A Two-Pronged Strategy for Enhanced Deep-Tumor Penetration and NIR-II Multimodal Imaging-Monitored Photothermal Therapy

ACS Appl Mater Interfaces. 2022 Sep 21;14(37):41684-41694. doi: 10.1021/acsami.2c08930. Epub 2022 Sep 12.

Abstract

The second near-infrared (NIR-II)-induced photothermal therapy (PTT) has attracted a great deal of attention in recent years due to its non-invasiveness and because it uses less energy. However, the penetration of photothermal agents into solid tumors is seriously impeded by the dense-tumor extracellular matrix (ECM) containing cross-linked hyaluronic acid (HA), thereby compromising the ultimate therapeutic effects. Herein, acid-labile metal-organic frameworks were employed as nanocarriers to efficiently mineralize hyaluronidase (HAase) and encapsulate Ag2S nanodots by a one-pot approach under mild conditions. The obtained nanocomposites (AHZ NPs) maintained enzyme activity and changed in size to prolong blood circulation and complete delivery of the cargo to the tumor. Moreover, the released HAase could specifically break out the HA to loosen ECM and enable the Ag2S nanodots to breeze through the tumor matrix space and gain access to the deep tumor. Under near-infrared laser irradiation, the AHZ NPs displayed remarkable fluorescence, outstanding photoacoustic signals, and excellent photothermal properties in the whole tumor. This work offers a promising two-pronged strategy via a decrease in nanoparticle size and the degradation of dense ECM for NIR-II multimodal imaging-guided PTT of deep tumors.

Keywords: Ag2S nanodots; NIR-II multimodal imaging; deep tumor; metal−organic frameworks; tumor extracellular matrix.

MeSH terms

  • Cell Line, Tumor
  • Humans
  • Hyaluronic Acid / pharmacology
  • Hyaluronoglucosaminidase
  • Metal-Organic Frameworks* / therapeutic use
  • Multimodal Imaging
  • Nanoparticles* / therapeutic use
  • Neoplasms* / drug therapy
  • Neoplasms* / therapy
  • Phototherapy
  • Photothermal Therapy

Substances

  • Metal-Organic Frameworks
  • Hyaluronic Acid
  • Hyaluronoglucosaminidase