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. 2017 Jun 9;25(7):1686–1696. doi: 10.1016/j.ymthe.2017.05.014

Figure 1.

Figure 1

Biodistribution of Anti-ICAM/ASM NCs Containing Different ASM Loads

Wild-type (C57BL/6) mice were i.v. injected with anti-ICAM/125I-ASM polystyrene NCs containing 0.06, 0.3, or 0.6 mg ASM/kg body weight (all at 1.8 × 1013 NCs/kg body weight). (A) The 125I content of blood samples taken 1, 15, and 30 min after injection was used to calculate the percent of the injected dose (%ID) in the circulation. (B) Similarly, the 125I content in the lungs, liver, and spleen isolated at sacrifice 30 min after injection, was used to determine the biodistribution (percent of the injected dose) in these organs. (C) The specificity index was calculated by normalizing tissue-over-blood accumulation for the targeted (anti-ICAM/ASM NCs) versus naked (ASM) enzyme, at matching ASM doses (see Materials and Methods). (D) The absolute amount of ASM delivered to these organs was calculated from their 125I-ASM content and specific radioactivity (counts per minute/milligram) of the enzyme. Data are mean ± SEM (n = 3–6 mice). *Compares formulations to the lowest ASM load; #compares highest load formulation to the intermediate ASM load (p ≤ 0.1 by Student’s t test).