2020
DOI: 10.1016/j.ijantimicag.2020.105976
|View full text |Cite
|
Sign up to set email alerts
|

Tetrahydroporphyrin-tetratosylate (THPTS)-based photodynamic inactivation of critical multidrug-resistant bacteria in vitro

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
11
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
7

Relationship

3
4

Authors

Journals

citations
Cited by 9 publications
(11 citation statements)
references
References 32 publications
0
11
0
Order By: Relevance
“…Modified translucent hydrogels can serve as a carrier system, allowing the release of PSs under local illumination [ 44 , 45 ] . This, and the increasing availability of inexpensive lasers and light-emitting diodes (LED) for optical excitation [ 46 , 47 ], may enable applications of PDT both in cancer therapy and against infections with multidrug-resistant bacteria.…”
Section: Introductionmentioning
confidence: 99%
“…Modified translucent hydrogels can serve as a carrier system, allowing the release of PSs under local illumination [ 44 , 45 ] . This, and the increasing availability of inexpensive lasers and light-emitting diodes (LED) for optical excitation [ 46 , 47 ], may enable applications of PDT both in cancer therapy and against infections with multidrug-resistant bacteria.…”
Section: Introductionmentioning
confidence: 99%
“…Both photosensitizers have been reported to have antibacterial properties previously. [19][20][21] Additionally, both photosensitizers are cationic. While anionic photosensitizers are ineffective against several bacteria, cationic photosensitizers have shown high efficiency in the past.…”
Section: Introductionmentioning
confidence: 99%
“…The feasibility of this approach was shown to depend, on the one hand, on the bacterial strain used, and on the other hand, on the optical properties of the PS. We found that the investigated luminescence-based method is feasible in many of the bacterial strains tested, and the aPDI effects determined by this approach were in good agreement with those obtained by manual counting of bacterial colonies after agar plate culturing [ 32 ]. In some bacterial strains, such as MDR Pseudomonas aeruginosa , however, the intrinsic properties of the bacteria precluded the use of luminescence-based cell density determination.…”
Section: Discussionmentioning
confidence: 68%
“…For TMPyP-treated samples, illumination was started for 0, 60, 90 and 120 min, as previously described [ 30 , 31 ]. For THPTS-based aPDI treatment, bacteria were illuminated for 0, 4, 12, 36 and 108 min in accordance with Ziganshyna et al [ 32 ]. Additional samples were stored under identical conditions but protected from light (dark control).…”
Section: Methodsmentioning
confidence: 99%