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Immobilization of Zinc Phthalocyanines in Silicate Matrices and Investigation of Their Photobactericidal Effect on E.coli

机译:酞菁锌在硅酸盐基质中的固定化及其对大肠杆菌的杀菌作用

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摘要

The aim of the present investigation was to immobilize zinc phthalocyanines in a silicate matrix and to test the photobactericidal properties of the matrices so prepared toward Esherichia coli in model aqueous media. For the purpose, tetra tertiary butyl zinc phthalocyanine (TBZnPc) and zinc phthalocyanine tetrasulfonic acid (ZnPcTS) were used. The abilities of these two photosensitizers to generate singlet oxygen in solution were compared by following the rate of photobleaching of 1,3-diphenylisobenzofuran (DPBF) at 430 nm in dimethylformamide (DMF).The results of this study show clearly that, under the conditions used here, the TBZnPc is the more effective generator of singlet oxygen; with it the DPBF was virtually completely photobleached in 4 min, while with the ZnPcTS under the same conditions, it took 12 min to reach this point. Glass conjugates with the two phthalocyanines were obtained by the sol-gel technique and were characterized by a well-defined color due to the phthalocyanine incorporated in the silicate matrix. Glasses with an intense, but inhomogeneous, green color were obtained when the tetrasulfonic derivative of the zinc phthalocyanine was used, while blue glasses of evenly distributed coloration were formed from the tetra tertiary butyl derivative.The ZnPcTS conjugate demonstrates more effective singlet oxygen evolution than is the case with the TBZnPc conjugate. These results are the opposite of those obtained for the free phthalocyanines in solution. The structural formulae of the compounds show that TBZnPc has a more pronounced hydrophobic character than the sulfonic derivative. In our view, the relative reactivities of the conjugates can be explained by the tetrasulfonic derivative being situated mainly in the surface parts of the glass matrix where the hydrophilic character is prevailing, while the tertiary butyl derivative is mainly present in the internal parts of the matrix as a result of which it is less accessible and therefore less activeThe results obtained on the effect of zinc phthalocyanine conjugates on E. coli show a trend similar to that observed with singlet oxygen evolution shown. Thus, for the ZnPcTS conjugate, the log kill is 1.32 and for the TBZnPc conjugate, it is 0.98, in each case after 120 min. The results obtained show that phthalocyanines can be immobilized successfully in a silicate matrix and used for photodisinfection of microbially polluted waters. The silicate matrix has some advantages in comparison with other organic matrices. It is insoluble in water, resistant towards microorganisms, easy to fabricate, and might be developed successfully for the photodisinfection of water, e.g., in swimming pools and in other open water reservoirs.
机译:本研究的目的是将酞菁锌固定在硅酸盐基质中,并测试在模型水性介质中如此制备的针对大肠杆菌的基质的光杀菌性能。为此目的,使用了四叔丁基锌酞菁锌(TBZnPc)和锌酞菁四磺酸锌(ZnPcTS)。通过跟踪1,430二甲基甲酰胺(DMF)中1,3-二苯基异苯并呋喃(DPBF)在430 nm处的光漂白速率,比较了这两种光敏剂在溶液中产生单线态氧的能力。此处使用的TBZnPc是更有效的单线态氧产生剂。 DPBF几乎在4分钟内就完全被光漂白,而ZnPcTS在相同条件下要花12分钟才能达到这一点。通过溶胶-凝胶技术获得了具有两种酞菁的玻璃共轭物,并且由于在硅酸盐基质中掺入了酞菁,因此具有明确定义的颜色。当使用酞菁锌的四磺酸衍生物时,获得的玻璃具有强烈但不均匀的绿色,而由四叔丁基衍生物形成的蓝玻璃具有均匀分布的颜色.ZnPcTS共轭物显示出比单态氧更有效的单线态氧放出。 TBZnPc共轭物的情况。这些结果与溶液中游离酞菁所获得的结果相反。化合物的结构式表明,TBZnPc具有比磺酸衍生物更明显的疏水性。我们认为,共轭物的相对反应性可以通过四磺酸衍生物主要位于玻璃基体的亲水性占主导的表面部分来解释,而叔丁基衍生物主要位于基体的内部部分中。锌酞菁结合物对大肠杆菌的影响所获得的结果显示出与单线态氧释放所观察到的趋势相似的趋势。因此,对于ZnPcTS共轭物,对数杀灭为1.32,对于TBZnPc共轭物,对数杀伤为0.98,在每种情况下均在120分钟后。所获得的结果表明,酞菁可以成功地固定在硅酸盐基质中,并用于对微生物污染的水进行光消毒。与其他有机基质相比,硅酸盐基质具有一些优势。它不溶于水,对微生物有抵抗力,易于制造,并且可能成功开发用于水的光消毒,例如在游泳池和其他开放水库中。

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