Chemistry:Temoporfin

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Short description: Chemical compound
Temoporfin
Temoporfin.png
Clinical data
AHFS/Drugs.comInternational Drug Names
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Legal status
  • In general: ℞ (Prescription only)
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Chemical and physical data
FormulaC44H32N4O4
Molar mass680.764 g·mol−1
3D model (JSmol)
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Temoporfin (INN) is a photosensitizer (based on chlorin) used in photodynamic therapy for the treatment of squamous cell carcinoma of the head and neck[1] .[2] It is marketed in the European Union under the brand name Foscan. The U.S. Food and Drug Administration (FDA) declined to approve Foscan in 2000. The EU approved its use in June 2001.[3]

Good results were obtained in 21 of 35 patients treated in Germany.[4]

It is photoactivated at 652 nm[2] i.e. by red light.

Patients can remain photosensitive for several weeks after treatment.[2]

References

  1. "[Squamous cell carcinoma of the head and neck. Photodynamic therapy with Foscan]" (in de). Hno 56 (4): 402–409. April 2008. doi:10.1007/s00106-007-1573-1. PMID 17516041. 
  2. 2.0 2.1 2.2 "Porphyrin and nonporphyrin photosensitizers in oncology: preclinical and clinical advances in photodynamic therapy". Photochemistry and Photobiology 85 (5): 1053–1074. 2009. doi:10.1111/j.1751-1097.2009.00585.x. PMID 19682322. 
  3. "Foscan approval saves Scotia's skin.". HighBeam. http://www.highbeam.com/doc/1P2-18794532.html. 
  4. "Photodynamic therapy with meta-tetrahydroxyphenylchlorin (Foscan) in the management of squamous cell carcinoma of the head and neck: experience with 35 patients". European Archives of Oto-Rhino-Laryngology 266 (12): 1937–1944. December 2009. doi:10.1007/s00405-009-0947-2. PMID 19290535. 

Further reading