首页 > 最新文献

Nano Life最新文献

英文 中文
Dexamethasone: Therapeutic Applications, Targets and Translation 地塞米松:治疗应用,靶点和翻译
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-06-30 DOI: 10.1142/s1793984422300035
Rishabh Hirday, Grace H. Tam, Audrey A. O'Neill, Mollie S Davis, R. Schloss
Dexamethasone is a synthetic corticosteroid that has historically been used to treat inflammation, such as from osteoarthritis, spinal cord injury and, more recently, COVID-19. The mechanism of action of dexamethasone is generally known to include attenuation of pro-inflammatory responses as well as upregulation of anti-inflammatory elements. A major issue with the use of dexamethasone is its delivery, as it is normally administered in large quantities via methods like bolus injection to attempt to maintain sufficient concentrations days or weeks after administration. In this review, we examine the mechanism of action of dexamethasone and its effects on three major cell types in the context of specific diseases: macrophages in the context of COVID, chondrocytes in the context of osteoarthritis, and astrocytes in the context of neuro-inflammatory disease. From this, we identify the key proinflammatory cytokines interleukin-1 (IL-1) and Tumor Necrosis Factor alpha (TNF-a) as universal effectors of inflammation that should be targeted alongside dexamethasone administration. Additionally, we review current extended release dosing mechanisms for dexamethasone to act over periods of weeks and months. We suggest that dual treatment of dexamethasone with IL-1 and/or TNF-a monoclonal antibodies will be an effective immediate treatment for inflammation, while the addition of fully developed dexamethasone extended release mechanisms will allow for effective long-term control of inflammatory disease. [ FROM AUTHOR] Copyright of Nano Life is the property of World Scientific Publishing Company and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)
地塞米松是一种合成皮质类固醇,历史上一直用于治疗炎症,如骨关节炎、脊髓损伤以及最近的COVID-19。众所周知,地塞米松的作用机制包括抑制促炎反应和上调抗炎因子。使用地塞米松的一个主要问题是它的给药,因为它通常是通过注射等方法大量给药,试图在给药后几天或几周内保持足够的浓度。在这篇综述中,我们研究了地塞米松的作用机制及其在特定疾病背景下对三种主要细胞类型的影响:巨噬细胞在COVID背景下,软骨细胞在骨关节炎背景下,星形胶质细胞在神经炎症疾病背景下。由此,我们确定了关键的促炎细胞因子白介素-1 (IL-1)和肿瘤坏死因子α (TNF-a)作为炎症的普遍效应物,应该与地塞米松一起靶向给药。此外,我们回顾了目前地塞米松在数周和数月时间内的缓释给药机制。我们建议,地塞米松与IL-1和/或TNF-a单克隆抗体的双重治疗将是炎症的有效即时治疗,而完全开发的地塞米松延长释放机制的添加将允许有效的长期控制炎症性疾病。纳米生命的版权是世界科学出版公司的财产,未经版权所有者的明确书面许可,其内容不得复制或通过电子邮件发送到多个网站或发布到listserv。但是,用户可以打印、下载或通过电子邮件发送文章供个人使用。这可以删节。对副本的准确性不作任何保证。用户应参阅原始出版版本的材料的完整。(版权适用于所有人。)
{"title":"Dexamethasone: Therapeutic Applications, Targets and Translation","authors":"Rishabh Hirday, Grace H. Tam, Audrey A. O'Neill, Mollie S Davis, R. Schloss","doi":"10.1142/s1793984422300035","DOIUrl":"https://doi.org/10.1142/s1793984422300035","url":null,"abstract":"Dexamethasone is a synthetic corticosteroid that has historically been used to treat inflammation, such as from osteoarthritis, spinal cord injury and, more recently, COVID-19. The mechanism of action of dexamethasone is generally known to include attenuation of pro-inflammatory responses as well as upregulation of anti-inflammatory elements. A major issue with the use of dexamethasone is its delivery, as it is normally administered in large quantities via methods like bolus injection to attempt to maintain sufficient concentrations days or weeks after administration. In this review, we examine the mechanism of action of dexamethasone and its effects on three major cell types in the context of specific diseases: macrophages in the context of COVID, chondrocytes in the context of osteoarthritis, and astrocytes in the context of neuro-inflammatory disease. From this, we identify the key proinflammatory cytokines interleukin-1 (IL-1) and Tumor Necrosis Factor alpha (TNF-a) as universal effectors of inflammation that should be targeted alongside dexamethasone administration. Additionally, we review current extended release dosing mechanisms for dexamethasone to act over periods of weeks and months. We suggest that dual treatment of dexamethasone with IL-1 and/or TNF-a monoclonal antibodies will be an effective immediate treatment for inflammation, while the addition of fully developed dexamethasone extended release mechanisms will allow for effective long-term control of inflammatory disease. [ FROM AUTHOR] Copyright of Nano Life is the property of World Scientific Publishing Company and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48033845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Performance Evaluation of SAW based Hydrogen Gas Sensors with different IDT Geometries 不同IDT几何结构的SAW型氢气传感器性能评价
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-06-30 DOI: 10.1142/s179398442250009x
Harath Nimmala, K. Subramanian, A. Sarkar, Rajakumar Selvarajan
{"title":"Performance Evaluation of SAW based Hydrogen Gas Sensors with different IDT Geometries","authors":"Harath Nimmala, K. Subramanian, A. Sarkar, Rajakumar Selvarajan","doi":"10.1142/s179398442250009x","DOIUrl":"https://doi.org/10.1142/s179398442250009x","url":null,"abstract":"","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45361948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Phyto-assisted Preparation of Fe2O3 Nanoflowers and Their Antimicrobial Studies Fe2O3纳米花的植物辅助制备及其抗菌研究
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-06-24 DOI: 10.1142/s1793984422500088
Ravinder, D. K. Das, Anuj Kumar
{"title":"Phyto-assisted Preparation of Fe2O3 Nanoflowers and Their Antimicrobial Studies","authors":"Ravinder, D. K. Das, Anuj Kumar","doi":"10.1142/s1793984422500088","DOIUrl":"https://doi.org/10.1142/s1793984422500088","url":null,"abstract":"","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45455151","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Quantification of Magnetic Nanoparticles in ex vivo Colorectal Lymph Nodes 磁性纳米颗粒在离体结肠直肠癌淋巴结中的定量研究
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-05-30 DOI: 10.1142/s1793984422500064
L. Molenaar, M. M. Horstman – van de Loosdrecht, L. Alic, J. Baarlen, J. Meijerink, B. Ten Haken, I. Broeders, D. Lips
En-bloc tumor resection is the standard treatment for locally advanced colorectal cancer (CRC). An extensive histopathological assessment is necessary to evaluate the metastatic spread and adjuvant therapy. Sentinel lymph node biopsy decreases the histopathological burden when only sentinel lymph nodes (SLNs) are examined. This study aims to evaluate the spread of a magnetic tracer throughout the lymphatic system after ex vivo injection in en-bloc resected specimens of patients with CRC. To achieve this, lymph nodes (LNs) were quantified using a new magnetic detection method. Fifteen patients with CRC diagnosed with clinically negative LNs were included in this study and received 2–4 ex vivo magnetic tracer injections (total volume of 2[Formula: see text]mL). Magnetic sample series were acquired to create a look-up table for magnetic tracer quantification. In 80% of the patients, at least one magnetic LN was detected. A total of 33 LNs were marked as magnetic, containing an average of 8.1[Formula: see text][Formula: see text]g iron. In 71% of the patients, metastases were found in nonmagnetic LNs. Ex vivo injection leads to sub-optimal tracer spread and therefore inaccurate diagnosis. This study presents a novel magnetic detection method to quantify magnetic tracer in lymph nodes. Detecting the SLNs in en-bloc resected specimens and involving only these LNs in histopathological investigation enable a decrease in healthcare costs or an increased diagnostic potential.
整体肿瘤切除术是局部晚期结直肠癌(CRC)的标准治疗方法。广泛的组织病理学评估是必要的,以评估转移扩散和辅助治疗。当只检查前哨淋巴结(sln)时,前哨淋巴结活检减少了组织病理学负担。本研究旨在评估在CRC患者整体切除标本中体外注射磁性示踪剂后在整个淋巴系统中的扩散。为了实现这一点,淋巴结(LNs)被量化使用一种新的磁检测方法。本研究纳入15例临床诊断为阴性LNs的结直肠癌患者,接受2 - 4次体外磁示踪剂注射(总体积2 mL[公式:见文]mL)。获取磁性样品系列,建立磁性示踪定量查表。在80%的患者中,至少检测到一个磁性LN。共有33个LNs被标记为磁性,平均含有8.1[公式:见文]g铁。71%的患者在非磁性LNs中发现转移。体外注射导致示踪剂扩散不理想,因此诊断不准确。本研究提出了一种新的磁检测方法来量化淋巴结中的磁示踪剂。在整体切除标本中检测sln,并在组织病理学调查中仅涉及这些ln,可以降低医疗费用或增加诊断潜力。
{"title":"Quantification of Magnetic Nanoparticles in ex vivo Colorectal Lymph Nodes","authors":"L. Molenaar, M. M. Horstman – van de Loosdrecht, L. Alic, J. Baarlen, J. Meijerink, B. Ten Haken, I. Broeders, D. Lips","doi":"10.1142/s1793984422500064","DOIUrl":"https://doi.org/10.1142/s1793984422500064","url":null,"abstract":"En-bloc tumor resection is the standard treatment for locally advanced colorectal cancer (CRC). An extensive histopathological assessment is necessary to evaluate the metastatic spread and adjuvant therapy. Sentinel lymph node biopsy decreases the histopathological burden when only sentinel lymph nodes (SLNs) are examined. This study aims to evaluate the spread of a magnetic tracer throughout the lymphatic system after ex vivo injection in en-bloc resected specimens of patients with CRC. To achieve this, lymph nodes (LNs) were quantified using a new magnetic detection method. Fifteen patients with CRC diagnosed with clinically negative LNs were included in this study and received 2–4 ex vivo magnetic tracer injections (total volume of 2[Formula: see text]mL). Magnetic sample series were acquired to create a look-up table for magnetic tracer quantification. In 80% of the patients, at least one magnetic LN was detected. A total of 33 LNs were marked as magnetic, containing an average of 8.1[Formula: see text][Formula: see text]g iron. In 71% of the patients, metastases were found in nonmagnetic LNs. Ex vivo injection leads to sub-optimal tracer spread and therefore inaccurate diagnosis. This study presents a novel magnetic detection method to quantify magnetic tracer in lymph nodes. Detecting the SLNs in en-bloc resected specimens and involving only these LNs in histopathological investigation enable a decrease in healthcare costs or an increased diagnostic potential.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41867155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Towards a More Theory-Driven BCI Using Source Reconstructed Dynamics of EEG Time-Series 利用脑电时间序列的源重构动力学实现理论驱动的脑机接口
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-05-09 DOI: 10.1142/s1793984422500052
Ravichander Janapati, Vishwas Dalal, Rakesh Sengupta, Usha Desai, P. V. Raja Shekar, Sreedhar Kollem
Currently, the operational electroencephalography (EEG)-based brain–computer interfaces (BCIs) suffer from problems of BCI latency/lag issues, which restricts the use of interfaces impractical scenarios. One of the reasons behind the present challenges is the application of a purely data-driven approach to the BCI pipeline. Although BCI applications have improved significantly with the research in the fields of artificial intelligence (AI) and machine learning (ML), fundamental issues of data-driven training restrict the latency that can be achieved under current BCI paradigms. This work explores the possibility of future BCI using a combination of data-driven and theory-driven methods. In this study, an EEG-BCI dataset from steady-state visually evoked potentials (SSVEPs) is applied, where the SSVEP signals contain, source components from the occipital, parietal and frontal regions of the brain. Source reconstruction is done with the combination of independent component analysis (ICA) and low-resolution electromagnetic tomography analysis (LORETA). This method was able to predict BCI classification labels 5[Formula: see text]s earlier, based on pre-recorded signals from the scalp. The novelty of the current contribution lies in utilizing the source reconstructed EEG time-series for BCI classification, which allows for retention of classification accuracy up to 70% while working with the reduced data dimensionality. Implementation of this algorithm will allow a significant reduction in lag in online BCIs.
目前,基于操作脑电图(EEG)的脑机接口(BCI)存在脑机接口延迟/滞后问题,这限制了接口在不切实际的场景中的使用。当前挑战背后的原因之一是将纯粹的数据驱动方法应用于脑机接口管道。尽管随着人工智能(AI)和机器学习(ML)领域的研究,脑机接口的应用有了显著改善,但数据驱动训练的基本问题限制了在当前脑机接口范式下可以实现的延迟。这项工作探索了未来使用数据驱动和理论驱动方法相结合的脑机接口的可能性。在这项研究中,应用了来自稳态视觉诱发电位(SSVEP)的EEG-BCI数据集,其中SSVEP信号包含来自大脑枕部、顶叶和额叶区域的源成分。源重建采用独立分量分析(ICA)和低分辨率电磁层析成像分析(LORETA)相结合的方法。该方法能够根据头皮的预先记录信号,提前5秒预测脑机接口分类标签[公式:见正文]。当前贡献的新颖性在于利用源重构的EEG时间序列进行脑机接口分类,这允许在降低数据维度的情况下保持高达70%的分类精度。该算法的实现将显著减少在线脑机接口中的滞后。
{"title":"Towards a More Theory-Driven BCI Using Source Reconstructed Dynamics of EEG Time-Series","authors":"Ravichander Janapati, Vishwas Dalal, Rakesh Sengupta, Usha Desai, P. V. Raja Shekar, Sreedhar Kollem","doi":"10.1142/s1793984422500052","DOIUrl":"https://doi.org/10.1142/s1793984422500052","url":null,"abstract":"Currently, the operational electroencephalography (EEG)-based brain–computer interfaces (BCIs) suffer from problems of BCI latency/lag issues, which restricts the use of interfaces impractical scenarios. One of the reasons behind the present challenges is the application of a purely data-driven approach to the BCI pipeline. Although BCI applications have improved significantly with the research in the fields of artificial intelligence (AI) and machine learning (ML), fundamental issues of data-driven training restrict the latency that can be achieved under current BCI paradigms. This work explores the possibility of future BCI using a combination of data-driven and theory-driven methods. In this study, an EEG-BCI dataset from steady-state visually evoked potentials (SSVEPs) is applied, where the SSVEP signals contain, source components from the occipital, parietal and frontal regions of the brain. Source reconstruction is done with the combination of independent component analysis (ICA) and low-resolution electromagnetic tomography analysis (LORETA). This method was able to predict BCI classification labels 5[Formula: see text]s earlier, based on pre-recorded signals from the scalp. The novelty of the current contribution lies in utilizing the source reconstructed EEG time-series for BCI classification, which allows for retention of classification accuracy up to 70% while working with the reduced data dimensionality. Implementation of this algorithm will allow a significant reduction in lag in online BCIs.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":"1 1","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41825800","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
A Review on Silver and Zinc Oxide Nanoparticles as Antimicrobial Agents in Water Treatment Technologies 纳米氧化银和氧化锌在水处理技术中的抗菌剂研究进展
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-04-29 DOI: 10.1142/s1793984422300023
P. Aravindakshan, A. Krishnamoorthy, C. Pal, Yoon-Young Chang, N. P. Tan
{"title":"A Review on Silver and Zinc Oxide Nanoparticles as Antimicrobial Agents in Water Treatment Technologies","authors":"P. Aravindakshan, A. Krishnamoorthy, C. Pal, Yoon-Young Chang, N. P. Tan","doi":"10.1142/s1793984422300023","DOIUrl":"https://doi.org/10.1142/s1793984422300023","url":null,"abstract":"","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44319867","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Voltammetric Detection of Inositol Using a Platinum Based Electrode 用铂基电极伏安法检测肌醇
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-03-11 DOI: 10.1142/s1793984422500040
Dipan Bandyopadhyay, S. Nag, D. Das, Srikanta Acharya, B. Tudu, P. Pramanik, R. Bandyopadhyay, R. B. Roy
An electrochemical detection of inositol content using platinum (Pt)-based noble metal electrode is investigated. In this work, the electrochemical behavior of the platinum electrode has been studied and analyzed using a three-electrode system against a silver–silver chloride (Ag/AgCl) reference electrode and a steel counter electrode. Differential pulse voltammetry technique has been employed for this experimental study. A satisfactory linear range of operation was obtained from 50 to 400[Formula: see text][Formula: see text]M with [Formula: see text]M. Electrochemical responses for several inositol concentrations 50, 80, 100, 200, 300 and 400[Formula: see text][Formula: see text]M have also been analyzed using principal component analysis (PCA) with effective data clustering. A good class separability index (SI) was found to be 142.91. In addition, a prediction estimation of inositol contents using partial least square regression (PLSR) and principal component regression (PCR) algorithms were also evaluated and prediction accuracies of 93.69% and 93.71% were obtained, respectively. Moreover, the application of the Pt electrode over real orange juice sample extracts revealed satisfactory recovery rate of 96.18%. Thus, this technique of electrochemical system may be subjected for inositol detection in our daily-life food (especially juice, beverages) consumption.
研究了用铂基贵金属电极电化学检测肌醇含量的方法。在这项工作中,使用三电极系统对氯化银(Ag/AgCl)参比电极和钢制对电极研究和分析了铂电极的电化学行为。本实验采用了微分脉冲伏安法。从50到400[公式:见正文][公式:见文本]M和[公式:见图文本]M获得了令人满意的线性操作范围。还使用具有有效数据聚类的主成分分析(PCA)分析了几种肌醇浓度50、80、100、200、300和400的电化学响应[公式:见正文][公式:见文本]M。一个良好的类可分性指数(SI)为142.91。此外,还评估了使用偏最小二乘回归(PLSR)和主成分回归(PCR)算法对肌醇含量的预测估计,预测准确率分别为93.69%和93.71%。此外,Pt电极在真实橙汁样品提取物上的应用显示出96.18%的令人满意的回收率。因此,该电化学系统技术可用于我们日常生活食品(尤其是果汁、饮料)消费中的肌醇检测。
{"title":"Voltammetric Detection of Inositol Using a Platinum Based Electrode","authors":"Dipan Bandyopadhyay, S. Nag, D. Das, Srikanta Acharya, B. Tudu, P. Pramanik, R. Bandyopadhyay, R. B. Roy","doi":"10.1142/s1793984422500040","DOIUrl":"https://doi.org/10.1142/s1793984422500040","url":null,"abstract":"An electrochemical detection of inositol content using platinum (Pt)-based noble metal electrode is investigated. In this work, the electrochemical behavior of the platinum electrode has been studied and analyzed using a three-electrode system against a silver–silver chloride (Ag/AgCl) reference electrode and a steel counter electrode. Differential pulse voltammetry technique has been employed for this experimental study. A satisfactory linear range of operation was obtained from 50 to 400[Formula: see text][Formula: see text]M with [Formula: see text]M. Electrochemical responses for several inositol concentrations 50, 80, 100, 200, 300 and 400[Formula: see text][Formula: see text]M have also been analyzed using principal component analysis (PCA) with effective data clustering. A good class separability index (SI) was found to be 142.91. In addition, a prediction estimation of inositol contents using partial least square regression (PLSR) and principal component regression (PCR) algorithms were also evaluated and prediction accuracies of 93.69% and 93.71% were obtained, respectively. Moreover, the application of the Pt electrode over real orange juice sample extracts revealed satisfactory recovery rate of 96.18%. Thus, this technique of electrochemical system may be subjected for inositol detection in our daily-life food (especially juice, beverages) consumption.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46510081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Investigation on Metal Nanoparticles: Nickel Oxide, Cuprous Oxide and Tin Ferrite with Their Humidity Sensing at Room Temperature 金属纳米颗粒:氧化镍、氧化亚铜和铁酸锡的室温湿度传感研究
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-03-09 DOI: 10.1142/s1793984422500015
Swati Singh, P. Chaudhary, Sunanda Singh, Vandana Verma, R. Srivastava, R. K. Tripathi, Kaman Singh, B. Yadav
This paper deals with the facile approach to the synthesis of different metal oxide nanoparticles and their comparative study for humidity sensing application at room temperature. The synthesis of these metal oxide nanoparticles is through co-precipitation method for nickel oxide and tin ferrite and hydrothermal route for cuprous oxide. The SEM and EDX reveal the porous morphology and confirmed composition of the synthesized metal oxides. FTIR detects the presence of functional groups like –OH and confirms the inverse spinal structure in tin ferrite. The optical band gap was determined by UV spectroscopy: 3.86[Formula: see text]eV for NiO, 4.13[Formula: see text]eV for Cu2O, and 4.07[Formula: see text]eV for SnFe2O4. XRD gives the information about the average crystallite size for tin ferrite 2.42[Formula: see text]nm, cuprous oxide 12.88[Formula: see text]nm and nickel oxide 22.51[Formula: see text]nm as the size comes to nano range the surface area increases, which is a good indication for humidity sensing. The humidity sensing of materials was detected by electrical modes. The deposited thin films were prepared by spin coater and observed sensitivity of these films was 0.72[Formula: see text]M[Formula: see text]/%RH for NiO, 1.59[Formula: see text]M[Formula: see text]/%RH for Cu2O, and 2.07[Formula: see text]M[Formula: see text]/%RH for SnFe2O4. The experiments were repeated after few weeks and the aging effects of samples were found negligible which makes the sensor stable.
本文介绍了合成不同金属氧化物纳米颗粒的简单方法及其在室温湿度传感应用中的比较研究。这些金属氧化物纳米颗粒的合成是通过氧化镍和铁氧体锡的共沉淀法和氧化亚铜的水热法进行的。SEM和EDX揭示了合成的金属氧化物的多孔形态和确定的组成。FTIR检测到–OH等官能团的存在,并证实了锡铁氧体中的反向脊柱结构。通过UV光谱测定光学带隙:NiO为3.86[公式:见正文]eV,Cu2O为4.13[公式:见图正文]eV,SnFe2O4为4.07[公式:详见正文]eV。XRD给出了关于铁氧体锡2.42[公式:见正文]nm、氧化亚铜12.88[公式:见图正文]nm和氧化镍22.51[公式:参见正文]nm的平均晶粒尺寸的信息。随着尺寸达到纳米范围,表面积增加,这是湿度传感的良好指示。材料的湿度传感是通过电模式检测的。通过旋涂机制备沉积的薄膜,并且观察到的这些膜的灵敏度对于NiO为0.72[公式:参见文本]M[公式:见文本]/%RH,对于Cu2O为1.59[公式:见图文本]/%RH,对于SnFe2O4为2.07[公式:参阅文本]M]公式:见文本]/%RH。几周后重复实验,发现样品的老化影响可以忽略不计,这使得传感器稳定。
{"title":"Investigation on Metal Nanoparticles: Nickel Oxide, Cuprous Oxide and Tin Ferrite with Their Humidity Sensing at Room Temperature","authors":"Swati Singh, P. Chaudhary, Sunanda Singh, Vandana Verma, R. Srivastava, R. K. Tripathi, Kaman Singh, B. Yadav","doi":"10.1142/s1793984422500015","DOIUrl":"https://doi.org/10.1142/s1793984422500015","url":null,"abstract":"This paper deals with the facile approach to the synthesis of different metal oxide nanoparticles and their comparative study for humidity sensing application at room temperature. The synthesis of these metal oxide nanoparticles is through co-precipitation method for nickel oxide and tin ferrite and hydrothermal route for cuprous oxide. The SEM and EDX reveal the porous morphology and confirmed composition of the synthesized metal oxides. FTIR detects the presence of functional groups like –OH and confirms the inverse spinal structure in tin ferrite. The optical band gap was determined by UV spectroscopy: 3.86[Formula: see text]eV for NiO, 4.13[Formula: see text]eV for Cu2O, and 4.07[Formula: see text]eV for SnFe2O4. XRD gives the information about the average crystallite size for tin ferrite 2.42[Formula: see text]nm, cuprous oxide 12.88[Formula: see text]nm and nickel oxide 22.51[Formula: see text]nm as the size comes to nano range the surface area increases, which is a good indication for humidity sensing. The humidity sensing of materials was detected by electrical modes. The deposited thin films were prepared by spin coater and observed sensitivity of these films was 0.72[Formula: see text]M[Formula: see text]/%RH for NiO, 1.59[Formula: see text]M[Formula: see text]/%RH for Cu2O, and 2.07[Formula: see text]M[Formula: see text]/%RH for SnFe2O4. The experiments were repeated after few weeks and the aging effects of samples were found negligible which makes the sensor stable.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43039355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
PTEN: Sumoylation Function is the Key to the Maintenance of Genomic Stability of Cell PTEN:酰化功能是维持细胞基因组稳定性的关键
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-02-25 DOI: 10.1142/s1793984422500039
Ginia Ghosh, S. Misra, P. Karmakar
Phosphatase and tensin homolog deleted on chromosome 10 (PTEN), a tumor suppressor protein with dual phosphatase activity, is found to be frequently mutated in various cancers. PTEN is post-translationally modulated at various amino acid residues which are crucial for sub-cellular localization as well as its catalytic functions rendering genomic stability. Recent reports suggest that PTEN also acts as a DNA repair protein. But how post-translational modulation of PTEN affects cytological damage and aneuploidy is not studied in detail. Here, we focus on the role of sumoylation of PTEN in context with DNA damage induced cytological damage like micronucleus (MNi), nuclear bud (NB), and nuclear bridge formation. Our data suggest that wild type PTEN but not sumo-dead PTEN significantly reduces cytological damage in PTEN mutant PC3 cells. In case of sumo-dead PTEN, the cytological parameters are increased during 24[Formula: see text]h recovery time point after DNA damage. Next, we measured the effectiveness of the sumo-dead (PTEN-K254R) mutant on aneuploidy, where we found that sumoylation is essential for maintaining chromosome number. As chromosome number variation in daughter cell is due to multiple spindle pole formation, we qualitatively and quantitatively evaluate the [Formula: see text] tubulin pole formation in PTEN-K254R clone transfected cells. We found aberrant pole formation is significantly increased in PTEN-K254R transfected cells compared to wild-type PTEN. Further depletion of sumoylation activity of PTEN increases the expression of phosphorylated form of Aurora kinase A (AURKA) (T288) and PLK1 (T210) proteins with or without nocodazole, a microtubule depolymerizing agent compared to cells expressing wild-type PTEN. Thus, sumoylation of PTEN is essential for maintaining genomic stability.
10号染色体上缺失的磷酸酶和张力素同源物(PTEN)是一种具有双重磷酸酶活性的肿瘤抑制蛋白,在各种癌症中经常发生突变。PTEN在各种氨基酸残基上被翻译后调节,这些氨基酸残基对亚细胞定位及其提供基因组稳定性的催化功能至关重要。最近的报道表明PTEN也起到DNA修复蛋白的作用。但PTEN的翻译后调节如何影响细胞学损伤和非整倍体尚未详细研究。在这里,我们重点关注PTEN的酰化在DNA损伤诱导的细胞学损伤(如微核(MNi)、核芽(NB)和核桥形成)中的作用。我们的数据表明,野生型PTEN而不是相扑死亡的PTEN显著降低了PTEN突变PC3细胞的细胞学损伤。在相扑死亡的PTEN的情况下,在DNA损伤后的24小时恢复时间点[公式:见正文]内,细胞学参数增加。接下来,我们测量了相扑死亡(PTEN-K254R)突变体对非整倍体的有效性,我们发现相扑酰化对维持染色体数量至关重要。由于子细胞中染色体数量的变化是由于多纺锤体极的形成,我们对PTEN-K254R克隆转染细胞中微管蛋白极的形成进行了定性和定量评估。我们发现,与野生型PTEN相比,PTEN-K254R转染的细胞中异常极的形成显著增加。与表达野生型PTEN的细胞相比,PTEN的sumoyalization活性的进一步缺失增加了磷酸化形式的Aurora激酶A(AURKA)(T288)和PLK1(T210)蛋白在有或没有诺可唑的情况下的表达,诺可唑是一种微管解聚剂。因此,PTEN的酰化对于维持基因组稳定性是必不可少的。
{"title":"PTEN: Sumoylation Function is the Key to the Maintenance of Genomic Stability of Cell","authors":"Ginia Ghosh, S. Misra, P. Karmakar","doi":"10.1142/s1793984422500039","DOIUrl":"https://doi.org/10.1142/s1793984422500039","url":null,"abstract":"Phosphatase and tensin homolog deleted on chromosome 10 (PTEN), a tumor suppressor protein with dual phosphatase activity, is found to be frequently mutated in various cancers. PTEN is post-translationally modulated at various amino acid residues which are crucial for sub-cellular localization as well as its catalytic functions rendering genomic stability. Recent reports suggest that PTEN also acts as a DNA repair protein. But how post-translational modulation of PTEN affects cytological damage and aneuploidy is not studied in detail. Here, we focus on the role of sumoylation of PTEN in context with DNA damage induced cytological damage like micronucleus (MNi), nuclear bud (NB), and nuclear bridge formation. Our data suggest that wild type PTEN but not sumo-dead PTEN significantly reduces cytological damage in PTEN mutant PC3 cells. In case of sumo-dead PTEN, the cytological parameters are increased during 24[Formula: see text]h recovery time point after DNA damage. Next, we measured the effectiveness of the sumo-dead (PTEN-K254R) mutant on aneuploidy, where we found that sumoylation is essential for maintaining chromosome number. As chromosome number variation in daughter cell is due to multiple spindle pole formation, we qualitatively and quantitatively evaluate the [Formula: see text] tubulin pole formation in PTEN-K254R clone transfected cells. We found aberrant pole formation is significantly increased in PTEN-K254R transfected cells compared to wild-type PTEN. Further depletion of sumoylation activity of PTEN increases the expression of phosphorylated form of Aurora kinase A (AURKA) (T288) and PLK1 (T210) proteins with or without nocodazole, a microtubule depolymerizing agent compared to cells expressing wild-type PTEN. Thus, sumoylation of PTEN is essential for maintaining genomic stability.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45398418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Factorial Design-Based Nanocarrier Mediated Formulation of Efavirenz and Its Characterization 基于析因设计的纳米载体介导的依非韦伦处方及其表征
IF 0.8 Q4 MATERIALS SCIENCE, BIOMATERIALS Pub Date : 2022-02-25 DOI: 10.1142/s1793984422500027
Ruchi Chawla, V. Karri, V. Rani, Mohini Mishra, K. Kumar
Efavirenz (EFV) suffers from poor aqueous solubility which results in low bioavailability of the drug. Nanocarrier-based drug delivery systems offer a suitable alternative for improving the physico-chemical properties of the drug and hence its efficacy. Nanosuspension (NS) of EFV was formulated by solvent-anti solvent precipitation method using PVP K-30 as stabilizer and sodium lauryl sulphate (SLS) as the wetting agent. Multi-level factorial design was applied to select the optimal formulation which was further characterized. The optimal batch exhibited mean particle size of 305[Formula: see text]nm and polydispersity index (PDI) of 0.345. Solid-state characterization studies of the NS conducted using scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction, and differential scanning calorimetry (DSC) revealed compatibility between the drug and the excipients and modest alteration in the crystallinity of the drug. There was progressive increase in the solubility of the drug when incorporated in NS from 17.39[Formula: see text][Formula: see text]g/ml to 256[Formula: see text][Formula: see text]g/ml. Further, drug release studies showed significantly better and controlled drug release pattern in comparison to the free drug due to the presence of nanosized particles in the formulation.
依非韦伦(EFV)水溶性差,导致药物的生物利用度低。基于纳米载体的药物递送系统为改善药物的物理化学性质和疗效提供了一种合适的选择。以PVP K-30为稳定剂,十二烷基硫酸钠(SLS)为润湿剂,采用溶剂-反溶剂沉淀法制备了EFV纳米悬浮液(NS)。采用多因素设计筛选最佳配方,并对其进行进一步表征。最佳批次的平均粒径为305 nm,多分散性指数(PDI)为0.345。利用扫描电子显微镜、傅里叶变换红外光谱(FTIR)、x射线粉末衍射和差示扫描量热法(DSC)对NS进行了固态表征研究,发现药物与辅料之间的相容性以及药物结晶度的适度改变。加入NS后,该药的溶解度逐渐增加,从17.39 g/ml增至256 g/ml。此外,药物释放研究表明,由于配方中存在纳米级颗粒,与游离药物相比,药物释放模式明显更好且可控。
{"title":"Factorial Design-Based Nanocarrier Mediated Formulation of Efavirenz and Its Characterization","authors":"Ruchi Chawla, V. Karri, V. Rani, Mohini Mishra, K. Kumar","doi":"10.1142/s1793984422500027","DOIUrl":"https://doi.org/10.1142/s1793984422500027","url":null,"abstract":"Efavirenz (EFV) suffers from poor aqueous solubility which results in low bioavailability of the drug. Nanocarrier-based drug delivery systems offer a suitable alternative for improving the physico-chemical properties of the drug and hence its efficacy. Nanosuspension (NS) of EFV was formulated by solvent-anti solvent precipitation method using PVP K-30 as stabilizer and sodium lauryl sulphate (SLS) as the wetting agent. Multi-level factorial design was applied to select the optimal formulation which was further characterized. The optimal batch exhibited mean particle size of 305[Formula: see text]nm and polydispersity index (PDI) of 0.345. Solid-state characterization studies of the NS conducted using scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction, and differential scanning calorimetry (DSC) revealed compatibility between the drug and the excipients and modest alteration in the crystallinity of the drug. There was progressive increase in the solubility of the drug when incorporated in NS from 17.39[Formula: see text][Formula: see text]g/ml to 256[Formula: see text][Formula: see text]g/ml. Further, drug release studies showed significantly better and controlled drug release pattern in comparison to the free drug due to the presence of nanosized particles in the formulation.","PeriodicalId":44929,"journal":{"name":"Nano Life","volume":" ","pages":""},"PeriodicalIF":0.8,"publicationDate":"2022-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44437008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","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
Nano Life
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:481959085
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