Synthesis and Spectral Studies of CdTe-Dendrimer Conjugates

被引:18
|
作者
Ghosh, Srabanti [1 ]
Saha, Abhijit [1 ]
机构
[1] UGC DAE Consortium Sci Res, Kolkata Ctr, Kolkata 700098, India
来源
NANOSCALE RESEARCH LETTERS | 2009年 / 4卷 / 08期
关键词
Quantum dots; Dendrimer; Conjugate; Infrared spectroscopy; Luminescence; LUMINESCENT QUANTUM DOTS; ENERGY-TRANSFER; NANOCRYSTALS; SIZE;
D O I
10.1007/s11671-009-9339-1
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In order to couple high cellular uptake and target specificity of dendrimer molecule with excellent optical properties of semiconductor nanoparticles, the interaction of cysteine-capped CdTe quantum dots with dendrimer was investigated through spectroscopic techniques. NH2-terminated dendrimer molecule quenched the photoluminescence of CdTe quantum dots. The binding constants and binding capacity were calculated, and the nature of binding was found to be noncovalent. Significant decrease in luminescence intensity of CdTe quantum dots owing to noncovalent binding with dendrimer limits further utilization of these nanoassemblies. Hence, an attempt is made, for the first time, to synthesize stable, highly luminescent, covalently linked CdTe-Dendrimer conjugate in aqueous medium using glutaric dialdehyde (G) linker. Conjugate has been characterized through Fourier transform infrared spectroscopy and transmission electron microscopy. In this strategy, photoluminescence quantum efficiency of CdTe quantum dots with narrow emission bandwidths remained unaffected after formation of the conjugate.
引用
收藏
页码:937 / 941
页数:5
相关论文
共 50 条
  • [41] Glycopeptide dendrimer colchicine conjugates targeting cancer cells
    Johansson, Emma M. V.
    Dubois, Joelle
    Darbre, Tamis
    Reymond, Jean-Louis
    BIOORGANIC & MEDICINAL CHEMISTRY, 2010, 18 (17) : 6589 - 6597
  • [42] Avidity Mechanism of Dendrimer-Folic Acid Conjugates
    van Dongen, Mallory A.
    Silpe, Justin E.
    Dougherty, Casey A.
    Kanduluru, Ananda Kumar
    Choi, Seok Ki
    Orr, Bradford G.
    Low, Philip S.
    Holl, Mark M. Banaszak
    MOLECULAR PHARMACEUTICS, 2014, 11 (05) : 1696 - 1706
  • [43] Enhancement of gene expression by polyamidoamine dendrimer conjugates with α-, β-, and γ-cyclodextrins
    Arima, H
    Kihara, F
    Hirayama, F
    Uekama, K
    BIOCONJUGATE CHEMISTRY, 2001, 12 (04) : 476 - 484
  • [44] In Vitro Evaluation of Third Generation PAMAM Dendrimer Conjugates
    Najlah, Mohammad
    Freeman, Sally
    Khoder, Mouhamad
    Attwood, David
    D'Emanuele, Antony
    MOLECULES, 2017, 22 (10)
  • [45] Synthesis and spectral properties of estrogen-and androgen-BODIPY conjugates
    Osati, Samira
    Ali, Hasrat
    Guerin, Brigitte
    van Lier, Johan E.
    STEROIDS, 2017, 123 : 27 - 36
  • [46] SULFATE ESTER CONJUGATES - THEIR SYNTHESIS, PURIFICATION, HYDROLYSIS, AND CHEMICAL SPECTRAL PROPERTIES
    PAULSON, GD
    ACS SYMPOSIUM SERIES, 1976, (29): : 86 - 102
  • [47] Synthesis and Characterization of KKRK Peptide-PAMAM Dendrimer G2 Conjugates as Gene Carriers
    Kim, Younjin
    Choi, Joon-Sig
    POLYMER-KOREA, 2022, 46 (01) : 113 - 121
  • [48] Synthesis and In Vivo Antitumor Efficacy of PEGylated Poly(L-lysine) Dendrimer-Camptothecin Conjugates
    Fox, Megan E.
    Guillaudeu, Steve
    Frechet, Jean M. J.
    Jerger, Katherine
    Macaraeg, Nichole
    Szoka, Francis C.
    MOLECULAR PHARMACEUTICS, 2009, 6 (05) : 1562 - 1572
  • [49] Synthesis and spectral and luminescence properties of new conjugates of brassinosteroids for immunofluorescence analysis
    Raichenok, T. F.
    Litvinovskaya, R. P.
    Zhabinskii, V. N.
    Raiman, M. E.
    Kurtikova, A. L.
    Minin, P. S.
    CHEMISTRY OF NATURAL COMPOUNDS, 2012, 48 (02) : 267 - 271
  • [50] Synthesis of CpM(CO)3-DAB and -PAMAM Dendrimer Conjugates and Preliminary Evaluation of Their Biological Activity
    Hu, Wanning
    Hoyer, Jan
    Neundorf, Ines
    Govender, Preshendren
    Smith, Gregory S.
    Schatzschneider, Ulrich
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2015, (09) : 1505 - 1510