# Killing of Gold Nanorods-Loaded Human Cardiac Fibroblasts Mediated by Photo-Thermal Activation

**Authors:** Erica Floris, Flaminia Pompeo, Vittorio Picchio, Selenia Miglietta, Vincenzo De Mei, Claudia Cozzolino, Francesca Icolaro, Vincenzo Petrozza, Giacomo Frati, Francesca Petronella, Isotta Chimenti, Francesca Pagano, Luciano De Sio

PMC · DOI: 10.1021/acsomega.5c12235 · ACS Omega · 2026-02-04

## TL;DR

This study explores using gold nanorods and laser light to selectively destroy heart fibroblasts, which could help treat heart diseases.

## Contribution

The paper introduces a novel method for targeted cardiac cell ablation using plasmonic photothermal therapy with gold nanorods.

## Key findings

- Human cardiac fibroblasts internalize gold nanorods without cytotoxicity.
- Laser irradiation of AuNR-loaded cells causes temperature increases leading to cell death.
- Nonloaded cells in coculture remain unaffected, showing selective ablation.

## Abstract

Cardiac fibrosis
is a pathological process associated with several
heart diseases, characterized by extracellular matrix deposition by
cardiac fibroblasts. Photothermal therapy is a minimally invasive
medical treatment that uses nanomaterials to convert external light
into localized heating. On these premises, we report an innovative
approach that exploits gold nanorods (AuNRs)-mediated plasmonic photothermal
therapy (PPTT) for selective ablation of AuNR-loaded human cardiac
fibroblasts (hCFs). Cellular uptake is confirmed by treating hCFs
with AuNRs, irradiating them with an 808 nm continuous-wave (CW) laser,
and performing ultrastructural electron microscopy analysis. Measurements
of extinction spectra, temperature variation, and cell viability were
conducted. Results show that hCFs internalize AuNRs effectively without
cytotoxicity, and extinction spectra reveal a concentration-dependent
redshift of the longitudinal plasmon bands. Upon laser irradiation,
AuNR-loaded hCFs experience a temperature increase, leading to cell
death in proportion to AuNRs concentration. In coculture systems,
AuNR-loaded hCFs are ablated while the viability of surrounding nonloaded
cells (fibroblasts or cardiomyocytes) remains unaffected, demonstrating
that hCFs can internalize AuNRs and be effectively ablated through
PPTT. Our results highlight the potential of AuNRs for targeted cardiac
cell ablation with minimal impact on adjacent cells.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, FAP (fibroblast activation protein alpha) [NCBI Gene 2191] {aka DPPIV, FAPA, FAPalpha, SIMP}, HCFC1 (host cell factor C1) [NCBI Gene 3054] {aka CFF, HCF, HCF-1, HCF1, HFC1, MAHCX}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, SMAD3 (SMAD family member 3) [NCBI Gene 4088] {aka HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3}
- **Diseases:** metabolic syndrome (MESH:D024821), Cardiac fibrosis (MESH:D005355), prostate cancer (MESH:D011471), inflammation (MESH:D007249), cancer (MESH:D009369), diabetes (MESH:D003920), lung cancer (MESH:D008175), liver fibrosis (MESH:D008103), obesity (MESH:D009765), microbial infections (MESH:D015163), cardiomyopathies (MESH:D009202), hyperthermia (MESH:D005334), death (MESH:D003643), CVDs (MESH:D002318), infection (MESH:D007239), myocardial infarction (MESH:D009203), PPTT (MESH:D016609), Cytotoxicity (MESH:D064420), breast cancer (MESH:D001943), heart failure (MESH:D006333), CF (MESH:D006331), cardiac remodeling (MESH:D020257), necrosis (MESH:D009336), brain cancer (MESH:D001932)
- **Chemicals:** gold (MESH:D006046), Calcein AM (MESH:C085925), osmium tetroxide (MESH:D009993), EDTA (MESH:D004492), ethidium (MESH:D004996), streptomycin (MESH:D013307), rapamycin (MESH:D020123), water (MESH:D014867), copper (MESH:D003300), Norepinephrine (MESH:D009638), ethanol (MESH:D000431), CFs (MESH:D002142), PI (MESH:D011419), AuNR800 (-), penicillin (MESH:D010406), pirfenidone (MESH:C093844), epoxy resin (MESH:D004853), 2-mercaptoethanol (MESH:D008623), l-glutamine (MESH:D005973), propylene oxide (MESH:C009068), PMS (MESH:D011399), glutaraldehyde (MESH:D005976), lanthanides (MESH:D028581), nintedanib (MESH:C530716)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HEK-293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), hCFs — Homo sapiens (Human), Transformed cell line (CVCL_YJ37), HL-1 — Mus musculus (Mouse), Transformed cell line (CVCL_0303)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12917637/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917637/full.md

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Source: https://tomesphere.com/paper/PMC12917637