・ルフィマー
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- dihematoporphyrin ether、Photofrin、porfimer sodium
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/10/22 07:46:01」(JST)
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Porfimer sodium
|
Clinical data |
AHFS/Drugs.com |
Consumer Drug Information |
Licence data |
EMA:Link, US FDA:link |
Pregnancy
category |
- US: C (Risk not ruled out)
|
Legal status |
|
Routes of
administration |
Intravenous |
Pharmacokinetic data |
Bioavailability |
NA |
Protein binding |
~90% |
Biological half-life |
21.5 days (mean) |
Excretion |
Fecal |
Identifiers |
CAS Registry Number |
97067-70-4 N 87806-31-3 |
ATC code |
L01XD01 |
PubChem |
CID: 57166 |
DrugBank |
DB00707 N |
ChemSpider |
10482283 Y |
UNII |
Y3834SIK5F N |
ChEMBL |
CHEMBL1201707 N |
Chemical data |
Formula |
C68H74N8O11 (for n=0) |
Molecular mass |
1179.36 g/mol (for n=0) |
SMILES
-
[Na+].OC(=O)CC\C2=C(/C)c1cc%10nc(cc4nc(cc3nc(cc2n1)c(CCC(O)=O)c3C)/C(=C4/C)C(C)OC(C)c9c5nc(cc8nc(cc7nc(cc6nc(c5)C(\C)=C6\C(C)O)c(C)c7CCC(O)=O)C(\CCC(O)=O)=C8\C)c9C)c(C(C)O)c%10C
|
InChI
-
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-; Y
-
Key:CGQHMICGJYKFFJ-ZLJVSRBASA-N Y
|
N (what is this?) (verify) |
Porfimer sodium, sold as Photofrin, is a photosensitizer used in photodynamic therapy and radiation therapy and for palliative treatment of obstructing endobronchial non-small cell lung carcinoma and obstructing esophageal cancer.
Porfimer is a mixture of oligomers formed by ether and ester linkages of up to eight porphyrin units.[1] In practice, a red light source emitting at 630 nm is used to excite the Porfimer oligomers.[2]
Porfimer is Haematoporphyrin Derivative (HpD) (See PDT).
Approvals and indications
It was approved in Canada in 1993 for the treatment of bladder cancer.[2] It was approved in Japan in 1994 (for early stage lung cancer?).[2] It was approved by the U.S. FDA in December 1995 for esophageal cancer, and in 1998, it was approved for the treatment of early non-small cell lung cancer.[2]
In August 2003 the FDA approved its use for Barrett's esophagus.[3]
References
- ^ "Porfimer injection Prescribing information" (PDF).
- ^ a b c d "Photodynamic Therapy (PDT) for Lung Cancers". 2006.
- ^ "FDA Patient Safety News: Show #20, October 2003". October 2003. Retrieved 2009-08-17.
External links
- Photofrin
- Photofrin marketing info
- Side effects of PDT with Photofrin
- History of Photofrin
UpToDate Contents
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English Journal
- Long term efficacy of Photodynamic Therapy (PDT) as an ablative therapy of high grade dysplasia in Barrett's oesophagus.
- Gray J1, Fullarton GM.Author information 1Department of Oesophagogastric Surgery, Glasgow Royal Infirmary, 84 Castle St., Glasgow G4 0SF, United Kingdom. Electronic address: jojo.gray@gmail.com.AbstractBACKGROUND: Barrett's high grade dysplasia (HGD) is a pre-malignant condition which requires treatment with either oesophagectomy or ablative endoscopic therapy. Endoscopic ablative techniques have evolved through Photodynamic Therapy (PDT) to more recently radiofrequency ablation (RFA). Although RFA has superseded PDT due to improved efficacy and safety profile there remains a significant cohort of patients previously treated by PDT where the long term outcome is unclear. This study's aim was to assess the long term efficacy of PDT in patients with Barrett's HGD.
- Photodiagnosis and photodynamic therapy.Photodiagnosis Photodyn Ther.2013 Dec;10(4):561-5. doi: 10.1016/j.pdpdt.2013.06.002. Epub 2013 Sep 17.
- BACKGROUND: Barrett's high grade dysplasia (HGD) is a pre-malignant condition which requires treatment with either oesophagectomy or ablative endoscopic therapy. Endoscopic ablative techniques have evolved through Photodynamic Therapy (PDT) to more recently radiofrequency ablation (RFA). Although RF
- PMID 24284112
- Photodynamic therapy vs radiofrequency ablation for Barrett's dysplasia: efficacy, safety and cost-comparison.
- Ertan A1, Zaheer I, Correa AM, Thosani N, Blackmon SH.Author information 1Atilla Ertan, Nirav Thosani, Ertan Digestive Disease Center, Memorial Hermann Hospital, Texas Medical Center, Houston, TX 77030, United States.AbstractAIM: To compare effectiveness, safety, and cost of photodynamic therapy (PDT) and radiofrequency ablation (RFA) in treatment of Barrett's dysplasia (BD).
- World journal of gastroenterology : WJG.World J Gastroenterol.2013 Nov 7;19(41):7106-13. doi: 10.3748/wjg.v19.i41.7106.
- AIM: To compare effectiveness, safety, and cost of photodynamic therapy (PDT) and radiofrequency ablation (RFA) in treatment of Barrett's dysplasia (BD).METHODS: Consecutive case series of patients undergoing either PDT or RFA treatment at single center by a single investigator were compared. Thirty
- PMID 24222954
- Treatment of astrocytoma grade III with Photofrin II as a radiosensitizer. A case report.
- Schaffer M1, Hofstetter A, Ertl-Wagner B, Batash R, Pöschl J, Schaffer PM.Author information 1Department of Oncology, Baruch Padeh Medical Center, Bar-Ilan School of Medicine, Poria, Israel, mschaffer@poria.health.gov.il.AbstractINTRODUCTION: Astrocytomas are neoplasms that originate from glial cells. Anaplastic astrocytoma is classified as WHO III, with 27 % of the individuals with grade III astrocytoma living for at least 5 years even after treatment (radiation and chemotherapy). Photofrin II has been demonstrated to serve as a specific and selective radiosensitizing agent in both in vitro and in vivo tumor models.
- Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al].Strahlenther Onkol.2013 Nov;189(11):972-6. doi: 10.1007/s00066-013-0430-2. Epub 2013 Oct 26.
- INTRODUCTION: Astrocytomas are neoplasms that originate from glial cells. Anaplastic astrocytoma is classified as WHO III, with 27 % of the individuals with grade III astrocytoma living for at least 5 years even after treatment (radiation and chemotherapy). Photofrin II has been demonstrated to
- PMID 24158603
Japanese Journal
- 光線力学的治療の基礎と臨床の現状 (レーザー治療技術の現状と進展)
- 臼田 実男,石角 太一郎,池田 徳彦
- 光学 = Japanese journal of optics : a publication of the Optical Society of Japan, the Japan Society of Applied Physics 41(11), 556-560, 2012-11-00
- NAID 40019487852
- 子宮頸部初期癌ならびに異形成に対する光線力学療法の現状と展望
- 坂本 優,嘉屋 隆介,三宅 清彦,小屋松 安子,茂木 真,秋谷 司,落合 和徳,粟津 邦男,田中 忠夫,岡本 愛光
- 日本レーザー医学会誌 = The Journal of Japan Society for Laser Medicine 33(2), 117-121, 2012-08-31
- NAID 10031120446
- Tissue damage in the canine normal esophagus by photoactivation with talaporfin sodium (laserphyrin): a preclinical study.
- Horimatsu Takahiro,Muto Manabu,Yoda Yusuke,Yano Tomonori,Ezoe Yasumasa,Miyamoto Shinichi,Chiba Tsutomu
- PloS one 7(6), 2012-06-00
- … Photodynamic therapy (PDT) with porfimer sodium (Photofrin®) has some problems such as the requirement for shielding from light for several weeks and a high incidence of skin phototoxicity. …
- NAID 120004247254
Related Links
- Porfimer makes your body's tissues more sensitive to the effects of light. Porfimer is used together with "photodynamic" laser light therapy to reduce the size of tumors in the lungs or esophagus (the tube that connects your mouth ...
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