Lai Pei-Yu, Huang Chih-Ching, Chou Tzung-Han, Ou Keng-Liang, Chang Jia-Yaw
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan, ROC.
Institute of Bioscience and Biotechnology and Center for Marine Bioenvironment and Biotechnology, National Taiwan Ocean University, Keelung 20224, Taiwan, ROC.
Acta Biomater. 2017 Mar 1;50:522-533. doi: 10.1016/j.actbio.2016.12.028. Epub 2016 Dec 18.
Here, we present the microwave-assisted synthesis of InS/ZnS core/shell quantum dots (QDs) co-doped with Ag and Mn (referred to as AgMn:InS/ZnS). Ag altered the optical properties of the host QDs, whereas the spin magnetic moment (S=5/2) of Mn efficiently induced the longitudinal relaxation of water protons. To the best of our knowledge, this is the first report of the aqueous synthesis of color-tunable AgMn:InS/ZnS core/shell QDs with magnetic properties. The synthetic procedure is rapid, facile, reproducible, and scalable. The obtained QDs offered a satisfactory quantum yield (45%), high longitudinal relaxivity (6.84smM), and robust photostability. In addition, they exhibited excellent stability over a wide pH range (5-12) and high ionic strength (0.15-2.0M NaCl). As seen by confocal microscopy and magnetic resonance imaging, AgMn:InS/ZnS conjugated to hyaluronic acid (referred to as AgMn:InS/ZnS@HA) efficiently and specifically targeted cluster determinant 44, a receptor overexpressed on cancer cells. Moreover, AgMn:InS/ZnS@HA showed negligible cytotoxicity in vitro and in vivo, rendering it a promising diagnostic probe for dual-modal imaging in clinical applications.
In this manuscript, we reported a facial and rapid method to prepare InS/ZnS core/shell quantum dots (QDs) co-doped with Ag and Mn (referred to as AgMn:InS/ZnS). Ag dopants were used to alter the optical properties of the InS host, whereas Mn co-dopants with their unpaired electrons provided paramagnetic properties. The emission wavelength of the core/shell QDs could be tuned from 550 to 743nm with a maximum PL quantum yield of 45%. The resulting core/shell QDs also maintained a stable emission in aqueous solution at broad ranges of pH (5-12) and ionic strength (0.15-2.0M NaCl), as well as a high photostability under continuous irradiation. In vivo cytotoxicity experiments showed that up to 500μg/mL AgMn:InS/ZnS@HA did not cause obvious toxicity to zebrafish embryos. In vitro targeted cell luminescence and magnetic resonance imaging showed that AgMn:InS/ZnS conjugated to hyaluronic acid was selectively and efficiently internalized in CD44-expressing tumor cells, confirming that the resultant QDs could function as dual-modal imaging probes for accurate diagnosis.
在此,我们展示了微波辅助合成共掺杂银和锰的硫化铟/硫化锌核壳量子点(QDs)(称为AgMn:InS/ZnS)。银改变了主体量子点的光学性质,而锰的自旋磁矩(S = 5/2)有效地诱导了水质子的纵向弛豫。据我们所知,这是关于具有磁性的颜色可调AgMn:InS/ZnS核壳量子点水相合成的首次报道。合成过程快速、简便、可重复且可扩展。所获得的量子点具有令人满意的量子产率(45%)、高纵向弛豫率(6.84 s mM)和强大的光稳定性。此外,它们在宽pH范围(5 - 12)和高离子强度(0.15 - 2.0 M NaCl)下表现出优异的稳定性。通过共聚焦显微镜和磁共振成像观察到,与透明质酸共轭的AgMn:InS/ZnS(称为AgMn:InS/ZnS@HA)有效且特异性地靶向簇分化抗原44,这是一种在癌细胞上过度表达的受体。此外,AgMn:InS/ZnS@HA在体外和体内均显示出可忽略不计的细胞毒性,使其成为临床应用中双模态成像的有前景的诊断探针。
在本手稿中,我们报道了一种简便快速的方法来制备共掺杂银和锰的硫化铟/硫化锌核壳量子点(称为AgMn:InS/ZnS)。银掺杂剂用于改变硫化铟主体的光学性质,而具有未成对电子的锰共掺杂剂提供顺磁性。核壳量子点的发射波长可从550调至743 nm,最大PL量子产率为45%。所得核壳量子点在宽pH范围(5 - 12)和离子强度(0.15 - 2.0 M NaCl)的水溶液中也保持稳定发射,以及在连续照射下具有高光稳定性。体内细胞毒性实验表明,高达500 μg/mL的AgMn:InS/ZnS@HA对斑马鱼胚胎未造成明显毒性。体外靶向细胞发光和磁共振成像表明,与透明质酸共轭的AgMn:InS/ZnS被选择性且有效地内化到表达CD44的肿瘤细胞中,证实所得量子点可作为双模态成像探针用于准确诊断。