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Tin sulfide quantum dots for in vivo near infrared imaging

机译:硫化锡量子点用于体内近红外成像

摘要

An aqueous approach to synthesize capped SnS quantum dots (QDs) followed by optional capping molecule extension by attaching one or more extending molecules to the capping molecule via peptide bond formation at elevated temperature. The capped SnS QDs may have a capping molecule:Sn:S molar ratio of 16:3:1 to 16:12:1. A suspension of SnS QDs was heat-treated at 200° C. for 0.5-4 hrs. The obtained SnS QDs showed an NIR emission peak at 820-835 nm with an excitation wavelength at 690 nm. The as synthesized SnS QDs were found to have high positive zeta potential of ˜30 mV and thus were toxic to cells. By neutralizing the SnS QDs the cytotoxicity was reduced to an accepted level. The heat-treatment step can be obviated by adding a glycerol solution containing S2− anions and capping molecule to a glycerol solution of Sn2+ ions.
机译:一种合成封端的SnS量子点(QD)的水性方法,然后通过在高温下通过肽键形成将一个或多个扩展分子连接到封端分子上,从而进行可选的封端分子扩展。封端的SnS QD可具有16:3:1至16:12:1的封端分子:Sn:S摩尔比。 SnS QDs的悬浮液在200℃下热处理0.5-4小时。所获得的SnS QD在820-835 nm处显示NIR发射峰,激发波长在690 nm处。发现合成的SnS QD具有〜30 mV的高正ζ电势,因此对细胞有毒。通过中和SnS QD,细胞毒性降低至可接受的水平。通过将含有S 2-阴离子的甘油溶液和封端分子加到Sn 2 + 离子的甘油溶液中,可以省去热处理步骤。

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