Accumulation and photocytotoxicity of hypericin and analogs in two- and three-dimensional cultures of transitional cell carcinoma cells

被引:0
|
作者
Huygens, A
Huyghe, D
Bormans, G
Verbruggen, A
Kamuhabwa, AR
Roskams, T
de Witte, PAM
机构
[1] Katholieke Univ Leuven, Fac Farmaceut Wetenschappen, Lab Farmaceut Biol & Fytofarmacol, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Fac Farmaceut Wetenschappen, Lab Radiofarmaceut Chem, B-3000 Leuven, Belgium
[3] Katholieke Univ Leuven, Fac Geneeskunde, Afdeling Histochem & Cytochem, B-3000 Leuven, Belgium
关键词
D O I
10.1562/0031-8655(2003)078<0607:AAPOHA>2.0.CO;2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to investigate the in vitro cellular accumulation, distribution and photocytotoxic effect of hypericin in two-dimensional (2-D) and three-dimensional (3-D) cultured RT-112 transitional cell carcinoma cells of the bladder. In addition, two iodinated derivatives of hypericin were incorporated to investigate whether these analogs, with their increased lipophilicity and heavy-atom effect, display a different biological behavior and optimized photodynamic effect. The results indicate that hypericin and mono-iodohypericin behave similarly in terms of cellular accumulation, spheroidal distribution and photocytotoxic effect. In contrast, di-iodohypericin concentrated to a higher extent in monolayers and spheroids, but the accumulation was restricted to the outermost part of the spheroid. An inverse correlation therefore seems to exist between the extent of cellular uptake under 2-D conditions and the penetration of the compounds in multicellular systems. Moreover, a less pronounced photocytotoxic effect was observed for di-iodohypericin in both 2-D and 3-D cell culture systems. It can be concluded that iodinated derivatives of hypericin do not show an increased cytotoxic effect upon irradiation in either monolayers or spheroids. Moreover, this study shows that when new photosensitizers are preclinically developed, the use of 3-D cell aggregates is critical for a correct evaluation of their efficacy.
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页码:607 / 614
页数:8
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