Paper
4 December 1996 In vivo uptake and biodistribution of lipophilic and hydrophilic photosensitizers
Author Affiliations +
Abstract
Uptake and biodistribution of photosensitizers are crucial parameters for evaluating the efficacy of photodynamic therapy (PDT). We used the tumor baring chorioallantoic membrane (CAM) as an in vivo model system to study biodistribution of hydrophilic and lipophile compounds of natural porphyrins and pthalocyanines using confocal laser scanning microscopy (LSM) and time-gated microspectrometry. Simultaneously we observed tumor vessels and tumor cells after intravascular application at different incubation times. Differences in biodistribution of hydrophilic and lipophilic sensitizers could be observed. Hydrophilic compounds were characterized by selective accumulation in tumor cells. In contrast, more lipophilic sensitizers are accumulated in endothelial cells at short incubation times as well as in tumor cells. These facts are in correlation with our studies in tumor cells and endothelial cells in vitro, where hydrophilic sensitizers are characterized by low uptake and low phototoxicity towards endothelial cells. In contrast more lipophilic sensitizers were rapidly taken up and showed high phototoxicity.
© (1996) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Karin Kunzi-Rapp, Nermin Akguen, Herbert Schneckenburger, Angelika C. Rueck, and Rudolf W. Steiner "In vivo uptake and biodistribution of lipophilic and hydrophilic photosensitizers", Proc. SPIE 2924, Photochemotherapy: Photodynamic Therapy and Other Modalities II, (4 December 1996); https://doi.org/10.1117/12.260754
Lens.org Logo
CITATIONS
Cited by 2 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Luminescence

Content addressable memory

In vivo imaging

Photodynamic therapy

Tumors

Confocal microscopy

Tumor growth modeling

Back to Top