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Inventi Impact - Pharmacokinetics & Pharmacodynamics

Articles

  • Inventi:pkd/24844/18
    PHARMACOKINETIC AND TOXICODYNAMIC CHARACTERIZATION OF A NOVEL DOXORUBICIN DERIVATIVE
    Samaa Alrushaid, Casey L Sayre, Jaime A Yanez, M Laird Forrest, Sanjeewa N Senadheera, Frank J Burczynski, Raimar Lobenberg, Neal M Davies

    Doxorubicin (Dox) is an effective anti-cancer medication with poor oral bioavailability and systemic toxicities. DoxQ was developed by conjugating Dox to the lymphatically absorbed antioxidant quercetin to improve Dox’s bioavailability and tolerability. The purpose of this study was to characterize the pharmacokinetics and safety of Dox after intravenous (IV) and oral (PO) administration of DoxQ or Dox (10 mg/kg) and investigate the intestinal lymphatic delivery of Dox after PO DoxQ administration in male Sprague–Dawley rats. Drug concentrations in serum, urine, and lymph were quantified by HPLC with fluorescence detection. DoxQ intact IV showed a 5-fold increase in the area under the curve (AUC)—18.6 1.98 compared to 3.97 0.71 g * h/mL after Dox—and a significant reduction in the volume of distribution (Vss): 0.138 0.015 versus 6.35 1.06 L/kg. The fraction excreted unchanged in urine (fe) of IV DoxQ and Dox was ~5% and ~11%, respectively. Cumulative amounts of Dox in the mesenteric lymph fluid after oral DoxQ were twice as high as Dox in a mesenteric lymph duct cannulation rat model. Oral DoxQ increased AUC of Dox by ~1.5-fold compared to after oral Dox. Concentrations of -N-Acetylglucosaminidase (NAG) but not cardiac troponin (cTnI) were lower after IV DoxQ than Dox. DoxQ altered the pharmacokinetic disposition of Dox, improved its renal safety and oral bioavailability, and is in part transported through intestinal lymphatics.

    How to Cite this Article
    CC Compliant Citation: Alrushaid, Samaa, et al. "Pharmacokinetic and Toxicodynamic Characterization of a Novel Doxorubicin Derivative." Pharmaceutics 9.3 (2017): 35, doi:10.3390/pharmaceutics9030035, https://creativecommons.org/licenses/by/4.0/.
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