Development of HPLC-UV method for quantification of Kratom compounds mitragynine and its 7-hydroxy metabolite

Authors' Affiliations

Durbin, Kathryn, PharmD Candidate, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN. Jones, Madison, PharmD Candidate, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN. Brown, Stacy, Ph.D., Professor, Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN. Pond, Brooks, Ph.D., Professor, Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN.

Location

Culp Center Ballroom

Start Date

4-25-2023 9:00 AM

End Date

4-25-2023 11:00 AM

Poster Number

112

Faculty Sponsor’s Department

Pharmaceutical Sciences

Name of Project's Faculty Sponsor

Brooks Pond

Classification of First Author

Pharmacy Student

Competition Type

Competitive

Type

Poster Presentation

Project's Category

Nervous System

Abstract or Artist's Statement

Kratom is an herbal substance that produces opioid-like and stimulant-like effects. Kratom contains bioactive alkaloids that include mitragynine and 7-OH mitragynine. Both substances activate mu-opioid receptors as well as bind to adrenergic, dopaminergic, and serotonergic receptors, which may be responsible for the stimulant effects. There is no current approved use of kratom or kratom products by the USFDA, but it is currently being used by individuals for management of drug withdrawal, pain, fatigue, and mental health problems. Multiple serious but rare side-effects have been reported, including gastrointestinal, respiratory, psychiatric, cardiovascular issues. Thus, the USDEA considers it to be a Drug and Chemical of Concern and has warned the public against risks of Kratom use. As such, research on Kratom products is necessary to better understand risks and inform policy regarding regulation. Here, we sought to develop a method by which the pharmacologically active mitragynine and its active metabolite 7-OH mitragynine could be measured in various kratom products. The quantification of each utilized high pressure liquid chromatography with ultra-violet detection (HPLC-UV). An XBridge C18 column with 3.5 um particle size, 4.6 x 150 mm was used, and separation was achieved using a gradient elution with acetonitrile and 0.1% formic acid. The flow rate was 1 mL/min, and the oven temperature was set at 40oC. UV detection was at 254 nm. The 7-OH mitragynine peak was visible at 2.5 minutes and the mitragynine at 3.55 minutes. In conclusion, this method has potential to provide utility for detection and quantification of pharmacologically active compounds in kratom products.

This document is currently not available here.

Share

COinS
 
Apr 25th, 9:00 AM Apr 25th, 11:00 AM

Development of HPLC-UV method for quantification of Kratom compounds mitragynine and its 7-hydroxy metabolite

Culp Center Ballroom

Kratom is an herbal substance that produces opioid-like and stimulant-like effects. Kratom contains bioactive alkaloids that include mitragynine and 7-OH mitragynine. Both substances activate mu-opioid receptors as well as bind to adrenergic, dopaminergic, and serotonergic receptors, which may be responsible for the stimulant effects. There is no current approved use of kratom or kratom products by the USFDA, but it is currently being used by individuals for management of drug withdrawal, pain, fatigue, and mental health problems. Multiple serious but rare side-effects have been reported, including gastrointestinal, respiratory, psychiatric, cardiovascular issues. Thus, the USDEA considers it to be a Drug and Chemical of Concern and has warned the public against risks of Kratom use. As such, research on Kratom products is necessary to better understand risks and inform policy regarding regulation. Here, we sought to develop a method by which the pharmacologically active mitragynine and its active metabolite 7-OH mitragynine could be measured in various kratom products. The quantification of each utilized high pressure liquid chromatography with ultra-violet detection (HPLC-UV). An XBridge C18 column with 3.5 um particle size, 4.6 x 150 mm was used, and separation was achieved using a gradient elution with acetonitrile and 0.1% formic acid. The flow rate was 1 mL/min, and the oven temperature was set at 40oC. UV detection was at 254 nm. The 7-OH mitragynine peak was visible at 2.5 minutes and the mitragynine at 3.55 minutes. In conclusion, this method has potential to provide utility for detection and quantification of pharmacologically active compounds in kratom products.