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Inactivation of human viruses by povidone-iodine in comparison with other antiseptics

R Kawana1, T Kitamura, O Nakagomi

  • 1Morioka Yuuai General Hospital, Japan.

Dermatology (Basel, Switzerland)
|January 1, 1997
PubMed

Insights

Povidone-iodine (PVP-I) effectively inactivated all tested viruses, including enveloped and nonenveloped types, in vitro. Other antiseptics showed a narrower antiviral spectrum compared to PVP-I.

Area of Science:

  • Virology
  • Antimicrobial agents

Background:

  • Antiseptics are crucial for infection control.
  • Understanding the broad-spectrum virucidal activity of antiseptics is vital.

Purpose of the Study:

  • To evaluate the in vitro antiviral efficacy of povidone-iodine (PVP-I) and other antiseptics against a wide range of viruses.
  • To compare the virucidal spectrum of PVP-I with other commercial antiseptics.

Main Methods:

  • Standardized in vitro protocols were used to test antiseptics against various viruses.
  • Tested antiseptics included PVP-I formulations, chlorhexidine gluconate, benzalkonium chloride (BAC), and benzethonium chloride (BEC).

Main Results:

  • Povidone-iodine demonstrated broad-spectrum virucidal activity, inactivating all tested viruses (adeno-, mumps, rota-, polio-, coxsackie-, rhino-, herpes simplex, rubella, measles, influenza, HIV).
  • Rubella, measles, mumps viruses, and HIV were susceptible to all tested antiseptics.
  • BAC and BEC inactivated rotavirus, while adeno-, polio-, and rhinoviruses were resistant to other antiseptics besides PVP-I.
  • PVP-I exhibited a wider virucidal spectrum than the other antiseptics evaluated.

Conclusions:

  • Povidone-iodine possesses superior broad-spectrum antiviral efficacy against both enveloped and nonenveloped viruses compared to other common antiseptics.
  • PVP-I is a highly effective virucidal agent for a wide range of clinically relevant viruses.

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