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Photoantimicrobials and PACT: what's in an abbreviation?
1School of Pharmacy & Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 3AF, UK. mark_wainwright@hotmail.com.
Abstract:
The use of a separate nomenclature for the application of photosensitisers to the oncological and infectious disease fields represents a sensible approach. There is commonality, of course, in that both utilise light activation and act via the local generation of reactive oxygen species, but the difference in cellular targets is so great that different designs are required to achieve proper selectivity for a clinical end use, whether in human or veterinary medicine. The following represents a personal view, and perhaps a clarification of terms, in what might be considered a major etymological dichotomy existing within photodynamic research, on the 20th anniversary of "PACT".
Insights
A distinct nomenclature for photosensitizers in oncology and infectious diseases is proposed. This clarifies terminology in photodynamic research, acknowledging shared mechanisms but differing cellular targets for specialized applications.
Area of Science:
- Photodynamic Therapy
- Medicinal Chemistry
- Biomedical Research
Background:
- Photosensitizers are utilized in both oncological and infectious disease treatments.
- A shared mechanism involves light activation and the generation of reactive oxygen species.
- Existing research, particularly around the 20th anniversary of "PACT", highlights a need for terminological clarity.
Purpose of the Study:
- To propose a sensible, separate nomenclature for photosensitizers in distinct medical fields.
- To clarify the etymological dichotomy within photodynamic research.
- To emphasize the need for distinct photosensitizer designs based on cellular targets.
Main Methods:
- Conceptual analysis and review of photodynamic research terminology.
- Comparison of photosensitizer applications in oncology versus infectious diseases.
- Discussion of design requirements for clinical selectivity.
Main Results:
- Identifies a significant etymological dichotomy in photodynamic research nomenclature.
- Highlights the critical differences in cellular targets between oncological and infectious disease applications.
- Argues for distinct design strategies for photosensitizers based on their intended clinical use.
Conclusions:
- Advocates for separate nomenclature for photosensitizers in oncology and infectious diseases.
- Emphasizes that despite shared mechanisms (light activation, reactive oxygen species), distinct cellular targets necessitate different photosensitizer designs.
- Calls for greater precision in terminology to improve clarity and application in clinical settings for human and veterinary medicine.
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