Ferro Stefania, Jori Giulio, Sortino Salvatore, Stancanelli Rosanna, Nikolov Peter, Tognon Giuseppe, Ricchelli Fernanda, Mazzaglia Antonino
Department of Biology, University of Padova, Padova, Italy.
Biomacromolecules. 2009 Sep 14;10(9):2592-600. doi: 10.1021/bm900533r.
Recent findings suggest that visible light-promoted photooxidative processes mediated by sensitizers of appropriate chemical structure could represent a useful tool for properly addressing the problem of the increasing occurrence of infectious diseases caused by multiantibiotic-resistant microbial pathogens. The monocationic meso-substituted porphyrin 5-[4-(1-dodecanoylpyridinium)]-10,15,20-triphenyl-porphine (TDPyP) complexed into supramolecular aggregates of cationic amphiphilic beta-cyclodextrin (SC(6)NH(2)) (mean diameter = 20 nm) appeared to be endowed with favorable properties to act as a photosensitizing agent, including a very high quantum yield (Phi(Delta) = 0.90) for the generation of the highly reactive oxygen species, singlet oxygen ((1)O(2)). Although the yield of (1)O(2) generation was comparable to that obtained after TDPyP incorporation into cationic unilamellar liposomes of N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTAP) SC(6)NH(2)-bound TDPyP was more active than DOTAP-bound TDPyP in photosensitizing the inactivation of the Gram-positive methicillin-resistant bacterium Staphylococcus aureus (MRSA). At variance with DOTAP-bound TDPyP, photoactivated SC(6)NH(2)-bound TDPyP was efficient also in photokilling Gram-negative bacterial pathogens, such as Escherichia coli . These observations are in agreement with the well-known photobactericidal effect of positively charged porphyrin derivatives, which can be markedly enhanced after incorporation into carriers with multiple positive charges. In addition, transmission electron microscopy studies revealed that potentiation of the TDPyP-mediated photobactericidal effect by incorporation into SC(6)NH(2) is a consequence of the carrier's ability to promote an efficient crossing of the very tightly organized three-dimensional architecture of the bacterial outer wall by the embedded porphyrin so that a prompt interaction between the short-lived photogenerated (1)O(2) and the nearby targets, whose integrity is critical for cell survival, can take place.
最近的研究结果表明,由具有适当化学结构的敏化剂介导的可见光促进的光氧化过程,可能是一种有用的工具,可用于妥善解决由多重耐药微生物病原体引起的传染病日益增多的问题。与阳离子两亲性β-环糊精(SC(6)NH(2))(平均直径 = 20 nm)形成超分子聚集体的单阳离子中位取代卟啉5-[4-(1-十二烷酰基吡啶鎓)]-10,15,20-三苯基卟啉(TDPyP)似乎具有作为光敏剂的良好特性,包括产生高活性氧物种单线态氧((1)O(2))的非常高的量子产率(Phi(Delta) = 0.90)。尽管(1)O(2)的产生产率与TDPyP掺入N-[1-(2,3-二油酰氧基)丙基]-N,N,N-三甲基氯化铵(DOTAP)的阳离子单层脂质体后获得的产率相当,但与DOTAP结合的TDPyP相比,与SC(6)NH(2)结合的TDPyP在使革兰氏阳性耐甲氧西林金黄色葡萄球菌(MRSA)光灭活方面更具活性。与与DOTAP结合的TDPyP不同,光活化的与SC(6)NH(2)结合的TDPyP在光杀死革兰氏阴性细菌病原体(如大肠杆菌)方面也很有效。这些观察结果与带正电荷的卟啉衍生物的众所周知的光杀菌作用一致,在掺入具有多个正电荷的载体后,这种作用可以显著增强。此外,透射电子显微镜研究表明,通过掺入SC(6)NH(2)增强TDPyP介导的光杀菌作用是载体促进嵌入的卟啉有效穿过细菌外壁非常紧密组织的三维结构的能力的结果,从而使短寿命的光生(1)O(2)与附近对细胞存活至关重要的靶点之间能够迅速相互作用。