TY - JOUR
T1 - Theranostic gold-in-gold cage nanoparticles enable photothermal ablation and photoacoustic imaging in biofilm-associated infection models
AU - Hajfathalian, Maryam
AU - de Vries, Christiaan R.
AU - Hsu, Jessica C.
AU - Amirshaghaghi, Ahmad
AU - Dong, Yuxi C.
AU - Ren, Zhi
AU - Liu, Yuan
AU - Huang, Yue
AU - Li, Yong
AU - Knight, Simon A.B.
AU - Jonnalagadda, Pallavi
AU - Zlitni, Aimen
AU - Grice, Elizabeth A.
AU - Bollyky, Paul L.
AU - Koo, Hyun
AU - Cormode, David P.
N1 - Publisher Copyright:
Copyright: © 2023, Hajfathalian et al.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - Biofilms are structured communities of microbial cells embedded in a self-produced matrix of extracellular polymeric substances. Biofilms are associated with many health issues in humans, including chronic wound infections and tooth decay. Current antimicrobials are often incapable of disrupting the polymeric biofilm matrix and reaching the bacteria within. Alternative approaches are needed. Here, we described a complex structure of a dextran-coated gold-in-gold cage nanoparticle that enabled photoacoustic and photothermal properties for biofilm detection and treatment. Activation of these nanoparticles with a near infrared laser could selectively detect and kill biofilm bacteria with precise spatial control and in a short timeframe. We observed a strong biocidal effect against both Streptococcus mutans and Staphylococcus aureus biofilms in mouse models of oral plaque and wound infections, respectively. These effects were over 100 times greater than those seen with chlorhexidine, a conventional antimicrobial agent. Moreover, this approach did not adversely affect surrounding tissues. We concluded that photothermal ablation using theranostic nanoparticles is a rapid, precise, and nontoxic method to detect and treat biofilm-associated infections.
AB - Biofilms are structured communities of microbial cells embedded in a self-produced matrix of extracellular polymeric substances. Biofilms are associated with many health issues in humans, including chronic wound infections and tooth decay. Current antimicrobials are often incapable of disrupting the polymeric biofilm matrix and reaching the bacteria within. Alternative approaches are needed. Here, we described a complex structure of a dextran-coated gold-in-gold cage nanoparticle that enabled photoacoustic and photothermal properties for biofilm detection and treatment. Activation of these nanoparticles with a near infrared laser could selectively detect and kill biofilm bacteria with precise spatial control and in a short timeframe. We observed a strong biocidal effect against both Streptococcus mutans and Staphylococcus aureus biofilms in mouse models of oral plaque and wound infections, respectively. These effects were over 100 times greater than those seen with chlorhexidine, a conventional antimicrobial agent. Moreover, this approach did not adversely affect surrounding tissues. We concluded that photothermal ablation using theranostic nanoparticles is a rapid, precise, and nontoxic method to detect and treat biofilm-associated infections.
UR - http://www.scopus.com/inward/record.url?scp=85175741302&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85175741302&partnerID=8YFLogxK
U2 - 10.1172/JCI168485
DO - 10.1172/JCI168485
M3 - Article
C2 - 37651187
AN - SCOPUS:85175741302
SN - 0021-9738
VL - 133
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 21
M1 - e168485
ER -