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NIR light-activatable dissolving microneedle system for melanoma ablation enabled by a combination of ROS-responsive chemotherapy and phototherapy.
Liu, Fan; Cheng, Zeneng; Yi, Hanxi.
Affiliation
  • Liu F; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
  • Cheng Z; Division of Biopharmaceutics and Pharmacokinetics, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, China.
  • Yi H; Department of Pathology, School of Basic Medical Science, Central South University, Tongzipo Road 172, Changsha, 410000, China. hanxiyi2022@csu.edu.cn.
J Nanobiotechnology ; 21(1): 61, 2023 Feb 22.
Article in En | MEDLINE | ID: mdl-36814244
ABSTRACT

BACKGROUND:

As a consequence of the aggressive and recurrent nature of melanoma, repeated, multimodal treatments are often necessary to cure the disease. While microneedle (MN)-based transdermal drug delivery methods can allow drugs to avoid first-pass metabolism and overcome the stratum corneum barrier, the main challenges of these delivery methods entail the lack of controlled drug release/activation and effective imaging methods to guide the entire treatment process.

METHODS:

To enable a transdermal delivery method with controllable drug release/activation and effective imaging guidance, we designed a near-infrared (NIR) photoactivatable, dissolving MN system comprising dissolvable polyvinylpyrrolidone MNs arrays (MN-pB/I) containing liposomes that were co-loaded with the photosensitizer indocyanine green (ICG) and the reactive oxygen species (ROS)-activatable prodrug of doxorubicin (pB-DOX).

RESULTS:

After applying the MN patch to the tumor site, the liposomes concentrated in the needle tips were released into the tumor tissue and distributed evenly upon dissolution of the matrix to enable targeted delivery. Then, the ROS produced by ICG after exposure to NIR light performed photodynamic therapy and activated the pB-DOX for chemotherapy by cleaving the prodrug moiety and converting it to DOX. As a dye, ICG was also used to guide the treatment regimens and monitor the efficacy by fluorescence and photoacoustic imaging. The growth of the tumors in the MN-pB/I group were inhibited by 93.5%, while those were only partially inhibited in the control groups. Negligible treatment-induced side effects and cardiotoxicity were observed.

CONCLUSION:

The MN-pB/I represents a multimodal, biocompatible theragnostic system with spatiotemporal control that was capable of ablating melanoma tumors after a single dose, providing a promising candidate for clinical melanoma therapy.
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Full text: 1 Database: MEDLINE Main subject: Prodrugs / Melanoma Type of study: Guideline Language: En Journal: J Nanobiotechnology Year: 2023 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Prodrugs / Melanoma Type of study: Guideline Language: En Journal: J Nanobiotechnology Year: 2023 Type: Article Affiliation country: China