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三重态-三重态湮灭上转换随后通过荧光共振能量转移实现脂质体中光解离钌配合物的红光激活。

Triplet-triplet annihilation upconversion followed by FRET for the red light activation of a photodissociative ruthenium complex in liposomes.

作者信息

Askes Sven H C, Kloz Miroslav, Bruylants Gilles, Kennis John T M, Bonnet Sylvestre

机构信息

Leiden Institute of Chemistry, Gorlaeus Laboratories, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.

出版信息

Phys Chem Chem Phys. 2015 Nov 7;17(41):27380-90. doi: 10.1039/c5cp04352b.

Abstract

Upconversion is a promising way to trigger high-energy photochemistry with low-energy photons. However, combining upconversion schemes with non-radiative energy transfer is challenging because bringing several photochemically active components in close proximity results in complex multi-component systems where quenching processes may deactivate the whole assembly. In this work, PEGylated liposomes were prepared that contained three photoactive components: a porphyrin dye absorbing red light, a perylene moiety emitting in the blue, and a light-activatable ruthenium prodrug sensitive to blue light. Time-dependent spectroscopic studies demonstrate that singlet perylene excited states are non-radiatively transferred to the nearby ruthenium complex by Förster resonance energy transfer (FRET). Under red-light irradiation of the three-component membranes, triplet-triplet annihilation upconversion (TTA-UC) occurs followed by FRET, which results in a more efficient activation of the ruthenium prodrug compared to a physical mixture of two-component upconverting liposomes and liposomes containing only the ruthenium complex. This work represents a rare example where TTA-UC and Förster resonance energy transfer are combined to achieve prodrug activation in the phototherapeutic window.

摘要

上转换是一种利用低能量光子触发高能光化学的有前景的方法。然而,将上转换方案与非辐射能量转移相结合具有挑战性,因为将几种光化学活性成分紧密靠近会导致复杂的多组分系统,其中猝灭过程可能会使整个组件失活。在这项工作中,制备了聚乙二醇化脂质体,其包含三种光活性成分:一种吸收红光的卟啉染料、一种发射蓝光的苝部分以及一种对蓝光敏感的光可激活钌前药。时间相关光谱研究表明,单线态苝激发态通过福斯特共振能量转移(FRET)非辐射转移到附近的钌配合物。在三组分膜的红光照射下,发生三重态-三重态湮灭上转换(TTA-UC),随后是FRET,这导致与双组分上转换脂质体和仅含钌配合物的脂质体的物理混合物相比,钌前药的激活效率更高。这项工作代表了一个罕见的例子,其中TTA-UC和福斯特共振能量转移相结合,以在光治疗窗口中实现前药激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab7d/4642198/63c137b9bf74/c5cp04352b-f1.jpg

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