Mapping of drug distribution in the rabbit liver tumor model by complementary fluorescence and mass spectrometry imaging

JOURNAL OF CONTROLLED RELEASE

卷:269

Article

Fuchs, Katrin¹  Kiss, Andras²  Bize, Pierre E.^3,4  Duran, Rafael^3,4  Denys, Alban^3,4  Hopfgartner, Gerard²  Borchard, Gerrit¹  Jordan, Olivier¹ 

[1] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, Geneva, Switzerland

[2] Univ Geneva, Dept Analyt & Inorgan Chem, Life Sci Mass Spectrometry, Geneva, Switzerland

[3] CHU Vaudois, Dept Radiol, Lausanne, Switzerland

[4] CHU Vaudois, Dept Intervent Radiol, Lausanne, Switzerland

关键词: Fluorescence imaging;    MALDI-SRM mass spectrometry imaging;    Transarterial chemoembolization;    Sunitinib;    Drug-eluting beads;    Biodistribution;   

DOI  :  10.1016/j.jconrel.2017.10.042

来源: Elsevier

【 摘 要 】

This study describes the use of fluorescence imaging and mass spectrometry imaging, for imaging the anti-angiogenic drug sunitinib, used to treat liver cancer. These techniques allowed for the assessment of local delivery of the unlabeled therapeutic drug. More specifically, the spatial distribution of the drug and its metabolites after local administration was investigated, and drug levels in tumor and liver tissue over time were quantified. For this purpose, sunitinib-eluting microspheres were locoregionally injected into the tumor feeding arteries of rabbits bearing liver tumors. In adjacent areas of tumor and non-targeted contralateral liver tissue, sunitinib distribution was mapped around beads in occluded vessels 7, 12, 13 and 14 days after embolization by means of the two imaging methods. Presence of sunitinib metabolites was assessed by mass spectrometry imaging. Sunitinib was found around microspheres in the tumor at day 7, 12, and 13. The drug was retained by the necrotic tumor tissue, resulting in homogeneously distributed and high levels of up to 40 mu g/g tissue in a 1.5 mm radius around the beads. The drug was almost completely eliminated from the contralateral liver tissue. Several of the drug's metabolites, including its primary active metabolite SU12662, were detected in the tumor tissue over 13 days. Sunitinib diffused from the beads and was retained at high, therapeutic levels during 13 days. This was confirmed independently by complementary fluorescence and mass spectrometry imaging, which served as tools to confirm effective drug delivery after hepatic transarterial administration in situ. Compound: Sunitinib: PubChem CID 5329102.

【 授权许可】

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