2,5-Diamino-5,5-diphosphonovaleric Acid as a Ligand for an Osteotropic <Superscript>188</Superscript>Re Radiopharmaceutical

A modified method for the preparation of 2,5-diamino-5,5-diphosphonovaleric acid (DADP5) has been developed in the search for new synthetically available organic ligands to produce ¹⁸⁸Re radiopharmaceuticals with an increased accumulation in the bone tissue. Interaction of the obtained acid with ¹⁸⁸Re was studied by radio-TLC. An optimal system for separating unbound ¹⁸⁸Re and labeled complex in a yield of at least 95% was found. The biological distribution of ¹⁸⁸Re-DADP5 was studied based on direct radiometric data. The osteotropicity of ¹⁸⁸Re-DADP5 and its increased accumulation in bone fracture sites, which represent oncological pathology models, was detected at a level comparable to known radiopharmaceuticals.     

Ionenaustausch

Ohne Zusammenfassung     

Log-periodic oscillations for biased diffusion of a polymer chain in a porous medium

A coarse-grained off-lattice bead-spring model is used to reveal the complex dynamics of a polymer chain in a quenched porous medium in the presence of an external field B. The behavior of the mean square displacement (MSD) of the center chain bead and that of the center of mass of the chain as a function of time is studied at different values of the barrier concentration C, the field strength B and the chain length N. In a field, important information on the way in which chains move between obstacles and overcome them is gained from the MSD vs. time analysis in the directions parallel and perpendicular to the flow. Instead of a steady approach to uniform drift-like motion at low C, for sufficiently strong field B we observe logarithmic oscillations in the effective exponents describing the time dependence of the MSD along and perpendicular to field. A common nature of this phenomenon with oscillatory behavior, observed earlier for biased diffusion of tracers on random lattices, is suggested. Received 7 August 1998     

Flow of polymer chains and segregation in a flow field with a hybrid simulation

Effects of a flow field (E) on segregation and flow of polymer chains are studied in two dimensions using a hybrid (discrete‐to‐continuum) simulation. The flow rate (j) of polymer chains is found to increase monotonically with E, a linear response in the low field regime followed by a slow approach to saturation in the high field regime. The effective chain permeability (ϕ_c = j/E) varies nonmonotonically on increasing the field E, with a maximum (ϕ_cm) at a characteristic value of the field (in the range 0.2 < E < 2); ϕ_cm depends on the chain length. Chain aggregates exhibit an anisotropic mass distribution due to the field with a molecular bridging at high fields. The longitudinal component of the radius of gyration (R_gx) exhibits a crossover from a random walk (RW) (R_gx ˜ L_c^1/2) at E = 0 to an elongated conformation (R_gx ˜L_c) at E ⪈ 0.2; the transverse component changes from R_gy ˜ L_c^1/2 to R_gy ˜ L_c^1/3. The width of the radial distribution function (ρ(r)) of the monomers increases while its peak varies nonmonotonically with E and is consistent with the observation of anisotropic mass distribution.     

Mesomorphic behaviors of a series of heterocyclic thiophene-imine-ester-based liquid crystals

The synthesis and characterization of a series of heterocyclic liquid crystal, 4-{[(thiophen-2-yl)methylidene]amino}phenyl 4-alkoxybenzoates possessing even number of carbon atoms at the alkoxy chain (C_nH_2n+1O-, n = 6, 8, 10, 12, 14, 16, 18) are reported. The molecular structures of title compounds were elucidated using Fourier-transform infrared spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopic techniques along with mass spectrometric analysis. The phase behavior of these compounds was characterized and studied by differential scanning calorimetry and polarizing optical microscopy. All members exhibited enantiotropic nematic phase except for the highest member (n = 18) which is a non-mesogen. Influence of alkoxy chain length on the transition temperatures of crystal-to-nematic (melting point) and nematic-to-isotropic (clearing point) was studied. Nematic phase range was found to increase from n = 6 to n = 10, then it started to descend from n = 12 to n = 16 and finally the nematic phase disappeared when n changed to 18.     

Enantioselective Sulfoxidation Catalyzed by a Bisguanidinium Diphosphatobisperoxotungstate Ion Pair

The first enantioselective tungstate‐catalyzed oxidation reaction is presented. High enantioselectivities were achieved for a variety of drug‐like phenyl and heterocyclic sulfides under mild conditions with H₂O₂, a cheap and environmentally friendly oxidant. Synthetic utility was demonstrated through the preparation of (S)‐Lansoprazole, a commercial proton‐pump inhibitor. The active ion‐pair catalyst was identified to be bisguanidinium diphosphatobisperoxotungstate using Raman spectroscopy and computational studies.     

Lectin affinity electrophoresis of alkaline phosphatase for the differentiation of bone and hepatobiliary disease

An affinity electrophoresis procedure is described for the separation and quantification of the bone- and liver-derived fractions of alkaline phosphatase in plasma. Separation is carried out on cellulose acetate membrane pre-soaked with buffer containing wheat germ lectin. The electrophoretic mobility of the bone enzyme is preferentially retarded by the lectin and this fraction is well separated from the liver fraction. After separation, enzyme activity is demonstrated by staining using an indigogenic alkaline phosphatase substrate incorporated in agar gel, and the stained fractions quantified by densitometry. The procedure has low imprecision, good linearity, and the activities of the bone and liver fractions correlate well with values obtained using nonelectrophoretic quantification methods. The procedure is especially suitable for use in the diagnostic laboratory.     

Photodecomposition of chromium tricarbonyl complexes with styrene, stilbene, and 1,4-diphenylbuta-1,3-diene in solution

Photolytic decomposition of styrene, stilbene, and 1,4-diphenylbuta-1,3-diene tricarbonyl chromium complexes in solution results in elimination of the carbonyl ligands and formation of binuclear alkenylarene chromium complexes. The quantum yields and activation and kinetic parameters of these processes were determined, and a scheme was proposed to rationalize photoinitiated transformations of the organochromium compounds under study.