Under continuous photolysis at 675 nm, liposomal zinc phthalocyanine associated with nitrosyl ruthenium complex [Ru(NH.NHq)(tpy)NO](3+) showed the detection and quantification of nitric oxide (NO) and singlet oxygen ((1)O(2)) release. Photophysical and photochemical results demonstrated that the interaction between the nitrosyl ruthenium complex and the photosensitizer can enable an electron transfer process from the photosensitizer to the nitrosyl ruthenium complex which leads to NO release. Synergistic action of both photosensitizers and the nitrosyl ruthenium complex results in the production of reactive oxygen species and reactive nitrogen species, which is a potent oxidizing agent to many biological tissues, in particular neoplastic cells.
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http://dx.doi.org/10.1111/j.1751-1097.2008.00481.x | DOI Listing |
ACS Omega
January 2025
Department of Chemical Engineering, Norwegian University of Science and Technology (NTNU), Sem Sælands vei 4, NO-7491 Trondheim, Norway.
The Ostwald process is one of the commercial pathways for the production of nitric acid (HNO), a key component in the production of nitrate fertilizers. The Ostwald process is a mature, extensively studied, and highly optimized process, and there is still room for further intensification. The process can be further intensified by catalyzing the homogeneous oxidation of nitric oxide to nitrogen dioxide.
View Article and Find Full Text PDFChem Biol Interact
January 2025
Department of Biological Chemistry, Regional University of Cariri, 63105-000, Crato, CE, Brazil.
Radiat Prot Dosimetry
November 2024
Department of Radioecology, Institute for Environmental Sciences, 1-7, Ienomae, Obuchi, Rokkasho, Kamikita, Aomori, 039-3212, Japan.
Inorg Chem
November 2024
São Carlos Institute of Chemistry, University of São Paulo, São Carlos 13560-970, SP,Brazil.
Ruthenium(II) tetraamine nitrosyl complexes with N-heterocyclic ligands are known for their potential as nitric oxide (NO) donors, capable of releasing NO through either direct photodissociation or one-electron reduction of the Ru(II)NO center. This study delivers a novel insight into the one-electron reduction mechanism for the model complex -[Ru(NO)(NH)(py)] (RuNOpy, py = pyridine) in phosphate buffer solution (pH 7.4).
View Article and Find Full Text PDFAdv Mater
December 2024
Songjiang Research Institute, Shanghai Key Laboratory of Emotions and Affective Disorders (LEAD), Songjiang Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 201600, China.
Conventional bone tissue engineering materials struggle to reinstate physiological bone remodeling in a diabetic context, primarily due to the compromised repolarization of proinflammatory macrophages to anti-inflammatory macrophages. Here, leveraging single-cell RNA sequencing (scRNA-seq) technology, the pivotal role of nitric oxide (NO) and reactive oxygen species (ROS) is unveiled in impeding macrophage repolarization during physiological bone remodeling amidst diabetes. Guided by scRNA-seq analysis, we engineer a multienzymatic bone tissue engineering hydrogel scaffold (MEBTHS) composed is engineered of methylpropenylated gelatin hydrogel integrated with ruthenium nanozymes, possessing both Ru and Ru components.
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