Application of DNA-Alkylating Pyrrole-Imidazole Polyamides for Cancer Treatment

Pyrrole-imidazole (PI) polyamides, which target specific DNA sequences, have been studied as a class of DNA minor-groove-binding molecules. To investigate the potential of compounds for cancer treatment, PI polyamides were conjugated with DNA-alkylating agents, such as seco-CBI and chlorambucil. DNA-alkylating PI polyamides have attracted attention because of their sequence-specific alkylating activities, which contribute to reducing the severe side effects of current DNA-damaging drugs. Many of these types of conjugates have been developed as new candidates for anticancer drugs. Herein, we review recent progress into research on DNA-alkylating PI polyamides and their sequence-specific action on targets associated with cancer development.     

Effects of spacing and arrangement of droplet on combustion characteristics of monodispersed suspended-droplet cluster model under microgravity

For bridging between knowledge on droplet combustion and spray combustion, an experimental study was performed on autoignition and combustion of multiple droplet clusters. The monodispersed suspended-droplet cluster (MSDC) model with which arrangement, spacing and initial diameter of the droplet are well controlled has been developed. The effects of spacing and arrangement of droplet on combustion characteristics of the MSDC model in a high-temperature air were examined using microgravity environment in a drop shaft. The ignition delay and the burning time increased with decreasing the droplet spacing, regardless of the droplet number and the model dimensions. Larger droplet number with three-dimensional (3D) hexagonal closest packing (HCP) structure model resulted in longer ignition delay and longer burning time. 3D cubic closest packing (CCP) structure model showed rather longer ignition delay and much shorter burning time than 2D model. For 3D HCP model, an individual flame which enveloped each droplet was formed whole in the combustion duration with larger droplet spacing, while the group flame was formed whole in the combustion duration with smaller droplet spacing. When the droplet spacing was in the intermediate range, each droplet was ignited to form the individual flame, and each flame merged into the group flame. The diameter of the burning sphere decreased at the beginning of combustion, and turned to increase afterward. The transition from the individual flame to the group flame occurred around the time when the burning sphere diameter reached its minimum. The burning sphere diameter relative to the model diameter increased with decreasing the droplet spacing in the middle stage of combustion.     

Chemical cross-linking of conducting poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) using poly(ethylene oxide) (PEO)

Hybrid films of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) were prepared with different molecular weights of poly(ethylene oxide) (PEO). The cross-linking reaction between PEO and PEDOT:PSS was performed at high temperature and confirmed by using differential scanning calorimeter (DSC), contact angle measurement, and solid-state ¹H NMR. The effect of chemical reaction on the conductivity and morphology of these hybrid films was studied by using 4-point probe and atomic force microscope (AFM), respectively. As-spun PEO/PEDOT:PSS films have lower electric conductivity due to the addition of nonconductive PEO, and exhibits no molecular weight dependence on conductivity. After chemical cross-linking reaction at high temperature, only PEDOT:PSS films with lowest molecular weight PEO additives show enhanced conductivity with increasing reaction time. AFM result indicates that the heat-treated PEO/PEDOT:PSS hybrid films show grain-like morphology compared to ethylene glycol treated PEDOT:PSS films which shows continuous PEDOT domain. In the present work we demonstrate that the cross-linking reaction can be used to improve the wet stability of PEDOT:PSS nanofiber, showing good water resistance and excellent dimensional stability.     

Synthesis and gas permeability of membranes of Poly(vinyl ether)s bearing oxyethylene segments

Cationic copolymerizations of vinyl ether monomers [2-methoxyethyl vinyl ether: MOVE, 2-(2-methoxyethoxy)ethyl vinyl ether: MEEVE, 2-adamantyl vinyl ether: AdVE, 2-(2-vinyloxyethoxy)ethyl methacrylate: VEEM] were performed to obtain three types of vinyl ether copolymers [poly(MOVE-AdVE)s, poly(MEEVE-AdVE)s, and poly(MEEVE-VEEM)s] with different composition rates. Poly(MOVE-AdVE) and poly(MEEVE-AdVE) obtained at monomer feed ratio of 1:1 exhibited the glass transition temperatures (T_g) of 55 and 28 °C, respectively, but the T_g's of copolymers were near or lower than room temperature when the feed ratio of AdVE decreased. Poly(MOVE-AdVE)s and poly(MEEVE-AdVE) with T_g's above room temperature afforded free-standing membranes by casting them from toluene solutions. They exhibited relatively high CO₂ permeability and high CO₂/N₂ separation factors (P(CO₂) = 22–36 barrers, P(CO₂)/P(N₂) = 19–40). The T_g's of poly(MEEVE-VEEM)s were very low and around ?70 °C irrespective of the difference of monomer feed ratio. Methacrylate groups in poly(MEEVE-VEEM)s partially reacted under heating to give crosslinked polymer membranes. The crosslinked membranes showed high CO₂/N₂ selectivity, especially the poly(MEEVE-VEEM) membrane possessing the highest ratio of MEEVE exhibited high CO₂ permeability and high selectivity (P(CO₂) = 120 barrers, P(CO₂)/P(N₂) = 55).     

Chiral specificity in responses by the bark beetleDendroctonus valens to host kairomones

The attraction of the red turpentine beetle,Dendroctonus valens, to the resin volatiles of its host,Pinus ponderosa, is elicited by three chiral monoterpenes. In field assays response was greatest to (S)-(–)--pinene; 92% (S)-(–)--pinene found inP ponderosa resin was not attractive. However, 75% (R)-(+)--pinene, which occurs inPinus lambertiana, a sympatric host ofD. valens, was attractive. (S)-(–)--Pinene interrupted response to (R)-(+)--pinene. (S)-(+)-3-Carene from both hosts was attractive at the (R)-(+)--pinene level. Three sympatric coniferous nonhosts each have the same attractive monoterpenes but produce less resin. These studies demonstrate the importance of chirality of host compounds in the host finding behavior of this bark beetle.     

Surface plasmon resonance immunosensor using Au nanoparticle for detection of TNT

In order to develop the fully integrated portable surface plasmon resonance (SPR) system for detection of explosives, the amplification strategy of SPR signal was investigated. Indirect competitive inhibition method allowed the middle-sized SPR sensor to detect trinitrotoluene (TNT) at ppt level. However, this enhanced SPR signal was not high enough to detect TNT at ppt level by a miniaturized SPR sensor. Therefore, localized surface plasmon resonance (LSPR) effect using Au nanoparticle as further signal amplification approach was used. The amplification method of indirect competitive inhibition and LSPR were combined together for fabrication of the immunosurface using Au nanoparticle. TNT detectable range of this immunosurface was from 10 ppt (10 pg/ml) to 100 ppb (100 ng/ml), which was almost comparable to that without Au nanoparticle. The observed resonance angle change due to binding monoclonal TNT antibody (M-TNT Ab) with the immunosurface modified with Au nanoparticle was amplified to four times higher than that in absence of Au nanoparticle.     

High efficiency ester condensation using hydrophobic zeolite membranes

We successfully developed zeolite membranes with hydrophilic character, by choosing appropriate zeolites in terms of hydrophilicity and high acid tolerance. We evaluated thus developed membranes by their pervaporation (PV) performance, dehydration from acidic organic solvent. The zeolite membranes we developed, based on merlinoite (MER), chabazite (CHA) or phillipsite (PHI), are shown to exhibit stable dehydration performance, respectively. We successfully applied the membranes to the selective removal of water in an ester condensation reaction starting from a stoichiometric mixture of a carboxylic acid and an alcohol. The availability of pervaporation-assisted ester condensation reaction was validated by various kinds of combinations of carboxylic acid and alcohols, which implies the general availability of pervaporation-assisted process intensification by zeolite membranes. This paper was presented at the 11th Korea-Japan Symposium on Catatysis held at Seoul, Korea, May 21–24, 2007.     

Experimental evaluation of a spherical aberration-corrected TEM and STEM

We have successfully developed a spherical aberration (Cs)-corrected electron microscope for probe- and image-forming systems using hexapole correctors. The performance of the microscope has been evaluated experimentally. The point resolution attained using the image-forming Cs-corrector is better than 0.12 nm. For scanning transmission electron microscopy, the Ronchigram flat area was >40 mrad in half-angle using the probe-forming Cs-corrector.