Photosensitizer and peptide-conjugated PAMAM dendrimer for targeted in vivo photodynamic therapy.

Challenges in photodynamic therapy (PDT) include development of efficient near infrared-sensitive photosensitizers (5,10,15,20-tetrakis(4-hydroxyphenyl)-21H,23H-porphine [PS]) and targeted delivery of PS to the tumor tissue. In this study, a dual functional dendrimer was synthesized for targeted PDT. For targeting, a poly(amidoamine) dendrimer (G4) was conjugated with a PS and a nitrilotriacetic acid (NTA) group.

Hierarchical mesoporous In2O3 with enhanced CO sensing and photocatalytic performance: distinct morphologies of In(OH)3 via self assembly coupled in situ solid-solid transformation.

The present investigation details our interesting findings and insights into the evolution of exotic hierarchical superstructures of In(OH)3 under solvothermal conditions. Controlled variation of reaction parameters such as, reactant concentration, solvent system, crystal structure modifiers, water content along with temperature and time, yielded remarkable architectures. Diverse morphologies achieved for the first time includes (i) raspberry-like hollow spheres, (ii) nanosheet-assembled spheres, (iii) nanoparticle-assembled spheres, (iv) nanocube-assembled hollow spheres, (v) yolk-like spheres, (vi) solid spheres, (vii) nanosheets/flakes, and (viii) ultrafine nanosheets.

Targeted in vivo photodynamic therapy with epidermal growth factor receptor-specific peptide linked nanoparticles.

In targeted photodynamic therapy (tPDT), photosensitizers (PS) are targeted to disease tissue to reduce the dosage of PS and in addition to reduce the photo damage to the non-target tissue. We synthesized iron oxide nanoparticles (NP) armored with tumor targeting peptide and PS for targeted PDT. Chitosan covered Fe3O4 NPs (30 nm) were deposited with gold NPs to generate two distinct chemical surfaces.

Structure and Li+ dynamics of Sb-doped Li7La3Zr2O12 fast lithium ion conductors.

Antimony-doped lithium stuffed garnets Li(7-x)La3Zr(2-x)Sb(x)O12 (x = 0.2-1.0) prepared using a conventional solid state reaction method are characterized using Powder X-ray Diffraction (PXRD), Scanning Electron Microscopy (SEM), Energy Dispersive Analysis by X-ray (EDAX), AC Impedance spectroscopy, Magic Angle Spinning Nuclear Magnetic Resonance (MAS NMR) and Raman spectroscopic techniques.