Abstract
In this study, two phthalocyanine-erlotinib conjugates linked by an oligoethylene glycol chain have been synthesised and fully characterised. Having erlotinib as the targeting moiety, the two conjugates exhibited high specific affinity to HepG2 cancer cells and tumour tissues, therefore leading to high photodynamic activity.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / administration & dosage*
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / pharmacology
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Drug Delivery Systems
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Erlotinib Hydrochloride
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Ethylene Glycol / chemistry
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Hep G2 Cells
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Humans
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Indoles / administration & dosage*
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Indoles / chemistry
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Indoles / pharmacology
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Isoindoles
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Neoplasms / drug therapy
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Organometallic Compounds / administration & dosage*
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Organometallic Compounds / chemistry
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Organometallic Compounds / pharmacology
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Photochemotherapy
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Photosensitizing Agents / administration & dosage*
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Photosensitizing Agents / chemistry
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Photosensitizing Agents / pharmacology
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Quinazolines / administration & dosage*
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Quinazolines / chemistry
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Quinazolines / pharmacology
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Zinc Compounds
Substances
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Antineoplastic Agents
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Indoles
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Isoindoles
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Organometallic Compounds
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Photosensitizing Agents
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Quinazolines
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Zinc Compounds
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Zn(II)-phthalocyanine
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Erlotinib Hydrochloride
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Ethylene Glycol