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Brucellosis is an intracellular infectious disease that is primarily treated with antibacterial therapy. However, most antibacterial drugs struggle to penetrate the cell membrane and may be excluded or inactivated within the cell. In a recent study, researchers developed a nanogel coated with polydopamine (PDA) that responds to reactive oxygen species (ROS) and has enhanced adhesion properties. This nanogel encapsulates photosensitized zinc phthalocyanine (ZnPc) and an antibacterial drug, and is further modified with folic acid (FA) for active targeting. The resulting ROS-responsive nanogel, termed PDA@PMAA@ZnPc@DH-FA, can reach temperatures up to 50°C under near-infrared light, leading to a 72.1% improvement in drug release through increased ROS production. Cell staining confirmed a cell survival rate above 75%, with a low hemolysis rate of only 4.633%, indicating excellent biocompatibility. Furthermore, the study's results showed that the nanogel exhibited stronger killing effects against Brucella compared to administering the drug alone. Under near-infrared irradiation, the nanogel achieved a bacteriostatic rate of 99.8%. The combined approach of photothermal therapy and photodynamic therapy offers valuable insights for treating Brucella. [ABSTRACT FROM AUTHOR]

This paper presents the results of quantum-chemical modeling performed by the Density Functional-Based Tight Binding (DFTB) method to investigate the change in the band structure of hybrid materials based on carbon nanotubes and unsubstituted, tetra-, or octa-halogen-substituted zinc phthalocyanines upon the adsorption of ammonia molecules. The study showed that the electrical conductivity of these materials and its changes in the case of interaction with ammonia molecules depend on the position of the impurity band formed by the orbitals of macrocycle atoms relative to the forbidden energy gap of the hybrids. The sensor response of the hybrids containing halogenated phthalocyanines was lower by one or two orders of magnitude, depending on the number of substituents, compared to the hybrid with unsubstituted zinc phthalocyanine. This result was obtained by calculations performed using the nonequilibrium Green's functions (NEGF) method, which demonstrated a change in the electrical conductivity of the hybrids upon the adsorption of ammonia molecules. The analysis showed that in order to improve the sensor characteristics of CNT-based hybrid materials, preference should be given to those phthalocyanines in which substituents contribute to an increase in HOMO energy relative to the unsubstituted macrocycles. [ABSTRACT FROM AUTHOR]

Laser thin layer deposition technologies were applied to develop organic heterostructures on flexible transparent conductive electrode (TCE). Flexible substrates such as flexible glass (FG), polyethersulfone (PES), amorphous polyethylene terephthalate (PET-A) and biaxially-oriented polyethylene terephthalate (PET-B) were employed to assess the influence of the substrate type on the optical and electrical characteristics of the organic devices. For comparison reason, the organic heterostructures were fabricated on rigid glass substrate and commercially available indium tin oxide (ITO)-coated PET. Hence, flexible and rigid glass substrates were coated with ITO film by pulsed laser deposition (PLD) at low fluence, subsequently a blend layer based on zinc phthalocyanine (ZnPc) and N, N′-bis-(1-dodecyl)perylene-3,4,9,10 tetracarboxylic diimide (AMC14) being deposited by matrix assisted pulsed laser evaporation (MAPLE) on the TCE film. The investigations evidenced that the roughness and the substrate type can strongly influence the properties of the ITO layer deposited by PLD as well as the optical and electrical characteristics of the organic heterostructures based on the blend layer deposited by MAPLE. Thus, the lowest roughness (0.8 nm) and the best Hall mobility (41.9 cm2/Vˑs) were achieved for ITO coatings deposited on flexible glass substrate. Also, the highest current density value (9.3 × 10− 4 A/cm2 at 0.5 V) was reached for the organic heterostructures fabricated on this type of flexible substrate. [ABSTRACT FROM AUTHOR]

The interest in research to enhance the ability of sensitizers to generate singlet oxygen using light and/or ultrasound in cancer treatment has increased significantly in recent years, and studies have attracted considerable interest. In addition, phthalocyanines (Pcs) have become increasingly important as sensitizers in photodynamic therapy (PDT) (stimulation source: light) and/or sonodynamic therapy (SDT) (stimulation source: light and ultrasound). Sonophotodynamic therapy (SPDT), a new technique that gives more effective results than PDT, is now gaining in importance. Although there are published articles on SPDT studies, studies in this field are limited. In this context, we synthesized a zinc(II) phthalocyanine molecule bearing 4-(pyridine-4-ylthio) substituents to determine its potential as a sensitizer in SPDT applications as well as PDT applications, and the structure of the synthesized complex was illuminated using FTIR,1H-NMR, UV-Vis, and MS spectroscopic techniques. When light and ultrasound were combined, the calculated ΦΔ value for zinc (II) phthalocyanine (3) increased to greater than 1, even though it was 0.76 after light excitation. When evaluating the two methods, it was observed that singlet oxygen production was greatly enhanced by the SPDT method. In this way, the research will add to the enhancement of knowledge on the subject of the SPDT method's enhancement of singlet oxygen generation.

Photodynamic therapy is an alternative method to surgical methods used in the treatment of cancer and one of its three basic components is photosensitizer. The high singlet oxygen generating capacity, high solubility in common organic solvents, low aggregation tendency and lightfastness are the characteristics that photosensitizers must have. Phthalocyanines with bulky substituents are candidate molecules that can be used as sensitizers in photodynamic therapy due to prevent aggregation in the solutions and improve solubility. Based on these facts in this study, singlet oxygen quantum yield and photodegradation quantum efficiency were calculated to evaluate the potential of bis(4-fluorophenyl)-methoxy-substituted zinc phthalocyanine, which does not form aggregation and has high solubility in organic solvents commonly used in photodynamic therapy applications. The metallo phthalocyanine generated higher singlet oxygen than unsubstitue zinc phthalocyanine. According to the singlet oxygen quantum yield, the addition of bis(4-fluorophenyl)-methoxy groups to the phthalocyanine ring increases the singlet oxygen production. The results show that this phthalocyanine may be suitable candidates as photosensitizers in photodynamic therapy with the singlet oxygen quantum yield values are 0.76 and 0.70 in DMSO and DMF, respectively. [ABSTRACT FROM AUTHOR]

This study proposes enhanced thermal stability and excellent electrochemical and photocatalytic performance of hierarchical structure of zinc-phthalocyanine (ZnPc) samples prepared through eco-friendly enhanced microwave (MW) synthesis over 5 min at T = 200 °C. The structure and morphology of the obtained ZnPc were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscope (TEM), and Atomic Force Microscope (AFM). At the same time, thermal stability was analyzed using thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The obtained ZnPc with high crystallinity, pure crystalline phases and reflection peaks related to the β-form of ZnPc. The average crystallite size (D) of 74 nm was determined using the Debye-Scherrer equation for a peak at 2θ = 9.30°. AFM image presented ZnPc material as a distinguished multilayered crystal with a rhombus-shaped crystal structure that seems very smooth on its surface, while TEM images showed a hierarchical structure of synthesized ZnPc self-organized assembles from the needle-like morphology which are aligned at different orientations having length up to approximately 500 nm and with 20 nm in diameter. TGA and DTA showed that the decomposition process occurred at a high temperature of 649 °C, for a heating rate of 15 °C/min, indicating good thermal stability of the investigated ZnPc. The photocatalytic activity of the hierarchically structured ZnPc was evaluated using different initial concentrations of Reactive Blue 19 (RB-19), pH value, and catalyst dose. Additionally, the electrochemical performance of ZnPc as electrode material was investigated. This study indicates facile, low-cost, and green MW method can be used for the preparation of the needle-like form of ZnPc as a promising multifunctional material for the potential applications: in thermal energy storage in future solar power technologies, as electrode material exhibiting superior voltammetric response, with cathodic and anodic current values and as photocatalyst for degradation of RB-19 and other organic dye-pollutants. [Display omitted] • Needle-like form of ZnPc were acquired through microwave-аssisted synthesis. • Thermal stability of ZnPc at high-temperature decomposition, at around 640 °C. • An electrochemical and photocatalytic properties of ZnPc were investigated. • Effects of RB-19 concentration and pH value on the decolorization rate were studied. [ABSTRACT FROM AUTHOR]

Context: The zinc (II) and silicon (IV) phthalocyanine adsorption on a TiO2 and SnO2 semiconductor surface was investigated using the density functional theory. Several effects were studied: the semiconductor (TiO2, SnO2), the central metal atom in the phthalocyanine (Zn, Si), the substituent groups in the phthalocyanine, and the anchor group (anhydrous, carboxyl) connecting the phthalocyanine with the semiconductor. The application of methodologies to study the intermolecular interactions predicted a stronger zinc and silicon phthalocyanine adsorption with carboxyl than anhydrous. Adsorption energies for phthalocyanines anchored by a carboxyl group indicate a stronger adsorption for TiO2 than for SnO2 with energy differences of up to 7 eV. The presence of coordinative and more van der Waals interactions in TiO2 can explain this. This work is carried out to understand the interaction between phthalocyanines and the semiconductor surface, a crucial aspect of the efficient performance of solar cells. Methods: We modeled two semiconductor surfaces in extended configuration (TiO2 and SnO2), which were optimized with the GGA-PBE exchange–correlation functional for solids, including the Grimme's correction dispersion (D3). The meta-GGA TB09LDA exchange–correlation functional was employed to calculate the band gap energy of the semiconductors. The adsorption energies of the phthalocyanines adsorbed on the semiconductors were determined with GGA-PBE-D3 and corrected by the counterpoise method. The nature of the intermolecular interactions in the adsorption was analyzed using the non-covalent interactions (NCI) based on the promolecular approximation of electron density. These interactions were quantifiable by employing the intrinsic bond strength index (IBSI). We used the QuantumATK and the Multiwfn packages for all the calculations. [ABSTRACT FROM AUTHOR]

Context: The zinc (II) and silicon (IV) phthalocyanine adsorption on a TiO2 and SnO2 semiconductor surface was investigated using the density functional theory. Several effects were studied: the semiconductor (TiO2, SnO2), the central metal atom in the phthalocyanine (Zn, Si), the substituent groups in the phthalocyanine, and the anchor group (anhydrous, carboxyl) connecting the phthalocyanine with the semiconductor. The application of methodologies to study the intermolecular interactions predicted a stronger zinc and silicon phthalocyanine adsorption with carboxyl than anhydrous. Adsorption energies for phthalocyanines anchored by a carboxyl group indicate a stronger adsorption for TiO2 than for SnO2 with energy differences of up to 7 eV. The presence of coordinative and more van der Waals interactions in TiO2 can explain this. This work is carried out to understand the interaction between phthalocyanines and the semiconductor surface, a crucial aspect of the efficient performance of solar cells. Methods: We modeled two semiconductor surfaces in extended configuration (TiO2 and SnO2), which were optimized with the GGA-PBE exchange–correlation functional for solids, including the Grimme's correction dispersion (D3). The meta-GGA TB09LDA exchange–correlation functional was employed to calculate the band gap energy of the semiconductors. The adsorption energies of the phthalocyanines adsorbed on the semiconductors were determined with GGA-PBE-D3 and corrected by the counterpoise method. The nature of the intermolecular interactions in the adsorption was analyzed using the non-covalent interactions (NCI) based on the promolecular approximation of electron density. These interactions were quantifiable by employing the intrinsic bond strength index (IBSI). We used the QuantumATK and the Multiwfn packages for all the calculations. [ABSTRACT FROM AUTHOR]

Phthalocyanines are versatile photodynamic therapy agents whose biological activity depends on their aggregation state, which is expected to be influenced by binding to biomolecules. Here, guanine‐rich nucleic acid binding of a water‐soluble cationic, regiopure C4h zinc phthalocyanine bearing four triethylene glycol methyl ether and four N‐methyl‐4‐pyridinium substituents (1) is reported. In contrast to double‐stranded DNA, guanine systems GpG, (GG)10, poly(G) and quadruplex DNA are shown to effectively disrupt phthalocyanine aggregates in buffered solution. This process is accompanied by evolution of the Q‐band absorbance and enhanced emission. Increasing the sequence length from GpG to (GG)10 increases the binding and confirms the importance of multiple binding interactions. Enhanced binding in the presence of KCl suggests the importance of nucleobase hydrogen‐bonded mosaics in phthalocyanine binding. Notably, the (GT)10 sequence is even more effective than quadruplex and pure guanine systems at disrupting the aggregates of 1. Significant time‐dependent binding of 1 with poly(G) reveals biexponential binding over minutes and hours, which is linked to local conformations of poly(G) that accommodate monomers of 1 over time. The study highlights the ability of biomacromolecules to disrupt phthalocyanines aggregates over time, which is an important consideration when rationalizing photoactivity of photosensitizers in‐vivo. [ABSTRACT FROM AUTHOR]

An asymmetric zinc phthalocyanine dye (ZnPcT3C), bearing three tetraethylene glycol donor groups and one carboxylic acid anchoring group, was synthesized as a photosensitizer dye for dye‐sensitized solar cells (DSSCs). The tetraethylene glycol (TEG), consisting of four ethoxy units, works as an amphiphilic long‐chain donor group that greatly helped in reducing the molecular aggregation. Carboxylic acid group, on the other hand, an acceptor, together with TEG in ZnPcT3C functions as a 'push–pullʼ system suitable for DSSCs. Absorption spectra of ZnPcT3C in DMSO showed a strong sharp Q band in the infrared region 600–700 nm with (λmax = 682 nm) and a less intense soret band appeared in the region 300–400 nm with λmax = 340 nm. The zinc phthalocyanine (ZnPcT3C) exhibited molar extinction coefficient (ε) of 72,727 L mol−1cm−1. The emission was observed at λem = 695 nm upon excitation at 650 nm and exhibited a fluorescence decay of 2.82 ns. The ZnPcT3C dye sensitised solar cell (c = 1 mM) exhibited the power conversion efficiency (η) of 3.52% in chloroform in I−/I3 electrolyte under simulated 100% brightness. Cosensitization of ZnPcT3C with another auxiliary dye D131 in 1:1 ratio in a cocktail‐type DSSC attained the power conversion efficiency of twice as high as η = 6.27% in an identical condition. A mixture of D131 (λmax = 470 nm) dye with the ZnPcT3C phthalocyanine harvests sunlight across the visible spectra, enabling DSSCs to attain a large photocurrent and photovoltage, enhancing power conversion efficiency. [ABSTRACT FROM AUTHOR]

The quantification of tyramine (Tyr) and spermidine (Spd) is essential to protect and ensure quality and safety for food and beverage consumers. In this work, an electrochemical study was carried out, and a new, rapid, sensitive, reliable, and selective square‐wave voltammetric method for simultaneously determining Tyr and Spd in wines was developed. A Chemically Modified Carbon Paste electrode with Zinc PhthaloCyanine (CMCPE‐ZnPC) was used as a sensor in the electrochemical study, and a standard addition procedure (SAP) was employed to solve the matrix effect in the quantification of Tyr and Spd in wines. These analytes were electroactive on the stable, sensitive, and selective CMCPE‐ZnPC sensor under study using SWV technique, displaying peak anodic potentials at around 400 mV for Tyr and 860 mV for Spd. Wine samples were analyzed using the proposed and reference methods. No statistically significant differences were observed among the results obtained for Tyr and Spd determinations, applying the paired t‐test at a confidence level of 95 %. The proposed method yielded low limits of detection (6.8 nmol L−1 for Tyr and 10.8 nmol L−1 for Spd), good recovery rates (from 86.1 to 107.5 %), and reproducibility (overall RSD of 2.6 %). The proposed method contributes to green analytical chemistry since it uses no chemical pretreatment of the wine samples. [ABSTRACT FROM AUTHOR]

A new nonperipheral zinc(II) phthalocyanine bearing octa carboxylic acid ethyl ester derivative substituted triazole attached propylmercaptothiobenzylmercapto derivative was synthesized via the tetramerization reaction of phthalonitrile. The photochemical in vitro photodynamic activity of zinc(II) phthalocyanine (ZnPc-I), such as human nonsmall cell lung carcinoma cell lines, was investigated in this study. The singlet oxygen generation property of novel zinc(II) phthalocyanine (ZnPc-I) was also examined due to the significantly high singlet oxygen quantum yield of ZnPc-I (FD = 0.66). The antiproliferative effects of ZnPc-I were also investigated on the A549 and H1299 cell lines, and the results demonstrated that ZnPc-I had a strong antiproliferative effect on both cell lines. [ABSTRACT FROM AUTHOR]

Nowadays, the development of devices based on organic materials is an interesting research challenge. The performance of such devices is strongly influenced by material selection, material properties, design, and the manufacturing process. Usually, buckminsterfullerene (C60) is employed as electron transport material in organic photovoltaic (OPV) devices due to its high mobility. However, considering its low solubility, there have been many attempts to replace it with more soluble non-fullerene compounds. In this study, bulk heterojunction thin films with various compositions of zinc phthalocyanine (ZnPc), a perylene diimide derivative, or C60 were prepared by matrix-assisted pulsed laser evaporation (MAPLE) technique to assess the influence of C60 replacement on fabricated heterostructure properties. The investigations revealed that the optical features and the electrical parameters of the organic heterostructures based on this perylene diimide derivative used as an organic acceptor were improved. An increase in the JSC value (4.3 × 10−4 A/cm2) was obtained for the structures where the perylene diimide derivative acceptor entirely replaced C60 compared to the JSC value (7.5 × 10−8 A/cm2) for the heterostructure fabricated only with fullerene. These results are encouraging, demonstrating the potential of non-fullerene compounds as electron transport material in OPV devices. [ABSTRACT FROM AUTHOR]

Herein, we designed and synthesized novel reactive oxygen species (ROS)-responsive glycol chitosan-doxorubicin (DOX) prodrug via a ROS-cleavable thioketal (TK) linker. The obtained GC-TK-DOX formed self-assembled nanoparticles of 312 nm in aqueous media. Photosensitizers zinc phthalocyanine (ZnPc)-loaded GC-TK-DOX (GC-TK-DOX/ZnPc) nanoparticles were fabricated by using a dialysis approach. The GC-TK-DOX and GC-TK-DOX/ZnPc nanoparticles were nearly spherical by transmission electron microscopy (TEM) observation. Under 660-nm laser irradiation, GC-TK-DOX/ZnPc could generate singlet oxygen. Further, GC-TK-DOX/ZnPc nanoparticles exhibited ROS-sensitive release of DOX and ZnPc in vitro. GC-TK-DOX/ZnPc with laser irradiation showed more drug uptake and higher cytotoxic effects than GC-TK-DOX/ZnPc without irradiation, free DOX and GC-TK-DOX in HeLa tumor cells. Overall, these findings suggested that GC-TK-DOX/ZnPc could be a promising nanoarchitecture for synergetic chemo-photodynamic therapy against tumors. [ABSTRACT FROM AUTHOR]

The most common method for metalated or metal-free phthalocyanines involves starting from phthalonitrile derivatives. These conventional reactions are generally carried out in high-boiling-point solvents (such as pentanol, DMF, DMSO, Quinoline, etc.) under reflux where they often have extended reaction times of up to 24 hours. New reaction methods with lower energy in short periods of time have been an issue to solve nowadays. Considering all, we aimed to synthesize substituted zinc phthalocyanine derivatives rapidly and with higher yields, without using any solvents. This study shows new synthesis methods for substituted phthalocyanine derivatives. ZnPc derivatives with different chain lengths functionalized with "O" and "S" donor atoms from the peripheral position have been synthesized in yields ranging from 52-75% in overall 3 minutes. Compared to conventional methods, which typically require extended reaction times and high energy consumption, this innovative approach reduces the reaction time from 18 hours to just 3 minutes and decreases energy consumption from 1.926 kWh to 0.063 kWh. The method achieves high reaction yields, highlighting its potential for sustainable chemical synthesis. [ABSTRACT FROM AUTHOR]

This work presents results on the efficiency of newly designed zinc phthalocyanine-mediated photodynamic therapy of both tumoral and nontumoral cell models using the MTT assay. Further detailed examinations of mechanistic and cell biological effects were focused on the HELA cervical cancer cell model. Here, ROS production, changes in the mitochondrial membrane potential, the determination of genotoxicity, and protein changes determined by capillary chromatography and tandem mass spectrometry with ESI were analyzed. The results showed that, in vitro, 5 Jcm−2 ZnPc PDT caused a significant increase in reactive oxygen species. Still, except for superoxide dismutase, the levels of proteins involved in cell response to oxidative stress did not increase significantly. Furthermore, this therapy damaged mitochondrial membranes, which was proven by a more than 70% voltage-dependent channel protein 1 level decrease and by a 65% mitochondrial membrane potential change 24 h post-therapy. DNA impairment was assessed by an increased level of DNA fragmentation, which might be related to the decreased level of DDB1 (decrease in levels of more than 20% 24 h post-therapy), a protein responsible for maintaining genomic integrity and triggering the DNA repair pathways. Considering these results and the low effective concentration (LC50 = 30 nM), the therapy used is a potentially very promising antitumoral treatment. [ABSTRACT FROM AUTHOR]

This paper reports the conjugation of (MeIt)8ZnPcCl8 to silver nanoparticles (AgNPs) through a metal-ligand coordination system. From the spectral and photophysical studies, the Stokes shift, the excited state lifetime, and the quantum yield are estimated. It was observed that the conjugation of (MeIt)8ZnPcCl8 to AgNPs in DMSO/H2O solution led to an increase in the absorption intensity of the Q band with a maximum at 675 nm and a shift of it of 10 nm. The fluorescence intensity of the (MeIt)8ZnPcCl8 is significantly higher than values obtained for (MeIt)8ZnPcCl8:AgNP compounds. The presence of AgNPs results in an increase in both triplet quantum yields and lifetimes, which is an advantage in the efficient generation of singlet oxygen quantum yields. The triplet quantum yield of 15.10% for (MeIt)8ZnPcCl8 conjugated to AgNP in DMSO/H2O was obtained (compared to 0.1% for the non-conjugated compound). [ABSTRACT FROM AUTHOR]

The interest in research to enhance the ability of sensitizers to generate singlet oxygen using light and/or ultrasound in cancer treatment has increased significantly in recent years, and studies have attracted considerable interest. In addition, phthalocyanines (Pcs) have become increasingly important as sensitizers in photodynamic therapy (PDT) (stimulation source: light) and/or sonodynamic therapy (SDT) (stimulation source: light and ultrasound). Sonophotodynamic therapy (SPDT), a new technique that gives more effective results than PDT, is now gaining in importance. Although there are published articles on SPDT studies, studies in this field are limited. In this context, we synthesized a zinc(II) phthalocyanine molecule bearing 4-(pyridine-4-ylthio) substituents to determine its potential as a sensitizer in SPDT applications as well as PDT applications, and the structure of the synthesized complex was illuminated using FTIR,1H-NMR, UV-Vis, and MS spectroscopic techniques. When light and ultrasound were combined, the calculated ΦΔ value for zinc (II) phthalocyanine (3) increased to greater than 1, even though it was 0.76 after light excitation. When evaluating the two methods, it was observed that singlet oxygen production was greatly enhanced by the SPDT method. In this way, the research will add to the enhancement of knowledge on the subject of the SPDT method's enhancement of singlet oxygen generation. [ABSTRACT FROM AUTHOR]

Abstract The inhibition effect of symmetrical Ball − type Zinc Phthalocyanine on Aluminum in 1mol/L hydrochloric acid was analyzed by electrochemical techniques. A novel ball-type zinc phthalocyanine (Zn-Pc) inhibitor has been synthesized and verified utilizing FTIR, nuclear magnetic resonance (1H NMR and 13C NMR), MALDI-TOF MS, and absorption spectroscopy (UV-Vis). In addition, laser-induced breakdown and photoluminescence spectroscopy were employed for additional study. Weight loss technique was employed to investigate the corrosion inhibition effectiveness of the synthesized Zn-Pc on Aluminum in 1mol/L hydrochloric acid at the range of variation temperatures (293–333 K). The inhibition efficiency of Zn-Pc increased with higher concentrations of Zn-Pc and decreased as the temperature increased. Furthermore, Zn-Pc demonstrated outstanding outcomes, achieving 72.9% at a very low inhibitor concentration (0.4 mmol/L) at 298 K. The experimental data for Zn-Pc Aluminum in 1mol/L hydrochloric acid obeys the Langmuir adsorption isotherm. Moreover, the corrosion system’s thermodynamic parameters and activation energy were determined. Quantum chemical calculations applying the (DFT) Density Functional Theory method was conducted and applied in this study. These calculations played a pivotal role in elucidating molecular structures and reactivity patterns. Through DFT, numerous reactivity indicators were computed, providing valuable insights into the chemical behavior of the studied compounds. These indicators, such as frontier molecular orbitals, electron density, and molecular electrostatic potential, were subsequently correlated with experimental data.

Nitroxide‐mediated polymerization (NMP) and nitroxide exchange reaction (NER) are very efficient methodologies that require only suitable alkoxyamine derivatives and create different polymeric architectures in a controlled manner. Herein, the synthesis of star polymers containing TEMPO‐substituted symmetric zinc phthalocyanine (ZnPc) is presented via NMP and NER. Moreover, linear polymer formation is conducted in a single arm on TEMPO‐substituted asymmetric ZnPc to elucidate the properties of star polymers. All linear and star polymers are characterized by FT‐IR, UV–vis, fluorescence, GPC, NMR, and EPR techniques. The results show that the proposed reactions are capable of forming controlled star‐shaped polymers. The increasing arm number (from a single to four arms) results in variable dispersity values (Đ) (1.2–3) due to different arm lengths, especially in NMP. However, this difficulty has been overcome via NER, and star polymers have been successfully synthesized with relatively low molecular weight (30 K > 10 K) and low dispersity (1.2–1.9). The results clearly indicate that while styrene and 4‐vinyl benzyl chloride monomers are introduced to the structure equally, star polymers with phthalocyanine can be synthesized in a controlled manner, and their quarternized derivatives have the potential to be effective as photoactive agents in photodynamic therapy. [ABSTRACT FROM AUTHOR]

The combination of metal–phthalocyanine complexes and axially coordinated organic molecules into polymer chains presents a significant challenge in the synthesis of hybrid materials. A calculated structure for one-dimensional coordinate polymers with N-donor ligands using ab initio (PM6) and DFT (LanL2Dz) methods is presented. DFT methods have shown that there is a linear, one-dimensional structure without distorted geometry for the two bipyridine ligands. The components of the proposed polymers consist of square-planar Zn complexes of phthalocyanine (PcZn) connected via bridging ligands (L). Electronic properties of the monomer PcZnL of zinc phthalocyanine with bidentate ligands have been analyzed using calculations based on density functional theory (B3LYP6-31G(d,p)). Molecular orbital calculations show that this connection between the metallomacrocycle and the conjugated ligand results in a small energy gap, promising molecularly active materials as conductors. The crystallographic reports indicate that obtaining this kind of polymer with the participation of Pc Zn and bidentate ligands is possible. [ABSTRACT FROM AUTHOR]

In this study, the spectroscopic measurements of the second generation dendritic zinc phthalocyanine (phthalocyanine dendrimer with tris) 2 were made and its potential to be used in optoelectronic applications was investigated. To examine the intramolecular energy transfer properties, fluorescence quantum yields were calculated and the contribution of first (phthalocyanine dendrimer with triethyl methanetricarboxylate) 1 and second 2 generation dendrimers to this energy transfer was investigated. The photoluminescence properties and optical band gap of the second generation zinc phthalocyanine 2 were investigated depending on the temperature. In addition, the quantum efficiency of singlet oxygen was calculated to evaluate the usability of this compound in photodynamic therapy. Also, aggregation behavior of compound 2 was examined in different solvents (DMF, DMSO and THF) and different concentrations in THF. To the best of our knowledge, this is the first study to examine the photoluminescence properties and temperature dependent changes of dendritic phthalocyanines. [ABSTRACT FROM AUTHOR]

Synthesis and properties of tetrahydroxy substituted zinc phthalocyanine is reported. UV–Visible spectrum for the aggregation properties of the compound and fluorescence properties were examined by excitation, emission spectra. This complex was an inhibitor of butyrylcholinesterase (BChE), α-Gly, α-Amy, and acetylcholinesterase (AChE) enzymes for tetra- hydroxy phthalocyaninato zinc (II) 3 with IC50 values of 49.18 μM for α-Amy, 110.85 μM for BChE, 35.13 μM for α-glycosidase and 54.63 μM for AChE, respectively. On the otherside, within the scope of computational study, in vitro activity behavior and states of the related complex, which cannot be explained experimentally, were evaluated at atomic level. The pharmacodynamics properties of the complex (3) were elucidated by molecular docking against four target enzymes, AChE, BChE, α-Gly and α-Amy. After that, its potential drug candidate was investigated based on its pharmacokinetic properties with help of in silico-ADMET analysis. As a result of all the applications, a desired goal in medicinal chemistry was to develop new, reliable and safe cholinesterase and α-glycosidase inhibitors with high efficacy. [ABSTRACT FROM AUTHOR]

The use of TiO2 as a photosensitizer in photodynamic therapy is limited due to TiO2 generates reactive oxygen species only under UV irradiation. The TiO2 surface has been modified with different functional groups to achieve activation at longer wavelengths (visible light). This work reports the synthesis, characterization, and biological toxicity assay of TiO2 nanoparticles functionalized with folic acid and combined with a zinc phthalocyanine to obtain a nano-photosensitizer for its application in photodynamic therapy for glioblastoma cancer treatment. The nano-photosensitizer was prepared using the sol-gel method. Folic acid and zinc phthalocyanine were added during the hydrolysis and condensation of titanium butoxide, which was the TiO2 precursor. The samples obtained were characterized by several microscopy and spectroscopy techniques. An in vitro toxicity test was performed using the MTT assay and the C6 cellular line. The results of the characterization showed that the structure of the nanoparticles corresponds mainly to the anatase phase. Successful functionalization with folic acid and an excellent combination with phthalocyanine was also achieved. Both folic acid-functionalized TiO2 and phthalocyanine-functionalized TiO2 had no cytotoxic effect on C6 cells (even at high concentrations) in comparison to Cis-Pt, which was very toxic to C6 cells. The materials behaved similarly to the control (untreated cells). The cell viability and light microscopy images suggest that both materials could be considered biocompatible and mildly phototoxic in these cells when activated by light. [ABSTRACT FROM AUTHOR]

Biohybrid membranes, combining a self-assembled lipid bilayer structure with functional nanomaterials/molecules, are promising candidates for ionic, optical, and electronic applications. However, information concerning the basic properties of these types of ultrathin hybrid membranes remains limited, primarily due to their low structural strength and low stability in air. In this work, we report on the successful formation of large-area ultrathin hybrid membranes composed of lipid and phthalocyanine molecules. The basic optical properties, mainly the light absorption and light emission properties, of the membranes were systematically investigated. The phthalocyanine molecules did not form an ordered crystal structure and were partially aggregated and dispersed in the hybrid membranes. Because the phthalocyanine molecules and the substrate were separated only by a monolayer of lipid molecules, the light-excited phthalocyanine molecules transferred the absorbed energy to the metal substrate, which led to the quenching of the emitted light. These unique properties of the hybrid membranes could be utilized in a variety of optoelectronic applications such as bioelectronic interfaces and photodetectors. [ABSTRACT FROM AUTHOR]

Herein, polycrystalline magnesium selenide (MgSe) thin films are deposited onto glass and monoclinic-structured zinc phthalocyanine (ZnPc) thin film substrates under high vacuum pressure using the thermal evaporation technique. ZnPc substrates improved the crystallinity of the MgSe films and decreased the stacking faults percentages and defect concentration by 31.57 and 52.49%, respectively. MgSe films deposited onto ZnPc substrates exhibited a notable increase of up to 32% in light absorption within the visible spectrum, while maintaining the energy band gap value of MgSe without significant alteration. In addition, as both the substrate and the epilayer exhibited p-type conductivity, an isotype heterojunction device structure is formed at the ZnPc/MgSe interfaces. The valence and conduction band offsets for this interface are 0.81 and 1.16 eV, respectively. On the other hand, re-fabrication of the ZnPc/MgSe heterojunctions onto Al thin film substrates and forming three Ag/MgSe, C/MgSe, and Au/MgSe Schottky channels on the epilayer surface allowed wide control of the negative capacitance effect and the resonance-antiresonance (RA) peaks in the capacitance spectra of the Al/ZnPc/MgSe/(Ag, C, Au) hybrid devices. These two important RA and NC features of the device can also be engineered by altering the DC biasing of the device. Moreover, Lorentz model analyses on the capacitance spectra showed an increased density of oscillators and increased scattering time constant with decreasing built-in potential at the metal/MgSe interfaces. The features of the hybrid devices presented make the device promising for microwave and electro-optical applications. [ABSTRACT FROM AUTHOR]

In recent years, photothermal (PTT) and photodynamic (PDT) therapy has become an important tumor treatment in the biomedical field due to its advantages of less side effects and higher targeting selectivity. However, the inherent toxicity of the formulations, poor biocompatibility, and long treatment cycle of monotherapy hinder their further clinical application. In this study, molybdenum disulfide nanosheets prepared by a hydrothermal method were used as a photothermal agent to enhance its biocompatibility by surface modification of bovine serum albumin (BSA). Afterward, the photosensitizer zinc phthalocyanine (ZnPc) and the target recognition molecule folic acid (FA) were sequentially loaded on the MoS2-BSA surface with the aid of hydrophobicity to obtain ZnPc-loaded MoS2 nanocomposites that possessed both the PTT/PDT performance and targeted binding to the folate receptor in tumor cells (FA-ZnPc-BSA/MoS2). The results of in vitro experiments, such as cytotoxicity and hemolysis, showed that the FA-ZnPc-BSA/MoS2 nanocomplexes possessed significant temperature-raising ability, good warming-cooling stability, and hemocompatibility and were of low cytotoxicity. The 808 nm near-infrared (NIR) laser-induced temperature increase and singlet oxygen generated by a FA-ZnPc-BSA/MoS2 nanocomplex in and outside breast cancer cells destroyed mitochondria and then induced apoptosis of tumor cells. The results of the FA-ZnPc-BSA/MoS2 nanocomposite PTT/PDT combined treatment on breast cancer tumor-bearing mice showed that the treatment time of 14 days was not only effective in ablating subcutaneous tumor tissue but also showed no signs of recurrence. The weight of tumor-bearing mice also increased steadily during treatment, and the five major organs of mice showed no obvious damage. The FA-ZnPc-BSA/MoS2 nanocomplex injected into the tail vein was basically metabolized out of the body within 7 days. In conclusion, the MoS2 nanocomposite loaded with ZnPc is a safe nanotherapeutic agent and has the potential to be used in PTT/PDT targeted synergistic therapy of tumor cells. [ABSTRACT FROM AUTHOR]

The inhibition effect of symmetrical Ball − type Zinc Phthalocyanine on Aluminum in 1mol/L hydrochloric acid was analyzed by electrochemical techniques. A novel ball-type zinc phthalocyanine (Zn-Pc) inhibitor has been synthesized and verified utilizing FTIR, nuclear magnetic resonance (1H NMR and 13C NMR), MALDI-TOF MS, and absorption spectroscopy (UV-Vis). In addition, laser-induced breakdown and photoluminescence spectroscopy were employed for additional study. Weight loss technique was employed to investigate the corrosion inhibition effectiveness of the synthesized Zn-Pc on Aluminum in 1mol/L hydrochloric acid at the range of variation temperatures (293–333 K). The inhibition efficiency of Zn-Pc increased with higher concentrations of Zn-Pc and decreased as the temperature increased. Furthermore, Zn-Pc demonstrated outstanding outcomes, achieving 72.9% at a very low inhibitor concentration (0.4 mmol/L) at 298 K. The experimental data for Zn-Pc Aluminum in 1mol/L hydrochloric acid obeys the Langmuir adsorption isotherm. Moreover, the corrosion system's thermodynamic parameters and activation energy were determined. Quantum chemical calculations applying the (DFT) Density Functional Theory method was conducted and applied in this study. These calculations played a pivotal role in elucidating molecular structures and reactivity patterns. Through DFT, numerous reactivity indicators were computed, providing valuable insights into the chemical behavior of the studied compounds. These indicators, such as frontier molecular orbitals, electron density, and molecular electrostatic potential, were subsequently correlated with experimental data. [ABSTRACT FROM AUTHOR]

ROS responsive nanodrug Z/B-PLS utilizes phototherapy and dual-metabolic regulation to promote complementary treatment, efficaciously breaking through the therapeutic challenges presented by KRAS mutation of PDAC. [Display omitted] Clinical pancreatic ductal adenocarcinoma (PDAC) treatment is severely limited by lack of effective KRAS suppression strategies. To address this dilemma, a reactive oxygen species (ROS)-responsive and PDAC-targeted nanodrug named Z/B-PLS was constructed to confront KRAS through dual-blockade of its downstream PI3K/AKT/mTOR and RAF/MEK/ERK for enhanced PDAC treatment. Specifically, photosensitizer zinc phthalocyanine (ZnPc) and PI3K/mTOR inhibitor BEZ235 (BEZ) were co-loaded into PLS which was constructed by click chemistry conjugating MEK inhibitor selumetinib (SEL) to low molecular weight heparin with ROS-responsive oxalate bond. The BEZ and SEL blocked PI3K/AKT/mTOR and RAF/MEK/ERK respectively to remodel glycolysis and non-canonical glutamine metabolism. ZnPc mediated photodynamic therapy (PDT) could enhance drug release through ROS generation, further facilitating KRAS downstream dual-blockade to create treatment-promoting drug delivery-therapeutic positive feedback. Benefiting from this broad metabolic modulation cascade, the metabolic symbiosis between normoxic and hypoxic tumor cells was also cut off simultaneously and effective tumor vascular normalization effects could be achieved. As a result, PDT was dramatically promoted through glycolysis-non-canonical glutamine dual-metabolism regulation, achieving complete elimination of tumors in vivo. Above all, this study achieved effective multidimensional metabolic modulation based on integrated smart nanodrug delivery, helping overcome the therapeutic challenges posed by KRAS mutations of PDAC. [ABSTRACT FROM AUTHOR]

Fouling and biofouling remain significant challenges in seawater desalination plants. One practical approach to address these issues is to develop anti-biofouling membranes. Therefore, novel hybrid zinc phthalocyanine/polyvinylidene fluoride-co-hexafluoropropylene (Zn(4-PPOx)4Pc/PVDF-HFP) membranes were prepared by electrospinning to evaluate their properties against biofouling. The hybrid nanofiber membrane was characterized by atomic force microscopy (AFM), attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, and contact angle measurements. The theoretical calculations of PVDF-HFP, Zn(4-PPOx)4Pc), and Zn(4-PPOx)4Pc/PVDF-HFP nanofibers were performed using a hybrid functional RB3LYP and the 6-31 G (d,p) basis set, employing Gaussian 09. DFT calculations illustrated that the calculated physical and electronic parameters ensured the feasibility of the interaction of PVDF-HFP with Zn(4-PPOx)4Pc via a halogen–hydrogen bond, resulting in a highly stable and remarkably reactive structure. Moreover, molecular electrostatic potential (MEP) maps were drawn to identify the reactive regions of the Zn(4-PPOx)4Pc and PVDF-HFP/Zn(4-PPOx)4Pc nanofibers. Molecular docking analysis revealed that Zn(4-PPOx)4Pc has highest binding affinity (−8.56 kcal/mol) with protein from S. aureus (1N67) mainly with ten amino acids (ASP405, LYS374, GLU446, ASN406, ALA441, TYR372, LYS371, TYR448, LYS374, and ALA442). These findings highlight the promising potential of Zn(4-PPOx) 4Pc/PVDF-HFP nanocomposite membranes in improving the efficiency of water desalination by reducing biofouling and providing antibacterial properties. [ABSTRACT FROM AUTHOR]

Psoriasis, a chronic immune-mediated skin disorder affecting over 125 million people globally, is characterized by abnormal keratinocyte proliferation and immune cell infiltration. Photodynamic therapy (PDT) remains underutilized in the treatment of psoriasis despite its potential as a promising and effective therapeutic approach. This study aimed to explore the efficacy of zinc phthalocyanine (ZnPc) and its sugar conjugates as potential antipsoriatic agents. We successfully synthesized protected and unprotected sugar-conjugated zinc phthalocyanines and evaluated their potential against cytokine-stimulated HaCaT keratinocytes, as well as an established IMQ psoriasis-like in vivo model. Tetrasubstituted protected glucose–ZnPc (Glu-4-ZnPc-P) demonstrated superior phototoxicity (IC50 = 2.55 µM) compared to unprotected glucose conjugate (IC50 = 22.7 µM), protected galactose–ZnPc (IC50 = 7.13 µM), and free ZnPc in cytokine-stimulated HaCaT cells (IC50 = 5.84 µM). Cellular uptake analysis revealed that IL-17A, a cytokine that plays a central role in the pathogenesis of psoriasis, enhanced unprotected Glu-4-ZnPc uptake by 56.3%, while GLUT1 inhibitor BAY-876 reduced its accumulation by 23.8%. Intracellular ROS generation following Glu-4-ZnPc-P-PDT was significantly increased after stimulation with IL-17A, correlating with in vitro photocytotoxicity. In vivo PDT using Glu-4-ZnPc-P exhibited significant improvement in Psoriasis Area and Severity Index (PASI), inhibiting splenomegaly and restoring normal skin morphology. This study highlights sugar-conjugated zinc phthalocyanines as potential candidates for targeted PDT in psoriasis, providing a basis for further clinical investigations. [ABSTRACT FROM AUTHOR]

Background: Tooth discoloration is a common concern in antimicrobial photodynamic therapy (aPDT) using various photosensitizers (PS). Toluidine Blue (TB), Methylene Blue (MB), Phthalocyanine (Pc), and 2-mercaptopyridine-substituted zinc phthalocyanine (TM-ZnPc) are among those studied, but their relative impacts on tooth discoloration remain unclear. Aim: This study aimed to compare the effects of TB, MB, Pc, and TM-ZnPc in aPDT on tooth discoloration, utilizing a controlled experimental setup. Materials and Methods: The study comprised seventy-five single-rooted incisors with root canals. Following meticulous preparation, a standardized area on the crown surface was designated for examination, and precise measurements of the initial tooth colors were recorded. Samples were randomly divided into five groups: Negative control, MB, TM, Pc, and TM-ZnPc. Photoactivation was performed using LED light, and color measurements were taken at multiple time points up to 90 days. Data were converted to Lab* color values of the CIE Lab* color system (International Commission on Illumination, Vienna, Austria), and ΔE values were calculated. Statistical analysis was performed using Two-way ANOVA and Post-Hoc Tukey tests (p < 0.05). Results: At day 7 and 30, TM-ZnPc and Pc caused less discoloration compared to MB and TB. TM-ZnPc caused more tooth discoloration compared to Pc (p < 0.05). Compared to baseline, MB and TM-ZnPc caused more tooth discoloration at 30 days and TB caused more tooth discoloration at 90 days (p < 0.05). No significant difference was observed in terms of tooth discoloration at all periods evaluated after Pc application (p > 0.05). All photosensitizers tested in the study caused tooth coloration. Conclusion: All PS induced clinically detectable tooth discoloration, with TB and MB causing more significant discoloration compared to Pc and TM-ZnPc at certain time points. TM-ZnPc and Pc demonstrated more stable coloration levels over time, suggesting their potential reliability in aPDT applications. This study highlights the importance of selecting appropriate PS to minimize tooth discoloration in aPDT, with Pc showing promise in this regard. [ABSTRACT FROM AUTHOR]

In this study, fluorescent zinc phthalocyanine compound was synthesized using 4-(2-(4-(2-phenylpropan-2-yl) phenoxy) phenoxy) phthalonitrile and zinc metal salt. The structure of compounds was characterized by using 1H, and 13C NMR, FT-IR, Mass, UV-Vis spectroscopy. The fluorescence emission, excitation and absorption properties of this phthalocyanine compound were studied in tetrahydrofuran and DMSO. Aggregation behaviors for different concentrations in the same solvent were investigated. Quantum chemical calculations were performed using 6-311G basis set of DFT (B3LYP and CAMB3LYP) methods. The structural optimization, molecular orbital analysis, and electronic properties of the synthesized phthalocyanine were then determined in the ground state and gas phase of the DFT method. Moreover, molecular electrostatic potential (MEP) maps were drawn to identify the reactive regions of the zinc phthalocyanine complex. The data of the study show that the phthalocyanine complex can be used as sensor agent for biological fluorescence analysis. [ABSTRACT FROM AUTHOR]

Quaternized zinc phthalocyanine (QZnPc) which is water soluable is a promising candidate for photo dynamic therapy (PDT) applications. The physicochemical properties like the stability, activity, particle size, surface charge of tetrakis-(4-[(1E)-3-iminoprop-1-en-1-yl]- N,N,N-trimethylphenylammonium) phthalocyaninato zinc(II)] tetraiodide (II) quaternized zinc phthalocyanine (fused extended conjugation, QZnPc-FE) were investigated. The Zeta Potential Analyzer was used for this purpose. QZnPc-FE is freshly synthesized, water soluble quaternized zinc phthalocyanine and used as potential photosensitizer for PDT application. The stability and activity behavior of QZnPc-FE was determined in vitro conditions such as different pHs and in simulated body fluids as function of time via Zetasizer measurements and UV/VIS absorbances, respectively. Morphology of the QZnPc-FE was determined via XRD and the organic solvent effect with different polarity on QZnPc-FE was checked by UV/VIS. The optimum stability and activity conditions of QZnPc-FE in vitro conditions were determined, and the obtained results showed that the studied compound can be used for medical (PDT) and pharmaceutical applications. [ABSTRACT FROM AUTHOR]

Breast cancer remains a formidable challenge in oncology despite significant advancements in treatment modalities. Conventional therapies such as surgery, chemotherapy, radiation therapy, and hormonal therapy have been the mainstay in managing breast cancer for decades. However, a subset of patient's experiences treatment failure, leading to disease recurrence and progression. Therefore, this study investigates the therapeutic potential of green-synthesized silver nanoparticles (AgNPs) using an African medicinal plant (Dicoma anomala methanol root extract) as a reducing agent for combating breast cancer. AgNPs were synthesized using the bottom-up approach and later modified with liposomes (Lip) loaded with photosensitizer (PS) zinc phthalocyanine tetrasulfonate (Lip@ZnPcS4) using thin film hydration method. The successful formation and Lip modification of AgNPs, alongside ZnPcS4, were confirmed through various analytical techniques including UV–Vis spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Following a 24 h treatment period, MCF-7 cells were assessed for viability using 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT viability assay), cell death analysis using mitochondrial membrane potential (MMP) (ΔΨm), Annexin V-fluorescein isothiocyanate (FITC)-propidium iodide (PI) kit, and caspase- 3, 8 and 9 activities. The experiments were repeated four times (n = 4), and the results were analyzed using SPSS statistical software version 27, with a confidence interval set at 0.95. The synthesized nanoparticles and nanocomplex, including AgNPs, AgNPs-Lip, Lip@ZnPcS4, and AgNPs-Lip@ZnPcS4, exhibited notable cytotoxicity and therapeutic efficacy against MCF-7 breast cancer cells. Notably, the induction of apoptosis, governed by the upregulation of apoptotic proteins i.e., caspase 8 and 9 activities. In addition, caspase 3 was not expressed by MCF-7 cells in both control and experimental groups. Given the challenging prognosis associated with breast cancer, the findings underscore the promise of liposomal nanoformulations in cancer photodynamic therapy (PDT), thus warranting further exploration in clinical settings.

Interfaces formed between monolayer transition metal dichalcogenides and (metallo)phthalocyanine molecules are promising in energy applications and provide a platform for studying mixed-dimensional molecule-semiconductor heterostructures in general. An accurate characterization of the frontier energy level alignment at these interfaces is key in the fundamental understanding of the charge transfer dynamics between the two photon absorbers. Here, we employ the first-principles substrate screening GW approach to quantitatively characterize the quasiparticle electronic structure of a series of interfaces: metal-free phthalocyanine (H2Pc) adsorbed on monolayer MX2 (M = Mo, W; X = S, Se) and zinc phthalocyanine (ZnPc) adsorbed on MoX2 (X = S, Se). Furthermore, we reveal the dielectric screening effect of the commonly used α-quartz (SiO2) substrate on the H2Pc:MoS2 interface using the dielectric embedding GW approach. Our calculations furnish a systematic set of GW results for these interfaces, providing the structure–property relationship across a series of similar systems and benchmarks for future experimental and theoretical studies. [ABSTRACT FROM AUTHOR]

AbstractPhthalocyanine is a safe and better biocompatible compound, and it has been used in diagnostic and cancer imaging. But the application in the treatment of colon and cervical cancer is elusive. In the present study, we have synthesized Iron (II) phthalocyanine and Zinc phthalocyanine respectively. The bonding, structure, and physical characteristics of the prepared products were analyzed and confirmed by FT-IR, XRD, SEM, EDX methods. We have also examined the anti-cancer properties of the compounds on two different cancer cells (colon cancer HCT-116 and cervical cancer HeLa) by MTT assay. The cell viability assay results showed that a noteworthy reduction in the cell viability post-treatments of Iron (II) phthalocyanine. However, treatment of Zinc phthalocyanine did not show any inhibitory action on both HCT-116 and HeLa cancer cells. We have also calculated the inhibitory concentration (IC50) post treatment of Zinc phthalocyanine and Iron (II) phthalocyanine on HCT-116 and HeLa cells. The IC50 was 30 µg/ml for HCT-116 cells treated with Iron (II) phthalocyanine, whereas it was 33 µg/ml for the HeLa cells. We have also examined the impact of Zinc phthalocyanine and Iron (II) phthalocyanine on non-cancerous cells (HEK-293), and MTT results showed that Iron (II) phthalocyanine and Zinc phthalocyanine induced no significant inhibitory action on HEK-293 cells. In addition, we have also examined the anti-fungal action of Zinc phthalocyanine and Iron (II) phthalocyanine. We have also examined the impact of Iron (II) phthalocyanine on cancer cells using DAPI staining, we have found that was a major reduction in cancer cells population, but there is no reduction in the Iron (II) phthalocyanine -treated cells. We have found that Iron (II) phthalocyanine induced significant antifungal activity against Candida albicans, whereas no significant antifungal activity was observed with Zinc phthalocyanine.

This research aims to examine the transdermal release of water-soluble indium and zinc metallo phthalocyanine (InPc and ZnPc) compounds from the poly(vinyl alcohol) (PVA) membrane and the cytotoxicity effect of these Pcs on normal mouse fibroblasts (L929 fibroblast) and human melanoma (SK-MEL-30) cells. For this purpose, the effects of temperature, pH, drug concentration and membrane thickness on transdermal release were investigated in order to obtain the optimum transdermal release profile by preparing PVA membranes with different thicknesses and crosslinked by heat treatment. Optimum drug release was found to be 85.36% using 6 µm thick PVA membrane at 37 ± 0.5 °C, when upper cell pH 1.2 and lower cell pH 5.5, for 3 mg/mL InPc drug concentration. Under the same conditions, the drug release value for ZnPc was found to be 69.78%. In addition, in vitro studies were performed on L929 and SK-MEL-30 cells. under optimized drug (InPc and ZnPc) and membrane conditions. It was found that no significant cytotoxic effect was observed in L929 and SK-MEL-30 cells in the dark. Photodynamic tests were also carried out with InPc and ZnPc. The results show that cell viability decreases in SK-MEL-30 cells at concentrations of 10 µg/mL and above. In addition, while the InPc IC50 value was determined as 4.058 µg/mL, this value was determined as 11.574 µg/mL for ZnPc. [ABSTRACT FROM AUTHOR]

Photodynamic therapy (PDT) is a potential treatment strategy for melanoma. As a second-generation photosensitizer, Zinc phthalocyanine (ZnPc) has many advantages for anti-tumor PDTs, such as strong absorption in the red and near infrared regions, high photo and chemical stability, etc. However, ZnPc has a poor water solubility and is apt to aggregate due to the π-π interaction between molecules, which limits its applications. In this study, various solvents and surfactants were screened for dissolving ZnPc and preparing ZnPc@SDC-TPGS micelle and thermosensitive in situ gel. After the cytotoxic effects of thermosensitive gels on PDT were tested, the antitumor effects on PDT of them in mice by intratumoral injection were evaluated, including body weight, and tumor weight, volume and morphology. The cell death pathway and the relationship of reactive oxygen species yield with apoptotic rate of tumor cells induced by ZnPc in situ gel were investigated. The results were that N-methyl-pyrrolidone (NMP) mixed with 2 % SDC and aqueous solution containing 2 % TPGS and 2 % SDC were used to synthesize ZnPc@SDC-TPGS micelle and the thermosensitive in situ gel. The cytotoxic effects of thermosensitive gels showed good tumor suppression of ZnPc@SDC-TPGS in situ gel and no toxicity of the blank gel. Intratumoral injection in situ gel containing 3 µg ZnPc under irradiation demonstrated good tumor inhibition in mice with melanoma. Apoptosis has been established as the primary pathway of cell death, and the production of reactive oxygen species (ROS) plays a crucial role in cellular apoptosis induced by ZnPc@SDC-TPGS in situ gel. In conclusion, the intratumoral injection of ZnPc@SDC-TPGS thermosensitive in situ gel provides a promising local treatment option for melanoma. [ABSTRACT FROM AUTHOR]

Cuproptosis is a recently identified copper-dependent form of nonapoptotic cell death and holds great prospect in cancer treatment. One of the most intriguing aspects of cuproptosis is its ability to synergize with apoptosis-based cancer treatments. Herein, we presented a novel approach using copper-coordinated nanoassemblies (CCNAs) that were constructed by incorporating a photosensitizer Zinc Phthalocyanine (ZnPc)-chemotherapeutic (DOX) prodrug with a thioketal (TK) spacer and an IDO inhibitor (1-methyl tryptophan, 1-MT) as building blocks for Cu2+-coordination self-assembly to achieve combinational apoptosis-cuproptosis and immunotherapy. Upon NIR laser irradiation, the ZnPc component of CCNAs exhibited a photodynamic effect that generated reactive oxygen species (ROS). This triggered the release of DOX, leading to enhanced tumor cell apoptosis. Additionally, the presence of Cu2+ in the CCNAs not only enhanced the photodynamic process by catalyzing oxygen generation but also promoted the aggregation of toxic mitochondrial proteins, leading to cell cuproptosis. Importantly, the intensified cuproptosis-apoptosis effect triggered an immunogenic cell death (ICD) response. The released 1-MT complemented this response by reversing the immunosuppressive tumor microenvironment (ITM), synergistically amplifying anti-tumor immunity and suppressing the growth of primary and distant tumors. The findings of this study provide a new perspective on potential cancer treatments based on cuproptosis-apoptosis synergistic immunotherapy and stimulate further research in the design of advanced metal-coordinated nanomedicines. The combination of cuproptosis and apoptosis that act with different mechanisms holds enormous potential in cancer treatment. Here, copper-coordinated nanoassemblies (CCNAs) based on photosensitizer-chemo prodrugs and checkpoint inhibitors were constructed for mediating cuproptosis-apoptosis and subsequently promoting cancer immunotherapy. CCNAs not only promoted the photodynamic effect and activation of chemotherapy through catalyzing the generation of oxygen but also induced toxic mitochondrial protein aggregation, leading to cell cuproptosis. These synergistic antitumor effects triggered robust immune responses with the aid of immune checkpoint blockade, almost eradicating primary tumors and inhibiting distant tumors by around 83 % without systemic toxicity. [Display omitted] [ABSTRACT FROM AUTHOR]

This article explores the use of novel zinc(II) phthalocyanine dyes as colorants in color photoresists for TFT-LCD modules. The dyes are being considered as an alternative to pigments, which have limitations in resolution and color performance. The article discusses the synthesis and properties of the dyes, including their spectral properties, thermal stability, and solubility. The results show that the synthesized dyes have promise for improving the color performance of color photoresists. Another document discusses the characterization and stability of green spin-coated color filters using zinc phthalocyanine dyes. The study evaluates the transmission spectra, color coordinates, and stability of the color filters. The results indicate that the filters have high transmittance in the green range and good stability and resistance to dye migration and aggregation. [Extracted from the article]

In this study, 4‐(2‐(4‐methylthiazol‐5‐yl) ethoxy) phthalonitrile (3) and zinc phthalocyanine complex (4) were synthesized and characterized. UV–vis and fluorescence spectra, aggregation, and fluorescence parameters of the zinc phthalocyanine compound were investigated. As biological properties, DPPH radical capture, antidiabetic, DNA cutting, antimicrobial, photodynamic antimicrobial, anti‐biofilm activities, and microbial cell viability parameters of the compounds were determined. The highest antioxidant activity was found as 62.80% at 100 mg/L concentration with compound 4, and compound 4 also showed the best antidiabetic activity as 65.17% at 400 mg/L concentration. In DNA cutting activity, it was determined that 3 and 4 cut DNA at all concentrations. For compounds 3–4, the minimum inhibitory concentration (MIC) values were found to be 32 and 16 mg/L for Enterococcus hirae and Enterococcus feacalis, respectively. The strongest MIC value of photodynamic antimicrobial activity was achieved as 4 mg/L for E. feacalis with 4. It was observed that both compounds inhibited the microbial viability activity of Escherichia coli by 100% at concentrations of 100 mg/L. Compound 4 inhibited biofilms of Pseudomonas aureginosa and Staphylococcus aureus as 92.48% and 98.56% at 50 mg/L concentration, respectively. [ABSTRACT FROM AUTHOR]

In this work, we showcase applications of single-molecule Fano resonance (SMFR) measurements beyond the determination of molecular excitonic energy and associated dipole orientation. We use the SMFR measurement to probe the local influence of a man-made single chlorine vacancy on the molecular transition of a single zinc phthalocyanine, which clearly reveals the lifting-up of the double degeneracy of the excited states due to defect-induced configurational changes. Furthermore, time-trace SMFR measurements at different excitation voltages are used to track the tautomerization process in a free-base phthalocyanine. Different behaviors in switching between two inner-hydrogen configurations are observed with decreasing voltages, which helps to reveal the underlying tautomerization mechanism involving both the molecular electronic excited states and vibrational excited states in the ground state. [ABSTRACT FROM AUTHOR]

We have investigated the morphological and optical properties of α- and β-phase Zinc Phthalocyanine (ZnPc) thin films for application to organic photovoltaic cells (OPVs). It was found that the α-phase is completely converted to the β-phase by thermal annealing at 220 °C under ultrahigh vacuum conditions. When the α- to β-phase transition takes place, the surface roughness of the ZnPc film became flat uniformly with a nanometer order of unevenness by anisotropic growth of crystalline grains along a lateral direction to substrates. Correspondingly, the optical absorbance of the β-phase film became greater by 1.5–2 times than that of the α-phase one in an ultraviolet–visible–near infrared (UV–vis–NIR) wavelength range, which plays a role in increasing the number of photogenerated excitons. On the contrary, time-resolved photoluminescence measurements showed that the average lifetime of excitons for the β-phase film became shorter by 1/6–1/7 than that for the α-phase one, which plays a role in decreasing the number of excitons achieving the donor/acceptor interface where excitons are separated to carriers (holes and electrons). Both the increase in the number and the shortening in the average lifetime have a trade-off relationship with each other for contribution to the photoelectric conversion efficiency of OPVs. Then, we examined an external quantum efficiency (EQE) of OPVs using the α- and β-phase films as a donor and obtained that the former OPV (α-phase) exhibits a higher EQE by ∼2 times than the latter one (β-phase) in the wavelength range of 400 nm–800 nm. [ABSTRACT FROM AUTHOR]

The vibrationally resolved absorption spectra of zinc phthalocyanine (ZnPc) aggregates (up to 70 monomers) are explored using the non-Markovian stochastic Schrödinger equation. Various types of local excitations, charge-transfer (CT) excitations, and exciton–phonon couplings are explicitly included in a comprehensive model Hamiltonian, which is parameterized by first-principles calculations. The absorption spectral simulations clarify that the two absorption bands in the Q-band region observed in experiments can be assigned to the contribution from the CT-mediated interactions, rather than the mixtures of different-type aggregates, as prevailingly assumed. Furthermore, the relative intensities of the two bands are found to be closely related to the intermolecular distance and molecular number in a ZnPc aggregate. From the investigation of the decoherence process after optical excitation, it is found that CT states can induce coherence regeneration as the time scale of charge separation is much faster than that of the vibration-induced decoherence. However, they would instead boost the decoherence process as the two time scales become comparable. The two different effects of CT states may suggest a novel way to regulate the decoherence process in excitation energy relaxation. [ABSTRACT FROM AUTHOR]

The increasing demand for energy and electricity and the depletion of fossil fuels are global problems. In recent years, dye-sensitized solar cell (DSSC) technologies have gained notoriety for their application in solar energy. DSSCs are considered a promising alternative renewable energy source to both inorganic and organic photovoltaic (PV) cells. Many types of dyes are being investigated to enhance the light-harvesting properties of DSSCs, but the actual realization of these absorbers in cell structure requires optimum parameters. The main aim of this study was to simulate proposed zinc phthalocyanine (ZnPC)-based structures to validate their design, assess their performance for commercial implementation, and optimize the cell parameters for optimum efficiency. To that end, Scaps-1D was employed to evaluate the performance of DSSCs to determine their optimum parameters. We found that ZnPC and isopropoxy ZnPC molecules outperform others molecules because of better optoelectronic properties. Several other parametric effects, such as photoactive layer thicknesses, doping densities, trap densities, and charge carrier mobilities, were also evaluated to observe their impact on device performance. The results show that moderate thickness, low defect density, moderate doping, and charge carrier mobility are favorable for better device performance due to low recombination losses, electrical losses, and better transport of charge carriers. The utmost power conversion efficiency values found for ZnPC- and ZnPC: PC70BM-based DSSCs after optimization were 9.50% and 9.81%. This paper also suggests a practical method for efficiently using DSSC cells by modifying factors that are significantly reliant on DSSC performance and output. [ABSTRACT FROM AUTHOR]

Phthalocyanine is a safe and better biocompatible compound, and it has been used in diagnostic and cancer imaging. But the application in the treatment of colon and cervical cancer is elusive. In the present study, we have synthesized Iron (II) phthalocyanine and Zinc phthalocyanine respectively. The bonding, structure, and physical characteristics of the prepared products were analyzed and confirmed by FT-IR, XRD, SEM, EDX methods. We have also examined the anti-cancer properties of the compounds on two different cancer cells (colon cancer HCT-116 and cervical cancer HeLa) by MTT assay. The cell viability assay results showed that a noteworthy reduction in the cell viability post-treatments of Iron (II) phthalocyanine. However, treatment of Zinc phthalocyanine did not show any inhibitory action on both HCT-116 and HeLa cancer cells. We have also calculated the inhibitory concentration (IC50) post treatment of Zinc phthalocyanine and Iron (II) phthalocyanine on HCT-116 and HeLa cells. The IC50 was 30 µg/ml for HCT-116 cells treated with Iron (II) phthalocyanine, whereas it was 33 µg/ml for the HeLa cells. We have also examined the impact of Zinc phthalocyanine and Iron (II) phthalocyanine on non-cancerous cells (HEK-293), and MTT results showed that Iron (II) phthalocyanine and Zinc phthalocyanine induced no significant inhibitory action on HEK-293 cells. In addition, we have also examined the anti-fungal action of Zinc phthalocyanine and Iron (II) phthalocyanine. We have also examined the impact of Iron (II) phthalocyanine on cancer cells using DAPI staining, we have found that was a major reduction in cancer cells population, but there is no reduction in the Iron (II) phthalocyanine -treated cells. We have found that Iron (II) phthalocyanine induced significant antifungal activity against Candida albicans, whereas no significant antifungal activity was observed with Zinc phthalocyanine. [ABSTRACT FROM AUTHOR]