Development of a Biosensor to Detect Venom of Malayan Krait (Bungarus candidus)

Author:

Choowongkomon Kiattawee12ORCID,Chaisakul Janeyuth3,Seetaha Supaphorn1,Vasaruchapong Taksa4ORCID,Hodgson Wayne C.5ORCID,Rasri Natchaya1ORCID,Chaeksin Katechawin2,Boonchaleaw Sattawat2ORCID,Sookprasert Nattapon6

Affiliation:

1. Department of Biochemistry, Faculty of Science, Kasetsart University, 50 Ngam Wong Wan Road, Chatuchak, Bangkok 10900, Thailand

2. Genetic Engineering Interdisciplinary Program, Graduate School, Kasetsart University, Bangkok 10900, Thailand

3. Department of Pharmacology, Phramongkutklao College of Medicine, Ratchawithi Road, Ratchathewi, Bangkok 10400, Thailand

4. Snake Farm, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok 10330, Thailand

5. Monash Venom Group, Department of Pharmacology, Biomedical Discovery Institute, Monash University, Clayton, VIC 3800, Australia

6. Department of Preclinical Science, Faculty of Medicine, Thammasat University, Rangsit Campus, Pathumthani 12120, Thailand

Abstract

Malayan krait (Bungarus candidus) envenoming is a cause of significant morbidity and mortality in many Southeast Asian countries. If intubation and specific antivenom administration are delayed, the most significant life-threatening outcome may be the inhibition of neuromuscular transmission and subsequent respiratory failure. It is recommended that krait-envenomed victims without indications of neurotoxicity, e.g., skeletal muscle weakness or ptosis, immediately receive 10 vials of antivenom. However, the administration of excess antivenom may lead to hypersensitivity or serum sickness. Therefore, monitoring venom concentrations in patients could be used as an indicator for snake antivenom treatment. In this study, we aimed to develop a screen-printed gold electrode (SPGE) biosensor to detect B. candidus venom in experimentally envenomed rats. The gold electrodes were coated with monovalent Malayan krait IgG antivenom and used as venom detection biosensors. Electrochemical impedance spectrometry (EIS) and square wave voltammetry (SWV) measurements were performed to detect the electrical characterization between B. candidus venom and monovalent IgG antivenom in the biosensor. The EIS measurements showed increases in charge transfer resistance (Rct) following IgG immobilization and incubation with B. candidus venom solution (0.1–0.4 mg/mL); thus, the antibody was immobilized on the electrode surface and venom was successfully detected. The lowest current signal was detected by SWV measurement in rat plasma collected 30 min following B. candidus experimental envenoming, indicating the highest level of venom concentration in blood circulation (4.3 ± 0.7 µg/mL). The present study demonstrates the ability of the SPGE biosensor to detect B. candidus venom in plasma from experimentally envenomed rats. The technology obtained in this work may be developed as a detection tool for use along with the standard treatment of Malayan krait envenoming.

Funder

Medical Council of Thailand

Kasetsart University Research and Development Institute

Publisher

MDPI AG

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