A new photoproduct of the drug furosemide in aqueous media

Authors: Greca, Marina1; Iesce, Maria1; Previtera, Lucio2; Rubino, Maria1; Temussi, Fabio1

Source: Environmental Chemistry Letters, Volume 2, Number 3, December 2004 , pp. 155-158(4)

Publisher: Springer

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

The solar phototransformation of furosemide has been investigated in aqueous media. Irradiation of the drug in distilled water, in water and humic acids or nitrate ions, and in sewage sludge water affords a new dehalogenated dimer. The formation of the dimer has been explained by the formation of a cation radical intermediate. The low-measured environmental concentration of furosemide with respect to predicted environmental concentration in the Po and Lambro Rivers could be justified by its phototransformation.

Keywords: Furosemide; Drug; Solar phototransformation; Solar-simulated irradiation

Document Type: Research article

DOI: 10.1007/s10311-004-0080-9

Affiliations: 1: Dipartimento di Chimica Organica e Biochimica, Università Federico II, Via Cynthia 4, 80126, Naples, Italy, 2: Dipartimento di Chimica Organica e Biochimica, Università Federico II, Via Cynthia 4, 80126, Naples, Italy, Email: previter@unina.it

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$47.00 plus tax      Refund Policy

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A