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Method development for the detection...

Brachtenbach, Travis.

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Method development for the detection of synthetic cathinones and investigation of their metabolism using human microsomes.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Method development for the detection of synthetic cathinones and investigation of their metabolism using human microsomes./
作者:	Brachtenbach, Travis.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:	70 p.
附註:	Source: Masters Abstracts International, Volume: 56-02.
Contained By:	Masters Abstracts International56-02(E).
標題:	Toxicology. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10191109
ISBN:	9781369365313

Method development for the detection of synthetic cathinones and investigation of their metabolism using human microsomes.
Brachtenbach, Travis.

Method development for the detection of synthetic cathinones and investigation of their metabolism using human microsomes. - Ann Arbor : ProQuest Dissertations & Theses, 2016 - 70 p.

Source: Masters Abstracts International, Volume: 56-02.

Thesis (M.S.)--Oklahoma State University, 2016.

Abuse of designer drugs such as synthetic cathinones presents a challenge to both medical and forensic experts. Detecting cathinone exposure in humans requires a sensitive, reliable method and treatment involves an understanding of the physiological response of the body to these novel compounds. This study focused on developing a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the detection and quantitation of sixteen popular synthetic cathinone analogues. The method was found to be linear from a lower limit of 1ng/ml-10ng/ml, depending on the drug, to an upper limit of 25ng/ml for all tested drugs. This LC-MS/MS method was then employed to study the interaction of specific bath salts, mephedrone (MEPH) and buphedrone (BUPH), with cytochrome p450 (CYP) enzyme systems. The IC50s of MEPH and BUPH were determined to be 10.1 microM and 61.7 microM, respectively, using a fluorescence-based CYP2D6 inhibitor screening kit, demonstrating an inhibiting interaction with CYP2D6. A human liver microsomal preparation consisting of 20 Phase I metabolic enzymes was then tested with MEPH and BUPH, which demonstrated no significant change in parent compound concentration over the course of an hour. These findings suggest that MEPH and BUPH act as a CYP2D6 inhibitors, but are not metabolized as a substrate by the enzymes in the test system.

ISBN: 9781369365313Subjects--Topical Terms:

556884
Toxicology.

Method development for the detection of synthetic cathinones and investigation of their metabolism using human microsomes.
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