首页> 外文期刊>Dyes and Pigments >Photophysics and photobiology of novel liposomal formulations of 2,9(10), 16(17),23(24)-tetrakis[(2-dimethylamino)ethylsulfanyl]phthalocyaninatozinc(II)
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Photophysics and photobiology of novel liposomal formulations of 2,9(10), 16(17),23(24)-tetrakis[(2-dimethylamino)ethylsulfanyl]phthalocyaninatozinc(II)

机译:2,9(10),16(17),23(24)-四[[2-(2-二甲基氨基)乙基硫烷基]邻苯二甲酰萘并锌(II)的脂质体新制剂的光物理和光生物学

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摘要

Six novel liposomal formulations of 2,9(10),16(17),23(24)-tetrakis[(2-dimethylamino)ethylsulfanyl] phthalocyaninatozinc(II) (Pc9) were investigated to establish how the environments affect their photo-physical and photobiological properties. The incorporation efficiency and solubility during a time period were evaluated. All Pc9-liposomal formulations were efficient singlet oxygen quantum yield generators. The photobiological potentials were evaluated on human nasopharynx KB carcinoma cells. None of the formulations studied showed cytotoxic effects in the absence of light, whereas all of them showed good performance after irradiation. The 50% inhibition of cell proliferation (IC50) was in the range of 0.21-0.47 μM for Pc9-loaded liposome formulations. A lysosomal localization was found for S-PEG as well as for S.
机译:研究了6,2,9(10),16(17),23(24)-四[[2-(2-二甲基氨基)乙基硫烷基]邻苯二甲酰萘并锌(II)(Pc9)的脂质体制剂,以确定环境如何影响其光物理性质和光生物学特性。评估一段时间内的掺入效率和溶解性。所有的Pc9-脂质体制剂都是有效的单线态氧量子产率产生剂。在人鼻咽KB癌细胞上评估了光生物学潜力。在没有光照的情况下,所研究的制剂均未显示出细胞毒性作用,而在辐射后它们均显示出良好的性能。对于负载Pc9的脂质体制剂,细胞增殖(IC50)的50%抑制作用在0.21-0.47μM的范围内。发现了S-PEG和S的溶酶体定位。

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