吲哚青绿
光热治疗
材料科学
体内
黑色素瘤
免疫疗法
生物医学工程
药物输送
透皮
纳米技术
癌症研究
医学
药理学
免疫系统
外科
生物技术
生物
免疫学
作者
Peipei Yang,Minglong Chen,Wanbing Qin,Chaonan Shi,Xuequn Bai,Guilan Quan,Xin Pan,Chuanbin Wu
标识
DOI:10.1021/acsanm.1c00832
摘要
Topical and targeted photothermal therapy (PTT) mediated by a microneedle system is a promising strategy to enhance checkpoint inhibitor immunotherapy in melanoma treatment by integrating the instant tumor ablation effect and persistent antitumor immune response. However, the amount of drug delivered into the tumor site by microneedles is limited by low drug loading efficiency and insufficient drug distribution in the microneedle tips. Here, a simple and ingenious microneedle design that makes use of nanotechnology and centrifugal force was developed for the effective loading of indocyanine green (ICG). ICG stability in aqueous solution was first improved by chitosan nanoparticle encapsulation and then mixed with oligomeric sodium hyaluronate, the microneedle matrix material, which increased the size of the nanoparticles and facilitated their enrichment in the microneedle tips under centrifugal force. The amount of ICG loaded into the designed microneedles was 7 times higher than that of the microneedles loaded directly with ICG without nanoparticle encapsulation. The higher drug loading amount and main distribution in the microneedle tips resulted in a higher transdermal delivery efficiency and finally contributed to better in vivo photothermal performance. An in vivo antitumor study showed that the combination of the designed microneedles and the previously established checkpoint inhibitor-loaded core–shell microneedle system exhibited instant tumor inhibition and a slower tumor growth rate in the later period, demonstrating a synergetic effect. Therefore, this microneedle system composed purely of clinically approved components is expected to have great potential for clinical translation to enhance checkpoint inhibitor immunotherapy.
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