van der Meulen F W, Ibrahim K, Sterenborg H J, Alphen L V, Maikoe A, Dankert J
Laser Centre, University of Amsterdam, Netherlands.
J Photochem Photobiol B. 1997 Oct;40(3):204-8. doi: 10.1016/s1011-1344(97)00057-2.
Bacterial resistance against antibiotic treatment is becoming an increasing problem in medicine. Therefore methods to destroy microorganisms by other means are being investigated, one of which is photodynamic therapy (PDT). It has already been shown that a variety of Gram-positive and Gram-negative bacteria can be killed in vitro by PDT using exogenous sensitizers. An alternative method of photosensitizing cells is to stimulate the production of endogenous sensitizers. The purpose of this study was to investigate the bactericidal efficacy of PDT for Haemophilus parainfluenzae with endogenously produced porphyrins, synthesized in the presence of delta-aminolaevulinic acid (delta-ALA). H. parainfluenzae incubated with increasing amounts of delta-ALA showed decreased survival after illumination with 630 nm light. No photodynamic effect on the bacterial viability was found when H. parainfluenzae was grown without added delta-ALA. H. influenzae, grown in the presence of delta-ALA, but not capable of synthesizing porphyrins from delta-ALA, was not affected by PDT. Of the range of incident wavelengths, 617 nm appeared to be the most efficient in killing the bacteria. Spectrophotometry of the bacterial porphyrins demonstrated that the maximum fluorescence occurred at approximately 617 nm, with a much lower peak around 680 nm. We conclude that a substantial killing of H. parainfluenzae by PDT in vitro after endogenous sensitization with delta-ALA can be achieved.
细菌对抗生素治疗的耐药性在医学领域正成为一个日益严重的问题。因此,人们正在研究通过其他手段消灭微生物的方法,其中之一就是光动力疗法(PDT)。已经表明,使用外源性敏化剂,多种革兰氏阳性菌和革兰氏阴性菌可在体外被PDT杀死。使细胞产生内源性敏化剂是另一种光致敏方法。本研究的目的是探讨在δ-氨基乙酰丙酸(δ-ALA)存在下合成内源性卟啉的情况下,PDT对副流感嗜血杆菌的杀菌效果。用不同量的δ-ALA孵育副流感嗜血杆菌后,用630nm光照射,其存活率降低。当副流感嗜血杆菌在不添加δ-ALA的情况下生长时,未发现对细菌活力有光动力效应。在δ-ALA存在下生长但不能从δ-ALA合成卟啉的流感嗜血杆菌不受PDT影响。在入射波长范围内,617nm似乎是杀灭细菌最有效的波长。对细菌卟啉进行分光光度测定表明,最大荧光出现在约617nm处,在680nm左右有一个低得多的峰值。我们得出结论,在用δ-ALA进行内源性致敏后,PDT在体外可大量杀灭副流感嗜血杆菌。