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Porfimer sodium

From Wikipedia, the free encyclopedia
Pharmaceutical drug
Pharmaceutical compound
Porfimer sodium
Clinical data
Trade namesPhotofrin
AHFS/Drugs.comConsumer Drug Information
License data
Routes of
administration
Intravenous
ATC code
Legal status
Legal status
Pharmacokinetic data
BioavailabilityNA
Protein binding~90%
Eliminationhalf-life21.5 days (mean)
ExcretionFecal
Identifiers
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC68H74N8O11 (for n=0)
Molar mass1179.36 g/mol (for n=0) g·mol−1
3D model (JSmol)
  • [Na+].CC(O)C1=C(C)C=2C=C5NC(=CC4=NC(=CC=3NC(C=C1N=2)=C(C)C=3CCC(O)=O)C(CCC(O)=O)=C4C)C(C)=C5C(C)OC(C)C6=C(C)C=7C=C%10NC(=CC9=NC(=CC=8NC(C=C6N=7)=C(C)C=8CCC(O)=O)C(CCC(O)=O)=C9C)C(C)=C%10C(C)O
  • InChI=1S/C68H74N8O11.Na/c1-29-41(13-17-61(79)80)53-28-56-44(16-20-64(85)86)32(4)48(72-56)24-59-68(36(8)52(76-59)25-58-65(37(9)77)33(5)49(73-58)21-45(29)69-53)40(12)87-39(11)67-35(7)50-22-46-30(2)42(14-18-62(81)82)54(70-46)27-55-43(15-19-63(83)84)31(3)47(71-55)23-57-66(38(10)78)34(6)51(74-57)26-60(67)75-50;/h21-28,37-40,71-73,75,77-78H,13-20H2,1-12H3,(H,79,80)(H,81,82)(H,83,84)(H,85,86);/q;+1/b45-21-,46-22-,47-23-,48-24-,49-21-,50-22-,51-26-,52-25-,53-28-,54-27-,55-27-,56-28-,57-23-,58-25-,59-24-,60-26-; checkY
  • Key:CGQHMICGJYKFFJ-ZLJVSRBASA-N checkY
 ☒NcheckY (what is this?)  (verify)

Porfimer sodium, sold asPhotofrin, is aphotosensitizer used inphotodynamic therapy andradiation therapy and forpalliative treatment of obstructing endobronchialnon-small cell lung carcinoma and obstructingesophageal cancer.

Porfimer is a mixture ofoligomers formed by ether and ester linkages of up to eightporphyrin units.[1] In practice, a red light source emitting at 630 nm is used to excite the Porfimer oligomers.[2]

Porfimer isHaematoporphyrin Derivative (HpD) (SeePDT).

Approvals and indications

[edit]

It was approved in Canada in 1993 for the treatment ofbladder cancer.[2]It was approved in Japan in 1994 (for early stage lung cancer?).[2]It was approved by theU.S. FDA in December 1995 foresophageal cancer, and in 1998, it was approved for the treatment of earlynon-small cell lung cancer.[2]

In August 2003 the FDA approved its use forBarrett's esophagus.[3]

References

[edit]
  1. ^"Porfimer injection Prescribing information"(PDF). Archived fromthe original(PDF) on October 16, 2012.
  2. ^abcdUsuda J, Kato H, Okunaka T, Furukawa K, Tsutsui H, Yamada K, et al. (June 2006)."Photodynamic therapy (PDT) for lung cancers".Journal of Thoracic Oncology.1 (5):489–93.doi:10.1016/S1556-0864(15)31616-6.PMID 17409904.
  3. ^"FDA Patient Safety News: Show #20, October 2003". October 2003. Archived fromthe original on October 19, 2010. Retrieved2009-08-17.

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