4.2 Article

Multimodal Applications of Zinc Gallate-Based Persistent Luminescent Nanoparticles in Cancer Treatment: Tumor Margining, Diagnosis, and Boron Neutron Capture Therapy

期刊

ACS APPLIED BIO MATERIALS
卷 5, 期 7, 页码 3134-3145

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.2c00081

关键词

zinc gallate; PLNPs; B-1(0)(OH)(3); poly(vicinal-dioal); BNCT; photon-imaging; fibrosarcoma

资金

  1. University Grants Commission (UGC) , New Delhi [BAEC/12/2020, BAEC/27/2021]

向作者/读者索取更多资源

Based on boron neutron capture therapy (BNCT), researchers have developed a zinc gallate-based nanoformulation for cancer treatment and diagnosis. The nanoformulation, with its functionalized surface, effectively targets tumor cells and demonstrates excellent therapeutic efficacy in in vitro and in vivo studies.
On the basis of the boron neutron capture therapy (BNCT) modality, we have designed and synthesized a zinc gallate (ZnGa2O4)-based nanoformulation for developing an innovative theranostic approach for cancer treatment. Initially, the (ZnGa1.995Cr0.005O4 or ZnGa2O4:(0.5%)Cr persistent luminescence nanopartides (PLNPs) embedded on silica matrix were synthesized. Their surface functionalization was performed using organic synthesis strategies to attach the amine functional moieties which were further coupled with poly(vicinal diol). These diols were helpful for conjugation with B-1(0)(OH)(3), which subsequently served to couple with an in-house-synthesized variant of pH-(low)-insertion peptide (pHLIP) finally giving a tumor-targeting nanoformulation. Most importantly, the polymeric diols helped in conjugation of a substantial number of B-10 to provide the therapeutic dose required for effective BNCT. This nanoformulation internalized substantially (similar to 80%) to WEHI-164 cancer cells within 6 h. Tumor homing studies indicated that the accumulation of this formulation at the acidic tumor site was within 2 h. The in vitro evaluation of the formulation against WEHI-164 cancer cells followed by neutron irradiation revealed its potent cytotoxicity with IC50 similar to 25 mu M. In the case of studies on animal models, the melanoma-induced CS7BL/6 and fibrosarcoma-induced BALB/c mice were treated with formulations through intratumoral and intravenous injections, respectively, followed by neutron irradiation, leading to a significant killing of the cancer cells, which was evidenced by a reduction in tumor volume (75-80%) as compared with a control tumor. Furthermore, the histopathological studies confirmed a damaging effect only on tumor cells, while there was no sign of damage to the vital organs in treated mice as well as in controls.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据