Male Sprague Dawley rats were given an intravenous bolus injection of 0.5, 1, 1.5, and 2 mg·kg−1 of ADCs. Body weights and general clinical observations were recorded daily over the entire 21 days of the study. Blood samples for pharmacokinetics (PK) were drawn predose, 4, 24, 48, 96, 168, 336, and 504 h after injection of test articles and collected in heparin‐coated tubes, followed by 14 000 g centrifugation for 5 min. Plasma concentrations of ADCs were measured by ELISA. Noncompartmental pharmacokinetic parameters were calculated using WinNonlin software (Pharsight, Mountain View, CA, USA).
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