Dissolving Microneedles with Spatiotemporally controlled pulsatile release Nanosystem for Synergistic Chemo-photothermal Therapy of Melanoma

被引:81
|
作者
Qin, Wanbing [1 ]
Quan, Guilan [2 ]
Sun, Ying [1 ]
Chen, Minglong [1 ]
Yang, Peipei [3 ]
Feng, Disang [2 ]
Wen, Ting [1 ]
Hu, Xinyu [1 ]
Pan, Xin [1 ]
Wu, Chuanbin [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
[2] Jinan Univ, Coll Pharm, Guangzhou 510632, Peoples R China
[3] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Pharm, Guangzhou 510623, Peoples R China
来源
THERANOSTICS | 2020年 / 10卷 / 18期
基金
中国国家自然科学基金;
关键词
melanoma; dissolving microneedles; solid lipid nanoparticles; triggered release; chemo-photothermal therapy; ALBUMIN NANOPARTICLES; DELIVERY; CANCER; NANOPLATFORM; CHEMOTHERAPY; GRAPHENE; PATCH;
D O I
10.7150/thno.44194
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
High aggressiveness and recurrence of melanoma tumors require multiple systemic drug administrations, causing discomfort and severe side effects to the patients. Topical treatment strategies that provide repetitively controllable and precise drug administrations will greatly improve treatment effects. Methods: In this study, a spatiotemporally controlled pulsatile release system, which combined dissolving microneedles (DMNs) and thermal-sensitive solid lipid nanoparticles (SLNs), was constructed to realize multiple doses of dual-modal chemo-photothermal therapy in a single administration. Paclitaxel (PTX) and photothermal agent IR-780 were encapsulated into SLNs and were concentrated in the tips of DMNs (PTX/IR-780 SLNs @DMNs). Equipped with several needles, the DMN patch could be directly inserted into the tumor site and provide a stable "Zone accumulation" to constrain the PTX/IR-780 SLNs at the tumor site with uniform distribution. Results: In vitro experiments showed that after irradiation with near-infrared light, the PTX/IR-780 SLNs gradually underwent phase transition, thereby accelerating the release of PTX. When irradiation was switched off, the PTX/IR-780 SLNs cooled to re-solidify with limited drug release. Compared with intravenous and intratumoral injections, very few SLNs from PTX/IR-780 SLNs @DMNs were distributed into other organs, resulting in enhanced bioavailability at the tumor site and good safety. In vivo analysis revealed that PTX/IR-780 SLNs @DMNs exhibited significant anti-tumor efficacy. In particular, the primary tumor was completely eradicated with a curable rate of 100% in 30 days and the highest survival rate of 66.67% after 100 days of treatment. Conclusion: Herein, we developed a DMN system with a unique spatiotemporally controlled pulsatile release feature that provides a user-friendly and low-toxicity treatment route for patients who need long-term and repeat treatments.
引用
收藏
页码:8179 / 8196
页数:18
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