In Vitro Evaluation of Photodynamic Activity of Plant Extracts from <i>Senna</i> Species against Microorganisms of Medical and Dental Interest
Background: Bacterial resistance requires new treatments for infections. In this context, antimicrobial photodynamic therapy (aPDT) is an effective and promising option. Objectives: Three plant extracts (<i>Senna splendida</i>, <i>Senna alata</i>, and <i>Senna macranthe...
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Main Authors: | , , , , , , , |
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Format: | Book |
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MDPI AG,
2023-01-01T00:00:00Z.
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Summary: | Background: Bacterial resistance requires new treatments for infections. In this context, antimicrobial photodynamic therapy (aPDT) is an effective and promising option. Objectives: Three plant extracts (<i>Senna splendida</i>, <i>Senna alata</i>, and <i>Senna macranthera</i>) were evaluated as photosensitizers for aPDT. Methods: <i>Cutibacterium acnes</i> (ATCC 6919), <i>Streptococcus mutans</i> (ATCC 35668), <i>Staphylococcus aureus</i> (ATCC 25923), <i>Escherichia coli</i> (ATCC 25922), and <i>Candida albicans</i> (ATCC 90028) were evaluated. Reactive oxygen species production was also verified. Oral keratinocytes assessed cytotoxicity. LC-DAD-MS analysis identified the chemical components of the evaluated extracts. Results: Most species cultured in the planktonic phase showed total microbial reduction (>6 log10 CFU/mL/<i>p</i> < 0.0001) for all extracts. <i>C. albicans</i> cultured in biofilm showed total microbial reduction (7.68 log10 CFU/mL/<i>p</i> < 0.0001) for aPDT mediated by all extracts. Extracts from <i>S. macranthera</i> and <i>S. alata</i> produced the highest number of reactive oxygen species (<i>p</i> < 0.0001). The <i>S. alata</i> extract had the highest cell viability. The LC-DAD-MS analysis of active extracts showed one naphthopyrone and seven anthraquinones as potential candidates for photoactive compounds. Conclusion: This study showed that aPDT mediated by <i>Senna</i> spp. was efficient in microbial suspension and biofilm of microorganisms of medical and dental interest. |
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Item Description: | 10.3390/pharmaceutics15010181 1999-4923 |