Photoinduced Reactive Oxygen Species Generation Research Articles

Precise ligand engineering of Ir(III)-based photosensitizer with aggregation-induced emission for image-guided photodynamic therapy.

Photodynamic therapy (PDT), which relies on the production of reactive oxygen species (ROS) induced by a photosensitizer to kill cancer cells, has become a non-invasive approach to combat cancer. However, the conventional aggregation-caused quenching effect, as well as the low ROS generation ability of photosensitizers, restrict their biological applications. In this work, a new Ir(III) complex with a dendritic ligand has been strategically designed and synthesized by ingenious modification of the ancillary ligand of a reported Ir(III) complex (Ir-1). The extended π-conjugation and multiple aromatic donor moieties endow the resulting complex Ir-2 with obvious aggregation-induced emission (AIE) activity and bathochromic emission. In in vitro experiments, importantly, Ir-2 nanoparticles exhibit the excellent photoinduced ROS generation capabilities of O2 •- and 1 O2 , as well as excellent biocompatibility and the lipid droplets (LDs) targeting feature. This study would provide useful guidance to design efficient Ir(III)-based photosensitizers used in biological applications in the future.

Metal–organic framework- and graphene quantum dot-incorporated nanofibers as dual stimuli-responsive platforms for day/night antibacterial bio-protection

Development of advanced antibacterial nanomaterials is important to prevent pathogenic microbial contamination and achieve bioprotection. Herein, we developed dual-stimuli-responsive nanoplatforms with efficient antibacterial activity based on electrospun polycaprolactone/hydroxypropyltrimethylammonium chloride chitosan (PQ) nanofiber membranes (NFMs) incorporated with naringenin-loaded zeolitic imidazolate framework-8 (NAR@ZIF-8) and graphene quantum dots (GQDs). These NFM nanoplatforms could simultaneously be used as “smart” pH-responsive controlled-release and photocatalytic systems. NAR was encapsulated in the microporous structure of the ZIF-8 channel, with a loading capacity of 22.57%. NAR@ZIF-8- and GQD-incorporated PQ (PQZG) nanofibers exhibited enhanced thermal stability and mechanical properties. The release kinetics and microstructure of the nanocarriers demonstrated that the acid-sensitive cleavable crystal structure of ZIF-8 resulted in the pH-responsive release of NAR from PQZG NFMs. Moreover, the presence of GQDs significantly enhanced the photoinduced reactive oxygen species (ROS) generation by NFMs. pH-triggered NAR release and photoinduced ROS generation improved the antibacterial efficacy of PQZG NFMs, forming the synergetic chemical-photodynamic strategies of the dual stimuli-responsive nanoplatforms. Additionally, cytotoxicity experiments revealed that the PQZG NFMs were non-toxic and had good biocompatibility. Therefore, the designed composite nanomaterials combined with the two antibacterial strategies can aid in the development of biosafe nanofibrous membranes for antibacterial or multifunctional bio-protection.

Isomeric sp2-C-conjugated porous organic polymer-mediated photo- and sono-catalytic detoxification of sulfur mustard simulant under ambient conditions

Isomeric sp2-C-conjugated porous organic polymer-mediated photo- and sono-catalytic detoxification of sulfur mustard simulant under ambient conditions

Multifunctional AIE iridium (III) photosensitizer nanoparticles for two-photon-activated imaging and mitochondria targeting photodynamic therapy

Developing novel photosensitizers for deep tissue imaging and efficient photodynamic therapy (PDT) remains a challenge because of the poor water solubility, low reactive oxygen species (ROS) generation efficiency, serve dark cytotoxicity, and weak absorption in the NIR region of conventional photosensitizers. Herein, cyclometalated iridium (III) complexes (Ir) with aggregation-induced emission (AIE) feature, high photoinduced ROS generation efficiency, two-photon excitation, and mitochondria-targeting capability were designed and further encapsulated into biocompatible nanoparticles (NPs). The Ir-NPs can be used to disturb redox homeostasis in vitro, result in mitochondrial dysfunction and cell apoptosis. Importantly, in vivo experiments demonstrated that the Ir-NPs presented obviously tumor-targeting ability, excellent antitumor effect, and low systematic dark-toxicity. Moreover, the Ir-NPs could serve as a two-photon imaging agent for deep tissue bioimaging with a penetration depth of up to 300 μm. This work presents a promising strategy for designing a clinical application of multifunctional Ir-NPs toward bioimaging and PDT.

Photocatalytic TiO2/CdS/ZnS nanocomposite induces Bacillus subtilis cell death by disrupting its metabolism and membrane integrity.

The online version contains supplementary material available at 10.1007/s12088-021-00973-z.

Unexpected Disparity in Photoinduced Reactions of C60 and C70 in Water with the Generation of O2 •- or 1O2.

Well-defined fullerene-PEG conjugates, C60-PEG (1) and two C70-PEG (2 and 3 with the addition sites on ab-[6,6] and cc-[6,6]-junctions), were prepared from their corresponding Prato monoadduct precursors. The resulting highly water-soluble fullerene-PEG conjugates 1–3 were evaluated for their DNA-cleaving activities and reactive oxygen species (ROS) generation under visible light irradiation. Unexpectedly, photoinduced cleavage of DNA by C60-PEG 1 was much higher than that by C70-PEG 2 and 3 with higher absorption intensity, especially in the presence of an electron donor (NADH). The preference of photoinduced ROS generation from fullerene-PEG conjugates 1–3 via the type II (energy transfer) or the type I (electron transfer) photoreaction was found to be dependent on the fullerene core (between C60 and C70) and functionalization pattern of C70 (between 2 and 3). This was clearly supported by the electron transfer rate obtained from cyclic voltammetry data and computationally estimated relative rate of each step of the type II and the type I reactions, with the finding that type II energy transfer reactions occurred in the inverted Marcus regime while type I electron transfer reactions proceeded in the normal Marcus regime. This finding on the disparity in the pathways of photoinduced reactions (type I versus type II) provides insights into the behavior of photosensitizers in water and the design of photodynamic therapy drugs.

(Invited) Water-soluble fullerenes (C60 and C70) with photoinduced ROS generation

Three types of water-soluble fullerene derivatives were prepared from their Prato adducts by conjugation with PEG. One Prato derivative of C60 ([6,6]-addition) and two Prato derivatives of C70 (ab-[6,6] and cc-[6,6]-addition) with carboxylic acids were synthesized, purified and subjected to the amide-forming conjugation with amine-PEG to form corresponding C60- or C70-PEG conjugates (Figure (a)). All the conjugates showed photoinduced DNA cleavage by reactive oxygen species (ROS) formed by type II energy transfer pathway or type I electron transfer pathway (Figure (d)). The responsible ROS were measured by ESR spin-trapping methods using 4-oxo-TEMP (for singlet oxygen) and DEPMPO (for superoxide radical anion), and were shown to be significantly different in three materials (Figure (b)-(c)). To understand the mechanism of these differences, redox potentials of the precursor molecules were analyzed by cyclic voltammetry in order to determine the difference in electron transfer rates. The lifetimes of the triplet excited states were measured by laser-flash photolysis. Finally, calculations were performed to obtain rate constants for each step in the type I and II pathways. The data will be explained in detail. Figure 1

In Vivo Bioimaging and Photodynamic Therapy Based on Two-Photon Fluorescent Conjugated Polymers Containing Dibenzothiophene-S,S-dioxide Derivatives.

As a critical component for photodynamic therapy toward cancer treatment, photosensitizers require high photoinduced reactive oxygen species generation efficiency, good biocompatibility, and high phototoxicity. Herein, a series of donor-acceptor conjugated polymers containing dibenzothiophene-S,S-dioxide derivatives are designed and synthesized, which can be used as effective photosensitizers. The resulting copolymer PTA5 shows strong green light emission with high photoluminescence quantum yields owing to the intercrossed excited state of local existed and charge transfer states. The PTA5 nanoparticles can be fabricated by encapsulation with a biocompatible polymer matrix. Upon excitation at 800 nm, these nanoparticles present a relatively large two-photon absorption cross section of 3.29 × 106 GM. These nanoparticles also exhibit good photostability in water and thus can be utilized for bioimaging. The tissue-penetrating depths of up to 170 μm for hepatic vessels and 380 μm for blood vessels of mouse ear were achieved using PTA5 nanoparticles. Furthermore, PTA5 nanoparticles show impressive reactive oxygen species generation capability under the irradiation of a white light source. This can be attributed to the effective intersystem crossing between high-level excited state. Upon irradiation with white light (400-700 nm) at 50 mW cm-2 for 5 min every other day, the tumor growth can be effectively suppressed in the presence of PTA5 nanoparticles. These findings demonstrate that PTA5 nanoparticles can be used as a photosensitizer for photodynamic therapy.

Enhanced Water Stability and Photoresponsivity in Metal-Organic Framework (MOF): A Potential Tool to Combat Drug-resistant Bacteria

In this work, we have successfully synthesized a bimetallic (Zinc and Cobalt) Zeolitic Imidazolate Framework (Zn50Co50-ZIF), a class in a wider microporous Metal-Organic Framework (MOF) family. The synthesized nanostructures maintain both water stability like ZIF-8 (solely Zn containing) and charge transfer electronic band in the visible optical spectrum as ZIF-67 (solely Co containing). Crystal structure from XRD, high resolution transmission electron microscopy (HRTEM) followed by elemental mapping (EDAX) confirm structural stability and omnipresence of the metal atoms (Zn and Co) across the nanomaterial with equal proportion. Existence of charge transfer state consistent with ZIF67 and intact ultrafast excited state dynamics of the imidazolate moiety in both ZIF-8 and ZIF-67, is evidenced from steady state and time resolved optical spectroscopy. The thermal and aqueous stabilities of Zn50Co50-ZIF are found to be better than ZIF-67 but comparable to ZIF-8 as evidenced by solubility, scanning electron microscopy (SEM) and XRD studies of the material in water. We have evaluated the photoinduced ROS generation by the mixed ZIF employing dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay. We have also explored the potentiality of the synthesized material for the alternate remediation of methicillin resistant Staphylococcus aureus (MRSA) infection through the photoinduced reactive oxygen species (ROS) generation and methylene blue (MB) degradation kinetics.

Multifunctional Nanosystem for Synergistic Tumor Therapy Delivered by Two-Dimensional MoS2.

A multifunctional nanosystem based on two-dimensional molybdenum disulfide (MoS2) was developed for synergistic tumor therapy. MoS2 was stabilized with lipoic acid (LA)-modified poly(ethylene glycol) and modified with a pH-responsive charge-convertible peptide (LA-K11(DMA)). Then, a positively charged photosensitizer, toluidine blue O (TBO), was loaded on MoS2 via physical absorption. The negatively charged LA-K11(DMA) peptide was converted into a positively charged one under acidic conditions. Charge conversion of the peptide could reduce the binding force between positively charged TBO and MoS2, leading to TBO release. Furthermore, the positively charged nanosystem was easily endocytosed by cells. Photo-induced hyperthermia of MoS2 in the tumor areas could promote TBO release and exhibited photothermal therapy. In vitro and in vivo results demonstrated that fluorescence and photo-induced reactive oxygen species (ROS) generation of TBO were severely decreased by MoS2 under normal conditions. While in the acidic condition, the pH-responsive nanosystem exhibited a highly specific and efficient antitumor effect with TBO release and photo-induced ROS generation, suggesting to be a promising accessory for synergistic tumor therapy.

Well-Defined Water-Soluble C60-PVP Conjugate

Based on their high photosensitivity, the potential medical application of fullerenes (C60 and C70) such as photodynamic therapy agents has been discussed for decades. Due to their high hydrophobicity, it is necessary to find a good method to solubilize fullerenes in water or water-miscible solvents for such application. We have been using a biocompatible and water-soluble polymer, poly(vinylpyrrolidone) (PVP) to prepare water-soluble C60/ or C70/PVP complex1 and C60- or C70-PVP conjugates2. 3 with efficient reactive oxygen species (ROSs) generation under visible light.4,5 However, in the clinical use, well-defined compounds with narrower molecular weight distribution are favored. In this study, we synthesized a RAFT reagent 1 for the preparation of well-defined PVP. The terminal moiety was converted to an amine 2 to connect to a C60 acid anhydride derivative 3 which was obtained through a Prato reaction.6 Obtained C60-PVP conjugate had a narrower molecular distribution, high water-solubility and photoinduced ROS generation.7 (1) Yamakoshi, Y.; Yagami, T.; Fukuhara, K.; Sueyoshi, S.; Miyata, N. J. Chem. Soc., Chem. Commun. 1994, 517. (2) Iwamoto, Y.; Yamakoshi, Y. Chem. Commun. 2006, 4805. (3) Oriana, S.; Aroua, S.; Söllner, J. O. B.; Ma, X.; Iwamoto, Y.; Yamakoshi, Y. Chem. Comm. 2013, 49, 9302. (4) Yamakoshi, Y.; Sueyoshi, S.; Fukuhara, K.; Miyata, N. J. Am. Chem. Soc. 1998, 120, 12367. (5) Yamakoshi, Y.; Umezawa, N.; Ryu, A.; Arakane, K.; Miyata, N.; Goda, Y.; Masumizu, T.; Nagano, T. J. Am. Chem. Soc. 2003, 125, 12803. (6) Aroua, S.; Schweizer, W. B.; Yamakoshi, Y. Org. Lett. 2014, 16, 1688. (7) Aroua, S.; Tiu, E. G. V.; Ayer, M.; Ishikawa, T.; Yamakoshi, Y. Polymer Chem. 2015, 6, 2616. Figure 1

Li-Doped ZnO Nanoparticles as Novel Direct Generator of Singlet Oxygen for Potential Photodynamic Therapy Applications

ABSTRACTPhotodynamic therapy (PDT) is an alternative to traditional cancer treatments. This approach involves the use of photosensitizer (PS) agents and their interaction with light. As a consequence, cytotoxic reactive oxygen species (ROS) are generated that, in turn will destroy tumors. On the other hand, ZnO is a biocompatible, nontoxic, and biodegradable material with the capability to generate ROS, specifically singlet oxygen (SO), which makes this material a promising candidate for 2-photon PDT. Doping ZnO with Li species is expected to induce defects in the host oxide structure that favors the formation of trap states that should affect the electronic transitions related to the generation of SO. The present work reports the effect of the level of Li-doping on the ZnO structure and its capability to generate SO. Li-doped ZnO nanoparticles were synthesized under size-controlled conditions using a modified version of the polyol method. XRD measurements confirmed the development of well-crystallized ZnO Wurtzite; the average crystallite sizes ranged between 13.3nm and 14.2 nm, with an increase in Li content. The corresponding band gap energy values, estimated from UV-vis measurements, decreased from 3.33 to 3.25 eV. Photoluminescence (PL) measurements of Li-ZnO revealed the presence of emission peaks centered on 363nm, 390nm, and 556 nm; these emission peaks correspond to the exciton emission, transition of shallow donor levels near of the conduction band to valence band such as interstitial Zn, and oxygen vacancies, respectively. The observed increase of the emission intensity of the 390 nm emission peak, relative to the intensity of the main emission peak at 363nm, was attributed to the promote of trap states due to interstitial Zn or Li-incorporation into the host oxide lattice. SO measurements evidenced the enhancing effect of the Li concentration on the capability of the doped ZnO to generate this species. This Li-dependence of SO generation can be attributed to the enhancement of the concentration of trap states in the host ZnO, as suggested by PL measurements. Accordingly, Li-ZnO would become cytotoxic to cancer cells via photo-induced ROS generation enabling this nanomaterial to be considered as a potential direct PS agent for the 2-photon PDT route.

Water-soluble fullerene materials for bioapplications: photoinduced reactive oxygen species generation.

The photoinduced reactive oxygen species (ROS) generation from several water-soluble fullerenes was examined. Macromolecular or small molecular water-soluble fullerene complexes/derivatives were prepared and their (1)O(2) and O(2)˙(-) generation abilities were evaluated by ESR spin-trapping methods. As a result, efficient (1)O(2) generation was detected from photoexcited C(60), not only in organic solvents, but also in aqueous media and especially from small molecule C(60)-carboxylic acid derivatives. Whereas efficient O(2)˙(-) generation was observed in the aqueous solution of the C(60)/γ-CD complex under photoirradiation.