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Gold Nanomaterial Engineering for Macrophage-Mediated Inflammation and Tumor Treatment
- Source :
- Advanced healthcare materials. 10(5)
- Publication Year :
- 2020
-
Abstract
- Macrophages play an important role in the body's immune defense process. Phenotype imbalance between M1 and M2 macrophages induced by inflammation-related disorders and tumor can also be reversibly converted to treat these diseases. As exogenous substances, a large part of gold-based nanomaterials interact with macrophages once they enter the body, which provides gold nanomaterials a huge advantage to act as imaging contrasts, active substance carriers, and therapeutic agents for macrophage modulation. By cutting off macrophage recruitment, inhibiting macrophage activities, and modulating M1/M2 polarization, gold nanomaterial engineering exerts therapeutic effects on inflammation-related diseases at target sites. In this review, biological functions of macrophages in inflammation-related diseases are introduced, the effect of physicochemical factors of gold nanomaterials including size, shape, and surface chemistry is focused on the interaction between macrophages and gold nanomaterials, and the applications of gold nanomaterials are elaborated for tracking and treating these diseases by macrophages. The rational and smart engineering of gold nanomaterials allows a promising platform for macrophage-mediated inflammation and tumor imaging and treatment.
- Subjects :
- Immune defense
Biomedical Engineering
Pharmaceutical Science
Inflammation
02 engineering and technology
010402 general chemistry
01 natural sciences
Nanomaterials
Biomaterials
Neoplasms
medicine
Macrophage
Humans
Tumor imaging
Chemistry
Macrophages
Tumor therapy
M2 polarization
021001 nanoscience & nanotechnology
0104 chemical sciences
Cell biology
Nanostructures
Gold
medicine.symptom
0210 nano-technology
Macrophage recruitment
Subjects
Details
- ISSN :
- 21922659
- Volume :
- 10
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Advanced healthcare materials
- Accession number :
- edsair.doi.dedup.....4725e5d06f5cbfe8bf40395e7574c25e