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含新型十二硼烷的吉西他滨类似物的设计用于基于白蛋白的治疗组合物。

Design of the New -Dodecarborate-Containing Gemcitabine Analogue for the Albumin-Based Theranostics Composition.

机构信息

Institute of Chemical Biology and Fundamental Medicine, SB RAS, 630090 Novosibirsk, Russia.

Faculty of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russia.

出版信息

Molecules. 2023 Mar 15;28(6):2672. doi: 10.3390/molecules28062672.

Abstract

Combination therapy is becoming an increasingly important treatment strategy because multi-drugs can maximize therapeutic effect and overcome potential mechanisms of drug resistance. A new albumin-based theranostic containing gemcitabine -dodecaborate analogue has been developed for combining boron neutron capture therapy (BNCT) and chemotheraphy. An exo-heterocyclic amino group of gemcitabine was used to introduce dodecaborate, and a 5'-hydroxy group was used to tether maleimide moiety through an acid-labile phosphamide linker. The -trifluoroacylated homocysteine thiolactone was used to attach the gemcitabine analogue to human serum albumin (HSA) bearing Cy5 or Cy7 fluorescent dyes. The half-maximal inhibitory concentration (IC) of the designed theranostic relative to T98G cells was 0.47 mM with the correlation coefficient R = 0.82. BNCT experiments resulted in a decrease in the viability of T98G cells, and the survival fraction was ≈ 0.4.

摘要

联合治疗正成为一种日益重要的治疗策略,因为多药物治疗可以最大限度地提高治疗效果,并克服潜在的耐药机制。一种新型基于白蛋白的治疗药物,包含吉西他滨-十二硼酸盐类似物,已被开发用于硼中子俘获治疗(BNCT)和化疗的联合治疗。吉西他滨的外环杂环氨基被用来引入十二硼酸盐,而 5'-羟基通过酸不稳定的磷酰胺连接物与马来酰亚胺部分连接。-三氟乙酰化高半胱氨酸硫内酯用于将吉西他滨类似物连接到携带 Cy5 或 Cy7 荧光染料的人血清白蛋白(HSA)上。相对于 T98G 细胞,设计的治疗药物的半最大抑制浓度(IC)为 0.47mM,相关系数 R = 0.82。BNCT 实验导致 T98G 细胞活力下降,存活分数约为 0.4。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfcf/10056911/508be94502df/molecules-28-02672-g001.jpg

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