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Updated: Jun 16, 2026

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation
Published on: March 27, 2016
Solvent-induced virus inactivation by acidic arginine solution.
Kazuko Tsujimoto1, Misao Uozaki, Keiko Ikeda
1Division of Virology, Department of Cellular and Molecular Medicine, Wakayama Medical University Graduate School of Medicine, Wakayama 641-8509, Japan.
Acidic arginine effectively inactivates herpes simplex virus type 2 (HSV-2) at lower pH and higher temperatures. This arginine solution shows unique properties for irreversible virus damage, suggesting potential for treating superficial infections.
Area of Science:
- Biochemistry
- Virology
- Pharmaceutical Science
Background:
- Viral clearance is critical for parenteral protein biopharmaceuticals.
- Current virus inactivation methods include low pH, detergent/solvent wash, and pasteurization.
- Detergent/solvent wash is also used for superficial infections like herpes simplex virus (HSV).
Purpose of the Study:
- To investigate the virus inactivation effects of acidic arginine on HSV type 2 (HSV-2).
- To determine the influence of pH and temperature on arginine's antiviral efficacy.
- To identify conditions for effective virus inactivation compatible with in vivo applications.
Main Methods:
- Aqueous arginine solutions (0.7 M) were tested against HSV-2.
- Experiments were conducted varying pH and temperature.
- Antiviral efficacy was compared to citrate-based solutions.
Main Results:
- 0.7 M aqueous arginine demonstrated high efficacy in HSV-2 inactivation.
- Inactivation was more pronounced at lower pH and higher temperatures.
- Arginine's effects surpassed those of 0.1 M citrate, 0.1 M citrate/0.6 M NaCl, and 0.7 M citrate across tested conditions.
- Arginine's efficacy is attributed to unique properties causing irreversible virus particle damage, not solely ionic strength or concentration.
Conclusions:
- Arginine exhibits potent, unique virus inactivation properties.
- Acidic arginine conditions are effective against HSV-2.
- These findings suggest potential in vivo applications for treating superficial viral infections, such as genital herpes.
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