首页 > 最新文献

Journal of hazardous materials advances最新文献

英文 中文
Association between urinary benzotriazole ultraviolet stabilizers and lung cancer risk: A case-control study 尿中苯并三唑紫外线稳定剂与肺癌风险的关系:一项病例对照研究
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2026-01-10 DOI: 10.1016/j.hazadv.2026.101018
Chengli Du , Yunhao Chen , Zhentao Yang , Linping Cao , Zhengliang Tu
As emerging environmental contaminants with suspected human health impacts, benzotriazole ultraviolet stabilizers (BUVSs) lack empirical evidence regarding pulmonary carcinogenicity in exposed populations, highlighting the need to investigate their potential association with lung cancer. This study aimed to analyze the relationship between urinary BUVSs concentrations and lung cancer risk within the general population of Hangzhou, China. This case-control study included 397 newly diagnosed lung cancer patients and an equivalent cohort of age- and sex-matched healthy controls. Urine samples were analyzed for five different types of BUVSs, with total concentrations ranging from 0.46 to 36.40 μg/g creatinine. 2-(2′-Hydroxy-3′,5′-di‑tert-butylphenyl)-5‑chloro-benzotriazole (UV-327) was the most prevalent, with a mean concentration of 5.09 μg/g creatinine. Logistic regression models were employed to estimate odds ratios (ORs) and 95 % confidence intervals (CIs) for assessing lung cancer risk in relation to urinary BUVSs concentrations. Following adjustment for covariates including sex, smoking status, alcohol intake, and dietary habits, urinary 2-(2H-benzotriazol-2-yl)-p-cresol (UV-P) was the only BUVS demonstrating a significant correlation with lung cancer risk. Participants in the highest urinary UV-P concentration group exhibited a 4.5-fold higher risk of lung cancer relative to those in the lowest group (adjusted OR = 4.55, 95 % CI:2.84–7.28, p for trend < 0.01). The link between elevated UV-P exposure and a higher risk of lung cancer was affected by factors such as smoking status and dietary habits. These findings provide novel evidence of a potential association between BUVSs exposure—particularly UV-P—and lung cancer in the general Chinese population, and highlight the need for future longitudinal and mechanistic studies to confirm these associations and elucidate the underlying biological pathways.
作为疑似对人类健康有影响的新兴环境污染物,苯并三唑紫外线稳定剂(BUVSs)在暴露人群中缺乏肺致癌性的经验证据,因此有必要调查其与肺癌的潜在关联。本研究旨在分析中国杭州普通人群尿液中BUVSs浓度与肺癌风险之间的关系。这项病例对照研究包括397名新诊断的肺癌患者和一组年龄和性别匹配的健康对照组。尿样分析5种不同类型BUVSs,总浓度范围为0.46 ~ 36.40 μg/g肌酐。2-(2 ' -羟基-3 ',5 ' -二叔丁基苯基)-5 -氯苯并三唑(UV-327)含量最高,平均浓度为5.09 μg/g肌酐。采用Logistic回归模型来估计比值比(ORs)和95%置信区间(CIs),以评估与尿中BUVSs浓度相关的肺癌风险。在调整了包括性别、吸烟状况、饮酒和饮食习惯在内的协变量后,尿中2-(2h -苯并三唑-2-酰基)-对甲酚(UV-P)是唯一显示与肺癌风险显著相关的BUVS。尿液中UV-P浓度最高组的参与者患肺癌的风险是最低组的4.5倍(调整后OR = 4.55, 95% CI: 2.84-7.28, p为趋势值<; 0.01)。UV-P暴露增加与肺癌风险增加之间的联系受到吸烟状况和饮食习惯等因素的影响。这些发现提供了新的证据,证明暴露于BUVSs(特别是uv - p)与中国普通人群的肺癌之间存在潜在关联,并强调未来需要进行纵向和机制研究来证实这些关联并阐明潜在的生物学途径。
{"title":"Association between urinary benzotriazole ultraviolet stabilizers and lung cancer risk: A case-control study","authors":"Chengli Du ,&nbsp;Yunhao Chen ,&nbsp;Zhentao Yang ,&nbsp;Linping Cao ,&nbsp;Zhengliang Tu","doi":"10.1016/j.hazadv.2026.101018","DOIUrl":"10.1016/j.hazadv.2026.101018","url":null,"abstract":"<div><div>As emerging environmental contaminants with suspected human health impacts, benzotriazole ultraviolet stabilizers (BUVSs) lack empirical evidence regarding pulmonary carcinogenicity in exposed populations, highlighting the need to investigate their potential association with lung cancer. This study aimed to analyze the relationship between urinary BUVSs concentrations and lung cancer risk within the general population of Hangzhou, China. This case-control study included 397 newly diagnosed lung cancer patients and an equivalent cohort of age- and sex-matched healthy controls. Urine samples were analyzed for five different types of BUVSs, with total concentrations ranging from 0.46 to 36.40 μg/g creatinine. 2-(2′-Hydroxy-3′,5′-di‑tert-butylphenyl)-5‑chloro-benzotriazole (UV-327) was the most prevalent, with a mean concentration of 5.09 μg/g creatinine. Logistic regression models were employed to estimate odds ratios (ORs) and 95 % confidence intervals (CIs) for assessing lung cancer risk in relation to urinary BUVSs concentrations. Following adjustment for covariates including sex, smoking status, alcohol intake, and dietary habits, urinary 2-(2H-benzotriazol-2-yl)-<em>p</em>-cresol (UV-P) was the only BUVS demonstrating a significant correlation with lung cancer risk. Participants in the highest urinary UV-P concentration group exhibited a 4.5-fold higher risk of lung cancer relative to those in the lowest group (adjusted OR = 4.55, 95 % CI:2.84–7.28, <em>p</em> for trend &lt; 0.01). The link between elevated UV-P exposure and a higher risk of lung cancer was affected by factors such as smoking status and dietary habits. These findings provide novel evidence of a potential association between BUVSs exposure—particularly UV-P—and lung cancer in the general Chinese population, and highlight the need for future longitudinal and mechanistic studies to confirm these associations and elucidate the underlying biological pathways.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101018"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077264","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
Organochlorine pesticides in placenta, blood and breast milk of mothers in Uganda: Concentrations and health risks to breast fed infants 乌干达母亲胎盘、血液和母乳中的有机氯农药:浓度和对母乳喂养婴儿的健康风险
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2025-12-03 DOI: 10.1016/j.hazadv.2025.100949
Daniel Omoding , Teddy Nantume , John Wasswa , Silver Odongo , Christine Kyarimpa , Ibrahim Karume , Henry Matovu , Mika Sillanpää , Charles Drago Kato , Josephine Nabuuma , Ashirafu Miiro , Patrick Ssebugere
Exposure to organochlorine pesticides (OCPs) remains a major public health concern in low-income countries, where historical usage and poor regulation continue to result in maternal and early-life exposures. This study assessed concentration profiles of selected OCPs, namely; p,p′-DDT, p,p′-DDE, o,p′-DDE, p,p′-DDD, o,p′-DDD, aldrin, dieldrin, lindane, α-endosulfan, β-endosulfan, and endosulfan-sulfate in maternal blood, breast milk, and placenta samples collected from 52 healthy mothers residing in the rural Kanungu District and urban Kampala District in Uganda. Analytical quantification was performed using gas chromatography-electron capture detection (GC-ECD), and compound identity was confirmed by gas chromatography–mass spectrometry (GC-MS). Concentrations of total DDTs (∑DDTs) were 63.0, 27.1, and 35.0 ng g-1 lipid weight (l.w) in blood, breast milk, and placenta, respectively. o,p′-DDE was the predominant metabolite in blood (67% of ∑DDTs), while p,p′-DDE dominated in placenta and milk (34% and 70%, respectively), possibly due to degradation of technical DDT applied in past decades. Other OCPs were generally low (<Limit of detection, LOD to 88.4 ng g-1 l.w), except for dieldrin, which reached 130 ng g-1 l.w in breast milk. OCP levels were significantly higher in Kanungu than Kampala, attributable to ongoing informal pesticide use in agriculture. In general, the estimated hazard quotients were <1, which indicated that the health risks posed to infants due to ingestion of OCPs in breast milk was negligible. Our findings underscore the need for rural pesticide regulation and continuous maternal exposure monitoring.
在低收入国家,接触有机氯农药仍然是一个主要的公共卫生问题,这些国家的历史使用和监管不力继续导致孕产妇和生命早期接触有机氯农药。本研究评估了所选ocp的浓度分布,即;对居住在乌干达卡农古农村地区和坎帕拉城市地区的52名健康母亲血液、母乳和胎盘样本中的p,p ' -滴滴涕、p,p ' -DDE、o,p ' -DDE、p,p ' -DDD、o,p ' -DDD、艾氏剂、狄氏剂、林丹、α-硫丹、β-硫丹和硫丹硫酸盐进行了研究。采用气相色谱-电子捕获检测(GC-ECD)进行分析定量,采用气相色谱-质谱(GC-MS)进行化合物鉴定。血液、母乳和胎盘中总DDTs(∑DDTs)浓度分别为63.0、27.1和35.0 ng g-1脂质重(l.w)。o,p′-DDE是血液中的主要代谢物(占∑DDTs的67%),而p,p′-DDE在胎盘和乳液中占主导地位(分别为34%和70%),可能是由于过去几十年使用的技术滴滴涕降解所致。其他ocp普遍较低(检出限,LOD为88.4 ng g-1 l.w),但狄氏剂在母乳中的检出限为130 ng g-1 l.w。卡农古的OCP水平明显高于坎帕拉,这是由于农业中持续非正式使用农药造成的。总的来说,估计的危害商数为<;1,这表明由于母乳中摄入ocp对婴儿造成的健康风险可以忽略不计。我们的研究结果强调了农村农药监管和持续监测孕产妇暴露的必要性。
{"title":"Organochlorine pesticides in placenta, blood and breast milk of mothers in Uganda: Concentrations and health risks to breast fed infants","authors":"Daniel Omoding ,&nbsp;Teddy Nantume ,&nbsp;John Wasswa ,&nbsp;Silver Odongo ,&nbsp;Christine Kyarimpa ,&nbsp;Ibrahim Karume ,&nbsp;Henry Matovu ,&nbsp;Mika Sillanpää ,&nbsp;Charles Drago Kato ,&nbsp;Josephine Nabuuma ,&nbsp;Ashirafu Miiro ,&nbsp;Patrick Ssebugere","doi":"10.1016/j.hazadv.2025.100949","DOIUrl":"10.1016/j.hazadv.2025.100949","url":null,"abstract":"<div><div>Exposure to organochlorine pesticides (OCPs) remains a major public health concern in low-income countries, where historical usage and poor regulation continue to result in maternal and early-life exposures. This study assessed concentration profiles of selected OCPs, namely; <em>p,p′</em>-DDT, <em>p,p′</em>-DDE, <em>o,p′</em>-DDE, <em>p,p′</em>-DDD, <em>o,p′</em>-DDD, aldrin, dieldrin, lindane, α-endosulfan, β-endosulfan, and endosulfan-sulfate in maternal blood, breast milk, and placenta samples collected from 52 healthy mothers residing in the rural Kanungu District and urban Kampala District in Uganda. Analytical quantification was performed using gas chromatography-electron capture detection (GC-ECD), and compound identity was confirmed by gas chromatography–mass spectrometry (GC-MS). Concentrations of total DDTs (∑DDTs) were 63.0, 27.1, and 35.0 ng g<sup>-1</sup> lipid weight (l.w) in blood, breast milk, and placenta, respectively. <em>o,p′</em>-DDE was the predominant metabolite in blood (67% of ∑DDTs), while <em>p,p′</em>-DDE dominated in placenta and milk (34% and 70%, respectively), possibly due to degradation of technical DDT applied in past decades. Other OCPs were generally low (&lt;Limit of detection, LOD to 88.4 ng g<sup>-1</sup> l.w), except for dieldrin, which reached 130 ng g<sup>-1</sup> l.w in breast milk. OCP levels were significantly higher in Kanungu than Kampala, attributable to ongoing informal pesticide use in agriculture. In general, the estimated hazard quotients were &lt;1, which indicated that the health risks posed to infants due to ingestion of OCPs in breast milk was negligible. Our findings underscore the need for rural pesticide regulation and continuous maternal exposure monitoring.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100949"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685539","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
Assessment of arsenic exposure through dietary sources and drinking water in Gallbladder cancer patients of Bihar 比哈尔邦胆囊癌患者通过饮食来源和饮用水接触砷的评估
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2025-11-19 DOI: 10.1016/j.hazadv.2025.100947
Shivam Kumar , Arun Kumar , Megha Sharma , Kanhaiya Kumar , Manishankar Kumar , Dhruv Kumar , Akhouri Bishwapriya , Maiko Sakamoto , Ashok Kumar Ghosh
In the recent times, there has been significant rise in the Gallbladder cancer (GBC) incidences globally. The present study examines the relationship between dietary arsenic exposure and GBC risk in n=141 inhabitants of Bihar. A total of n=705 samples were collected from n=141 subject’s households which included rice, wheat, pulse, potato and their household water samples. The study revealed that 11% of rice samples, 2% of potato samples, 6% of pulse samples, and 33% of wheat samples exceeded FAO permissible limits (200 µg/kg for rice, potatoes, and pulses; 100 µg/kg for wheat), with maximum concentrations of 574.8 µg/kg, 912 µg/kg, 267.2 µg/kg, and 376.4 µg/kg, respectively. Additionally, 21% of 141 handpump water samples had arsenic concentration more than the WHO limit of 10 µg/L, with maximum concentration as 91.6 µg/L. Health risk assessments indicated significant non-carcinogenic (Hazard Quotient > 1) and carcinogenic (Cancer Risk > 1 × 10⁻⁶) risks, with rice emerging as the primary dietary contributor, followed by wheat, while pulses and potatoes posed lower risks. Pearson correlation coefficients (r = 0.2590–0.4446, p < 0.01) among staple food consumptions. In the present study, the human health risk assessment based on food samples showed that 17.73% of wheat samples exceeded the non-carcinogenic risk limit, and 58.15% exceeded the carcinogenic risk limit. Similarly, for rice samples, 39% of the exposed population showed potential non-carcinogenic risk, while 59.57% were at risk of carcinogenic effects. Rice showed the highest non-carcinogenic (HQ) and carcinogenic (CR) risks, with HQ values frequently exceeding the threshold of 1 and CR values surpassing the acceptable safety limit (1 × 10⁻⁶). This establishes rice as the primary dietary contributor to arsenic-related gallbladder cancer risk in the study population. Wheat presented moderate risk, with some HQ values exceeding 1 and CR values approaching the risk boundary, suggesting a secondary but significant contribution. In contrast, pulses demonstrated very low HQ and CR values, both well within safe limits, indicating negligible health risk from arsenic exposure through this food group. Overall, these findings highlight rice as the dominant dietary source of arsenic exposure among gallbladder cancer patients, followed by wheat, while pulses and potatoes pose comparatively lower risks. The study emphasizes the need for continuous biomonitoring and public health interventions, including safe irrigation and dietary diversification, to mitigate GBC risk in this arsenic-endemic region, with further research required to understand the impact of other confounding risk factors.
近年来,全球胆囊癌(GBC)发病率显著上升。本研究调查了比哈尔邦141名居民膳食砷暴露与GBC风险之间的关系。共从n=141个被试家庭中收集了n=705个样本,包括水稻、小麦、豆类、马铃薯及其家庭用水样本。研究表明,11%的大米样品、2%的土豆样品、6%的豆类样品和33%的小麦样品超过粮农组织允许的限值(大米、土豆和豆类为200微克/公斤;小麦为100微克/公斤),最高浓度分别为574.8微克/公斤、912微克/公斤、267.2微克/公斤和376.4微克/公斤。此外,141个手泵水样中有21%的砷浓度超过世界卫生组织10µg/L的限值,最高浓度为91.6µg/L。健康风险评估显示了显著的非致癌性(危险系数>; 1)和致癌性(癌症风险>; 1 × 10 - 6)风险,其中大米是主要的饮食来源,其次是小麦,而豆类和土豆的风险较低。主食消费之间的Pearson相关系数(r = 0.2590-0.4446, p < 0.01)。在本研究中,基于食品样品的人体健康风险评估显示,17.73%的小麦样品超过非致癌风险限值,58.15%超过致癌风险限值。同样,在大米样本中,39%的暴露人群显示出潜在的非致癌风险,而59.57%的暴露人群存在致癌风险。大米显示出最高的非致癌性(HQ)和致癌性(CR)风险,HQ值经常超过1的阈值,CR值超过可接受的安全限值(1 × 10⁻26)。这表明大米是研究人群中砷相关胆囊癌风险的主要饮食因素。小麦呈中等风险,部分HQ值超过1,CR值接近风险边界,表明小麦有次要但显著的贡献。相比之下,豆类显示出非常低的HQ和CR值,两者都在安全范围内,表明通过这类食物接触砷的健康风险可以忽略不计。总的来说,这些发现突出表明,在胆囊癌患者中,大米是砷暴露的主要饮食来源,其次是小麦,而豆类和土豆的风险相对较低。该研究强调需要持续的生物监测和公共卫生干预措施,包括安全灌溉和饮食多样化,以减轻砷流行地区的GBC风险,并需要进一步研究以了解其他混杂风险因素的影响。
{"title":"Assessment of arsenic exposure through dietary sources and drinking water in Gallbladder cancer patients of Bihar","authors":"Shivam Kumar ,&nbsp;Arun Kumar ,&nbsp;Megha Sharma ,&nbsp;Kanhaiya Kumar ,&nbsp;Manishankar Kumar ,&nbsp;Dhruv Kumar ,&nbsp;Akhouri Bishwapriya ,&nbsp;Maiko Sakamoto ,&nbsp;Ashok Kumar Ghosh","doi":"10.1016/j.hazadv.2025.100947","DOIUrl":"10.1016/j.hazadv.2025.100947","url":null,"abstract":"<div><div>In the recent times, there has been significant rise in the Gallbladder cancer (GBC) incidences globally. The present study examines the relationship between dietary arsenic exposure and GBC risk in n=141 inhabitants of Bihar. A total of n=705 samples were collected from n=141 subject’s households which included rice, wheat, pulse, potato and their household water samples. The study revealed that 11% of rice samples, 2% of potato samples, 6% of pulse samples, and 33% of wheat samples exceeded FAO permissible limits (200 µg/kg for rice, potatoes, and pulses; 100 µg/kg for wheat), with maximum concentrations of 574.8 µg/kg, 912 µg/kg, 267.2 µg/kg, and 376.4 µg/kg, respectively. Additionally, 21% of 141 handpump water samples had arsenic concentration more than the WHO limit of 10 µg/L, with maximum concentration as 91.6 µg/L. Health risk assessments indicated significant non-carcinogenic (Hazard Quotient &gt; 1) and carcinogenic (Cancer Risk &gt; 1 × 10⁻⁶) risks, with rice emerging as the primary dietary contributor, followed by wheat, while pulses and potatoes posed lower risks. Pearson correlation coefficients (r = 0.2590–0.4446, p &lt; 0.01) among staple food consumptions. In the present study, the human health risk assessment based on food samples showed that 17.73% of wheat samples exceeded the non-carcinogenic risk limit, and 58.15% exceeded the carcinogenic risk limit. Similarly, for rice samples, 39% of the exposed population showed potential non-carcinogenic risk, while 59.57% were at risk of carcinogenic effects. Rice showed the highest non-carcinogenic (HQ) and carcinogenic (CR) risks, with HQ values frequently exceeding the threshold of 1 and CR values surpassing the acceptable safety limit (1 × 10⁻⁶). This establishes rice as the primary dietary contributor to arsenic-related gallbladder cancer risk in the study population. Wheat presented moderate risk, with some HQ values exceeding 1 and CR values approaching the risk boundary, suggesting a secondary but significant contribution. In contrast, pulses demonstrated very low HQ and CR values, both well within safe limits, indicating negligible health risk from arsenic exposure through this food group. Overall, these findings highlight rice as the dominant dietary source of arsenic exposure among gallbladder cancer patients, followed by wheat, while pulses and potatoes pose comparatively lower risks. The study emphasizes the need for continuous biomonitoring and public health interventions, including safe irrigation and dietary diversification, to mitigate GBC risk in this arsenic-endemic region, with further research required to understand the impact of other confounding risk factors.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100947"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145618470","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
Detection and characterization of microplastics in commercial eye drops: A novel ocular exposure pathway 商业滴眼液中微塑料的检测和表征:一种新的眼部暴露途径
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2026-01-10 DOI: 10.1016/j.hazadv.2026.101019
Yixiang Que , Zhilei Zhang , Yunchou Wu , Weyland Cheng , Longfei Wang , Yanfan Wang , Yaodong Zhang , Kuo Lu
Microplastics (MPs), as emerging contaminants, have infiltrated various environments and consumer products, and are widely present in human tissues and bodily fluids. Currently, there is limited research on microplastic contamination in pharmaceuticals, particularly in eye drops that directly contact the ocular surface, where the risk of microplastic exposure urgently requires evaluation. This study investigated microplastic contamination in eye drops, aiming to assess the presence of microplastics in over-the-counter eye drops used directly on the ocular surface. The study employed multiple analytical methods, including laser direct infrared spectroscopy (LDIR), pyrolysis gas chromatography-mass spectrometry (Py-GC/MS), and scanning electron microscopy (SEM), to test commercially available eye drop samples. The results revealed that microplastics were present in all tested brands of eye drops, with most particles being smaller than 100 µm and primarily composed of polymers such as polyvinyl chloride (PVC), polyethylene (PE), and polypropylene (PP). Variations in the quantity, type, and morphology of microplastics were observed among different brands, suggesting that production processes or packaging may be sources of contamination. The study indicates that microplastic contamination in eye drops, which are formulations that directly contact the ocular surface, may pose potential risks to ocular health. Current pharmaceutical quality control standards do not yet cover such contaminants, highlighting the urgent need for attention from regulatory authorities, manufacturers, and medical professionals.
微塑料作为一种新兴污染物,已经渗透到各种环境和消费品中,广泛存在于人体组织和体液中。目前,关于药物中微塑料污染的研究有限,特别是直接接触眼表的滴眼液,其中微塑料暴露的风险迫切需要评估。本研究调查了眼药水中的微塑料污染,旨在评估直接用于眼表的非处方眼药水中微塑料的存在。本研究采用多种分析方法,包括激光直接红外光谱(LDIR)、热解气相色谱-质谱(Py-GC/MS)和扫描电子显微镜(SEM),对市售滴眼液样品进行测试。结果显示,所有测试品牌的眼药水中都含有微塑料,大多数颗粒小于100微米,主要由聚氯乙烯(PVC)、聚乙烯(PE)和聚丙烯(PP)等聚合物组成。在不同品牌中观察到微塑料的数量、类型和形态的变化,这表明生产过程或包装可能是污染源。研究表明,眼药水是直接接触眼表的配方,其中的微塑料污染可能对眼部健康构成潜在风险。目前的药品质量控制标准尚未涵盖此类污染物,这突出了监管当局、制造商和医疗专业人员迫切需要予以关注。
{"title":"Detection and characterization of microplastics in commercial eye drops: A novel ocular exposure pathway","authors":"Yixiang Que ,&nbsp;Zhilei Zhang ,&nbsp;Yunchou Wu ,&nbsp;Weyland Cheng ,&nbsp;Longfei Wang ,&nbsp;Yanfan Wang ,&nbsp;Yaodong Zhang ,&nbsp;Kuo Lu","doi":"10.1016/j.hazadv.2026.101019","DOIUrl":"10.1016/j.hazadv.2026.101019","url":null,"abstract":"<div><div>Microplastics (MPs), as emerging contaminants, have infiltrated various environments and consumer products, and are widely present in human tissues and bodily fluids. Currently, there is limited research on microplastic contamination in pharmaceuticals, particularly in eye drops that directly contact the ocular surface, where the risk of microplastic exposure urgently requires evaluation. This study investigated microplastic contamination in eye drops, aiming to assess the presence of microplastics in over-the-counter eye drops used directly on the ocular surface. The study employed multiple analytical methods, including laser direct infrared spectroscopy (LDIR), pyrolysis gas chromatography-mass spectrometry (Py-GC/MS), and scanning electron microscopy (SEM), to test commercially available eye drop samples. The results revealed that microplastics were present in all tested brands of eye drops, with most particles being smaller than 100 µm and primarily composed of polymers such as polyvinyl chloride (PVC), polyethylene (PE), and polypropylene (PP). Variations in the quantity, type, and morphology of microplastics were observed among different brands, suggesting that production processes or packaging may be sources of contamination. The study indicates that microplastic contamination in eye drops, which are formulations that directly contact the ocular surface, may pose potential risks to ocular health. Current pharmaceutical quality control standards do not yet cover such contaminants, highlighting the urgent need for attention from regulatory authorities, manufacturers, and medical professionals.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101019"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146022488","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
Leveraging molecular mechanisms of desorption to enhance PFAS bioavailability in contaminated soils 利用分子解吸机制提高PFAS在污染土壤中的生物利用度
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2026-01-02 DOI: 10.1016/j.hazadv.2025.100999
Husam Kafeenah , Margaret D. Taiwo , Patrica-Ivy Agorsor , Michael O. Eze
Per- and polyfluoroalkyl substances (PFAS) are known for their strong binding properties to soil matrices owing to their amphiphilic properties. While most studies focus on the search for novel PFAS biodegraders, our knowledge of sustainable biomolecules that could drive PFAS desorption and make them more bioavailable is limited. This study investigated the effectiveness of rhamnolipids and organic acids in desorbing PFAS compounds from contaminated soil. Rhamnolipids (25 mg/L) significantly enhanced the release of PFAS compounds from soil, achieving up to 90 % desorption. Acetic acid provided 60–90 % desorption efficiency for most of the PFAS studied, except for PFDA and three sulfonic PFAS (L-PFBS, L-PFHxS, and L-PFOS), suggesting acid-induced charge modification and reduced sorption affinity. Increasing the concentration of either additive enhanced desorption across all PFAS types, with acetic acid achieving maximum desorption at 0.5 M. Desorption kinetics revealed that rhamnolipids and acetic acid accelerated the kinetics of slow-desorbing PFAS. While oxalic and malic acids hindered the desorption of carboxylic PFAS, they enhanced the desorption of sulfonates. Considering the higher sorption capacity of sulfonates to sediment and soil, with greater potential for bioconcentration, the sorption reversibility of oxalic and malic acids can be harnessed for enhanced remediation of sulfonic PFAS in situations where rhamnolipids and acetic acids are inapplicable. Our findings will potentially stimulate research aimed at identifying suitable biomolecule-producing plants and microbes for enhanced PFAS desorption. Leveraging eco-friendly molecular mechanisms of desorption will complement the activities of novel microbes and facilitate PFAS biodegradation and site reclamation.
全氟和多氟烷基物质(PFAS)由于其两亲性而具有与土壤基质的强结合特性。虽然大多数研究都集中在寻找新型PFAS生物降解剂上,但我们对能够驱动PFAS解吸并使其更具生物可利用性的可持续生物分子的了解有限。本研究考察了鼠李糖脂和有机酸对污染土壤中PFAS化合物的解吸效果。鼠李糖脂(25 mg/L)显著提高了PFAS化合物从土壤中的释放,达到90%的解吸率。除PFDA和三种磺酸型PFAS (L-PFBS、L-PFHxS和L-PFOS)外,乙酸对大多数PFAS的解吸效率为60 - 90%,表明酸诱导的电荷修饰和吸附亲和力降低。增加任何一种添加剂的浓度都能增强所有PFAS类型的解吸,其中乙酸在0.5 m时达到最大解吸,解吸动力学表明鼠李糖脂和乙酸加速了缓慢解吸的PFAS动力学。草酸和苹果酸阻碍了羧基PFAS的脱附,而促进了磺酸盐的脱附。考虑到磺酸盐对沉积物和土壤具有较高的吸附能力,具有更大的生物浓缩潜力,在鼠李糖脂和乙酸不适用的情况下,草酸和苹果酸的吸附可逆性可以用于加强磺酸型PFAS的修复。我们的发现将潜在地激发旨在确定合适的生物分子产生植物和微生物来增强PFAS解吸的研究。利用生态友好的分子解吸机制将补充新型微生物的活性,促进PFAS的生物降解和场地回收。
{"title":"Leveraging molecular mechanisms of desorption to enhance PFAS bioavailability in contaminated soils","authors":"Husam Kafeenah ,&nbsp;Margaret D. Taiwo ,&nbsp;Patrica-Ivy Agorsor ,&nbsp;Michael O. Eze","doi":"10.1016/j.hazadv.2025.100999","DOIUrl":"10.1016/j.hazadv.2025.100999","url":null,"abstract":"<div><div>Per- and polyfluoroalkyl substances (PFAS) are known for their strong binding properties to soil matrices owing to their amphiphilic properties. While most studies focus on the search for novel PFAS biodegraders, our knowledge of sustainable biomolecules that could drive PFAS desorption and make them more bioavailable is limited. This study investigated the effectiveness of rhamnolipids and organic acids in desorbing PFAS compounds from contaminated soil. Rhamnolipids (25 mg/L) significantly enhanced the release of PFAS compounds from soil, achieving up to 90 % desorption. Acetic acid provided 60–90 % desorption efficiency for most of the PFAS studied, except for PFDA and three sulfonic PFAS (L-PFBS, <span>L</span>-PFHxS, and <span>L</span>-PFOS), suggesting acid-induced charge modification and reduced sorption affinity. Increasing the concentration of either additive enhanced desorption across all PFAS types, with acetic acid achieving maximum desorption at 0.5 M. Desorption kinetics revealed that rhamnolipids and acetic acid accelerated the kinetics of slow-desorbing PFAS. While oxalic and malic acids hindered the desorption of carboxylic PFAS, they enhanced the desorption of sulfonates. Considering the higher sorption capacity of sulfonates to sediment and soil, with greater potential for bioconcentration, the sorption reversibility of oxalic and malic acids can be harnessed for enhanced remediation of sulfonic PFAS in situations where rhamnolipids and acetic acids are inapplicable. Our findings will potentially stimulate research aimed at identifying suitable biomolecule-producing plants and microbes for enhanced PFAS desorption. Leveraging eco-friendly molecular mechanisms of desorption will complement the activities of novel microbes and facilitate PFAS biodegradation and site reclamation.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100999"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924654","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
In-vehicle toluene exposure affects functional connectivity of working memory retrieval networks 车内接触甲苯影响工作记忆检索网络的功能连通性
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2025-12-17 DOI: 10.1016/j.hazadv.2025.100982
Jiajing Wang , Fangfang Hao , Peiran Yu , Wenjuan Wu , Junjie Liu , Yijun Song
With the aim to investigate the impact of in-vehicle toluene exposure on working memory (WM) retrieval networks, twenty-three healthy adults underwent 4-hour exposures to toluene at concentrations of 0, 17.5, 35, or 70 ppb within a simulated vehicle. After exposure, all participants completed a WM task while cortical electroencephalography signals were recorded. The functional connectivity (FC) strengths of WM retrieval networks were compared across the four groups using direct transfer function (DTF) analysis. Results indicated that exposure to 70 ppb toluene significantly increased the FC strengths of the WM retrieval network, particularly in the frontal cortex (P < 0.05). Specifically, DTF values for FZ-T5, FZ-F3, F3-T5, F4-T6, and F7-T5 were higher at 70 ppb than those at 0 ppb (P < 0.05, P < 0.01, P < 0.001, P < 0.05, P < 0.05, respectively). The DTF values for FZ-F3 and F3-T5 at 35 ppb were higher than those at 0 ppb (P < 0.01). The DTFFZ-F3 value at 17.5 ppb was higher than that at 0 ppb (P < 0.01). The results suggest that even ppb-level, in-vehicle toluene exposure can significantly impact WM retrieval networks. The observed increase in FC strengths involved the medial prefrontal-to-left dorsolateral prefrontal cortex network, and several prefrontal-to-inferior temporal gyrus pathways. This dose-dependent enhancement of FC within critical cognitive networks presents a plausible neurophysiological mechanism for how in-vehicle toluene exposure may disrupt normal WM retrieval processes.
为了研究车内甲苯暴露对工作记忆(WM)检索网络的影响,23名健康成年人在模拟车辆中暴露于浓度为0、17.5、35或70 ppb的甲苯4小时。暴露后,所有参与者都完成了一项WM任务,同时记录了皮质脑电图信号。采用直接传递函数(DTF)分析比较四组WM检索网络的功能连通性(FC)强度。结果表明,暴露于70 ppb的甲苯显著增加了WM检索网络的FC强度,特别是在额叶皮层(P < 0.05)。其中,FZ-T5、FZ-F3、F3-T5、F4-T6和F7-T5在70 ppb时的DTF值高于0 ppb(分别为P <; 0.05、P < 0.01、P < 0.001、P < 0.05、P < 0.05)。FZ-F3和F3-T5在35 ppb下的DTF值高于0 ppb (P < 0.01)。17.5 ppb时DTFFZ-F3值高于0 ppb时(P < 0.01)。结果表明,即使是ppb水平的车内甲苯暴露也会显著影响WM检索网络。观察到的FC强度增加涉及内侧前额叶到左背外侧前额叶皮层网络,以及几个前额叶到下颞回通路。这种关键认知网络中FC的剂量依赖性增强提供了一种合理的神经生理学机制,说明车内甲苯暴露如何破坏正常的WM检索过程。
{"title":"In-vehicle toluene exposure affects functional connectivity of working memory retrieval networks","authors":"Jiajing Wang ,&nbsp;Fangfang Hao ,&nbsp;Peiran Yu ,&nbsp;Wenjuan Wu ,&nbsp;Junjie Liu ,&nbsp;Yijun Song","doi":"10.1016/j.hazadv.2025.100982","DOIUrl":"10.1016/j.hazadv.2025.100982","url":null,"abstract":"<div><div>With the aim to investigate the impact of in-vehicle toluene exposure on working memory (WM) retrieval networks, twenty-three healthy adults underwent 4-hour exposures to toluene at concentrations of 0, 17.5, 35, or 70 ppb within a simulated vehicle. After exposure, all participants completed a WM task while cortical electroencephalography signals were recorded. The functional connectivity (FC) strengths of WM retrieval networks were compared across the four groups using direct transfer function (DTF) analysis. Results indicated that exposure to 70 ppb toluene significantly increased the FC strengths of the WM retrieval network, particularly in the frontal cortex (<em>P</em> &lt; 0.05). Specifically, DTF values for FZ-T5, FZ-F3, F3-T5, F4-T6, and F7-T5 were higher at 70 ppb than those at 0 ppb (<em>P</em> &lt; 0.05, <em>P</em> &lt; 0.01, <em>P</em> &lt; 0.001, <em>P</em> &lt; 0.05, <em>P</em> &lt; 0.05, respectively). The DTF values for FZ-F3 and F3-T5 at 35 ppb were higher than those at 0 ppb (<em>P</em> &lt; 0.01). The DTF<sub>FZ-F3</sub> value at 17.5 ppb was higher than that at 0 ppb (<em>P</em> &lt; 0.01). The results suggest that even ppb-level, in-vehicle toluene exposure can significantly impact WM retrieval networks. The observed increase in FC strengths involved the medial prefrontal-to-left dorsolateral prefrontal cortex network, and several prefrontal-to-inferior temporal gyrus pathways. This dose-dependent enhancement of FC within critical cognitive networks presents a plausible neurophysiological mechanism for how in-vehicle toluene exposure may disrupt normal WM retrieval processes.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100982"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924730","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
Interactions of microplastics with heavy metals in the aquatic environment: Mechanisms and mitigation 水生环境中微塑料与重金属的相互作用:机制和缓解
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2025-12-22 DOI: 10.1016/j.hazadv.2025.100984
Atta Rasool, Jan Halfar, Kateřina Brožová, Kristina Čabanová, Jitka Chromíková, Petra Malíková, Oldřich Motyka, Eva Pertile, Silvie Drabinová, Silvie Heviánková
Microplastics (MPs) and heavy metals (HMs) are significant pollutants in aquatic ecosystems, posing substantial risks to both environmental and human health. Despite growing research interest, the quantitative understanding of MPs-HMs interactions remains limited due to methodological inconsistencies and insufficient cross-study data synthesis. This review presents a data-driven and mechanistic evaluation of these interactions, focusing on sorption and desorption mechanisms and the impact of key physicochemical parameters, including pH, salinity, temperature, and dissolved organic matter. Experimental data are analyzed to reveal trends in adsorption capacity across different polymers, particle sizes, and metal species. The review also synthesizes toxicological effects on aquatic organisms and humans and assesses recent advances in modeling and remediation approaches. Hybrid techniques integrating conventional and emerging technologies show promise for the simultaneous removal of MPs and HMs, though challenges persist for large-scale implementation. By linking quantitative trends with mechanistic insights, this review identifies critical knowledge gaps, outlines directions for future experimental validation, and supports the development of standardized protocols for environmental monitoring, risk assessment, and remediation.
微塑料(MPs)和重金属(HMs)是水生生态系统中的重要污染物,对环境和人类健康构成重大风险。尽管研究兴趣日益浓厚,但由于方法不一致和交叉研究数据合成不足,对MPs-HMs相互作用的定量理解仍然有限。本文综述了这些相互作用的数据驱动和机制评价,重点关注吸附和解吸机制以及关键物理化学参数(包括pH,盐度,温度和溶解有机质)的影响。实验数据进行分析,以揭示趋势的吸附能力跨越不同的聚合物,颗粒大小,和金属物种。该综述还综合了对水生生物和人类的毒理学影响,并评估了模拟和补救方法的最新进展。结合传统技术和新兴技术的混合技术有望同时去除MPs和HMs,尽管大规模实施仍然存在挑战。通过将定量趋势与机制见解联系起来,本综述确定了关键的知识差距,概述了未来实验验证的方向,并支持制定环境监测、风险评估和补救的标准化方案。
{"title":"Interactions of microplastics with heavy metals in the aquatic environment: Mechanisms and mitigation","authors":"Atta Rasool,&nbsp;Jan Halfar,&nbsp;Kateřina Brožová,&nbsp;Kristina Čabanová,&nbsp;Jitka Chromíková,&nbsp;Petra Malíková,&nbsp;Oldřich Motyka,&nbsp;Eva Pertile,&nbsp;Silvie Drabinová,&nbsp;Silvie Heviánková","doi":"10.1016/j.hazadv.2025.100984","DOIUrl":"10.1016/j.hazadv.2025.100984","url":null,"abstract":"<div><div>Microplastics (MPs) and heavy metals (HMs) are significant pollutants in aquatic ecosystems, posing substantial risks to both environmental and human health. Despite growing research interest, the quantitative understanding of MPs-HMs interactions remains limited due to methodological inconsistencies and insufficient cross-study data synthesis. This review presents a data-driven and mechanistic evaluation of these interactions, focusing on sorption and desorption mechanisms and the impact of key physicochemical parameters, including pH, salinity, temperature, and dissolved organic matter. Experimental data are analyzed to reveal trends in adsorption capacity across different polymers, particle sizes, and metal species. The review also synthesizes toxicological effects on aquatic organisms and humans and assesses recent advances in modeling and remediation approaches. Hybrid techniques integrating conventional and emerging technologies show promise for the simultaneous removal of MPs and HMs, though challenges persist for large-scale implementation. By linking quantitative trends with mechanistic insights, this review identifies critical knowledge gaps, outlines directions for future experimental validation, and supports the development of standardized protocols for environmental monitoring, risk assessment, and remediation.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100984"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924809","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
Reengineering electrokinetics: EDTA-enhanced mobilization of organic soil pollutants 再造电动力学:edta增强有机土壤污染物的动员
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2025-12-30 DOI: 10.1016/j.hazadv.2025.100994
Bryan A. Tiban-Anrango , Carolina De los Santos , J. Fernández-Cascán , Cristina Sáez , Manuel A. Rodrigo
The lack of mobility of chlorinated organic compounds in electrokinetic systems requires enhancement of the operational parameters. In this study, we investigated the role of ethylenediaminetetraacetic acid (EDTA) as a catholyte additive in enhancing the electrokinetic remediation (EKR) of real-contaminated soils containing chlorinated organic compounds (COCs). Initial soil washing experiments confirmed EDTA’s chelating efficacy, with extraction increasing from 0.006 mmol using pure water to 0.15 mmol with 0.1 M EDTA. Subsequent EKR trials at varying temperatures revealed that EDTA significantly improves COC mobilization, particularly toward the anode, where a 120% increase in molar transport was observed at 10 °C. This enhancement is attributed to the interaction between negatively charged EDTA complexes and chloro-substituted aromatic and alicyclic compounds, facilitating directional migration under an electric field. Temperature played a critical role in optimizing electro-osmotic flux and minimizing evaporation, with sub-25 °C conditions favoring contaminant transport. However, EDTA’s anionic nature also contributed to reduced soil electrical resistance, indirectly supporting electrokinetic performance. Notably, COC mobilization toward the cathode was less pronounced, with only a 20% increase, primarily driven by water movement rather than electrophoretic or electromigration. The study quantified EDTA demand, indicating that 26 mmol and 8 mmol of EDTA are required per mmol of COC mobilized at 10 °C and 25 °C, respectively. Despite lower extraction yields in EKR (0.086 mmol L⁻¹) compared to soil washing (0.149 mmol L⁻¹), the findings underscore EDTA’s potential to enhance organic pollutant mobility in electrokinetic systems. This work expands the applicability of chelating agents beyond heavy metals, offering new pathways for remediating complex organic-contaminated matrices.
氯化有机化合物在电动系统中缺乏流动性,需要提高操作参数。在本研究中,我们研究了乙二胺四乙酸(EDTA)作为阴极电解质添加剂对含氯有机化合物(COCs)污染土壤的电动修复(EKR)的作用。初步的土壤洗涤实验证实了EDTA的螯合作用,提取量从纯水时的0.006 mmol增加到0.1 M EDTA时的0.15 mmol。随后在不同温度下进行的EKR试验表明,EDTA显著改善了COC的动员,特别是向阳极的转移,在10°C时观察到摩尔转移增加了120%。这种增强是由于带负电荷的EDTA配合物与氯取代的芳香和脂环化合物之间的相互作用,促进了电场下的定向迁移。温度在优化电渗透通量和减少蒸发方面起着关键作用,低于25°C的条件有利于污染物的运输。然而,EDTA的阴离子性质也有助于降低土壤电阻,间接支持电动性能。值得注意的是,COC向阴极的迁移不太明显,仅增加了20%,主要是由水运动驱动,而不是电泳或电迁移。该研究量化了EDTA需求,表明在10°C和25°C条件下,每调动mmol COC分别需要26 mmol和8 mmol EDTA。尽管与洗土(0.149 mmol L⁻)相比,EKR (0.086 mmol L⁻)的萃取率较低,但研究结果强调了EDTA在电动系统中增强有机污染物迁移的潜力。这项工作扩大了螯合剂在重金属以外的适用性,为修复复杂的有机污染基质提供了新的途径。
{"title":"Reengineering electrokinetics: EDTA-enhanced mobilization of organic soil pollutants","authors":"Bryan A. Tiban-Anrango ,&nbsp;Carolina De los Santos ,&nbsp;J. Fernández-Cascán ,&nbsp;Cristina Sáez ,&nbsp;Manuel A. Rodrigo","doi":"10.1016/j.hazadv.2025.100994","DOIUrl":"10.1016/j.hazadv.2025.100994","url":null,"abstract":"<div><div>The lack of mobility of chlorinated organic compounds in electrokinetic systems requires enhancement of the operational parameters. In this study, we investigated the role of ethylenediaminetetraacetic acid (EDTA) as a catholyte additive in enhancing the electrokinetic remediation (EKR) of real-contaminated soils containing chlorinated organic compounds (COCs). Initial soil washing experiments confirmed EDTA’s chelating efficacy, with extraction increasing from 0.006 mmol using pure water to 0.15 mmol with 0.1 M EDTA. Subsequent EKR trials at varying temperatures revealed that EDTA significantly improves COC mobilization, particularly toward the anode, where a 120% increase in molar transport was observed at 10 °C. This enhancement is attributed to the interaction between negatively charged EDTA complexes and chloro-substituted aromatic and alicyclic compounds, facilitating directional migration under an electric field. Temperature played a critical role in optimizing electro-osmotic flux and minimizing evaporation, with sub-25 °C conditions favoring contaminant transport. However, EDTA’s anionic nature also contributed to reduced soil electrical resistance, indirectly supporting electrokinetic performance. Notably, COC mobilization toward the cathode was less pronounced, with only a 20% increase, primarily driven by water movement rather than electrophoretic or electromigration. The study quantified EDTA demand, indicating that 26 mmol and 8 mmol of EDTA are required per mmol of COC mobilized at 10 °C and 25 °C, respectively. Despite lower extraction yields in EKR (0.086 mmol L⁻¹) compared to soil washing (0.149 mmol L⁻¹), the findings underscore EDTA’s potential to enhance organic pollutant mobility in electrokinetic systems. This work expands the applicability of chelating agents beyond heavy metals, offering new pathways for remediating complex organic-contaminated matrices.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100994"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924750","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
Sustainable dual-mechanism arsenic remediation by Rhodopseudomonas palustris: Synergistic adsorption-methylation and life cycle assessment 古红假单胞菌对砷的持续双机制修复:协同吸附-甲基化和生命周期评价
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2026-01-27 DOI: 10.1016/j.hazadv.2026.101040
Nishan Sengupta , Monika Sogani , Anees Y. Khan , Keshava Balakrishna , Jayana Rajvanshi , Zainab Syed , Samiksha Verma
Arsenic pollution in groundwater is a global health concern that requires long-term cleanup techniques. This study presents Rhodopseudomonas palustris biomass as a unique, eco-friendly option for arsenic detoxification, achieving levels below the WHO/EPA limit of 10 µg L⁻¹ through synergistic adsorption and enzymatic methylation. The biomass can successfully adsorb arsenate [As(V)] and arsenite [As(III)], with capacities of 92 ± 0.5 µg g⁻¹ and 127 ± 0.5 µg g⁻¹, respectively, following pseudo-first-order kinetics at near-neutral pH (6.7). HPLC-ICP-MS analysis showed that As(III) transforms into less dangerous dimethylarsinic acid (DMA) at 1.30 ± 0.28 µg L⁻¹, whereas As(V) displays minor methylation (<0.01 µg L⁻¹ DMA) as estimated by mass balance calculations, thus emphasising As(III)'s higher reactivity. FTIR and FESEM-EDAX confirm that arsenic binds to carboxyl and phosphate groups on the biomass surface. The technique maintains 70 % efficiency after three repetitive adsorption cycles, increasing cost-effectiveness. Life Cycle Assessment reveals an environmental footprint of 2.34 kg CO₂-eq/m³, 0.015 kg PO₄³⁻-eq, and 0.00015 kg 1,4-DCB-eq, offering a significant improvement over reverse osmosis (3.5 kg CO₂-eq/m³) and adsorption-only systems (2.8 kg CO₂-eq/m³) by leveraging biological methylation to minimize emissions and toxicity. This dual-functional strategy, which combines strong adsorption and biotransformation, provides a scalable, long-term sustainable solution for arsenic remediation in resource-constrained areas, aligning with global water safety goals and advancing bioremediation paradigms.
地下水中的砷污染是一个全球性的健康问题,需要长期的清理技术。这项研究表明,palustris红脓单胞菌的生物量是一种独特的、生态友好的砷解毒选择,通过协同吸附和酶甲基化,可以达到低于WHO/EPA 10µg L的限制。在接近中性的pH值(6.7)下,生物质可以成功地吸附砷酸盐[As(V)]和亚砷酸盐[As(III)],其吸附量分别为92±0.5µg⁻¹和127±0.5µg⁻¹。HPLC-ICP-MS分析表明,As(III)在1.30±0.28µg L -毒血症时转化为危险性较低的二甲基larsinic酸(DMA),而As(V)则表现出轻微的甲基化(<;0.01µg L -毒血症),从而强调As(III)具有较高的反应性。FTIR和FESEM-EDAX证实,砷与生物质表面的羧基和磷酸基团结合。该技术在三次重复吸附循环后仍保持70%的效率,提高了成本效益。生命周期评估显示,环境足迹为2.34 kg CO₂-eq/m³,0.015 kg PO₄³-eq和0.00015 kg 1.4 - dcb -eq,通过利用生物甲基化来减少排放和毒性,显着改善了反渗透(3.5 kg CO₂-eq/m³)和仅吸附系统(2.8 kg CO₂-eq/m³)。这一双重功能战略结合了强吸附和生物转化,为资源受限地区的砷修复提供了可扩展的、长期可持续的解决方案,与全球水安全目标保持一致,并推进了生物修复范例。
{"title":"Sustainable dual-mechanism arsenic remediation by Rhodopseudomonas palustris: Synergistic adsorption-methylation and life cycle assessment","authors":"Nishan Sengupta ,&nbsp;Monika Sogani ,&nbsp;Anees Y. Khan ,&nbsp;Keshava Balakrishna ,&nbsp;Jayana Rajvanshi ,&nbsp;Zainab Syed ,&nbsp;Samiksha Verma","doi":"10.1016/j.hazadv.2026.101040","DOIUrl":"10.1016/j.hazadv.2026.101040","url":null,"abstract":"<div><div>Arsenic pollution in groundwater is a global health concern that requires long-term cleanup techniques. This study presents <em>Rhodopseudomonas palustris</em> biomass as a unique, eco-friendly option for arsenic detoxification, achieving levels below the WHO/EPA limit of 10 µg L⁻¹ through synergistic adsorption and enzymatic methylation. The biomass can successfully adsorb arsenate [As(V)] and arsenite [As(III)], with capacities of 92 ± 0.5 µg g⁻¹ and 127 ± 0.5 µg g⁻¹, respectively, following pseudo-first-order kinetics at near-neutral pH (6.7). HPLC-ICP-MS analysis showed that As(III) transforms into less dangerous dimethylarsinic acid (DMA) at 1.30 ± 0.28 µg L⁻¹, whereas As(V) displays minor methylation (<strong>&lt;</strong>0.01 µg L⁻¹ DMA) as estimated by mass balance calculations, thus emphasising As(III)'s higher reactivity. FTIR and FESEM-EDAX confirm that arsenic binds to carboxyl and phosphate groups on the biomass surface. The technique maintains 70 % efficiency after three repetitive adsorption cycles, increasing cost-effectiveness. Life Cycle Assessment reveals an environmental footprint of 2.34 kg CO₂-eq/m³, 0.015 kg PO₄³⁻-eq, and 0.00015 kg 1,4-DCB-eq, offering a significant improvement over reverse osmosis (3.5 kg CO₂-eq/m³) and adsorption-only systems (2.8 kg CO₂-eq/m³) by leveraging biological methylation to minimize emissions and toxicity. This dual-functional strategy, which combines strong adsorption and biotransformation, provides a scalable, long-term sustainable solution for arsenic remediation in resource-constrained areas, aligning with global water safety goals and advancing bioremediation paradigms.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101040"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147385188","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
Polymer‑specific hazard profiling and risk indexing of microplastics in coastal sediments of St. Martin’s Island: A multivariate and machine learning approach 圣马丁岛海岸沉积物中微塑料的聚合物特定危害分析和风险指数:多变量和机器学习方法
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2026-02-01 Epub Date: 2026-01-11 DOI: 10.1016/j.hazadv.2026.101017
Mahir Tajwar , Sidratul Muntaha , Asif Ashraf , Md Sahidul Islam , Subrota Kumar Saha
Microplastic (MP) contamination poses an emerging ecological threat in small-island environments, yet polymer-specific risk assessments remain limited for the Bay of Bengal region. This study provides the first integrated, polymer-resolved evaluation of microplastics in coastal sediments of St. Martin’s Island, Bangladesh. A total of 298 suspected MPs were isolated through stereomicroscopy, of which 250 particles were confirmed through ATR-FTIR (≥89% spectral match). Fibres and fragments dominated the assemblage, with high abundances observed in tourism-intensive beaches (S1–S4, S12) and fishing-dominated zones (S8–S11). Polymer profiles were characterized by the predominance of PE, PP, PET, and PVC. Four complementary ecological risk metrics, Pollution Load Index (PLI), Polymer Hazard Index (PHI), Sediment Polymer Hazard Index (SPHI), and the Microplastic Pollution Risk Index (MPRI), identified localized hotspots of elevated risk, particularly at tourism and active fishing sites. Multivariate analyses (PCA, HCA) revealed clear clustering patterns associated with site-use categories, while machine-learning classifiers (Random Forest, SVM, KNN) accurately distinguished tourism, fishing, and low-use zones based on MP morphology, color, polymer type, and abundance. Collectively, these findings demonstrate that anthropogenic pressure strongly shapes microplastic composition and hazard profiles on St. Martin’s Island. The integrated risk-index and ML framework presented here provides a robust, reproducible approach for coastal microplastic monitoring in data-limited regions and can support targeted management and mitigation strategies in vulnerable island ecosystems.
微塑料(MP)污染在小岛屿环境中构成了新的生态威胁,但孟加拉湾地区聚合物特异性风险评估仍然有限。本研究首次对孟加拉国圣马丁岛沿海沉积物中的微塑料进行了综合、聚合物分解评估。通过体视显微镜分离到298个疑似MPs,其中250个通过ATR-FTIR确认(光谱匹配度≥89%)。在旅游密集的海滩(S1-S4, S12)和渔业为主的区域(S8-S11)中,纤维和碎片的丰度较高。高分子型材以PE、PP、PET和PVC为主。四个互补的生态风险指标,即污染负荷指数(PLI)、聚合物危害指数(PHI)、沉积物聚合物危害指数(SPHI)和微塑料污染风险指数(MPRI),确定了局部风险升高的热点,特别是在旅游和活跃的捕鱼地点。多变量分析(PCA, HCA)揭示了与站点使用类别相关的清晰聚类模式,而机器学习分类器(随机森林,SVM, KNN)根据MP形态,颜色,聚合物类型和丰度准确区分了旅游,渔业和低利用区域。总的来说,这些发现表明,人为压力强烈地影响了圣马丁岛上的微塑料成分和危害概况。本文提出的综合风险指数和ML框架为数据有限地区的沿海微塑料监测提供了一种可靠、可重复的方法,并可支持脆弱岛屿生态系统中有针对性的管理和缓解战略。
{"title":"Polymer‑specific hazard profiling and risk indexing of microplastics in coastal sediments of St. Martin’s Island: A multivariate and machine learning approach","authors":"Mahir Tajwar ,&nbsp;Sidratul Muntaha ,&nbsp;Asif Ashraf ,&nbsp;Md Sahidul Islam ,&nbsp;Subrota Kumar Saha","doi":"10.1016/j.hazadv.2026.101017","DOIUrl":"10.1016/j.hazadv.2026.101017","url":null,"abstract":"<div><div>Microplastic (MP) contamination poses an emerging ecological threat in small-island environments, yet polymer-specific risk assessments remain limited for the Bay of Bengal region. This study provides the first integrated, polymer-resolved evaluation of microplastics in coastal sediments of St. Martin’s Island, Bangladesh. A total of 298 suspected MPs were isolated through stereomicroscopy, of which 250 particles were confirmed through ATR-FTIR (≥89% spectral match). Fibres and fragments dominated the assemblage, with high abundances observed in tourism-intensive beaches (S1–S4, S12) and fishing-dominated zones (S8–S11). Polymer profiles were characterized by the predominance of PE, PP, PET, and PVC. Four complementary ecological risk metrics, Pollution Load Index (PLI), Polymer Hazard Index (PHI), Sediment Polymer Hazard Index (SPHI), and the Microplastic Pollution Risk Index (MPRI), identified localized hotspots of elevated risk, particularly at tourism and active fishing sites. Multivariate analyses (PCA, HCA) revealed clear clustering patterns associated with site-use categories, while machine-learning classifiers (Random Forest, SVM, KNN) accurately distinguished tourism, fishing, and low-use zones based on MP morphology, color, polymer type, and abundance. Collectively, these findings demonstrate that anthropogenic pressure strongly shapes microplastic composition and hazard profiles on St. Martin’s Island. The integrated risk-index and ML framework presented here provides a robust, reproducible approach for coastal microplastic monitoring in data-limited regions and can support targeted management and mitigation strategies in vulnerable island ecosystems.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101017"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145976538","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
Journal of hazardous materials advances
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