Bacteriophages as therapeutic and diagnostic vehicles in cancer

Evolution of nanomedicine is the re-design of synthetic and biological carriers to implement novel theranostic platforms. In recent years, bacteriophage research favors this process, which has opened up new roads in drug and gene delivery studies. By displaying antibodies, peptides, or proteins on the surface of different bacteriophages through the phage display technique, it is now possible to unravel specific molecular determinants of both cancer cells and tumor-associated microenvironmental molecules. Downstream applications are manifold, with peptides being employed most of the times to functionalize drug carriers and improve their therapeutic index. Bacteriophages themselves were proven, in this scenario, to be good carriers for imaging molecules and therapeutics as well. Moreover, manipulation of their genetic material to stably vehiculate suicide genes within cancer cells substantially changed perspectives in gene therapy. In this review, we provide examples of how amenable phages can be used as anticancer agents, especially because their systemic administration is possible. We also provide some insights into how their immunogenic profile can be modulated and exploited in immuno-oncology for vaccine production

Bartlett pear unsaturated ethyl deconoates and C9 compounds among components characterizing cv. Catalan roxo grape marc distillates

Catalan roxo marc distillates contain compounds at an unusual level in a grape derivate. The most peculiar are several unsaturated ethyl decanoates typical of Bartlett pear distillates and derived from ethyl esters found in the grape skins, some of which partially modified in the stereoisomery probably by the fermentation process. Remarkable compounds are unbranched aliphatic C-9 compounds at different oxidation state as well as ethyl nonanoate. At sensorially interesting levels methyl and ethyl salicylate and ethyl cinnamate, monoterpenols typical of floral-like varieties, vitispiranes and 4-ethylguaiacol are detected. Methyl salicylate is found in the berry as free and bound compound as several monoterpenols

Operability and Results of Retro and On-Going Commission Tools Applied to an Existing Building

Several tools in the scope of Annex 40 (PECI Model Commissioning Plan and Guide specification, Emma-CTA, IPMVP) have been used to realise the retro and the on-going commissioning of an existing building. The aim of the work was to evaluate operability, consumed time, results of these tools used by HVAC operation technicians. Analysis of making use of the different tools in a common framework is proposed, giving feedback information to creative authors

Phosphine Oxide Porous Organic Polymers Incorporating Cobalt(II) Ions: Synthesis, Characterization, and Investigation of H2Production

Suitably functionalized porous matrices represent versatile platforms to support well-dispersed catalytic centers. In the present study, porous organic polymers (POPs) containing phosphine oxide groups were fabricated to bind transition metals and to be investigated for potential electrocatalytic applications. Cross-linking of mono- and di-phosphine monomers with multiple phenyl substituents was subject to the Friedel-Crafts (F-C) reaction and the oxidation process, which generated phosphine oxide porous polymers with pore capacity up to 0.92 cm3/g and a surface area of about 990 m2/g. The formation of the R3P·BH3 borohydride adduct during synthesis allows to extend the library of phosphine-based monomeric entities when using FeCl3. The porous polymers were loaded with 0.8-4.2 w/w % of cobalt(II) and behaved as hydrogen evolution reaction (HER) catalysts with a Faradaic efficiency of up to 95% (5.81 × 10-5 mol H2 per 11.76 C) and a stable current density during repeated controlled potential experiments (CPE), even though with high overpotentials (0.53-0.68 V to reach a current density of 1 mA·cm-2). These studies open the way to the effectiveness of tailored phosphine oxide POPs produced through an inexpensive and ecofriendly iron-based catalyst and for the insertion of transition metals in a porous architecture, enabling electrochemically driven activation of small molecules

Insight into the Properties of Heteroleptic Metal Dithiolenes: Multistimuli Responsive Luminescence, Chromism, and Nonlinear Optics

A comprehensive investigation of the functional properties of heteroleptic donor-M-acceptor dithiolene complexes Bu4N[MII(L1)(L2)] is presented (M = Pd, Pt). The acceptor L1 consists of the chiral (R)-(+)α-methylbenzyldithiooxamidate ((R)-α-MBAdto), the donor L2 is 2-thioxo-1,3-dithiole-4,5-dithiolato (dmit) in 1 (Pd) and 2 (Pt), 1,2-dicarbomethoxyethylenedithiolate (ddmet) in 3 (Pd) and 4 (Pt), or [4′,5′:5,6][1,4]dithiino[2,3-b]quinoxaline-1′,3′-dithiolato (quinoxdt) in 5 (Pd) and 6 (Pt). L1 is capable of undergoing proton exchange and promoting crystal formation in noncentrosymmetric space groups. L2 has different molecular structures while it maintains similar electron-donating capabilities. Thanks to the synergy of the ligands, 1-6 behave as H+ and Ag+ switchable linear chromophores. Moreover, the compounds exhibit a H+-switchable second-order NLO response in solution, which is maintained in the bulk for 1, 3, and 4 when they are embedded into a PMMA poled matrix. 5 and 6 show unique anti-Kasha H+ and Ag+ tunable colored emission originating from the quinoxdt ligand. A correlation between the electronic structure and properties is shown through density functional theory (DFT) and time-dependent DFT calculations

Au(III)-Proline derivatives exhibiting selective antiproliferative activity against HepG2/SB3 apoptosis-resistant cancer cells

This paper deals with the combination of a proline-based moiety with biologically active gold centers in the oxidation states +1 and +3. In particular, six Au(i)/(iii)-proline dithiocarbamato (DTC) complexes with general formulae [AuI2(DTC)(2)] and [(AuX2)-X-III(DTC)] (X = Cl, Br) are reported here. After the synthesis of the ligand and the complexes, all derivatives were characterized via several techniques and tested for their stability in DMSO/water media. This study was focused on the demonstration of a peculiar behavior of Au(iii)-DTC species in solution. Finally, the complexes were screened for their antiproliferative activity against 2 human cancer cell lines, namely HepG2 and HepG2/SB3, taken as models of hepatocellular carcinoma. The latter, chosen for its aggressiveness due to the upregulation of the anti-apoptotic protein SerpinB3, was selectively inhibited in terms of growth by some Au(iii)-DTC complexes

Anti-Kasha Conformational Photoisomerization of a Heteroleptic Dithiolene Metal Complex Revealed by Ultrafast Spectroscopy

We investigated the anti-Kasha photochemistry and anti-Kasha emission of d8-metal donor-acceptor dithiolene with femtosecond UV-vis transient absorption spectroscopy and molecular modeling. Experimentally, we found a lifetime of 1.4 ps for higher excited states, which is exceptionally long when compared to typical values for internal conversion (IC) (10 s of fs or less). Consequently, a substantial emission originates from the second excited state. Molecular modeling suggests this to be a consequence of the spatially separated molecular orbitals of the first and second excited states, which gives a charge transfer character to the IC. More surprisingly, we found that the inherent flexibility of the molecule allows the metal complex to access different configurations depending on the photoexcited state. We believe that this unique manifestation of anti-Kasha photoinduced conformational isomerization is facilitated by the exceptionally long lifetime of the second excited state