Cat. No. Name Size Price Add Cart
KI0818Verteporfin10 mg$512
Verteporfin50 mg$1552
Verteporfin100 mg$2672

Chemical Characteristic

Product NameVerteporfin
SynonymsVisudyne
CAS No.129497-78-5
Molecular Weight 718.79
FormulaC41H42N4O8
Chemical Structure

Biological activities

Verteporfin is a benzoporphyrin derivative. Verteporfin is a medication used as a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels. In vitro, cytotoxic effect of photodynamic therapy using verteporfin (2 µg/mL) can be augmented by paclitaxel in gastric cancer cells (NCI-N87) and bile duct cancer cells (YGIC-6B).[1] A panel of pancreatic cancer cell lines (AsPC-1, BxPC-3, Capan-1, PANC-1 and Capan-2) have gemcitabine non-responsive populations (17 to 33%) at doses up to 1mM while moderate total verteporfin photodynamic therapy (PDT) doses (1閳?µMJ/cm2) produce nearly complete killing. Verteporfin-based PDT also decreases Bcl-XL and increases the bax/Bcl-XL ratio toward a pro-apoptotic balance.[2] In vivo, verteporfin incorporated into small nanoparticles effectively controls tumor growth for 20 days in mice with early light irradiation times following verteporfin administration.[3]

Protocols

In vivo: Verteporfin is dissolved in dimethyl sulfoxide (DMSO) or 5% dextrose solution.[4]

References

[1] Park S, et al. Paclitaxel augments cytotoxic effect of photodynamic therapy using verteporfin in gastric and bile duct cancer cells. Photochem Photobiol Sci. 2008, 7(7): 769-774. 閵嗏偓閵嗏偓
[2] Celli JP, et al. Verteporfin-based photodynamic therapy overcomes gemcitabine insensitivity in a panel of pancreatic cancer cell lines. Lasers Surg Med. 2011, 43(7): 565-574. 閵嗏偓閵嗏偓
[3] Konan-Kouakou YN, et al. In vitro and in vivo activities of verteporfin-loaded nanoparticles. J Control Release. 2005, 103(1): 83-91. 閵嗏偓閵嗏偓
[4] Ota J, et al. Local photodynamic therapy for equine squamous cell carcinoma: evaluation of a novel treatment method in a murine model. Vet J. 2008, 176(2): 170-176. 閵嗏偓閵嗏偓

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