Activity of Drill® lozenges on the main microorganisms responsible for upper respiratory tract infections
C Michel1, S Salvatico1, H Belkhelfa1
1Fonderephar, faculté des sciences pharmaceutiques, 35, chemin des Maraîchers, 31062 Toulouse cedex 9, France.
Objectives:
The treatment of sore throat, considered to be essentially due to viral infection, does not require the use of antibiotics. The recommended treatment is therefore based on the use of topical anaesthetics and antiseptics. Throat lozenges play a leading role in topical treatment by allowing immediate, massive and persistent release of the active molecule at the site of infection. The objective of this study was to demonstrate the short-term and long-term in vitro antimicrobial efficacy of Drill(®) lozenges in relation to the main pathogens responsible for upper respiratory tract infections.
Material And Method:
The bactericidal and virucidal activity in relation to the main microorganisms responsible for upper respiratory tract infections, including the H1N1 influenza virus, was evaluated after short (5 minutes) and long (3h) contact times, according to a methodology complying with European standards for the evaluation of chemical antiseptics and disinfectants. In parallel, the global antibacterial activity was determined on 30 strains representative of the resident flora by determination of maximum inhibitory dilutions (MID) and maximum bactericidal dilutions (MBD).
Results:
Drill(®) lozenges presented an antibacterial activity inducing significant (>90%) destruction of the main upper respiratory tract pathogens after a 5-minute contact time at high concentration and after a 3-hour contact time after dilution. Drill(®) lozenges also exerted an antiviral activity inducing 2 log (99%) destruction of the H1N1 virus after a 5-min contact time at high concentration, with maintenance of this activity after dilution (3h). A homogeneous antibacterial activity was observed on the resident flora.
Conclusion:
These in vitro tests confirm the value of chlorhexidine lozenges in the treatment of upper respiratory tract infections such as sore throat.
Insights
Drill® lozenges demonstrate significant in vitro antimicrobial and antiviral efficacy against common upper respiratory tract pathogens. These findings support their use in treating infections like sore throat, complementing antibiotic-free approaches.
Area of Science:
- Microbiology
- Pharmacology
- Infectious Diseases
Background:
- Sore throat is often viral, not requiring antibiotics.
- Topical treatments like lozenges offer localized relief.
- Throat lozenges provide immediate and sustained release of active ingredients.
Purpose of the Study:
- To evaluate the in vitro antimicrobial and antiviral effectiveness of Drill® lozenges.
- To assess both short-term and long-term efficacy against key respiratory pathogens.
- To support the use of topical antiseptics in upper respiratory tract infections.
Main Methods:
- Bactericidal and virucidal activity testing against major respiratory pathogens, including H1N1 influenza virus.
- Evaluation of efficacy after short (5 minutes) and long (3 hours) contact times.
- Assessment of antibacterial activity on resident flora using maximum inhibitory and bactericidal dilutions.
Main Results:
- Drill® lozenges showed significant antibacterial activity (>90% pathogen destruction) within 5 minutes at high concentration and after 3 hours when diluted.
- Effective antiviral activity against H1N1 virus (2 log destruction) within 5 minutes, maintained after dilution for 3 hours.
- Homogeneous antibacterial effect observed on the resident flora.
Conclusions:
- In vitro results confirm Drill® lozenges' value in treating upper respiratory tract infections.
- Chlorhexidine-based lozenges are effective against common sore throat pathogens.
- Supports topical antiseptic use as an alternative to antibiotics for viral infections.
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