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

被引:44
作者
Askes, Sven H. C. [1 ]
Kloz, Miroslav [2 ]
Bruylants, Gilles [3 ]
Kennis, John T. M. [2 ]
Bonnet, Sylvestre [1 ]
机构
[1] Leiden Univ, Gorlaeus Labs, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
[2] Vrije Univ Amsterdam, Laserlab Amsterdam, NL-1081 HV Amsterdam, Netherlands
[3] Univ Libre Bruxelles, Engn Mol NanoSyst, B-1050 Brussels, Belgium
基金
欧洲研究理事会;
关键词
PHOTODYNAMIC THERAPY; LIPID-BILAYER; TO-BLUE; CANCER; NANOCAPSULES; STRATEGY;
D O I
10.1039/c5cp04352b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 multicomponent 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 Forster 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 Forster resonance energy transfer are combined to achieve prodrug activation in the phototherapeutic window.
引用
收藏
页码:27380 / 27390
页数:11
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