Aggregation-induced emission photosensitizer microneedles for enhanced melanoma photodynamic therapy.
Ling LiangTuokai PengXin Yao GengWenping ZhuChaoyong LiuHui-Qing PengBo Zhi ChenXin Dong GuoPublished in: Biomaterials science (2024)
The incidence and mortality rates of skin melanoma have been increasing annually. Photodynamic therapy (PDT) enables effective destruction of tumor cells while minimizing harm to normal cells. However, traditional photosensitizers (PSs) suffer from photobleaching, photodegradation and the aggregation-caused quenching (ACQ) effect, and it is challenging for light to reach the deep layers of the skin to maximize the efficacy of PSs. Herein, we developed dissolving microneedles (MNs) loaded with PSs of TPE-EPy@CB[7] through supramolecular assembly. The PSs effectively enhanced the type-I reactive oxygen species (ROS) generation capacity, with a concentration of 2 μM possessing nearly half of the tumor cell-killing ability under 10 min white light irradiation. The MNs were successfully pierced into the targeted site for precise drug delivery. Additionally, the conical structure of the MNs, as well as the lens-like structure after dissolution, facilitated the transmission of light in the subcutaneous tissue, achieving significant inhibition of tumor growth with a tumor suppression rate of 97.8% and no systemic toxicity or side effects in melanoma mice. The results demonstrated the potent melanoma inhibition and biosafety of this treatment approach, exhibiting a new and promising strategy to conquer malignant melanoma.
Keyphrases
- photodynamic therapy
- drug delivery
- reactive oxygen species
- fluorescence imaging
- skin cancer
- cancer therapy
- induced apoptosis
- wound healing
- risk factors
- basal cell carcinoma
- cardiovascular disease
- oxidative stress
- single cell
- dna damage
- radiation therapy
- adipose tissue
- signaling pathway
- high fat diet induced
- endoplasmic reticulum stress
- mesenchymal stem cells
- coronary artery disease
- energy transfer
- skeletal muscle
- anti inflammatory
- drug release
- pi k akt
- quantum dots