Theranostic nanoemulsions suppress macrophage-mediated acute inflammation in rats

In inflammatory diseases or following an injury, dysregulated inflammation is a common driver of pain and tissue damage. Macrophages are immune cells that contribute to the initiation, maintenance, and resolution of inflammation due to their phenotypic plasticity in response to signals from inflammatory microenvironments. Macrophages infiltrate and polarize toward a pro-inflammatory phenotype (M<sub>1</sub>-like), thereby increasing the severity of inflammation. Therefore, we aimed to suppress the pro-inflammatory activity of M<sub>1</sub>-like macrophages and decrease their infiltration at the site of inflammatory insult to resolve tissue inflammation. To achieve this, we developed a theranostic curcumin-loaded nanoemulsion platform that delivers a low dose of curcumin, a known anti-inflammatory phytochemical, to macrophages and allows in vivo tracking of macrophages by near-infrared fluorescence (NIRF) imaging technique. In vitro, we showed that curcumin-loaded nanoemulsion suppressed polarization of macrophages towards M<sub>1</sub>-like phenotype, consequently decreasing the release of pro-inflammatory cytokines and mediators like IL-6, IL-[Formula: see text] TNF-[Formula: see text], and nitric oxide (NO). Furthermore, curcumin-loaded nanoemulsion increased the level of IL-10, an anti-inflammatory cytokine, and protected macrophages against ferroptosis compared to drug-free nanoemulsion. In a rodent model of Complete Freund's adjuvant (CFA)-induced inflammation, we demonstrated that infiltrating macrophages sequestered curcumin-loaded nanoemulsion droplets and acted as cellular drug depots at the site of inflammation. This consequently decreased macrophage infiltration at the CFA-induced inflammation site in both sexes compared to drug-free nanoemulsion, as demonstrated by NIRF imaging, H&E staining, and immunofluorescence. Taken together, our results indicated that the anti-inflammatory efficacy of curcumin was significantly improved when directly delivered to pro-inflammatory macrophages via theranostic nanoemulsion. This work opens an avenue for exploring theranostic nanoemulsions as a platform for delivering natural anti-inflammatory products for immune modulation.

Authors

Institutions

Publication Details

Journal
Journal of Nanobiotechnology
Published
2025-02-04
DOI
https://doi.org/10.1186/s12951-025-03164-w
Citations
5
Primary Topic
Curcumin's Biomedical Applications
Type
article
Field-Weighted Citation Impact
2.96

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Theranostic nanoemulsions suppress macrophage-mediated acute inflammation in rats

James M. Nichols, Fatih Zor, Michele Herneisey, Andrew J. Shepherd et al.
5 citations
Journal of Nanobiotechnology
Curcumin's Biomedical Applications
2.96
article

Theranostic nanoemulsions suppress macrophage-mediated acute inflammation in rats

James M. Nichols, Fatih Zor, Michele Herneisey, Andrew J. Shepherd, Caitlin Crelli, Fatma Nurefsan Selek, Yalçın Külahçi, Riddhi Vichare, Rebecca McCallin, Jelena M. Janjic, Anneliese Troidle, Lu Liu, Vijay S. Gorantla
article en
5 citations

Abstract

In inflammatory diseases or following an injury, dysregulated inflammation is a common driver of pain and tissue damage. Macrophages are immune cells that contribute to the initiation, maintenance, and resolution of inflammation due to their phenotypic plasticity in response to signals from inflammatory microenvironments. Macrophages infiltrate and polarize toward a pro-inflammatory phenotype (M<sub>1</sub>-like), thereby increasing the severity of inflammation. Therefore, we aimed to suppress the pro-inflammatory activity of M<sub>1</sub>-like macrophages and decrease their infiltration at the site of inflammatory insult to resolve tissue inflammation. To achieve this, we developed a theranostic curcumin-loaded nanoemulsion platform that delivers a low dose of curcumin, a known anti-inflammatory phytochemical, to macrophages and allows in vivo tracking of macrophages by near-infrared fluorescence (NIRF) imaging technique. In vitro, we showed that curcumin-loaded nanoemulsion suppressed polarization of macrophages towards M<sub>1</sub>-like phenotype, consequently decreasing the release of pro-inflammatory cytokines and mediators like IL-6, IL-[Formula: see text] TNF-[Formula: see text], and nitric oxide (NO). Furthermore, curcumin-loaded nanoemulsion increased the level of IL-10, an anti-inflammatory cytokine, and protected macrophages against ferroptosis compared to drug-free nanoemulsion. In a rodent model of Complete Freund's adjuvant (CFA)-induced inflammation, we demonstrated that infiltrating macrophages sequestered curcumin-loaded nanoemulsion droplets and acted as cellular drug depots at the site of inflammation. This consequently decreased macrophage infiltration at the CFA-induced inflammation site in both sexes compared to drug-free nanoemulsion, as demonstrated by NIRF imaging, H&E staining, and immunofluorescence. Taken together, our results indicated that the anti-inflammatory efficacy of curcumin was significantly improved when directly delivered to pro-inflammatory macrophages via theranostic nanoemulsion. This work opens an avenue for exploring theranostic nanoemulsions as a platform for delivering natural anti-inflammatory products for immune modulation.

Journal of NanobiotechnologyVol. 23(1)
The University of Texas MD Anderson Cancer Center (US), Duquesne University (US), Wake Forest University (US)
Congressionally Directed Medical Research Programs
Good health and well-being
Openalex Percentile: Top 10%
Curcumin's Biomedical Applications
2.96
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.