31 January 1996 Independent pathway for inclusion complexes of porphyrinoid drugs in tumors: the separation from the lipoprotein pathway in plasma
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Abstract
Phthalocyanines and m-TPPs were substituted with two or three t-butyl phenyl anchor groups to build up inclusion complexes with dimeric (beta) -cyclodextrins. These complexes proved to be stable enough to hinder complexation of the porphyrinoids with plasma lipoproteins and, so, offer an independent pathway to transfer porphyrinoids to photosensitize tumor tissue.
© (1996) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Joerg G. Moser, Anja Ruebner-Heuermann, Andrea Weitemeyer, Ulrike Michelsen, Dieter Woehrle, Angelika C. Rueck, Wolfgang S. L. Strauss, Dieter Kirsch, Sonja Andrees, Chrs. Schroers, "Independent pathway for inclusion complexes of porphyrinoid drugs in tumors: the separation from the lipoprotein pathway in plasma", Proc. SPIE 2625, Photochemotherapy: Photodynamic Therapy and Other Modalities, (31 January 1996); doi: 10.1117/12.230980; https://doi.org/10.1117/12.230980
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