrahim , Mohamed Maddeh , Nadeem Sarwar , Nazik Alturki
This study presents an IoT-based framework for real-time diabetes monitoring and management, addressing key limitations identified in previous studies by integrating four datasets: BVH Dataset, PIMA Diabetes Dataset, Simulated Dataset, and an Integrated Dataset. The proposed approach ensures diverse demographic representation and a wide range of features including real-time vital signs (e.g., oxygen saturation, pulse rate, temperature) and subjective variables (e.g., skin color, moisture, consciousness level). Advanced preprocessing techniques, including Kalman Filtering for noise reduction, KNN imputation for addressing missing data, and SMOTE-ENN for improving data quality and class balance, were employed. These methods resulted in a 25 % improvement in Recall and a 20 % increase in the F1-score, demonstrating the model's effectiveness and robustness.
By applying PCA and SHAP for feature engineering, high-impact features were identified, enabling the tuning of models such as Random Forest, SVM, and Logistic Regression, which achieved an accuracy of 97 % and an F1-score of 0.98. A novel triage system, integrated with edge and cloud computing, classifies health status in real-time (Green, Yellow, Red, Black), reducing latency by 35 %. The proposed system sets a new benchmark for scalable, individualized diabetes care in IoT-based healthcare solutions, demonstrating significant improvements in accuracy, response time, and feature incorporation compared to prior works.
本研究提出了一个基于物联网的糖尿病实时监测和管理框架,通过整合四个数据集:BVH数据集、PIMA糖尿病数据集、模拟数据集和集成数据集,解决了先前研究中发现的关键局限性。所提出的方法确保了多样化的人口统计学表征和广泛的特征,包括实时生命体征(例如,氧饱和度、脉搏率、温度)和主观变量(例如,肤色、湿度、意识水平)。采用了先进的预处理技术,包括用于降噪的卡尔曼滤波,用于寻寻缺失数据的KNN输入,以及用于提高数据质量和类平衡的SMOTE-ENN。这些方法使召回率提高了25%,f1得分提高了20%,证明了模型的有效性和稳健性。通过应用PCA和SHAP进行特征工程,识别出高影响特征,实现随机森林、支持向量机和Logistic回归等模型的调优,准确率达到97%,f1得分为0.98。一种新型的分类系统,集成了边缘和云计算,实时分类健康状态(绿色、黄色、红色、黑色),减少了35%的延迟。该系统为基于物联网的医疗保健解决方案中可扩展的个性化糖尿病护理设定了新的基准,与之前的工作相比,在准确性、响应时间和功能整合方面有了显着改善。
{"title":"IoT-based approach for diabetes patient monitoring using machine learning","authors":"Sarra Ayouni ,&nbsp;Muhammad Hamza Khan ,&nbsp;Muhammad Ibrahim ,&nbsp;Mohamed Maddeh ,&nbsp;Nadeem Sarwar ,&nbsp;Nazik Alturki","doi":"10.1016/j.slast.2025.100348","DOIUrl":"10.1016/j.slast.2025.100348","url":null,"abstract":"<div><div>This study presents an IoT-based framework for real-time diabetes monitoring and management, addressing key limitations identified in previous studies by integrating four datasets: BVH Dataset, PIMA Diabetes Dataset, Simulated Dataset, and an Integrated Dataset. The proposed approach ensures diverse demographic representation and a wide range of features including real-time vital signs (e.g., oxygen saturation, pulse rate, temperature) and subjective variables (e.g., skin color, moisture, consciousness level). Advanced preprocessing techniques, including Kalman Filtering for noise reduction, KNN imputation for addressing missing data, and SMOTE-ENN for improving data quality and class balance, were employed. These methods resulted in a 25 % improvement in Recall and a 20 % increase in the F1-score, demonstrating the model's effectiveness and robustness.</div><div>By applying PCA and SHAP for feature engineering, high-impact features were identified, enabling the tuning of models such as Random Forest, SVM, and Logistic Regression, which achieved an accuracy of 97 % and an F1-score of 0.98. A novel triage system, integrated with edge and cloud computing, classifies health status in real-time (Green, Yellow, Red, Black), reducing latency by 35 %. The proposed system sets a new benchmark for scalable, individualized diabetes care in IoT-based healthcare solutions, demonstrating significant improvements in accuracy, response time, and feature incorporation compared to prior works.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100348"},"PeriodicalIF":3.7,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145071195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High-throughput cytokine detection platform for evaluation of chemical induced microglial activation 评价化学诱导的小胶质细胞活化的高通量细胞因子检测平台。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-09-10 DOI: 10.1016/j.slast.2025.100347
Shu Yang , Kelly E. Carstens , Ibukunoluwa Ipaye , Xing Chen , Helena T. Hogberg , Nicole Kleinstreuer , Thomas B. Knudsen , Menghang Xia
Environmental chemical exposure, such as pesticides and heavy metals, may contribute to neurodegenerative disorders through neuroinflammation. This study aims to identify suitable in vitro microglial models for assessing cytokine responses to potential neurotoxicants, particularly focusing on human induced pluripotent stem cell-derived microglia (hiMG). In this study, we evaluated the cytokine secretion profiles of four microglial cell types—hiMG, HMC3, IM-HM, and BV2—upon stimulation with lipopolysaccharides (LPS) using cytokine arrays. Our findings showed cytokine response patterns in hiMG cells that most closely resemble in vivo conditions, with significant increases in interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-α) levels, the latter being uniquely expressed after LPS treatment. Consequently, we developed a homogeneous time-resolved fluorescence (HTRF) assay platform in a 1536-well plate format for high-throughput screening of environmental chemicals using hiMG cells. After LPS treatment, the assay window for secretion of IL-6 and TNF-α increased 3.71-fold and 2.62-fold over the vehicle control group, respectively, with respective EC50 values of approximately 50 ng/mL and 90 ng/mL for IL-6 and TNF-α. We also assessed the response activity of hiMG to other stimuli, including interferon gamma and various catecholamine compounds, and nine environmental chemicals with evidence of cytokine-inducing potential in other in vitro assays. While all nine tested agents stimulated IL-6 and TNF-α production, three compounds (e.g., picoxystrobin) showed significant stimulation of both cytokines. ​This study establishes a reliable high-throughput platform for detecting inflammatory effects of environmental toxicants in a microglial cell assay, contributing valuable insights into their neuroinflammatory potential and possible implications for neurodegenerative disorders.
环境中的化学物质暴露,如杀虫剂和重金属,可能通过神经炎症导致神经退行性疾病。本研究旨在确定合适的体外小胶质细胞模型,以评估细胞因子对潜在神经毒物的反应,特别是关注人诱导多能干细胞来源的小胶质细胞(hiMG)。在这项研究中,我们使用细胞因子阵列评估了四种小胶质细胞类型(himg, HMC3, IM-HM和bv2)在脂多糖(LPS)刺激下的细胞因子分泌谱。我们的研究结果显示,细胞因子在hiMG细胞中的反应模式与体内条件最相似,白细胞介素6 (IL-6)和肿瘤坏死因子α (TNF-α)水平显著升高,后者在LPS处理后唯一表达。因此,我们开发了1536孔板格式的均匀时间分辨荧光(htf)检测平台,用于使用hiMG细胞进行高通量筛选环境化学物质。LPS处理后,IL-6和TNF-α分泌的测定窗口分别比对照增加了3.71倍和2.62倍,IL-6和TNF-α的EC50值分别约为50 ng/mL和90 ng/mL。我们还评估了hiMG对其他刺激的反应活性,包括干扰素γ和各种儿茶酚胺化合物,以及在其他体外实验中具有细胞因子诱导潜力的九种环境化学物质。虽然所有九种被测试的药物都能刺激IL-6和TNF-α的产生,但三种化合物(如皮氧嘧啶)对这两种细胞因子都有显著的刺激作用。本研究建立了一个可靠的高通量平台,用于在小胶质细胞试验中检测环境毒物的炎症效应,为其神经炎症潜力和神经退行性疾病的可能含义提供了有价值的见解。
{"title":"High-throughput cytokine detection platform for evaluation of chemical induced microglial activation","authors":"Shu Yang ,&nbsp;Kelly E. Carstens ,&nbsp;Ibukunoluwa Ipaye ,&nbsp;Xing Chen ,&nbsp;Helena T. Hogberg ,&nbsp;Nicole Kleinstreuer ,&nbsp;Thomas B. Knudsen ,&nbsp;Menghang Xia","doi":"10.1016/j.slast.2025.100347","DOIUrl":"10.1016/j.slast.2025.100347","url":null,"abstract":"<div><div>Environmental chemical exposure, such as pesticides and heavy metals, may contribute to neurodegenerative disorders through neuroinflammation. This study aims to identify suitable <em>in vitro</em> microglial models for assessing cytokine responses to potential neurotoxicants, particularly focusing on human induced pluripotent stem cell-derived microglia (hiMG). In this study, we evaluated the cytokine secretion profiles of four microglial cell types—hiMG, HMC3, IM-HM, and BV2—upon stimulation with lipopolysaccharides (LPS) using cytokine arrays. Our findings showed cytokine response patterns in hiMG cells that most closely resemble <em>in vivo</em> conditions, with significant increases in interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-α) levels, the latter being uniquely expressed after LPS treatment. Consequently, we developed a homogeneous time-resolved fluorescence (HTRF) assay platform in a 1536-well plate format for high-throughput screening of environmental chemicals using hiMG cells. After LPS treatment, the assay window for secretion of IL-6 and TNF-α increased 3.71-fold and 2.62-fold over the vehicle control group, respectively, with respective EC<sub>50</sub> values of approximately 50 ng/mL and 90 ng/mL for IL-6 and TNF-α. We also assessed the response activity of hiMG to other stimuli, including interferon gamma and various catecholamine compounds, and nine environmental chemicals with evidence of cytokine-inducing potential in other <em>in vitro</em> assays. While all nine tested agents stimulated IL-6 and TNF-α production, three compounds (<em>e.g.</em>, picoxystrobin) showed significant stimulation of both cytokines. ​This study establishes a reliable high-throughput platform for detecting inflammatory effects of environmental toxicants in a microglial cell assay, contributing valuable insights into their neuroinflammatory potential and possible implications for neurodegenerative disorders.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100347"},"PeriodicalIF":3.7,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145056195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Staining Triad: A fully automated and zero-waste flow cytometry staining system fostering the 3R to 4R transition 三合一染色:一个全自动和零浪费的流式细胞术染色系统,促进3R到4R的过渡。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-08-27 DOI: 10.1016/j.slast.2025.100345
Santosh Dhule , Eric Corriveau , Christopher Lepsy , Sophie Tourdot
Despite significant advances in instrumentation and robotics, the automation of cell staining in flow cytometry remains largely unaddressed. While sample acquisition in flow cytometry has been fully automated, sample staining continues to be a predominantly manual process—requiring substantial time, labor, and cost. Additionally, the repetitive nature of manual staining introduces monotony and increases the likelihood of human error. The Staining Triad presented here achieves full automation of the staining process, requiring only the input of samples and reagents, with no manual intervention. Staining performed using the Staining Triad showed a comparable biomarker profile to that of conventional manual staining. The modular and adaptable system design enables the flexibility to tailor throughput and accommodate assay-specific requirements, thereby extending its applicability to plate-based ligand binding assays. Moreover, the system eliminates the need for pipette tips, exemplifying a sophisticated and sustainable solution that enhances laboratory efficiency while reducing human error and the primary source of plastic waste in flow cytometry staining. Although 3R initiatives (Reduce, Reuse, Recycle) have helped decrease laboratory plastic waste volumes, substantial amounts are still incinerated or end up in landfills, where they persist in the environment for decades. This limitation underscores the need to incorporate a fourth R—"Remove/Replace"—into sustainability strategies. As flow cytometry becomes increasingly integral across various biotechnology disciplines, it is imperative to streamline associated workflows to accelerate drug discovery while preserving the environment that sustains life.
尽管在仪器和机器人技术方面取得了重大进展,但流式细胞术中细胞染色的自动化在很大程度上仍未得到解决。虽然流式细胞术中的样品采集已经完全自动化,但样品染色仍然是一个主要的人工过程-需要大量的时间,劳动力和成本。此外,手工染色的重复性引入了单调性,增加了人为错误的可能性。这里介绍的染色三合一实现了染色过程的完全自动化,只需要输入样品和试剂,无需人工干预。使用染色三合一进行的染色显示出与传统手工染色相当的生物标志物特征。模块化和适应性强的系统设计提供了灵活性,以定制吞吐量和适应分析特定的要求,从而扩展其适用于基于板的配体结合分析。此外,该系统消除了对移液头的需求,体现了一个复杂和可持续的解决方案,提高了实验室效率,同时减少了人为错误和流式细胞术染色中塑料废物的主要来源。尽管3R倡议(减少、再利用、再循环)帮助减少了实验室塑料废物的数量,但仍有大量塑料被焚烧或最终进入垃圾填埋场,在那里它们在环境中存留了几十年。这一限制强调了将第四个R——“移除/替换”——纳入可持续发展战略的必要性。随着流式细胞术在各种生物技术学科中越来越不可或缺,简化相关工作流程以加速药物发现,同时保护维持生命的环境势在必行。
{"title":"Staining Triad: A fully automated and zero-waste flow cytometry staining system fostering the 3R to 4R transition","authors":"Santosh Dhule ,&nbsp;Eric Corriveau ,&nbsp;Christopher Lepsy ,&nbsp;Sophie Tourdot","doi":"10.1016/j.slast.2025.100345","DOIUrl":"10.1016/j.slast.2025.100345","url":null,"abstract":"<div><div>Despite significant advances in instrumentation and robotics, the automation of cell staining in flow cytometry remains largely unaddressed. While sample acquisition in flow cytometry has been fully automated, sample staining continues to be a predominantly manual process—requiring substantial time, labor, and cost. Additionally, the repetitive nature of manual staining introduces monotony and increases the likelihood of human error. The Staining Triad presented here achieves full automation of the staining process, requiring only the input of samples and reagents, with no manual intervention. Staining performed using the Staining Triad showed a comparable biomarker profile to that of conventional manual staining. The modular and adaptable system design enables the flexibility to tailor throughput and accommodate assay-specific requirements, thereby extending its applicability to plate-based ligand binding assays. Moreover, the system eliminates the need for pipette tips, exemplifying a sophisticated and sustainable solution that enhances laboratory efficiency while reducing human error and the primary source of plastic waste in flow cytometry staining. Although 3R initiatives (Reduce, Reuse, Recycle) have helped decrease laboratory plastic waste volumes, substantial amounts are still incinerated or end up in landfills, where they persist in the environment for decades. This limitation underscores the need to incorporate a fourth R—\"Remove/Replace\"—into sustainability strategies. As flow cytometry becomes increasingly integral across various biotechnology disciplines, it is imperative to streamline associated workflows to accelerate drug discovery while preserving the environment that sustains life.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100345"},"PeriodicalIF":3.7,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144978504","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Application of 3D printing imaging technology in the treatment of bronchopleural fistula with individual customized bronchial occluder 3D打印成像技术在个性化支气管封堵器治疗支气管胸膜瘘中的应用
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-08-27 DOI: 10.1016/j.slast.2025.100344
Zelin Xiao , Jianqi Gao , Hui Zhang , Linyao Wang

Background

Bronchopleural fistula (BPF) is a common and severe complication in thoracic surgery, characterized by its complex nature and high mortality rate. Bronchial occluder is one of the effective methods for the interventional treatment of BPF under bronchoscopy.

Objective

This work was to evaluate the adoption and efficacy of individualized bronchial occluder designed with the assistance of 3D printing technology in the treatment of BPF.

Material and Methods

This single-center, retrospective study included 60 patients (35 males and 25 females, aged 40–78 years, without severe dysfunction of major organs or history of mental disorders) diagnosed with BPF between January 2020 and December 2023, who received different treatment and were divided into the Control Group (CG, receiving thoracotomy treatment), Therapy group-I (TG-I, receiving septal occluder treatment), and Therapy group-II (TG-II, receiving treatment with 3D-printed individualized bronchial occluder). Serum levels of high-sensitivity C-reactive protein (hs-CRP) and procalcitonin (PCT) were measured by enzyme-linked immunosorbent assay preoperatively and at 1, 4, and 12 weeks postoperatively. Daytime cough scores were assessed according to guidelines, pain scores were evaluated using a visual analog scale, clinical efficacy was determined based on consensus criteria, and complications were recorded. Quantitative variables were compared using one-way ANOVA with Bonferroni correction, while categorical variables were analyzed by chi-square or Fisher’s exact test.

Results

the overall clinical efficacy was higher in TG-I and TG-II versus CG, with TG-II showing a greatly higher efficacy after twelve weeks of treatment (P < 0.05). Relative to CG, both TG-I and TG-II demonstrated lower serum levels of hs-CRP and PCT, markedly reduced cough and pain symptom scores, and markedly lower complication rates (P < 0.05). Additionally, TG-II resulted in notably lower serum inflammatory markers, cough and pain symptom scores, and complication rates versus TG-I (P < 0.05).

Conclusion

The 3D-printed personalized occluder (TG-II) significantly reduced postoperative inflammatory responses and alleviated cough-associated pain, demonstrating superior short-term efficacy and safety compared to conventional treatment (CG) and commercially available occluders (TG-I). This approach offers distinct advantages for the personalized precision treatment of BPF. However, further clinical studies are required to validate its potential as an alternative to surgical repair.
背景:支气管胸膜瘘(BPF)是胸外科手术中常见且严重的并发症,其性质复杂,死亡率高。支气管闭塞术是支气管镜下介入治疗BPF的有效方法之一。目的:评价3D打印技术辅助设计的个体化支气管封堵器在BPF治疗中的应用及疗效。材料和方法:本单中心回顾性研究纳入2020年1月至2023年12月诊断为BPF的患者60例(男35例,女25例,年龄40-78岁,无严重主要器官功能障碍或精神障碍史),接受不同治疗,分为对照组(CG,接受开胸治疗)、治疗组i (TG-I,接受间隔闭塞治疗)和治疗组ii (TG-II,接受3d打印个性化支气管封堵器治疗)。术前、术后1、4、12周采用酶联免疫吸附法测定血清高敏c反应蛋白(hs-CRP)和降钙素原(PCT)水平。根据指南评估日间咳嗽评分,使用视觉模拟量表评估疼痛评分,根据共识标准确定临床疗效,并记录并发症。定量变量比较采用Bonferroni校正的单因素方差分析,分类变量分析采用卡方或Fisher精确检验。结果:与CG相比,TG-I和TG-II的总体临床疗效更高,其中TG-II在治疗12周后的疗效明显更高(p结论:3d打印个性化封口器(TG-II)显著降低了术后炎症反应,缓解了咳嗽相关疼痛,与常规治疗(CG)和市售封口器(TG-I)相比,具有更优越的短期疗效和安全性。这种方法为BPF的个性化精确治疗提供了明显的优势。然而,需要进一步的临床研究来验证其作为手术修复替代方案的潜力。
{"title":"Application of 3D printing imaging technology in the treatment of bronchopleural fistula with individual customized bronchial occluder","authors":"Zelin Xiao ,&nbsp;Jianqi Gao ,&nbsp;Hui Zhang ,&nbsp;Linyao Wang","doi":"10.1016/j.slast.2025.100344","DOIUrl":"10.1016/j.slast.2025.100344","url":null,"abstract":"<div><h3>Background</h3><div>Bronchopleural fistula (BPF) is a common and severe complication in thoracic surgery, characterized by its complex nature and high mortality rate. Bronchial occluder is one of the effective methods for the interventional treatment of BPF under bronchoscopy.</div></div><div><h3>Objective</h3><div>This work was to evaluate the adoption and efficacy of individualized bronchial occluder designed with the assistance of 3D printing technology in the treatment of BPF.</div></div><div><h3>Material and Methods</h3><div>This single-center, retrospective study included 60 patients (35 males and 25 females, aged 40–78 years, without severe dysfunction of major organs or history of mental disorders) diagnosed with BPF between January 2020 and December 2023, who received different treatment and were divided into the Control Group (CG, receiving thoracotomy treatment), Therapy group-I (TG-I, receiving septal occluder treatment), and Therapy group-II (TG-II, receiving treatment with 3D-printed individualized bronchial occluder). Serum levels of high-sensitivity C-reactive protein (hs-CRP) and procalcitonin (PCT) were measured by enzyme-linked immunosorbent assay preoperatively and at 1, 4, and 12 weeks postoperatively. Daytime cough scores were assessed according to guidelines, pain scores were evaluated using a visual analog scale, clinical efficacy was determined based on consensus criteria, and complications were recorded. Quantitative variables were compared using one-way ANOVA with Bonferroni correction, while categorical variables were analyzed by chi-square or Fisher’s exact test.</div></div><div><h3>Results</h3><div>the overall clinical efficacy was higher in TG-I and TG-II versus CG, with TG-II showing a greatly higher efficacy after twelve weeks of treatment (<em>P</em> &lt; 0.05). Relative to CG, both TG-I and TG-II demonstrated lower serum levels of hs-CRP and PCT, markedly reduced cough and pain symptom scores, and markedly lower complication rates (<em>P</em> &lt; 0.05). Additionally, TG-II resulted in notably lower serum inflammatory markers, cough and pain symptom scores, and complication rates versus TG-I (<em>P</em> &lt; 0.05).</div></div><div><h3>Conclusion</h3><div>The 3D-printed personalized occluder (TG-II) significantly reduced postoperative inflammatory responses and alleviated cough-associated pain, demonstrating superior short-term efficacy and safety compared to conventional treatment (CG) and commercially available occluders (TG-I). This approach offers distinct advantages for the personalized precision treatment of BPF. However, further clinical studies are required to validate its potential as an alternative to surgical repair.</div></div>","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"35 ","pages":"Article 100344"},"PeriodicalIF":3.7,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144978420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bio-inspired computing and Machine learning analytics for future-oriented mental well-being 面向未来的心理健康的生物启发计算和机器学习分析。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-08-14 DOI: 10.1016/j.slast.2025.100343
Chinmay Chakraborty , Bhuvan Unhelkar , Saïd Mahmoudi
{"title":"Bio-inspired computing and Machine learning analytics for future-oriented mental well-being","authors":"Chinmay Chakraborty ,&nbsp;Bhuvan Unhelkar ,&nbsp;Saïd Mahmoudi","doi":"10.1016/j.slast.2025.100343","DOIUrl":"10.1016/j.slast.2025.100343","url":null,"abstract":"","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"34 ","pages":"Article 100343"},"PeriodicalIF":3.7,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144862686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Life sciences and artificial intelligence 生命科学与人工智能。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-08-11 DOI: 10.1016/j.slast.2025.100342
Kerstin Thurow
{"title":"Life sciences and artificial intelligence","authors":"Kerstin Thurow","doi":"10.1016/j.slast.2025.100342","DOIUrl":"10.1016/j.slast.2025.100342","url":null,"abstract":"","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"34 ","pages":"Article 100342"},"PeriodicalIF":3.7,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144849637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Life sciences and society – an alphabetical journey 生命科学与社会——按字母顺序排列的旅程。
IF 3.7 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Pub Date : 2025-08-10 DOI: 10.1016/j.slast.2025.100341
Kerstin Thurow
{"title":"Life sciences and society – an alphabetical journey","authors":"Kerstin Thurow","doi":"10.1016/j.slast.2025.100341","DOIUrl":"10.1016/j.slast.2025.100341","url":null,"abstract":"","PeriodicalId":54248,"journal":{"name":"SLAS Technology","volume":"34 ","pages":"Article 100341"},"PeriodicalIF":3.7,"publicationDate":"2025-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144838578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
SLAS Technology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1