Beilstein J. Org. Chem.2010,6, No. 58, doi:10.3762/bjoc.6.58
-22), 66.93 (C-14), 62.05 (C-24), 58.07 (C-10), 50.65 (C-13), 48.40 (C-1), 40.04 (C-7), 35.00 (C-2), 31.48 (C-4), 26.00–26.50 (C-6, C-8), 18.27 (C-3).
Nanoparticle formation
Ethyl acetate and water were contacted for 2 h in order to obtain mutually saturated solutions. Polycaprolactone (80000 g/mol
emulsified by sonication (ultrasonic processor Vibra Cell VCX-750) for 2 min at 525 W. De-ionized water (175 mL) was then added while stirring the solution at 700–800 rpm. The nanoparticle suspension was then concentrated at atmospheric pressure to 30–35 mL by stirring and heating to 70–80 °C.
The sizes of
containing D-mannose with con A
In a 20 mL flask, 8.7 mg of concanavalin A was dissolved without stirring in 10 mL of phosphate-buffered saline (PBS, pH = 6.8, 0.1 M) over 16 hours. The flask was then stored at 4 °C. The nanoparticle stock solution (200 mg of dry matter in 3.5 mL H2O) was diluted in PBS and
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Graphical Abstract
Figure 1:
Preparation of the 8-azido-3,6-dioxaoctyl α-D-mannopyranoside.