Journal: Acta biomaterialia
Article Title: Modeling the kinetics of lymph node retention and exposure of a cargo protein delivered by biotin-functionalized nanoparticles.
doi: 10.1016/j.actbio.2023.08.048
Figure Lengend Snippet: Fig. 2. In vivo Near Infrared Imaging following Subcutaneous Administration. C57/black mice were administered SA + saline, SA-bNP or bNP + saline SC into the right footpad ( n = 3 each group). Injection volume was 40 μL in each group through a 28G needle. SA was loaded onto bNPs by incubation with an approximately 2x molar excess of SA: bNP surface biotin for 30 minutes. Unbound SA was washed from particles by centrifugation and decanting supernatant 2x. SA + saline was injected at the calculated maximum biotin binding on bNPs. T = 0 SA + saline dose was higher than SA-bNP dose due to incomplete binding of SA on bNP and washing steps to remove unbound SA. Observed fluorescence in the 700 nm channel for SA + saline (A) and SA in SA-bNP (B), and in the 800nm channel for bNP in SA-bNP (C) and unloaded bNPs (D). Normalized injection site elimination profiles vs time for SA + Saline (E ), SA in SA-bNP (F) bNP in SA-bNP (G ), and bNP + saline (H). I, Elimination rate constants from injection site. Data was fitted to a 1-compartment PK model utilizing Matlab symbiology. J, Area under the curve for free and bound SA in the injection site were calculated from concentration vs time data. ∗, ∗∗, ∗∗∗p < 0.05, < 0.01, and < 0.001 respectively, by 1-way ANOVA or two-tailed T-test.
Article Snippet: Modeling and simulations MATLAB Simbiology 2018 (Natick, MA) module was utilized to imulate the elimination of SA and bNP from the SC injections.
Techniques: In Vivo, Imaging, Saline, Injection, Incubation, Centrifugation, Binding Assay, Concentration Assay, Two Tailed Test