Abstract:
:The di-methyl-, di-ethyl-, di-propyl-, di-normal butyl-, and di-iso-butyl-ethers of hematoporphyrin were synthesized and shown to possess chromatographic properties similar to those of the tumorlocalizing components of hematoporphyrin derivative (Hpd). The cellular uptake of these ethers, as well as their retention in cells during incubation with porphyrin free medium, increased with decreasing polarity and so did their efficiency in sensitizing cultured cells to photoinactivation. The least polar of the porphyrin ethers tested showed up to a 10-fold stronger efficiency in sensitizing cultured cells to photoinactivation than Hpd and Photofrin II (P II).
journal_name
Cancer Lettjournal_title
Cancer lettersauthors
Moan J,Rimington C,Sommer Sdoi
10.1016/0304-3835(87)90178-9subject
Has Abstractpub_date
1987-03-01 00:00:00pages
283-9issue
3eissn
0304-3835issn
1872-7980pii
0304-3835(87)90178-9journal_volume
34pub_type
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