4.8 Article

Self-assembly nanomicelle-microneedle patches with enhanced tumor penetration for superior chemo-photothermal therapy

期刊

NANO RESEARCH
卷 15, 期 3, 页码 2335-2346

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-3817-x

关键词

dissolving microneedle; tumor penetration; nanomicelle; superficial tumor; chemo-photothermal therapy

资金

  1. National Natural Science Foundation of China [81803466]
  2. Key Areas Research and Development Program of Guangdong Province [2019B020204002]
  3. Natural Science Foundation of Guangdong Province [2021A1515012525]

向作者/读者索取更多资源

The study developed a self-assembly nanomicelle dissolving microneedle (DMN) patch to enhance drug accumulation in tumors and improve penetration into deep tumor tissue for synergetic chemo-photothermal therapy against melanoma. The results showed that the nanomicelles could efficiently eliminate tumors without causing damage to normal tissues, providing a versatile approach for superficial cancer treatment.
Nanomedicine with high specificity has been a promising tool for cancer diagnosis and therapy. However, the successful application of nanoparticle-based superficial cancer therapy is severely hindered by restricted deep tumor tissue accumulation and penetration. Herein, a self-assembly nanomicelle dissolving microneedle (DMN) patch according to the nano in micro strategy was conducted to co-deliver a first-line chemotherapeutic agent paclitaxel (PTX), and a photosensitizer IR780 (PTX/IR780-NMs @DMNs) for chemo-photothermal synergetic melanoma therapy. Upon direct insertion into the tumor site, DMNs created a regular and multipoint three-dimensional drug depot to maximize the tumor accumulation. Accompanied by the DMN dissolution, the composition of the needle matrixes self-assembled into nanomicelles, which could efficiently penetrate deep tumor tissue. Upon laser irradiation, the nanomicelles could not only ablate tumor cells directly by photothermal conversion but also trigger PTX release to induce tumor cell apoptosis. In vivo results showed that compared with intravenous injection, IR780 delivered by PTX/IR780-NMs @DMNs was almost completely accumulated at the tumor site. The antitumor results revealed that the PTX/IR780-NMs @DMNs could effectively eliminate tumors with an 88% curable rate without any damage to normal tissues. This work provides a versatile and generalizable framework for designing self-assembly DMN-mediated combination therapy to fight against superficial cancer.

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