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Intracellularly and controllably biosynthesizing nanomaterials by 'Space-Time Coupling' of intracellular irrelated biochemical reaction pathways

机译:细胞内触发生化反应途径的“时空耦合”细胞内和可控地生物化纳米材料

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Intrinsic properties of nanomaterials are mainly determined by their composition, crystallinity, structure, size, and shape. In principle, the properties of nanomaterials can be finely tuned by controlling any of these parameters. Quantum dots (QDs) with fantastic optical properties, such as broad excitation, size-dependent photoluminescence, unusual photochemical stability, single-excitation/multiple-emission, etc., have attracted much attention in biological imaging. QDs based bioprobes used in clinical practice or biosystems should be of biocompatibility, nontoxicity and small size. In general, existing QDs which usually contain toxic heavy metals are close to or larger than most biomacromolecules in size. The use of QDs in biolabeling may be limited due to their large size, which would interfere with both the recognition between QD-labeled bioprobes and target molecules due to steric hindrance and the movement of the bioprobes. So far, it is still a big challenge to controllably synthesize QDs with less toxicity and small size for bioimaging and biodetection.
机译:纳米材料的固有性质主要由它们的组成,结晶度,结构,尺寸和形状决定。原则上,可以通过控制这些参数来精细调整纳米材料的性质。具有奇妙光学性质的量子点(QDS),如广泛的激发,尺寸依赖性光致发光,不寻常的光化学稳定性,单激发/多排放等,在生物成像中引起了很多关注。临床实践或生物系统中使用的基于QDS的生物体团应该具有生物相容性,无毒和小尺寸。通常,通常含有有毒重金属的现有QD近于或大于大多数尺寸的大多数生物致荷荷。由于其大尺寸可能受到限制的QDS在生物标记中的使用,这将在QD标记的生物体和靶分子之间干扰由于空间阻断和生物部的运动来干扰QD标记的生物体和靶分子之间的识别。到目前为止,可控制地合成QDS仍然是一个很大的挑战,并对生物体和生物触发的毒性较小和小尺寸。

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