Optimized microwave-assisted functionalization and quantification of superficial amino groups on porous silicon nanostructured microparticles.

This work presents an optimized microwave (MW)-assisted method for the chemical functionalization of porous silicon particles (PSip). 3-(Aminopropyl)triethoxysilane (APTES) was grafted on previously stabilized PSip. The functionalization efficiency was studied and optimized in terms of reaction time (Rt) and reaction temperature (RT) using a central composite design (CCD). The effect of MW irradiation on the surface coverage was found to strongly depend on the PSip surface chemistry, Rt, RT, and percentage of APTES. Quantification of grafted amino groups was performed by the ninhydrin method (NHIM); confirming the results by thermogravimetric analysis (TGA). Reacting with 5% APTES solution at 95 °C for 26 min was the best functionalization conditions. The efficiency of PSip-APTES prepared under the optimized conditions was compared to those functionalized by the traditional method; MW irradiation increases by 39% the number of functional groups grafted onto the PSip surfaces with the additional benefit of having a drastic reduction in Rt.

Non-Covalently Pre-Assembled High-Performance Near-Infrared Fluorescent Molecular Probes for Cancer Imaging.

New fluorescent molecular probes, which can selectively target specific cell surface receptors, are needed for microscopy, in vivo imaging, and image guided surgery. The preparation of multivalent probes using standard synthetic chemistry can be a laborious process due to low reaction yields caused by steric effects. In this study, fluorescent molecular probes were prepared by a programmed non-covalent pre-assembly process that used a near-infrared fluorescent squaraine dye to thread a macrocycle bearing a cyclic arginine-glycine-aspartate peptide antagonist (cRGDfK) as a cancer targeting unit. Cell microscopy studies using OVCAR-4 (ovarian cancer) and A549 (lung cancer) cells that express high levels of the integrin αvß3 or αvß5 receptors, respectively, revealed a multivalent cell targeting effect. That is, there was comparatively more cell uptake of a pre-assembled probe equipped with two copies of the cRGDfK antagonist than a pre-assembled probe with only one appended cRGDfK antagonist. The remarkably high photostability and low phototoxicity of these near-infrared probes allowed for acquisition of long-term fluorescence movies showing endosome trafficking in living cells. In vivo near-infrared fluorescence imaging experiments compared the biodistribution of a targeted and untargeted probe in a xenograft mouse tumor model. The average tumor-to-muscle ratio for the pre-assembled targeted probe was 3.6 which matches the tumor targeting performance reported for analogous cRGDfK-based probes that were prepared entirely by covalent synthesis. The capability to excite these pre-assembled near-infrared fluorescent probes with blue or deep-red excitation light makes it possible to determine if a target site is located superficially or buried in tissue, a probe performance feature that is likely to be very helpful for eventual applications such as fluorescence guided surgery.

Structural Control of Kinetics for Macrocycle Threading by Fluorescent Squaraine Dye in Water.

While the general concept of steric speed bumps has been demonstrated in rotaxane shuttles and macrocycle threading systems, the sensitivity of speed bump effects has not been evaluated as a function of structural geometry. Values of Ka and kon for macrocycle threading in water are reported for a series of homologous squaraine dyes with different substituents (speed bumps) on the flanking chains and two macrocycles with different cavity sizes. Sensitivity to a steric speed bump effect was found to depend on (a) structural location, being lowest when the speed bump was near the end of a flanking chain, and (b) macrocycle cavity size, which was enhanced when the cavity was constricted. This new insight is broadly applicable to many types of molecular threading systems.