出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/09/01 08:47:48」(JST)
Systematic (IUPAC) name | |
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1-(3-iodobenzyl)guanidine
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Clinical data | |
Routes of administration |
Intravenous |
Legal status | |
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Identifiers | |
CAS Number | 77679-27-7 N |
ATC code | V09IX01 (WHO) (123I) V09IX02 (WHO) (131I, diagnostic) |
PubChem | CID 60860 |
ChemSpider | 54847 N |
UNII | 35MRW7B4AD Y |
ChEMBL | CHEMBL818 N |
Synonyms | meta-iodobenzylguanidine mIBG, MIBG |
Chemical data | |
Formula | C8H10IN3 |
Molar mass | 275.09 g/mol |
SMILES
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InChI
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NY (what is this?) (verify) |
Iobenguane, also known as metaiodobenzylguanidine or mIBG, or MIBG (tradename Adreview) is a radiopharmaceutical,[1] used in a scintigraphy method called MIBG scan. Iobenguane is a radiolabeled molecule similar to noradrenaline.
The radioisotope of iodine used for the label can be iodine-123 (for imaging purposes only) or iodine-131 (which must be used when tissue destruction is desired, but is sometimes used for imaging also).
It localizes to adrenergic tissue and thus can be used to identify the location of tumors[2] such as pheochromocytomas and neuroblastomas. With I-131 it can also be used to eradicate tumor cells that take up and metabolize norepinephrine.
Thyroid blockade with (nonradioactive) potassium iodide is indicated for nuclear medicine scintigraphy with iobenguane/mIBG. This competitively inhibits radioiodine uptake, preventing excessive radioiodine levels in the thyroid and minimizing the risk of thyroid ablation ( in the case of I-131). The minimal risk of thryoid carcinogenesis is also reduced as a result.
The FDA-approved dosing of potassium iodide for this purpose are as follows: infants less than 1 month old, 16 mg; children 1 month to 3 years, 32 mg; children 3 years to 18 years, 65 mg; adults 130 mg.[3] However, some sources recommend alternative dosing regimens.[4]
Not all sources are in agreement on the necessary duration of thyroid blockade, although agreement appears to have been reached about the necessity of blockade for both scintigraphic and therapeutic applications of iobenguane. Commercially available iobenguane is labeled with iodine-123, and product labeling recommends administration of potassium iodide 1 hour prior to administration of the radiopharmaceutical for all age groups,[5] while the European Associated of Nuclear Medicine recommends (for iobenguane labeled with either I-131 or I-123,) that potassium iodide administration begin one day prior to radiopharmaceutical administration, and continue until the day following the injection, with the exception of new-borns, who do not require potassium iodide doses following radiopharmaceutical injection.[4]
Product labeling for diagnostic iodine-131 iobenguane recommends potassium iodide administration one day before injection and continuing 5 to 7 days following.[6] Iodine-131 iobenguane used for therapeutic purposes requires a different pre-medication duration, beginning 24–48 hours prior to iobenguane injection and continuing 10–15 days following injection.[7]
The FDOPA PET/CT scan has proven to be nearly 100% sensitive for detection of pheochromocytomas, vs. 90% for MIBG scans.[8][9][10] Centers which offer FDOPA PET/CT, however, are more rare.
Diagnostic radiopharmaceuticals (V09)
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Central nervous system |
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Skeletal system |
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Renal |
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Hepatic/reticuloendothelial |
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Respiratory system |
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Cardiovascular system |
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Inflammation/infection |
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Tumor |
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Adrenal cortex |
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Radionuclides (including tracers) |
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Therapeutic radiopharmaceuticals (V10)
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Pain palliation |
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Adrenergic tumors |
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CD20 antibodies |
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Radionuclides |
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リンク元 | 「褐色細胞腫」「シンチ」「甲状腺髄様癌」「123I-メタヨードベンジルグアニジン」「メタヨードベンジルグアニジン」 |
拡張検索 | 「131I-MIBG scintigraphy」「131I-MIBGシンチグラフィ」 |
関連記事 | 「131I」「MI」「MIBG」 |
Location | Phenotype | Phenotype | Gene/Locus | Gene/Locus |
MIM number | MIM number | |||
1p36.22 | Pheochromocytoma | 171300 | KIF1B | 605995 |
1p36.13 | Pheochromocytoma | 171300 | SDHB | 185470 |
2q11.2 | {Pheochromocytoma, susceptibility to} | 171300 | TMEM127 | 613403 |
3p25.3 | Pheochromocytoma | 171300 | VHL | 608537 |
5p13.2 | {Pheochromocytoma, modifier of} | 171300 | GDNF | 600837 |
10q11.21 | Pheochromocytoma | 171300 | RET | 164761 |
11q23.1 | Pheochromocytoma | 171300 | SDHD | 602690 |
14q23.3 | {Pheochromocytoma, susceptibility to} | 171300 | MAX | 154950 |
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