RESUMO
Melanins are a family of heterogeneous polymeric pigments that provide ultraviolet (UV) light protection, structural support, coloration, and free radical scavenging. Formed by oxidative oligomerization of catecholic small molecules, the physical properties of melanins are influenced by covalent and noncovalent disorder. We report the use of tyrosine-containing tripeptides as tunable precursors for polymeric pigments. In these structures, phenols are presented in a (supra-)molecular context dictated by the positions of the amino acids in the peptide sequence. Oxidative polymerization can be tuned in a sequence-dependent manner, resulting in peptide sequence-encoded properties such as UV absorbance, morphology, coloration, and electrochemical properties over a considerable range. Short peptides have low barriers to application and can be easily scaled, suggesting near-term applications in cosmetics and biomedicine.
Assuntos
Melaninas/química , Peptídeos/química , Cromatografia Líquida de Alta Pressão , Espectrometria de Massas , Oxirredução , Conformação Proteica , Multimerização Proteica , Tirosina/química , Raios UltravioletaRESUMO
Photoelectrochemical conversion of solar energy is explored for many diverse applications but suffers from poor efficiencies due to limited solar absorption, inadequate charge carrier separation, redox half-reactions occurring in close proximity, and/or long ion diffusion lengths. We have taken a drastically different approach to the design of photoelectrochemical cells (PECs) to spatially isolate reaction sites at the nanoscale to different materials and flow channels, suppressing carrier recombination and back-reaction of intermediates while shortening ion diffusion paths and, importantly, avoiding mixed product generation. We developed massively parallel nano-PECs composed of an array of open-ended carbon nanotubes (CNTs) with photoanodic reactions occurring on the outer walls, uniformly coated with titanium dioxide (TiO2), and photocathodic reactions occurring on the inner walls, decorated with platinum (Pt). We verified the redox reaction isolation by demonstrating selective photodeposition of manganese oxide on the outside and silver on the inside of the TiO2/CNT/Pt nanotubes. Further, the nano-PECs exhibit improved solar absorption and efficient charge transfer of photogenerated carriers to their respective redox sites, leading to a 1.8% photon-to-current conversion efficiency (a current density of 4.2 mA/cm2) under white-light irradiation. The design principles demonstrated can be readily adapted to myriads of photocatalysts for cost-effective solar utilization.
RESUMO
In the previous article we have reported that 3,4-dihydroquinazoline 1 is a potent and selective T-type calcium channel blocker that exhibited strong anti-cancer activity in vitro. Compound 1·2HCl was further in vivo evaluated against A549 xenograft in BALB/c nude mice, which exhibited 49% tumor-weight inhibition through intravenous administration of 2 mg/kg of body weight and was more potent than doxorubicin. Moreover, compound 1·2HCl has an oral bioavailability of 98% with LD(50) values of 693 mg/kg (p.o. route) and 40.0 mg/kg (i.v. route) of body weight. In addition, its efficient scale-up synthetic method was developed.
Assuntos
Antineoplásicos/farmacologia , Quinazolinas/farmacologia , Animais , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Dose Letal Mediana , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Nus , Transplante HeterólogoRESUMO
3,4-Diphenyl-substituted 1H-furan-2,5-dione and 1H-pyrrole-2,5-dione derivatives were synthesized and evaluated for the inhibitory activities on LPS-induced PGE(2) production in RAW 264.7 macrophage cells. Both 1H-furan-2,5-dione and 1H-pyrrole-2,5-dione rings as main scaffolds were easily obtained using one of three synthetic methods. Among the compounds investigated, 1H-3-(4-sulfamoylphenyl)-4-phenyl-pyrrole-2,5-dione (6l) showed a strong inhibitory activity (IC(50)=0.61microM) of PGE(2) production.