Cobalt Ferrite-Gossypol Coordination Nanoagents with High Photothermal Conversion Efficiency Sensitizing Chemotherapy against Bcl-2 to Induce Tumor Apoptosis.
Yun ZengHuifang LiuJingwen MaKe LiPeng ChangChenying WangLei LiDan ChenChanghu LiuNa LiWenhua ZhanYonghua ZhanPublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
Gossypol is a chemotherapeutic drug that can inhibit the anti-apoptotic protein Bcl-2, but the existing gossypol-related nanocarriers cannot well solve the problem of chemotherapy resistance. Based on the observation that gossypol becomes black upon Fe 3+ coordination, it is hypothesized that encasing gossypol in glyceryl monooleate (GMO) and making it coordinate cobalt ferrite will not only improve its photothermal conversion efficiency (PCE) but also help it enter tumor cells. As the drug loading content and drug encapsulation efficiency of gossypol are 10.67% (w/w) and 96.20%, the PCE of cobalt ferrite rises from 14.71% to 36.00%. The synergistic therapeutic effect finally induces tumor apoptosis with a tumor inhibition rate of 96.56%, which is 2.99 and 1.47 times higher than chemotherapy or photothermal therapy (PTT) alone. PTT generated by the GMO nanocarriers under the irradiation of 808 nm laser can weaken tumor hypoxia, thereby assisting gossypol to inhibit Bcl-2. In addition, the efficacy of nanocarriers is also evaluated through T 2 -weighted magnetic resonance imaging. Observations of gossypol-induced apoptosis in tissue slices provide definitive proof of chemotherapy sensitization, indicating that such coordination nanocarriers can be used as an effective preclinical agent to enhance chemotherapy.
Keyphrases
- drug delivery
- cancer therapy
- locally advanced
- drug release
- endoplasmic reticulum stress
- induced apoptosis
- oxidative stress
- magnetic resonance imaging
- cell death
- photodynamic therapy
- squamous cell carcinoma
- signaling pathway
- stem cells
- cell cycle arrest
- computed tomography
- magnetic resonance
- drug induced
- reduced graphene oxide
- cell therapy
- metal organic framework
- bone marrow
- endothelial cells
- contrast enhanced
- anti inflammatory
- protein protein