๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Application of I-123 HIPDM as a lung imaging agent

โœ Scribed by Wei-Jen Shih; John J. Coupal; Marcus L. Dillon; Hank F. Kung


Publisher
Springer
Year
1988
Tongue
English
Weight
470 KB
Volume
14
Category
Article
ISSN
0340-6997

No coin nor oath required. For personal study only.

โœฆ Synopsis


N,N,N'-Trimethyl-N'-(2-Hydroxyl-3-Methyl-5-123I Iodobenzyl)-1,3-Propanediamine.Hcl (123I-HIPDM) has been used for diagnosis of patients with strokes and dementias. Since this radiopharmaceutical is also accumulated in the lung, we routinely performed a lung image or images immediately prior to cerebral planar and SPECT images after a 3-5 mCi 123I-HIPDM injection. During the past 14 months, we obtained 78 (age from 41 to 92 years, average 66.7 +/- 8.9 years; 64 males, 14 females) suspected stroke or dementia patients' lung images. All lung images were correlated to chest X-ray (CXR) or CT and other clinical data. Sixty five of 78 patients had normal lungs showing homogeneous distribution of activity throughout the lungs which correlated well to normal CXR and/or CT studies. Abnormal scintigraphic patterns of the 13 patients included lung defect (5 bronchogenic carcinoma with or without atelectasis) and decreased uptake in apices (8 chronic obstructive pulmonary disease). The findings of pulmonary intrathoracic pathologies on lung images with 123I-HIPDM suggests further evaluation of the agent for detection of localized pulmonary diseases and pulmonary physiological studies relating to amine metabolism.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis and preliminary evaluation of
โœ Michael J. Adam; Yolanda Zea Ponce; Joffre M. Berry; Kevin Hoy ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 483 KB ๐Ÿ‘ 1 views

A bst rnct in buffer(pH 4) for 35 minutes at 97ยฐC. The synthesis was complete in approximately 1 hour with a radiochemical yield of 50% , a specific activity of 65 Ci/mmol and a radiochemical purity of >95%. A non radioactive standard of L-6-iododopa was synthesized by the iododemercuration of a mer

Synthesis and evaluation of [123I]-indom
โœ Md. Jashim Uddin; Brenda C. Crews; Anna L. Blobaum; Philip J. Kingsley; Kebreab ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 243 KB

## Abstract A novel series of iodinated indomethacin derivatives was synthesized, and evaluated as selective inhibitors of COXโ€2. Two candidate compounds __N__โ€(__p__โ€iodobenzyl)โ€2โ€(1โ€(__p__โ€chlorobenzoyl)โ€5โ€methoxyโ€2โ€methylโ€1__H__โ€indolโ€3โ€yl)acetamide (3) and 1โ€(__p__โ€iodobenzyl)โ€5โ€methoxyโ€2โ€methy

Synthesis of L-6-[123I]iodo-m-tyrosine a
โœ Michael J. Adam; Yolanda Zea Ponce; Joffre M. Berry ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 295 KB ๐Ÿ‘ 1 views

## Abstract Lโ€6โ€[^123^I]Iodoโ€__m__โ€tyrosine was synthesized by the direct iodination of Lโ€__m__โ€tyrosine with [^123^I]โ€NaI and Chloramineโ€T. The product was purified by reverse phase HPLC to give the final product in 57% radiochemical yield with a radiochemical purity of greater than 97%.