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用于近红外触发协同癌症治疗的负载MXene/阿霉素复合物的超分子水凝胶

MXene/Doxorubicin Complex-Loaded Supramolecular Hydrogels for Near Infrared-Triggered Synergistic Cancer Therapy.

作者信息

Yang Seung Min, Bae Hanseo, Kim Seong-Jong, Kim Mungu, Hong Sang Hoon, Choi Hyunsik, Hahn Sei Kwang

机构信息

Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongbuk 37673, Republic of Korea.

出版信息

Biomater Res. 2025 Apr 9;29:0163. doi: 10.34133/bmr.0163. eCollection 2025.

Abstract

Photothermal therapy (PTT) has attracted great interest due to the high spatial precision and reduced general toxicity compared to conventional cancer therapies. However, PTT often faces challenges such as incomplete tumor eradication and collateral damage to healthy tissues. Here, we report an injectable MXene-doxorubicin (MD) complex-loaded supramolecular hydrogel (MDGel) for dual synergistic cancer therapy of near-infrared (NIR) PTT and chemotherapy. MDGel is prepared by the host-guest interaction between gelatin-cyclodextrin (GE-CD) and hyaluronic acid-adamantane (HA-AD), facilitating the efficient dispersion of MD complexes in the hydrogel. NIR irradiation triggers the PTT and the release of doxorubicin with increasing temperature. In vitro therapeutic effect is confirmed by achieving nearly 80% cancer cell death via the synergistic effect, compared to the single-modality treatment. In vivo tumor inhibition (68.9% volume reduction) is further validated in skin cancer-bearing model mice with no substantial negative side effect. With its prolonged retention, NIR light-controlled release, and localized therapeutic effect, the MDGel system would provide a notable paradigm as a versatile platform for dual synergistic cancer therapy.

摘要

与传统癌症治疗方法相比,光热疗法(PTT)因其高空间精度和较低的全身毒性而备受关注。然而,PTT常常面临诸如肿瘤根除不完全以及对健康组织的附带损伤等挑战。在此,我们报道了一种用于近红外(NIR)光热疗法和化疗双重协同癌症治疗的可注射的负载有MXene-阿霉素(MD)复合物的超分子水凝胶(MDGel)。MDGel是通过明胶-环糊精(GE-CD)与透明质酸-金刚烷(HA-AD)之间的主客体相互作用制备而成,有助于MD复合物在水凝胶中有效分散。近红外照射会随着温度升高触发光热疗法并促使阿霉素释放。与单模态治疗相比,通过协同效应实现近80%的癌细胞死亡,从而证实了体外治疗效果。在荷皮肤癌模型小鼠中进一步验证了体内肿瘤抑制效果(体积减少68.9%),且无明显负面副作用。凭借其延长的保留时间、近红外光控释放以及局部治疗效果,MDGel系统将作为双重协同癌症治疗的通用平台提供一个显著的范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aac/11979340/daa47a32dc20/bmr.0163.fig.001.jpg

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