Bacterial elimination via the photodynamic activity of a fullerene/light-harvesting antenna molecule assembled system integrated into liposome membranes

Ease of transmission and exceptionally high mortality rates make pathogen-based infections an ongoing global threat. Herein, a facile bacterial elimination process is described which is based on the photodynamic activity of fullerenes composed of light-harvesting antenna molecules integrated into liposome membranes. This was done to expand the absorption capabilities of fullerene derivatives. Efficient energy transfer from the photoactivated antenna molecules to the fullerenes enhanced antimicrobial activity without any harmful lytic activity against red blood cells even under irradiation.

The frequency and severity of serious pathogenic infections globally is of concern because of their rapid transmission rates and high mortality. [1][2][3] Since the discovery of penicillin by Dr Fleming in 1928, researchers have developed various types of small molecule antibiotics, 4,5 peptides, 5,6 polymers, 7 and nanomaterials 8 in an attempt to combat and eliminate this omnipresent threat. The emergence of drug-resistant bacteria due to antibiotic misuse poses a serious risk to global health and safety. 9,10 Recently, it was revealed that drug resistance can be acquired by E. coli aer as little as 3 h of exposure. 11 With this in mind, it is critical that alternative approaches for the elimination of bacteria and other harmful microbes must be developed. [8][9][10] Photodynamic therapy (PDT) has been proposed as a candidate for the treatment of cancer, 12-14 rheumatoid arthritis, 15 and infections 16 because of its excellent spatiotemporal selectivity and invasiveness. The therapeutic effects of PDT are achieved through oxidative stress caused by the presence of cytotoxic reactive oxygen species (ROS) such as the singlet oxygen ( 1 O 2 ) and the superoxide anion (O 2 À c); these are produced by photosensitizers via light irradiation. 17 In comparison with conventional antibiotic courses, PDT has also been proposed as a treatment option for infectious diseases as it requires a relatively short-term treatment course, inicts severe damage due to oxidative stress, and offers non-specic targeting of the microbial cellular structures and metabolic pathways related to the appropriate receptors. 16 Of course, the key to successful PDT is highly dependent on the deliverability of the photosensitizers to the right recipient cells. 18 Many types of photosensitizers have been developed, 18 including fullerenes, 19 porphyrins, 20,21 chlorines, 22,23 phthalocyanines, 20,23 and their derivatives. Because of their ability to remain in the excited state for a long time and excellent capacity to generate ROS, fullerenes, and their derivatives are extensively used as possible photosensitizers in PDT. 19 Despite their fascinating potential for PDT, their bioavailability is oentimes limited because of poor water solubility and low absorption capacity at longer wavelengths. 24 Thus, the development of more effective fullerene delivery systems is a necessary step in accessing the full therapeutic potential of these compounds as antimicrobial agents. 25 To address these issues, we used a liposome as a delivery platform via two approaches; in one strategy, the target location could be manipulated through the use of polarized fullerenes (catC 60 ), whereas the other approach focused on facilitating more efficient energy transfer from the photo activated antenna molecules to catC 60 at longer wavelengths. In this study, bacterial elimination was achieved via excellent photodynamic activity using a catC 60 /light-harvesting antenna molecule assembly, which was integrated into liposomal membranes (LMIcatC 60light-harvesting antenna molecule) (Fig. 1). Natural products, including cyclodextrins, 27 polysaccharides, 28,29 and liposomes, [30][31][32] were developed based on solubilizing techniques to utilize fullerenes in applications as photosensitizers. 26 In particular, liposomal membranes are attractive platforms for designing and constructing assembled systems of fullerenes with dialkylated light-harvesting antenna molecules. [32][33][34] Previously, the poor absorption capacity of our photosensitizers over the longwavelength range between 600 and 700 nm was improved and the photoinduced cytotoxicity toward HeLa cells of these types of assembled systems was enhanced. Without the need for complicated synthesis of fullerenes, we used our system, which is based on LMI systems, to maximize and expand the availability of our photosensitizers at will by combining them with commercially available light-harvesting molecules. These results encouraged us to apply our system for bacterial elimination processes.
Furthermore, 94% of the uorescence signals from DiO were quenched via complexation ( Fig. 2B and Table 1). This was conrmation that DiO had been successfully introduced into the liposomal membrane via the DMSO injection method and that the distance between DiO and catC 60 facilitated efficient energy transfer. The z potential of the liposome decreased slightly as a result of the complexation of DiO from +36 to +30 mV, whereas the hydrodynamic diameter of the liposomes remained relatively unchanged at 80 nm.
To evaluate whether our systems were suitable photosensitizers, the quantity of 1 O 2 generated by our system under white light irradiation (>400 nm) was determined. Initially, we conducted a stability check against photo-irradiation by measuring the UV-vis spectra. As shown in Fig. S2, † catC 60 showed excellent stability in all the systems against photo-irradiation under the current conditions. In contrast, photobleaching was observed in all the systems (Fig. S3 †). Aer 40 min of irradiation, the absorbance at the maximum absorption wavelength from DiO of LMIcatC 60 -DiO (490 nm), DiI of LMIcatC 60 -DiI (552.5 nm), and DiD of LMIcatC 60 -DiD (648 nm) decreased to 53%, 90%, and 45%, respectively (Fig. S4 †). Similar trends were observed in all dyes in the case with the mixture of these three systems. Furthermore, we examined the colloidal stability during photo-  irradiation using DLS. The results revealed that the hydrodynamic diameter and PDI value did not signicantly change via photo-irradiation. A time course of 1 O 2 generation was established by monitoring the conversion of the anthracene derivative 9,10-anthracenediyl-bis(methylene)dimalonic acid (ABDA) into endoperoxide (Scheme S2 †). 35 As 1 O 2 oxidized ABDA, the maximum absorbance peaks at 360, 380, and 400 nm that were characteristic of ABDA decreased as shown in Fig. S5. † The ratio of absorbance of ABDA at 400 nm, which was expressed as the amount of ABDA at each time point relative to the total concentration of ABDA, was quantied as a measure of the system's ability to generate 1 O 2 under white light irradiation in an O 2 -saturated aqueous solution (Fig. 2C). The LMIDiD, catC 60free control systems, did not generate 1 O 2 under irradiation with white light (Fig. S5A †). The 1 O 2 expression level of catC 60 (Fig. 2C, black line) was accelerated by combining it with photoharvesting antenna molecules, which indicated that the energy transfer process from the photo activated photo-antenna molecules to catC 60 was efficient. When comparing the photodynamic activity of these LMIcatC 60 -dyad systems, the LMIcatC 60 -DiO and LMIcatC 60 -DiI systems generated the largest amount of 1 O 2 via photo irradiation under the prevailing conditions (ABDA, 25 mM; lipids, 1 mM; catC 60 , 2.5 mM; lightharvesting molecules, 1.25 mM) (Fig. 2C, yellow and red lines, respectively). In contrast, the photodynamic activity of the LMIcatC 60 -DiD system was lower than that of the other dyad systems (Fig. 2C, blue line). These results suggested that enhancing the photodynamic activities of the LMIcatC 60 systems was highly dependent on the activation frequencies of the light-harvesting antenna molecules attained via irradiation. These differences were observed in the quenching efficiencies (Table 1). To expand the absorption capacity for white light across a wide range of wavelengths and improve the availability of catC 60 , we examined a mixture of these three dyes with the same concentration of total catC 60 as that used for the other dyad systems (lipids, 1 mM; catC 60 , 0.05 mM; DiO, 0.08 mM; DiI, 0.08 mM; DiD, 0.08 mM; Fig. 2C, purple line). We found that they all exhibited the same level function as the LMIcatC 60 -DiO and LMIcatC 60 -DiI systems.
The antibacterial activity of our systems was tested against Escherichia coli (E. coli) as a measure of their photodynamic character. Under the prevailing conditions, the nonionic LMI catC 60 -DiD system did not work well as an antibacterial agent even during irradiation ( Fig. S6 and S7 †). It was theorized that the electrically negative character of E. coli (approximately À15 mV) prevented maximum interaction between the dyad systems and the E. coli colony (Fig. S8 †). To enhance the interaction of dyad systems with E. coli, cationic lipids (2) were prepared using the aforementioned method and tested; the solution properties of these lipids, including their hydrodynamic diameter and z potential, are summarized in Table 1 (1, 45 mM; 2, 5 mM). Unfortunately, both the hydrodynamic diameter and the z potential of samples containing DiD could not be measured accurately since its absorption interfered with the DLS instrument. We addressed the morphological observation of our systems using transmission electron microscopy; the analysis revealed a spherical morphology with a lipid-bilayer. The size of our dyad systems agreed with the results of the DLS measurements (Fig. S9 †). In addition, it was revealed that the diameter of LMIcatC 60 -DiD is similar to that of the other systems. Thus, the antimicrobial activity was established based on the photodynamic character of our LMIcatC 60 -light-harvesting antenna molecule using the cationic lipids. Initially, the minimum bactericidal concentration (MBC 90 ), which is dened as the lowest concentration of the antibacterial agent needed to destroy 90% of a particular bacterial colony in broth media, was determined. 36 Briey, aer co-incubation with our dyad systems for 30 min, the E. coli cells were irradiated with white light for 30 min. A 24 h incubation period then followed, aer which the viability of the E. coli was estimated by measuring the optical density of the colony at 600 nm.
As shown in Fig. 3A, no apparent cytotoxicity against E. coli was established for the "dark" (no irradiation) conditions. In contrast, antimicrobial activities were obtained under irradiation except for the LMIcatC 60 systems in which the concentration of catC 60 was between 0 and 2.5 mM (Fig. 3B). The MBC 90 values for the LMIcatC 60 -DiO, LMIcatC 60 -DiI, LMIC 60 -DiD, and dyad mixture were 5.1, 2.4, 3.2, and 1.2 mM, respectively ( Table  1). As expected, the LMIcatC 60 -light-harvesting molecules enhanced the antimicrobial activity of catC 60 . Moreover, the system containing a mixture of LMIcatC 60 -DiO, LMIcatC 60 -DiI, and LMIcatC 60 -DiD showed the highest antimicrobial activity, whereas the lowest antimicrobial activity was associated with the LMIcatC 60 -DiO dyad despite its excellent 1 O 2 production The hydrodynamic diameter was determined by conducting dynamic light scattering (DLS) measurements in Milli-Q water (25 C; pH, 7.4). The PDI value was calculated using the cumulant method from an auto-correlation curve. b The z potential was determined using capillary cells. c MBC 90 is dened as the concentration of the antimicrobial agent required to kill 90% of the bacterial colony within 1 h with irradiation. d MIC is dened as the minimum inhibitory concentration of bacterial growth with irradiation using white light. e Lysis of red blood cells was determined at 2.5 mM and carried out under irradiation. f The absorption of DiD interfered with the DLS instruments. g The quenching efficiencies of LMIcatC 60 -DiI and LMIcatC 60 -DiD were previously reported. 32 capacity. The reason for this is discussed in the next paragraph.
To address their availability as photoinduced antimicrobial agents, the minimal inhibitory concentration was investigated using an agar-based colony-forming assay ( Fig. S10-S14 †). Here similar trends in the dyads' antimicrobial prole were found ( Fig. 3C and D), 36 namely, colony formation was drastically suppressed even at low concentrations (catC 60 <1.25 mM) upon exposure to LMIcatC 60 -DiI, LMIC 60 -DiD, and the dyad mixture with irradiation (400-800 nm). The MIC value of our systems is summarized in Table 1; here, it was noted that the antimicrobial activity of the DiO systems was quite low when compared with the other catC 60 -photo-harvesting antenna molecule assembled systems. We hypothesized that these differences in performance were caused by variations in the extent of the interaction and the uptake of the appropriate concentrations.
To verify our hypothesis, interaction of the LMI system with E. coli was studied using confocal laser scanning microscopy (Fig. 4). Aer co-incubation with LMIDiO, LMIDiI, LMIDiD  (Fig. 4B, D, F, and H-J). Fluorescence signals for DiO were quite faint compared with the signals from the other systems; however, these signals were much brighter when the mixture was used regardless of the extent of dilution. Thus, the strong interactions of our systems with E. coli enhanced the photoinduced damage caused by the 1 O 2 molecules that had been generated via photodynamic activity. These differences in the extent of the interaction between the system and the bacteria may be caused by the electrostatic character of the respective systems.
To determine the hemolytic effect of each system, the lytic activity against red blood cells (RBCs) 36 was quantied aer a 1 h period of exposure of a veried concentration of the dyad against E. coli. The E. coli (2 Â 10 7 cfu) cells were co-incubated with the fullerene/photo-antenna molecule-liposome hybrid for 30 min, after which they were irradiated (300-740 nm) for 30 min. After a 24 h incubation period in the culture media, the survival rate was quantified by measuring the optical density at 600 nm using a microplate reader. Three independent experiments were conducted in duplicate. (C and D) Minimal inhibitory concentration assay of the fullerene/photoantenna molecule-liposome hybrid system without irradiation (C) and with irradiation (D) against E. coli. The E. coli (4 Â 10 5 cfu) cells were co-incubated with the fullerene/photo-antenna molecule-liposome hybrid for 30 min, after which they were subjected to irradiation (300-740 nm) for 30 min. After incubation for 24 h on MHB agar gel, the survival rate was quantified. The three independent experiments were conducted in duplicate. systems to RBCs by measuring the absorbance of the leaked myoglobin. No apparent lytic activity was observed even at the highest concentration of the dyad aer irradiation with white light (Table 1 and Fig. S15 †), suggesting that our system was a potentially safe alternative for eliminating bacterial content under white light irradiation.
In conclusion, we present a facile method for the elimination of bacteria based on the photodynamic activity of cationic fullerene-photo-harvesting antenna molecules integrated into a liposome membrane. We were able to expand the absorption capacity of these fullerene derivatives mainly via the development of more efficient energy transfer processes from the photo activated antenna molecules to the fullerene derivatives. As noted in this study, our strategy has great potential for use in the photo dynamically inuenced elimination of bacterial content.

Conflicts of interest
There are no conicts to declare.