Fig. 1Design of fluorescent QDs, measurement of hydrodynamic diameter, and interaction of the organic coating with serum proteins
a. Chemical compositions of CdSe/ZnS QDs with DHLA (anionic), cysteamine (cationic), cysteine (zwitterionic), and DHLA-PEG (neutral) coatings.
b. GFC (mobile phase = PBS, pH 7.4) of QDs (CdSe/ZnS core/shell, diameter 3.02 nm) with organic coatings shown in (a) after treatment with PBS, pH 7.4 (blue line) or FBS (red line). λexc = 414 nm. λem = 534 nm. Molecular weight markers M1 (thyroglobulin; 669 kDa, 18.0 nm HD), M2 (γ-globulin; 158 kDa, 11.9 nm HD), M3 (ovalbumin; 44 kDa, 6.13 nm HD), and M4 (myoglobin; 17 kDa, 3.83 nm HD) are shown by arrows.
c. GFC (mobile phase = PBS, pH 7.4) of QD-Cys of various hydrodynamic diameters. λexc = 414 nm. λem = 554 nm. Molecular weight markers (arrows) are as described in (a). Also shown are the peak emission wavelengths as a function of core/shell diameter measured by TEM, DLS, and GFC. TEM size data for each sample was determined from the average of at least 150 measurements. DLS and GFC measurements (mean ± S.D.) were from N = 3 independent experiments. %PD = poly-dispersity.
d. TEM pictures of QD515 (left, core/shell 2.85 nm) and QD574 (right, core/shell 4.31 nm). Scale bar = 20 nm.