Evidence map›Paper›PMID 41459758›Full record

ArticlePhotochemistry and photobiology

Evaluation of antibacterial photodynamic efficacy of a novel cationic near infrared chlorophyll derivative against planktonic and biofilm-borne methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa.

Sucharita Chatterjee, Alok Dube, Shovan Kumar Majumder

Abstract read
In one paragraph

Article in Photochemistry and photobiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sucharita ChatterjeeDepartment of Atomic Energy, Homi Bhabha National Institute, Mumbai, India.
Alok DubeDepartment of Atomic Energy, Homi Bhabha National Institute, Mumbai, India.ORCID https://orcid.org/0000-0001-7664-4492
Shovan Kumar MajumderDepartment of Atomic Energy, Homi Bhabha National Institute, Mumbai, India.

Funding

Department of Atomic Energy, Government of IndiaHomi Bhabha National Institute
6 · The paper itself

Abstract

Antibacterial photodynamic therapy (aPDT) is a promising approach for inactivation of antibiotic-resistant bacteria; however, its effectiveness is compromised, particularly when bacteria hide within biofilm and if infection spreads deeper in tissue. To overcome this limitation, photosensitizers having absorption in the near-infrared region (NIR) (650-800 nm), where light penetrates deeper in tissue, need to be developed. We report aPDT efficacy of Cycloimide Purpurin-18 betaine hydrazide conjugate (CIPp-18-BH), a cationic chlorophyll derivative, against Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa (PAO). CIPp-18-BH was synthesized by conjugating CIPp-18 to betaine hydrazide (BH) using a carbodiimide coupling reaction. CIPp-18-BH, as compared to CIPp-18, exhibited lower lipophilicity; thereby, it did not aggregate in aqueous conditions and generated a substantial amount of singlet oxygen upon photo-excitation with red light. CIPp-18-BH exhibited no fluorescence in water and substantial fluorescence in less polar solvents. CIPp-18-BH bound to planktonic bacteria did not show fluorescence; whereas remarkable fluorescence was seen in biofilms, indicating it lies on the surface of bacteria and accumulates within the apolar micro-environment of biofilms. PDT of planktonic MRSA and PAO with 40 μM CIPp-18-BH led to ~7 log and ~2.5 log reduction in cell viability, respectively. Confocal microscopy showed that PDT led to substantial bacterial inactivation within MRSA and PAO biofilms, resulting in inhibition of biofilm growth by ~50% and ~20%, respectively. Results demonstrate that CIPp-18-BH is a promising photosensitizer for photodynamic inactivation of planktonic and biofilm-borne bacteria.

Indexed as

Anti-Bacterial AgentsBiofilmsChlorophyllMethicillin-Resistant Staphylococcus aureusPhotosensitizing AgentsPseudomonas aeruginosaCationsInfrared RaysMicrobial Sensitivity TestsPhotochemotherapyPlanktonAnti-Bacterial AgentsCationsChlorophyllPhotosensitizing Agentsantibacterialbiofilmcationic photosensitizerchlorophyll derivativenear infraredphotodynamic treatment

Identifiers

PMID41459758
PMCPMC13575724

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.