One-Step Detection of Vancomycin in Whole Blood Using the Lateral Flow Immunoassay

Author:

Jung Yugyung1,Kim Seonjong2ORCID,Kim Min-Gon23ORCID,Lee Young-Eun45ORCID,Shin Myung-Geun45ORCID,Yang Sung16

Affiliation:

1. Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea

2. Department of Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea

3. GMD Biotech, Inc., Gwangju 61005, Republic of Korea

4. Department of Laboratory Medicine, Chonnam National University Hwasun Hospital (CNUHH), Hwasun 58128, Republic of Korea

5. Accelerator Platform of Precision Medicine, Chonnam National University Hwasun Hospital (CNUHH), Hwasun 58128, Republic of Korea

6. School of Mechanical Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea

Abstract

Vancomycin (VAN) is an effective antibiotic against Gram-positive bacteria and the first-line therapy to prevent and treat methicillin-resistant Staphylococcus aureus (MRSA) and severe infections. However, low concentrations of VAN can result in resistant strains. High doses of VAN can cause nephrotoxicity and ototoxicity; thus, VAN is a representative drug for which drug monitoring is recommended. Several methods have been proposed to detect VAN. Among them, lateral flow immunoassays (LFIAs) have advantages, such as simple and user-friendly operation, low sample volume requirement, and cost effectiveness. In this study, we developed an LFIA capable of rapid on-site detection such that the VAN concentration in plasma could be monitored within 20 min by a one-step detection process using whole blood without plasma separation. VAN can be detected in whole blood over a wide range of concentrations (20−10,000 ng/mL), and the LFIA reported here has a detection limit of 18 ng/mL. The applicability of the developed LFIA compared to the results of measuring VAN with a commercial enzyme-linked immunosorbent assay kit showed a satisfactory correlation (Spearman’s rho, ρ = 0.891). Therefore, the developed LFIA enables rapid and wide-range VAN detection in whole blood and can aid in drug monitoring to evaluate patients’ responses to treatment.

Funder

National Research Foundation of Korea

Korea government

Publisher

MDPI AG

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