Drug release from hydroethanolic gels. Effect of drug's lipophilicity (logP), polymer-drug interactions and solvent lipophilicity.

We demonstrate drug release properties from hydroethanolic formulations as a function of the drug's lipophilicity (logP), solvent lipophilicity and drug-polymer interactions, for the first time. A hydrophilic polymer, hydroxypropyl cellulose (HPC), provides the non-Fickian slower release of the lipophilic drug, lidocaine (logP=2.6) and the burst (Fickian) release of hydrophilic drug, lidocaine hydrochloride (logP

In-depth nano-scale analysis of complex interactions of Hg with gold nanostructures using AFM-based power spectrum density method.

Atomic force microscopy based power spectrum density (PSD) method along with conventional methods such as line, grain height, root mean square (rms) roughness, is used to probe complex Hg-Au interactions i.e. the amalgamation of smooth gold nanostructures (Au-ns) and partial dissolution of irregular edges of interconnecting Au-ns networks due to Hg. We have demonstrated for the first time the use of the PSD method to gain significant insights into the directional anisotropy of resultant Hg-Au-ns and the range of Au-ns responsible.

Microbeads on microposts: an inverted architecture for bead microarrays.

The rapid development of genomics and proteomics requires accelerated improvement of the microarrays density, multiplexing, readout capabilities and cost-effectiveness. The bead arrays are increasingly attractive because of their self-assembly-based fabrication, which alleviates many problems of top-down microfabrication. Here we present a simple, reliable, robust and modular technique for the fabrication of bead microarrays, which combines the directed assembling of beads in microstructures and PDMS-based replica molding. The beads are first self-assembled in pyramidal microwells fabricated by anisotropic etching of silicon substrates, then transferred on the apex of PDMS pyramids that replicate the silicon microstructures. The arrays are chemically and biochemically robust; they are spatially addressable and have the potential for being informationally addressable; and they appear to offer better readout capabilities than the classical microarrays.

Two-step protocol to incorporate cells in thermoresponsive hydrogels.

One of the stumbling blocks in the formation of a thermoresponsive cell-hydrogel hybrid (TCH) is the efficient incorporation of cells in thermoresponsive hydrogels (TH) using traditional top-down (i.e., cells penetrate in the pre-set gels from top surface) approach. This approach is slow and tedious because the hydrogel needs to soak in the cells culture for a long time to allow cells to penetrate from the gel surface in to the bulk of the gel. In addition, cell incorporation into TH is difficult because elevated dissolution temperatures of gelators are detrimental to cell viability, whereas the highly viscous gel state that formed at ambient temperatures retards the penetration of cells. We propose a bottom-up approach (i.e., cells mixed prior to gel setting) using a novel two-step protocol. The first step is the rapid cooling of the agarose solution from its dissolution temperature (98 degrees C) to 37 degrees C and equilibrating for 3-4 min. The second step is the mixing of fibroblasts with the agarose solution and natural cooling to the room temperature to form the TCH. With this novel protocol, 90% of fibroblasts are found to be trapped in the cell-gel hybrid.

Capacity of nano-reactors of AOT micro-emulsions to form and sustain ultra small semiconductor quantum dots.

Microemulsions (MEs) are increasingly being used as nano-reactors for the formation and synthesis of nanoparticles or quantum dots (QDs). In this paper, we study the capacity of aqueous nanoreactors of AOT microemulsions for the formation of ultrasmall semiconductor QDs by fixing w = ([H2O]/[AOT]) and varying the concentration of CdS up to 100 mM. The CdS QDs in the MEs are evaluated using UV-vis spectroscopy, XRD, TEM, and light scattering. Particles are found to be controlled in 8.7 A-11.8 A. The UV-vis spectra are analysed using an accurate tight-binding (TB) approach and effective mass approximation (EMA). The TB method, being much more accurate than the EMA, gives results in good agreement with X-ray diffraction (XRD) and transmission electron microscopy (TEM). XRD reveals that the particles are mostly zinc-blend at low concentrations (> or =20 mM) but a mixture of zinc-blend and wurtzite at higher concentrations (100 mM). High concentrations of CdS are useful to improve the yield while best-utilizing nanoreactors and to give a tight control over size and polydispersity. MEs containing CdS are found to be stable over a month when kept in the dark.

Creating new supramolecular materials by architecture of three-dimensional nanocrystal fiber networks.

The architecture of three-dimensional interconnecting self-organized nanofiber networks from separate needlelike crystals of L-DHL (lanosta-8,24-dien-3beta-ol:24,25-dihydrolanosterol = 56:44) in di-isooctylphthalate has been achieved for the first time, on the basis of the completely new concept of branching creation by additives (branching promoters). [In this work, an additive, ethylene/vinyl acetate copolymer (EVACP), is used at a concentration of several 10 ppm.] We demonstrate that this novel technique enables us to produce previously unknown self-supporting supramolecular functional materials with tailormade micro- or nanostructures, possessing significantly modified macroscopic properties, by utilizing materials thus far considered to be "useless". In addition, both the self-organized structure and the properties of the new materials can be fine-tuned by altering the processing conditions. Our results show that the formation of the interconnecting 3D self-organized network structure is controlled by a new mechanism, so-called crystallographic mismatch branching mechanism, as opposed to the conventionally adopted molecular self-assembly mechanism. The principles and criteria for the selection of branching promoters are also discussed from the point of view of molecular structures.