Paper
6 March 2006 Synthesis and photodynamic activities of modified corrole derivatives on nasopharyngeal carcinoma cells
Chi K. Chang, Pak-Wing Kong, Hai-Yang Liu, Lam-Lung Yeung, Ho-Kee Koon, Nai-Ki Mak
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Abstract
Ten trans-A2B and A3-type corrole photosensitizers carrying functional groups were synthesized and screened for PDT activities. Photocytotoxicity was measured by the MTT cell reduction assay on a cultured human nasopharyngeal carcinoma (NPC) cell line (HONE-1). Experimental results indicated that corroles containing a single hydroxyphenyl substituent (3, 4 and 5) exhibit the highest activity among the corrole derivatives investigated. Confocal microscopy revealed that the site of cellular localization of the photosensitizers is predominantly at mitochondria. Also, nuclear staining detected apoptotic cell death.
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Chi K. Chang, Pak-Wing Kong, Hai-Yang Liu, Lam-Lung Yeung, Ho-Kee Koon, and Nai-Ki Mak "Synthesis and photodynamic activities of modified corrole derivatives on nasopharyngeal carcinoma cells", Proc. SPIE 6139, Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy XV, 613915 (6 March 2006); https://doi.org/10.1117/12.646328
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Cited by 12 scholarly publications.
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KEYWORDS
Chlorine

Magnesium

Photodynamic therapy

Chromatography

Silica

Cell death

Solids

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