Literature DB >> 28793756

Pharmacokinetics of Rhodamine 110 and Its Organ Distribution in Rats.

Shiau-Han Jiang1, Yung-Yi Cheng2, Teh-Ia Huo1, Tung-Hu Tsai2,3,4,5.   

Abstract

Rhodamine dyes have been banned as food additives due to their potential tumorigenicity. Rhodamine 110 is illegal as a food additive, although its pharmacokinetics have not been characterized, and no accurate bioanalytical methods are available to quantify rhodamine 110. The aim of this study was to develop and validate a fast, stable, and sensitive method to quantify rhodamine 110 using high-performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) to assess its pharmacokinetics and organ distribution in awake rats. Rhodamine 110 exhibited linear pharmacokinetics and slow elimination after oral administration. Furthermore, its oral bioavailability was approximately 34-35%. The distribution in the liver and kidney suggests that these organs are primarily responsible for rhodamine 110 metabolism and elimination. Our investigation describes the pharmacokinetics and a quantification method for rhodamine 110, improving our understanding of the food safety of rhodamine dyes.

Entities:  

Keywords:  HPLC-MS/MS; food additives; pharmacokinetics; rhodamine 110; rhodamine dyes; toxicokinetics

Mesh:

Substances:

Year:  2017        PMID: 28793756     DOI: 10.1021/acs.jafc.7b02685

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  1 in total

1.  Selective Activation of N,N'-Diacyl Rhodamine Pro-fluorophores Paired with Releasing Enzyme, Porcine Liver Esterase (PLE).

Authors:  Kristopher K Abney; Susan J Ramos-Hunter; Ian M Romaine; J Shawn Goodwin; Gary A Sulikowski; C David Weaver
Journal:  Chemistry       Date:  2018-05-25       Impact factor: 5.236

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.