Journal
JOURNAL OF CONTROLLED RELEASE
Volume 333, Issue -, Pages 487-499Publisher
ELSEVIER
DOI: 10.1016/j.jconrel.2021.04.005
Keywords
Psoriasis; Hyperproliferation; Gold nanorod; Isatin; Nanocomplex; Photothermal therapy
Funding
- Ministry of Science and Technology of Taiwan [MOST-107-2320-B-182-016-MY3]
- Chang Gung Memorial Hospital [CMRPD1K00512]
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This study designed a nanocomplex capable of treating psoriasis through hyperthermia induced by near-infrared irradiation. The nanocomplexes were shown to specifically induce keratinocyte apoptosis, inhibit the progression of lesions, and recover overexpressed cytokines in an in vivo psoriasiform murine model. The photothermal nanosystems show promise as a new therapeutic approach against psoriasis.
Psoriasis is a chronic autoimmune skin disorder that involves keratinocyte hyperproliferation and inflammatory cell recruitment. A strategy to mitigate psoriatic lesions is to induce keratinocyte apoptosis for proliferation suppression. Herein we designed a nanoformulation capable of treating psoriasis via hyperthermia-induced apoptosis in response to near-infrared (NIR) irradiation. To this end, gold nanorods (GNRs) and isatin, which is an anti-inflammatory agent for synergizing antipsoriatic activity, were loaded into a poly (lactic-co-glycolic acid) (PLGA) matrix to form the nanocomplexes. The physicochemical and photothermal properties of the nanocomplexes were determined in terms of size, surface charge, NIR-absorbing feature, isatin release, keratinocyte uptake, and cytotoxicity. The nanocomplexes showed a spherical shape with an average size of about 180 nm. The GNR-loaded nanoparticles can efficiently convert NIR light at 0.42 W/cm(2) into heat with an increased temperature of 10 degrees C. When combined with NIR exposure, the nanocomplexes were internalized into keratinocyte cytoplasm with an inhibition of keratinocyte viability to about 60%. Live/dead cell assay and flow cytometry confirmed that the nanocomplexes could serve as NIR-absorbers to specifically elicit keratinocyte apoptosis through caspase and poly ADP-ribose polymerase (PARP) pathways. The in vivo psoriasiform murine model indicated that the combined nanocomplexes and NIR inhibited epidermal hyperplasia and neutrophil infiltration. The overexpressed cytokines in the lesion could be recovered to normal baseline level after the photothermal management. The subcutaneous nanocomplexes remained in the skin for at least 5 days. The nanocomposites produced a negligible toxicity in the skin or liver of healthy mice. The photothermal nanosystems, as designed in this study, shed new light on the therapeutic approach against psoriasis.
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