不同灵芝子实体及其粗多糖中微量元素及重金属含量分析

利用电感耦合等离子发射光谱-质谱联用法（ICP-MS）、原子荧光法（AFS）和原子吸收法（AAS）对不同品种灵芝子实体中的生物必需微量元素。有毒的微量元素及重金属元素的含量进行了测定,并对其营养性和安全性进行了分析。与砷、镉、汞相比,在所有品种的灵芝中重金属铅的含量相对较高,但是在对全国各地收集的灵芝及其培养基分析,灵芝对铅没有生物富集的作用,另外,灵芝粗多糖中各种元素的含量均明显高于提取用的灵芝子实体,其中铅和砷含量高于国家标准,其安全性应该受到重视。     

栽培条件对灵芝子实体中四种重金属含量的影响

以不同灵芝品种、不同栽培基质、不同栽培方式、不同生长时期获得的菌草灵芝和木屑灵芝为原料,对栽培基质及灵芝子实体中铅、砷、汞、镉4种重金属的含量参照国际标准进行检测,结果表明虽然菌草栽培基质中重金属含量高于木屑栽培基质,但菌草灵芝对重金属富集率远低于木屑灵芝,成熟期的菌草灵芝与木屑灵芝中的重金属含量均低于农业行业标准和国家标准。因此菌草可以替代木屑用作灵芝栽培的营养来源。     

海南冰糖草中4种重金属元素含量分析

目的:建立海南产冰糖草中重金属元素含量测定方法,测定其重金属元素含量。方法:采用氢化物原子荧光法建立冰糖草中重金属砷、汞、铅、镉元素的分析检测方法。结果:4种重金属元素的线性相关系数为0.9991-0.9999,精密度小于2.74%,加标回收率为95%~102.3%,RSD≤3.36%。冰糖草中重金属元素含量均符合绿色中药标准。结论:该方法简便、准确、稳定,可用于冰糖草的质量控制。     

重庆市野生黄精中重金属含量分析与评价

目的：建立电感耦合等离子体质谱法（ICP-MS）测定不同产地黄精中砷、铅、铬、镉、汞含量的方法，进行含量分析，为黄精的医用和食疗安全提供理论基础。方法：采用ICP-MS法对52份野生黄精样品中5种重金属进行检测，内标法定量，并进行数据分析。结果：野生黄精中5种重金属的方法检出限为0.002～0.020 mg/kg，回收率为95.5%～104.4%，精密度为2.8%～4.6%；野生黄精根茎中含量高低依次为铬、铅、镉、砷和汞，各元素间呈正相关；巫山的铬和砷显著高于其他地区，奉节的铅最高，石柱的镉显著高于其他地区；黄精不同部位的重金属含量高低：根须>根茎>叶子>种子，其中根须的铬含量高达4.406±1.021 mg/kg。结论：野生黄精的重金属含量存在一定的地域性差异；不同部位的含量也有差异：地下部位（根须、根茎）含量大于地上部位（叶子、种子）。本研究可为黄精的外源性污染提供数据支撑。     

微波消解-ICP-AES法测定硫熏对党参重金属及微量元素含量的影响

采用硝酸消解党参,建立电感耦合等离子体原子发射光谱法(ICP-AES)测定党参及硫磺熏蒸党参药材的重金属(Cu、Cd、Pb、Hg、As)及微量元素(Al、Cr、Fe、Mg、Zn、P、K、Ca)含量变化,研究传统硫磺熏蒸方法对党参重金属及微量元素含量的影响。结果表明,党参经硫磺熏蒸后镉(Cd)含量增加63.51%,铅(Pb)含量增加35.47%,砷(As)含量增加108.63%。Fe含量减少36.64%,K含量减少20.48%。党参硫磺熏蒸后重金属及微量元素含量有显著变化,应加强检测,以便全面评价和控制党参药材质量,确保临床用药安全。     

冬虫夏草与产地植物及土壤的重金属含量测定

本文测定了野生采集和人工培育冬虫夏草、人工培育冬虫夏草子实体、冬虫夏草发酵菌液、冬虫夏草寄主蝙蝠蛾昆虫食物(蕨麻Potentilla anserine和珠芽蓼Polygonum viviparum),以及野生冬虫夏草产地土壤中5种重金属元素(铜Cu、铅Pb、砷As、镉Cd、汞Hg)的含量。结果表明,人工培育冬虫夏草、人工培育冬虫夏草子实体、冬虫夏草发酵菌液、蕨麻块根、珠芽蓼种子的5种重金属元素含量符合《中医药-中药材重金属限量》ISO国际标准;而野生冬虫夏草,除砷含量(6.170 mg/kg)超标外,铜、铅、镉、汞元素含量均符合要求。按国家标准《土壤环境质量农用地土壤污染风险管控标准(试行)》(GB 1516-2018),四川产地土壤(KDX)与青海产地土壤(GD、HN)的5种重金属含量均低于农用土壤污染风险筛选值;而四川产地土壤(KDT),除镉含量(0.923 mg/kg)高于风险筛选值而低于风险管制值外,其余4种元素含量均低于风险筛选值。结果为人工培育冬虫夏草的质量控制提供了参考。     

湘潭莲子种植区土壤和莲子重金属污染的生态风险评价

为探讨湘潭莲子种植区土壤重金属的污染特征及潜在生态风险, 以6个主要的莲子种植区为研究对象, 分析了土壤和莲子籽粒中锰、铜、砷、镉、铅和铬的含量和污染特征, 并利用潜在生态危害指数法评价了土壤重金属的综合潜在生态风险。结果表明: 6种重金属中镉含量平均值高于风险筛选值, 低于风险管制值, 其它重金属含量的平均值低于或接近风险筛选值。各元素生态风险从大到小依次是镉、铅、砷、铜、铬、锰。6个位点的综合生态危害指数平均值为224.7, 属于中等污染风险水平。各位点对应的莲子也受到一定程度的重金属污染, 籽粒中镉和铅存在超标现象。通过以上分析说明, 莲子种植区土壤重金属整体呈现出中等生态风险状态。为了确保莲子的安全生产, 有必要加强莲子种植区的土壤检测和治理。     

重金属污染土壤中微生物的多样性

<正>土壤重金属污染是指人类活动将重金属混入到土壤中,致使土壤中重金属含量明显高于原有含量,并造成生态环境质量恶化的现象[1]。污染土壤的重金属主要包括汞(Hg)、镉(Cd)、铅(Pb)、铬(Cr)和类金属砷(As)等生物毒性显著的元素,以及有一定毒性的锌(Zn)、铜(Cu)、镍(Ni)等元素。除了来自农药、废水、污泥和     

海南万宁海域海洋生物重金属分析与评价

海洋经济生物体内重金属含量直接影响到人类健康。根据2020年12月对万宁海域12个调查站、10种生物(鱼类7种、软体类1种、甲壳类2种)体内的7种重金属(Cu、Pb、Zn、Cd、Cr、As、Hg)含量监测结果,分析了重金属的含量特征,并分别利用单因子污染指数法和重金属富集系数对重金属污染水平和它在生物体内的富集情况进行了评价。结果表明:(1)各类生物体内重金属含量的高低顺序不一致,但三类生物体内锌和铜的含量均相对较高。生物对必需元素锌和铜的富集明显高于对非必需元素铅、镉和总汞的,主动吸收能力明显。(2)不同类生物同种重金属的含量存在一定差异,甲壳类的高于鱼类和软体类的。万宁海域鱼类和软体类生物重金属单因子污染指数均小于1,部分甲壳类生物的铬单因子污染指数大于1,超标率为41.7%。铬是万宁海域海洋生物的主要污染因子,影响其含量的原因可能是周围的围填海工程,以及所研究物种的生理特性。(3)万宁海域甲壳类生物体内总汞已呈轻污染状态,铬呈重污染状态。(4)甲壳类生物对重金属的富集能力强于鱼类和软体类的,各类生物对Cu的富集能力最高,对As的富集能力最低,且对重金属Cu、Cd和Zn有潜在的严重...     

四种重金属在金针菇栽培过程中的迁移规律

为了掌握铅、镉、砷、汞4种有害重金属元素在金针菇栽培过程中的富集和迁移,为金针菇产品质量控制提供依据。采用在培养料中添加一定量的铅、镉、汞、砷栽培金针菇,测定其在各栽培阶段培养料、金针菇子实体中的含量。结果表明,在试验的浓度范围内,金针菇子实体中4种重金属的含量随着培养料中添加量的增加而增加,说明金针菇子实体中4种重金属主要是来源于培养料,但金针菇子实体对不同重金属的吸收富集能力不同,对汞的吸收富集能力最强,富集系数最高达到7.590,富集能力大小依次为汞>镉>砷>铅。     

Heavy metal concentrations in,and human health risk assessment of,three commercially valuable fish species in the lower Niger River,Nigeria

The concentrations of Fe, Mn, Ni, Pb and V in water, sediment and the gill, liver and muscle tissues of Synodontis resupinatus, Heterotis niloticus and Clarias gariepinus, all commercially important fish species of the lower Niger River, were investigated in 2015. Water, sediment and fish samples were collected for six months and heavy metals were determined using an Atomic Absorption Spectrometer. Fe ranked highest in water and sediment, with concentrations of 2.74 mg l^?1 and 61.60 mg kg^?1, respectively. Metals followed the magnitude of Fe > Mn > Ni > V > Pb in the water and Fe > Mn > V > Ni > Pb in the sediments. Metal concentrations were higher in the tissues of S. resupinatus compared with H. niloticus and C. gariepinus. Fe was also highest in the gills, liver and muscle of the three fish species. Its highest concentration of 132.97 mg kg^?1 dry weight was recorded in the gills of S. resupinatus. Bioconcentration factors of metals ranged from 8.79 for Mn in H. niloticus muscle to 67.99 for Ni in S. resupinatus gills. The fish species studied pose no health risk for all metals studied, because the target hazard quotient was less than 1 and the estimated daily intakes of the metals were below the reference doses.     

Evaluation of blood mercury and serum selenium levels in the pregnant population of the Community of Madrid,Spain

BackgroundThe main exposure route to methylmercury (MeHg) is from eating fish and shellfish containing this compound. Since 2004, women of childbearing age in Spain have been urged not to eat some species (eg, tuna, shark, and swordfish), instead choosing low-MeHg seafood as part of a healthy diet.ObjectiveTo describe maternal total blood mercury (THg) and serum selenium (Se) in a cohort of pregnant women living in Spain as it relates to fish intake during the three trimesters and to assess whether or not Spanish women of childbearing age follow the recommendations listed in fish advisories and choose fish species with lower mercury levels.MethodsWe studied 141 female volunteers of childbearing age (16–45 years), interviewing all participants about their overall eating habits and seafood intake. Hg and Se levels were tested using cold-vapor atomic absorption spectrometry (CVAAS) and electrothermal atomic absorption spectrometry (ETAAS), respectively.ResultsAverage THg levels in pregnant women were 2.89 μg/L (standard deviation [SD], 2.75 μg/L, geometric mean [GM], 2.19 μg/L), and THg GM was positively associated with fish intake. Mean Se levels in pregnant women were 73.06 μg/L (SD, 13.38 μg/L), and Se levels were found to increase with tuna intake. In 16 (12%) pregnant women, THg was higher than the level recommended by the U.S. Environmental Protection Agency (EPA) (6.4 μg/L). A positive association was also found between THg and serum Se.ConclusionWomen of childbearing age in Spain had higher THg levels than women in other Western studies. Our study observed that 12% of women had THg levels above the safety limit set by the EPA (6.4 μg/L), and 31% had levels above the relevant benchmark level of 3.5 μg/L suggested by various researchers.     

Determination of copper in different chloroplast preparations

The determination of total Cu is not often correlated with states of deficiency in plant material. This fact makes it necessary to look for biologically active Cu. Suspensions of thylakoid membranes and photosystem II particles, properly diluted with 13 mM nitric acid, were used for this purpose. The presence of a minute quantity of an antifoaming agent, such as 1-octanol, is essential when an aliquot of the slurry is injected into the graphite furnace of the atomic absorption spectrophotometer. Good agreement was obtained between our results and those obtained by a classical dry combustion method. Reproducibility was better than 5% when expressed as relative standard deviation.     

Determination of trace elements in some natural drugs by atomic absorption spectrometry

Fifteen kinds of common plants, animals, and minerals used as traditional medicines by the Chinese people have been subjected to analysis by atomic absorption spectrometry for its content of seven metals: lead, cadmium, arsenic, mercury, copper, cobalt, and manganese. The concentrations of these elements are significantly different according to their vegetal, animal, or mineral origin. The average values found for lead, cadmium, arsenic, cobalt, and manganese in drugs of mineral origin are higher than those derived from plants and animals, except for copper, which was higher in drugs of animal origin. Our results suggest that the user of traditional Chinese crude drugs should be warned of the potential danger of heavy-metal poisoning because their concentrations seem to be higher than the maximum values allowed by health agencies in several countries.     

Studies on some trace and minor elements in blood

Blood is one of the widely used specimens for biological trace element research because of its biological significance and ease of sampling. We have conducted a study of the blood of the Kalpakkam township population for trace and minor elements. For this purpose, analytical methods have been developed and standardized in our laboratory for the elemental analysis of blood plasma and red cells. Inductively coupled plasma-mass spectrometry (ICP-MS), a relatively new technique, has been applied for the analysis of trace elements. Details regarding spectral interference and matrix interference encountered in the analysis of blood and the methods of correcting them have been discussed. Flame atomic absorption spectrometry (AAS)/atomic emission spectrometry (AES) has been applied for the determination of minor elements. Precision and accuracy of these methods have also been discussed.     

Chromium content in human milk,Cow's milk,and infant formulas

Chromium was measured by Electrothermal Atomic Absorption Spectrometry in human milk, cow's milk, and infant formulas. The mean levels found were 1.56, 0.83, and 4.84 (13%) μg/L, respectively. According to our data, the daily intake for the Spanish neonates is lower than the Recommended Dietary Allowances (RDAs) (10–40 μg/d) for this element.     

石墨炉原子吸收光谱法测定虾产品中铝的方法研究

目的:本文着重研究利用石墨炉原子吸收光谱法测定虾产品中铝,对测定条件进行优化选择,达到快速、准确,以弥补国家标准检测方法中没有虾产品中铝检测方法的不足。方法:利用混合酸硝酸-高氯酸对样品进行消化处理,无基体改进剂,利用石墨炉原子吸收光谱仪进行定量检测。结果:在优化干燥、灰化、原子化、除残四个步骤的时间和温度的实验条件后,铝含量在0.0-50.0μg/L范围内呈线性关系,相关系数达到r=0.9990,最低检出限为0.54 ng/mL,铝的特征质量为5.0 pg。相对标准偏差为3.83%-6.42%,虾产品中铝含量测定回收率为90.7%-105.6%。结论:本法方便准确,灵敏度高,并有较高的回收率,可作为日常检测使用。     

Evaluation of methods for total selenium determination in yeast

The selenium determination in biological materials by the classical fluorometric method (FM) is time-consuming and also hazardous, as it requires the destruction of the organic matrix samples with hot HNO₃/HClO₄ mixtures prior to analysis. Accordingly, commercial analytical laboratories are increasingly using faster instrumental methods; for sample digestion, avoid using HClO₄. Because of these procedural changes, the results obtained by commercial laboratories may be unreliable, especially for samples containing Se in organic forms. One such “difficult” substrate is Se yeast, which contains most of its Se as selenomethionine. To establish which methods for Se analysis and sample digestion are applicable, samples of Se yeast and of selenomethionine standards were sent to laboratories employing either flame atomic absorption spectrometry (FAAS), inductively coupled plasma-mass spectrometry (ICP-MS), or hydride generation atomic absorption spectrometry (HGAAS). The result were compared with those obtained by FM and non-destructive instrumental neutron activation analysis (INAA). ICP-MS, after microwave digestion of sample with HNO₃/H₂O₂, produced results within 5% of the expected values, as did those obtained by FM and INAA. With FAAS, acceptable results were obtained after digestion with HNO₃/HCl. With HGAAS, sample digestion with HNO₃/H₂O₂ produced values that were systematically elevated by about 10% and exhibited standard deviations of ≥10%. Thus, current methods of sample digestion are applicable for Se yeast analysis by ICP-MS and FAAS, but not by HGAAS.     

中药及其水煎液中微量元素含量研究

采用火焰原子吸收光谱法(flame atomic absorption spectrometry,FAAS)测定了黄芪、白术、防风及玉屏风散各次水煎液中铁、铜、锰、铅4种微量元素的含量。结果表明,中药各次水煎液中微量元素的浸出率各不相同,应合理用药,以更好地发挥中药的疗效。