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. Author manuscript; available in PMC: 2018 Jun 6.
Published in final edited form as: Anal Chem. 2017 May 22;89(11):5932–5939. doi: 10.1021/acs.analchem.7b00384

Figure 5.

Figure 5

SBK2-Lys-(Gd-DOTA) shows prolonged labeling of intracranial CNS-1 tumors at 0.2mmol Gd/kg compared to Scrambled-Lys-(Gd-DOTA). (A) The rate of agent clearance from 7 d CNS-1 tumors was determined by the change in T1 map value/time (min) from 20 to 35 min following intravenous injection of agent and is significantly different (p=0.026) between the mice treated with SBK2 and Scrambled agent. N=4 for each agent. (B) Normalized T1 map values over time for mice administered the indicated agent at 0.2mmol Gd/kg in CNS-1 intracranial tumor (top) or a contralateral control area (bottom). The agents were injected following acquisition of 5 baseline scans. Upon injection, the T1 map values decrease at a similar rate and to a similar extent but the SBK2 agent is cleared more slowly than the Scrambled agent in tumor. The lines show the mean +/− SE of 4 mice treated with SBK2 agent, and 4 mice treated with Scrambled agent. SBK2 and Scrambled agent show the same trend observed with flank tumors. The decrease in T1 signal is less pronounced in brains compared to flanks, despite twice the dose.