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配制成纳米颗粒的高度稳定的四酚氧基钛(IV)试剂具有抗肿瘤活性和选择性。

Highly Stable Tetra-Phenolato Titanium(IV) Agent Formulated into Nanoparticles Demonstrates Anti-Tumoral Activity and Selectivity.

作者信息

Meker Sigalit, Braitbard Ori, Margulis-Goshen Katrin, Magdassi Shlomo, Hochman Jacob, Tshuva Edit Y

机构信息

The Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

Department of Cell and Developmental Biology, Alexander Silberman Institute of Life Science, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

出版信息

Molecules. 2015 Oct 9;20(10):18526-38. doi: 10.3390/molecules201018526.

Abstract

Titanium(IV) complexes exhibit high potential as anti-tumor agents, particularly due to their low intrinsic toxicity and cytotoxicity toward cisplatin resistant cells. Nevertheless, Ti(IV) complexes generally undergo rapid hydrolysis that previously hampered their utilization as anticancer drugs. We recently overcame this difficulty by developing a highly stable Ti(IV) complex that is based on tetra-phenolato, hexadentate ligand, formulated into organic nanoparticles. Herein we investigated the activity of this complex in vitro and in vivo. Although inactive when tested directly due to poor solubility, when formulated, this complex displayed (a) high cytotoxicity toward cisplatin resistant human ovarian cells, A2780-cp, with resistance factor of 1.1; (b) additive behavior in combination with cisplatin toward ovarian and colon cancer cells; (c) selectivity toward cancer cells as implied by its mild activity toward non-cancerous, fibroblast lung cells, MRC-5; (d) high stability and durability as manifested by the ability to maintain cytotoxicity, even following one week of incubation in 100% aquatic medium solution; and (e) in vivo efficacy toward solid tumors of human colon cancer cells, HT-29, in nude mice without any clinical signs of toxicity. These features support the formulated phenolato Ti(IV) complex being an effective and selective anti-tumoral agent.

摘要

钛(IV)配合物作为抗肿瘤药物具有很高的潜力,特别是由于其固有毒性低,对顺铂耐药细胞具有细胞毒性。然而,Ti(IV)配合物通常会迅速水解,这以前阻碍了它们作为抗癌药物的应用。我们最近通过开发一种基于四酚盐六齿配体的高度稳定的Ti(IV)配合物克服了这一困难,该配合物被制成有机纳米颗粒。在此,我们研究了该配合物在体外和体内的活性。尽管由于溶解度差直接测试时无活性,但制成制剂后,该配合物表现出:(a)对顺铂耐药的人卵巢细胞A2780-cp具有高细胞毒性,耐药因子为1.1;(b)与顺铂联合使用时对卵巢癌和结肠癌细胞具有相加作用;(c)对癌细胞具有选择性,对非癌性成纤维细胞肺细胞MRC-5活性较弱即表明了这一点;(d)具有高稳定性和耐久性,即使在100%水性介质溶液中孵育一周后仍能保持细胞毒性;(e)对裸鼠体内人结肠癌细胞HT-29的实体瘤具有体内疗效,且无任何毒性临床症状。这些特性支持制成制剂的酚盐Ti(IV)配合物是一种有效且选择性的抗肿瘤药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c528/6331959/ff8a25939429/molecules-20-18526-g006.jpg

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