Graduate Institute of Biomedical Sciences, Chang Gung University, Kweishan, Taoyuan, Taiwan.
Department of Neurology, China Medical University Hospital, Taichung, Taiwan; School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan; Department of Neurology, An-Nan Hospital, China Medical University, Tainan, Taiwan.
J Control Release. 2021 May 10;333:487-499. doi: 10.1016/j.jconrel.2021.04.005. Epub 2021 Apr 13.
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 into heat with an increased temperature of 10 °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.
银屑病是一种慢性自身免疫性皮肤疾病,涉及角质形成细胞过度增殖和炎症细胞募集。减轻银屑病损伤的一种策略是诱导角质形成细胞凋亡以抑制增殖。在此,我们设计了一种纳米制剂,能够通过热诱导凋亡来治疗银屑病,以响应近红外 (NIR) 照射。为此,将金纳米棒 (GNR) 和异吲哚啉,一种用于协同抗银屑病活性的抗炎剂,负载到聚 (乳酸-共-乙醇酸) (PLGA) 基质中形成纳米复合物。从尺寸、表面电荷、NIR 吸收特性、异吲哚啉释放、角质形成细胞摄取和细胞毒性等方面确定了纳米复合物的物理化学和光热特性。纳米复合物呈球形,平均尺寸约为 180nm。负载 GNR 的纳米颗粒可以有效地将 0.42W/cm 的 NIR 光转化为 10°C 的热量。与 NIR 暴露结合时,纳米复合物被内吞到角质形成细胞质中,将角质形成细胞活力抑制到约 60%。活/死细胞检测和流式细胞术证实,纳米复合物可以作为 NIR 吸收剂,通过半胱天冬酶和多聚 ADP-核糖聚合酶 (PARP) 途径特异性诱导角质形成细胞凋亡。体内银屑病样小鼠模型表明,联合纳米复合物和 NIR 抑制表皮过度增生和中性粒细胞浸润。病变中过度表达的细胞因子在光热治疗后可恢复到正常基线水平。皮下纳米复合物在皮肤中至少保留 5 天。纳米复合材料在健康小鼠的皮肤或肝脏中几乎没有毒性。本研究设计的光热纳米系统为治疗银屑病提供了新的思路。