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ACS Appl Bio Mater ; 7(9): 6055-6064, 2024 Sep 16.
Article in English | MEDLINE | ID: mdl-39224079

ABSTRACT

Both boron neutron capture therapy (BNCT) and photothermal therapy (PTT) have been applied to tumor treatment in clinical. However, their therapeutic efficacy is limited. For BNCT, the agents not only exhibit poor targeting ability but also permit only a single irradiation session within a course due to significant radiation risks. In the context of PTT, despite enhanced selectivity, the limited photothermal effect fails to meet clinical demands. Hence, the imperative arises to combine these two therapies to enhance tumor-killing capabilities and improve the targeting of BNCT agents by leveraging the advantages of PTT agents. In this study, we synthesized a potential responsive agent by linking 4-mercaptophenylboronic acid (MPBA) and IR-780 dye that served as the agents for BNCT and PTT, respectively, which possesses the dual capabilities of photothermal effects and thermal neutron capture. Results from both in vitro and in vivo research demonstrated that IR780-MPBA effectively inhibits tumor growth through its photothermal effect with no significant toxicity. Furthermore, IR780-MPBA exhibited substantial accumulation in tumor tissues and superior tumor-targeting capabilities compared with MPBA, which demonstrated that IR780-MPBA possesses significant potential as a combined antitumor therapy of PTT and BNCT, presenting a promising approach for antitumor treatments.


Subject(s)
Antineoplastic Agents , Boron Neutron Capture Therapy , Photothermal Therapy , Animals , Mice , Humans , Antineoplastic Agents/pharmacology , Antineoplastic Agents/chemistry , Particle Size , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Biocompatible Materials/chemical synthesis , Drug Screening Assays, Antitumor , Materials Testing , Cell Survival/drug effects , Indoles/chemistry , Indoles/pharmacology , Cell Proliferation/drug effects , Molecular Structure , Cell Line, Tumor , Mice, Inbred BALB C , Boronic Acids/chemistry , Boronic Acids/pharmacology , Female
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