Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea

A high-performance liquid chromatography-ultraviolet detector (HPLC-UV) method has been used to quantify teicoplanin concentrations in human plasma. However, the limited analytical accuracy of previously bioanalytical methods for teicoplanin has given rise to uncertainty due to the use of an externa...

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Main Authors: Jaeok Lee, Eun-Kyoung Chung, Sung-Wook Kang, Hwa-Jeong Lee, Sandy-Jeong Rhie
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/13/4/572
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author Jaeok Lee
Eun-Kyoung Chung
Sung-Wook Kang
Hwa-Jeong Lee
Sandy-Jeong Rhie
author_facet Jaeok Lee
Eun-Kyoung Chung
Sung-Wook Kang
Hwa-Jeong Lee
Sandy-Jeong Rhie
author_sort Jaeok Lee
collection DOAJ
description A high-performance liquid chromatography-ultraviolet detector (HPLC-UV) method has been used to quantify teicoplanin concentrations in human plasma. However, the limited analytical accuracy of previously bioanalytical methods for teicoplanin has given rise to uncertainty due to the use of an external standard. In this study, an internal standard (IS), polymyxin B, was applied to devise a precise, accurate, and feasible HPLC-UV method. The deproteinized plasma sample containing teicoplanin and an IS of acetonitrile was chromatographed on a C18 column with an acidic mobile phase consisting of NaH<sub>2</sub>PO<sub>4</sub> buffer and acetonitrile (78:22, <i>v</i>/<i>v</i>) by isocratic elution and detection at 220 nm. The linearity was in the range 7.8–500 mg/L calculated by the ratio of the teicoplanin signal to the IS signal. This analytical method, validated by FDA guidelines with ICH Q2 (R1), was successfully applied to analyze the plasma samples of patients in the intensive care unit for treating serious resistant bacterial infectious diseases, such as those by methicillin-resistant <i>Staphylococcus aureus</i> and <i>Enterococcus faecalis</i>. The methods suggested the potential for use in routine clinical practice for therapeutic drug monitoring of teicoplanin, providing both improved accuracy and a wide range of linearity from lower than steady-state trough concentrations (10 mg/L) to much higher concentrations.
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spelling doaj.art-29a05529f3fb4486aacedf53db9e42332023-11-21T15:58:33ZengMDPI AGPharmaceutics1999-49232021-04-0113457210.3390/pharmaceutics13040572Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in KoreaJaeok Lee0Eun-Kyoung Chung1Sung-Wook Kang2Hwa-Jeong Lee3Sandy-Jeong Rhie4College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, KoreaDepartment of Pharmacy, College of Pharmacy, Kyung Hee University, Seoul 02453, KoreaDepartment of Pulmonary, Allergy and Critical Care Medicine, Kyung Hee University Hospital at Gangdong, School of Medicine, Kyung Hee University, Seoul 05278, KoreaCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, KoreaCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, KoreaA high-performance liquid chromatography-ultraviolet detector (HPLC-UV) method has been used to quantify teicoplanin concentrations in human plasma. However, the limited analytical accuracy of previously bioanalytical methods for teicoplanin has given rise to uncertainty due to the use of an external standard. In this study, an internal standard (IS), polymyxin B, was applied to devise a precise, accurate, and feasible HPLC-UV method. The deproteinized plasma sample containing teicoplanin and an IS of acetonitrile was chromatographed on a C18 column with an acidic mobile phase consisting of NaH<sub>2</sub>PO<sub>4</sub> buffer and acetonitrile (78:22, <i>v</i>/<i>v</i>) by isocratic elution and detection at 220 nm. The linearity was in the range 7.8–500 mg/L calculated by the ratio of the teicoplanin signal to the IS signal. This analytical method, validated by FDA guidelines with ICH Q2 (R1), was successfully applied to analyze the plasma samples of patients in the intensive care unit for treating serious resistant bacterial infectious diseases, such as those by methicillin-resistant <i>Staphylococcus aureus</i> and <i>Enterococcus faecalis</i>. The methods suggested the potential for use in routine clinical practice for therapeutic drug monitoring of teicoplanin, providing both improved accuracy and a wide range of linearity from lower than steady-state trough concentrations (10 mg/L) to much higher concentrations.https://www.mdpi.com/1999-4923/13/4/572teicoplaninpolymyxin BHPLC-UVinternal standardhuman plasmaclinical application
spellingShingle Jaeok Lee
Eun-Kyoung Chung
Sung-Wook Kang
Hwa-Jeong Lee
Sandy-Jeong Rhie
Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
Pharmaceutics
teicoplanin
polymyxin B
HPLC-UV
internal standard
human plasma
clinical application
title Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
title_full Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
title_fullStr Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
title_full_unstemmed Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
title_short Quantification of Teicoplanin Using the HPLC-UV Method for Clinical Applications in Critically Ill Patients in Korea
title_sort quantification of teicoplanin using the hplc uv method for clinical applications in critically ill patients in korea
topic teicoplanin
polymyxin B
HPLC-UV
internal standard
human plasma
clinical application
url https://www.mdpi.com/1999-4923/13/4/572
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