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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: Prostate. 2015 Jan 25;75(6):593–602. doi: 10.1002/pros.22941

Fig 1.

Fig 1

A Scheme of the molecular structure of TGX221 and its analog BL05, as well as nanomicellar TGX221-BL05 formulation. Circled in red line indicates the modified position on TGX221 for conjugation with micelle polymers. Scale bar, 50 nm.

B Microscopic images of mice organs. Mice were treated with the solvent (PPG, 200 μl), TGX221-BL05 in polypropylene glycol (PPG) solution (naked TGX221) and nanomicellar TGX221 formulation (nano-TGX221). Drugs were injected via tail vein at a dose of 100 mg/kg bodyweight in 200 μl PPG solution. Animals were sacrificed at day 5 after drug delivery and the major organs as indicated on the left side of the panels were dissected for histological analysis after H&E staining. Magnification, × 200.

C. Tissue distribution of the delivered drug TGX221. Mice tissues harvested at autopsy described in panel B were homogenized for quantitative measurement of the TGX221 compound. Data were presented as Mean (n = 3) and error bars indicate the SEM. The asterisk indicates significant difference compared to the naked drug (P < 0.05, Student t-test).