Analysis of the biomolecular profile by Fourier transform vibrational spectroscopy (FT-IR) in Acinetobacter baumannii after application of photodynamic therapy with curcumin "in vitro "

被引:0
|
作者
Marques, Camila Monteiro Santos [1 ,2 ]
Lyra, Lucas Ferreira [1 ,2 ]
Pinto, Juliana Guerra [2 ]
Sakane, Kumiko Koibuchi [1 ]
Ferreira-Strixino, Juliana [2 ]
机构
[1] Univ Vale Paraiba Univap, Res & Dev Inst R&DI, Infrared Spect Lab, Shishima Hifumi Ave 2911, BR-12244000 Sao Jose Dos Campos, SP, Brazil
[2] Univ Vale Paraiba Univap, Photobiol Appl Hlth PhotoBioS Res & Dev Inst R&DI, Shishima Hifumi Ave 2911, BR-12244000 Sao Jose Dos Campos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ESKAPE; Acinetobacter baumannii; photodynamic therapy (PDT); Curcumin; Fourier Transform Infrared Spectroscopy (FT-IR); Secondary structures of proteins; Biomolecules; INFRARED-SPECTROSCOPY; CELL-DEATH;
D O I
10.1016/j.saa.2025.125740
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Acinetobacter baumannii stands out for its antimicrobial resistance and high capacity to cause hospital infections, posing a severe threat to global public health. Thus, there is an urgent need for new therapeutic strategies. This work applied photodynamic therapy (PDT) with curcumin to Acinetobacter baumannii, and bacterial cell viability was assessed. Fourier transform infrared spectroscopy (FT-IR) was used to study changes in biomolecules after PDT application, comparing them with control groups that were only irradiated and only with curcumin photosensitizer. According to the results, there was an increase in the total amount of lipids ( 0.3 %), total proteins ( 0.6 %), and nuclear material ( 8.6 %), with a decrease in carbohydrates ( 3.0 %) after the application of PDT, compared to the control group. In the secondary structure of the proteins, a reduction in alpha-helix ( 3.0 %), disordered structure ( 7.0 %), and turns ( 5.0 %) was observed, with an increase in beta-sheets ( 8.8 %). The analysis of biomolecular changes by FT-IR after the application of PDT can contribute to understanding the mechanisms of action of cell death, enabling therapeutic strategies to improve diagnosis and clinical treatment.
引用
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页数:12
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