Abstract

On-site monitoring of carbamazepine (CBZ) that allows rapid, sensitive, automatic, and high-throughput detection directly from whole blood is of urgent demand in current clinical practice for precision medicine. Herein, we developed two types (being indirect vs. direct) of fiber-optic biolayer interferometry (FO-BLI) biosensors for on-site CBZ monitoring. The indirect FO-BLI biosensor preincubated samples with monoclonal antibodies towards CBZ (MA-CBZ), and the mixture competes with immobilized CBZ to bind towards MA-CBZ. The direct FO-BLI biosensor used sample CBZ and CBZ-horseradish peroxidase (CBZ-HRP) conjugate to directly compete for binding with immobilized MA-CBZ, followed by a metal precipitate 3,3′-diaminobenzidine to amplify the signals. Indirect FO-BLI detected CBZ within its therapeutic range and was regenerated up to 12 times with negligible baseline drift, but reported results in 25 min. However, Direct FO-BLI achieved CBZ detection in approximately 7.5 min, down to as low as 10 ng/mL, with good accuracy, specificity and negligible matric interference using a high-salt buffer. Validation of Direct FO-BLI using six paired sera and whole blood from epileptic patients showed excellent agreement with ultra-performance liquid chromatography. Being automated and able to achieve high throughput, Direct FO-BLI proved itself to be more effective for integration into the clinic by delivering CBZ values from whole blood within minutes.

Highlights

  • Epilepsy is a neurological disorder characterized by an enduring predisposition to spontaneous epileptic seizures, and affects over 70 million people worldwide [1,2]

  • This study investigates the potential of applying the fiber-optic biolayer interferometry (FO-BLI) technique for rapid, sensitive, and automated detection of small molecule CBZ in whole blood

  • This study reports the development of two types of FO-BLI biosensors for on-site monitoring CBZ in serum and whole blood

Read more

Summary

Introduction

Epilepsy is a neurological disorder characterized by an enduring predisposition to spontaneous epileptic seizures, and affects over 70 million people worldwide [1,2]. Antiepileptic drugs remain the firstline treatment, which a majority of epileptic patients needing to take them daily, despite being effective in only 60–70% of individuals [4]. Among the available antiepileptic drugs, carbamazepine (CBZ) is the most commonly used drug in clinical practice [5]. CBZ has a narrow therapeutic index and is a highly variable drug. Therapeutic drug monitoring (TDM) is considered a powerful tool for maximizing efficacy [6,7]. TDM helps to investigate the effectiveness, pharmacokinetics, tolerability, dosage, and the possibility of withdrawing during CBZ treatment [1]. The therapeutic reference range for CBZ is 4–12 μg/mL in plasma and 2–12 μg/mL in serum [8]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call