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   <subfield code="a">Pharmacokinetic Study of ZS-1, a Targeted Peptide to NCI-H1299, in Rats Following Intravenous Administration</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Junqiang Luo, Xun Li, Xuediao Pan, Jie Zhou, Wenbin Feng, Dalu Liu, Linquan Zang]</subfield>
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   <subfield code="a">To investigate the pharmacokinetics of ZS-1 following intravenous injection in rats, ZS-1 was administered at doses of 20, 30 and 45mgkg−1, respectively. Blood samples were collected at 0.5, 3, 8, 12, 15, 20, 30, 40 and 45min. ZS-1 in rat plasma was measured by LC. The limit of detection (LOD) was 0.02μgmL−1. The relative standard deviation (RSD) of intra- and inter-day precisions were &lt;10%, and the accuracy of intra- and inter-day were &gt;94%. The mean extraction recovery of ZS-1 was 86.1%. After intravenous injection at doses of 20, 30 and 45mgkg−1, the concentration-time curves of ZS-1 fitted well to one compartment model. Area under the concentration-time curves (AUC) increased with dose. Clearance rates (CL) and elimination half-lives (T 1/2) had no significant difference between different dose groups (P&gt;0.05). ZS-1 was stable in plasma after at 25°C for 2, 4, 6h, after three freeze-thaw cycles, after −20°C for a month, and after −80°C for 3months. The accuracy of ZS-1 was between 96.8 and 106.9%. The results indicated there was no significant degradation. These data indicated that the method for analysis of ZS-1 was reliable and the pharmacokinetic data could guide dosing regimens to be tested in future clinical pharmacokinetic study.</subfield>
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