I. Sondi et al., Preparation of aminodextran-CdS nanoparticle complexes and biologically active antibody-aminodextran-CdS nanoparticle conjugates, LANGMUIR, 16(7), 2000, pp. 3107-3118
Stable aqueous dispersions consisting of CdS nanoparticles having modal dia
meters, ranging between 2 and 8 nm, were prepared with amino-derivatized po
lysaccharides (aminodextrans, hence abbreviated as Amdex) as the stabilizin
g agents. The size, stability, and luminescence intensity of such dispersio
ns were shown to be dependent on the types of the cadmium salts and aminode
xtrans used, as well as on the reactant concentrations. Specifically, it wa
s demonstrated that the degree of substitution of amino groups in the amino
dextran molecules greatly affected the properties of the dispersions; i.e.,
with higher degree of substitution, smaller CdS particles and higher lumin
escence intensity were achieved. It was also shown that the Amdex-CdS nanop
article complexes could be activated and conjugated with antibody by conven
tional means. Molecular weight ranges of the Amdex and their complexes with
CdS nanoparticles and the purity of antibody-Amdex-CdS nanoparticle conjug
ates were determined by polyacrylamide gel electrophoresis combined with Co
omassie blue staining of resultant gel bands. The purified conjugate of the
aminodextran-CdS nanoparticle complex with anti-CD4 monoclonal antibody wa
s mixed with a whole blood control, followed by indirect sheep antimouse an
tibody-phycoerythrin (SAM-PE) labeling of washed cells incubated with T4-5X
-Amdex-CdS. Red blood cells were then lysed and quenched, and the resulting
mixture, which was run on a flow cytometer with 488.0 nm argon ion laser e
xcitation, suggested that the T4 antibody from the conjugate was present sp
ecifically on lymphocytes.