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用于超灵敏检测生物流体和活细胞中有机汞、无机汞及元素汞的水溶性硒化镉量子点

Water soluble cadmium selenide quantum dots for ultrasensitive detection of organic, inorganic and elemental mercury in biological fluids and live cells.

作者信息

Bala Subramaniyan Siva, Veerappan Anbazhagan

机构信息

Department of Chemistry, School of Chemical & Biotechnology, SASTRA Deemed University Thanjavur - 613401 Tamil Nadu India

出版信息

RSC Adv. 2019 Jul 18;9(39):22274-22281. doi: 10.1039/c9ra04753k. eCollection 2019 Jul 17.

Abstract

Mercury exists in organic, inorganic, and elemental forms; all of them are highly toxic. A sensor which could detect all forms of mercury below the permissible level in environmental and biological samples would be advantageous. A facile method to synthesize -acetyl cysteine capped cadmium selenide quantum dots (CdSe QDs) with an emission at 554 nm was reported. CdSe QDs showed high sensitivity and selectivity toward Hg in aqueous media as well as biological fluids like simulated cerebrospinal fluid, saliva, and urine, and also in natural fluids like juices of tomato, sugarcane, and lime. The sensing mechanism is attributed to the interactions between Hg and CdSe QDs inducing fluorescence quenching. The limit of detection is 1.62, 0.75, and 1.27 ppb for organic, inorganic and elemental mercury, respectively, which is below WHO guidelines. The suitability of the sensor for estimating Hg in biological fluids was demonstrated by recovery experiments. Besides sensing, a two color cell imaging method was developed employing CdSe QDs and acridine orange. Using this method, the uptake of Hg in living cells was demonstrated.

摘要

汞以有机、无机和元素形式存在;它们都具有剧毒。一种能够检测环境和生物样品中低于允许水平的所有形式汞的传感器将具有优势。据报道,有一种简便的方法可合成发射波长为554 nm的乙酰半胱氨酸包覆的硒化镉量子点(CdSe QDs)。CdSe QDs在水性介质以及生物流体(如模拟脑脊液、唾液和尿液)中,以及在天然流体(如番茄汁、甘蔗汁和酸橙汁)中对汞表现出高灵敏度和选择性。传感机制归因于汞与CdSe QDs之间的相互作用导致荧光猝灭。有机汞、无机汞和元素汞的检测限分别为1.62、0.75和1.27 ppb,低于世界卫生组织的指导方针。通过回收率实验证明了该传感器在生物流体中估算汞的适用性。除了传感,还开发了一种使用CdSe QDs和吖啶橙的双色细胞成像方法。使用这种方法,证明了活细胞中汞的摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a91/9066711/6b837d8c49a7/c9ra04753k-f1.jpg

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