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21.
Lectin affinity electrophoresis of serum alpha-fetoprotein (AFP) was carried out on samples obtained from patients with benign and malignant diseases and on cord blood, and separated AFP bands were detected by antibody-affinity blotting. The following major bands were identified by determination of kinetic constants: AFP-C1 and -C2 with concanavalin A, AFP-L1, -L2 and -L3 with Lens culinaris agglutinin A, AFP-P1, -P2, -P3, -P4 and -P5 with erythroagglutinating phytohemagglutinin, and AFP-A1, -A2 and -A3 with Allomyrina dichotoma lectin. AFP bands with the lowest number had either low or no affinity and those with higher numbers had higher affinities for respective lectins. AFP from cord blood and chronic liver disease was characterized by the predominance of AFP-C2, AFP-L1, AFP-P2 and AFP-A3. Hepatocellular carcinoma was differentiated from the benign liver disease by increased proportions of AFP-L3 and AFP-P4. Extrahepatic tumors had additional increases of AFP-C1, AFP-L2, AFP-P5 and AFP-A1 (or slow-migrating AFP-Als, particularly in yolk sac tumor). 相似文献
22.
Hidefumi Hirai Tsuneaki Tanabe Hideomi Koinuma 《Journal of polymer science. Part A, Polymer chemistry》1980,18(1):203-222
Triad cotacticities of alternating copolymers of methyl methacrylate with styrene prepared in the presence of zinc chloride, ethylaluminium sesquichloride, and ethylboron dichloride are investigated from the mechanistic point of view by means of 1H- and 13C-NMR. The cotacticities from 1H-NMR spectra are obtained accurately by using α-d-styrene in the place of styrene and by measuring the spectra on the copolymer in o-dichlorobenzene at 170°C. The relative intensities of three peaks of the splitting signal for the methoxy protons in the nonalternating copolymers obtained by the use of benzoyl peroxide in the absence of metal halides agree well with the cotacticity distribution calculated theoretically by the Lewis-Mayo mechanism with the stereoregulation following Bernoullian statistics. The splitting signals in the 1H- and 13C-NMR spectra of the alternating copolymers prepared in the presence of metal halides cannot be explained by the same mechanism. The relative intensities of three peaks of the splitting signals for the methoxy protons and for the carbonyl carbon in the methyl methacrylate unit (the contents of cotactic triads centered by the methyl methacrylate unit) are not equal to those for the aromatic C1 carbon in the styrene unit (the contents of cotactic triads centered by styrene unit). The value of f2Y - 4fxfz is not equal to zero, where fx, fy, and fz are the cosyndiotactic, coheterotactic, and coisotactic triad contents, respectively, in the alternating copolymer. Copolymers obtained in the presence of zinc chloride are not exactly equimolar alternating but always contain a methyl methacrylate unit in excess, and the relative intensities of the three peaks for the aromatic C1 carbon change with the copolymer composition. These results are explained by a proposed mechanism: the alternating copolymerization proceeds through the homopolymerization of a ternary molecular complex composed of a metal halide, methyl methacrylate, and styrene, accompanied with the stereoregulation following first-order Markovian statistics; the increase of methyl methacrylate content in the copolymer prepared in the presence of zinc chloride is caused by the participation of the binary molecular complex composed of a metal halide and methyl methacrylate in addition to the ternary molecular complex. 相似文献
23.
A new C3-unit substitution reaction at C-4 position of 4- acetoxyazetidinone derivative ( and ) by tetraallyltin () in the presence of 1/10 eq. of BF3-ether in methylene chloride is described. From 4-allylazetidinone derivative () via ylid intermediate () dethiathienamycin () was synthesized. 相似文献
24.
K. Hashimoto S. Hirota Y. Kanari Y. Hirai 《Journal of Radioanalytical and Nuclear Chemistry》2002,252(2):287-291
More than 200 samples of marine products have been collected and analyzed for plutonium and almost 100 samples for americium around Hitachi, Tokai and Oarai in the pacific coast of Ibaraki prefecture. The data have shown that the concentration factor (CF) values for plutonium were 330 for bivalve, 770 for abalone (muscle) and 610 for brown algae. For americium, the CF was calculated as 2400 for bivalve, 1000 for abalone (muscle) and 420 for brown algae. 相似文献
25.
26.
Takuo Kosuge Kuniro Tsuji Koichi Hirai Kentaro Yamaguchi Toshihiko Okamoto Yoichi Iitaka 《Tetrahedron letters》1981,22(35):3417-3420
A new toxin, named neosurugatoxin, was isolated from the toxic Japanese Ivory Shell and its structure was determined by X-ray crystallographic analysis. 相似文献
27.
Shinji Suzuki Furitsu Suzuki Yasumasa Kanie Koji Tsujitani Asako Hirai Hironori Kaji Fumitaka Horii 《Cellulose (London, England)》2012,19(3):713-727
The structure and crystallization of carefully isolated sub-elementary fibrils (SEFs) of bacterial cellulose have been investigated
using TEM, WAXD, and high-resolution solid-state 13C NMR. The addition of a suitable amount of fluorescent brightener (FB) to the incubation medium of Acetobacter xylinum effectively suppressed the aggregation of the SEFs into the microfibrils, as previously reported. However, this study confirmed
for the first time that serious structural change in the SEFs occurs during the removal of excess FB by washing with buffer
solutions having pH values higher than 6 or with the alkaline aqueous solution that was frequently used in previous studies.
In contrast, the isolation of unmodified SEFs was successfully performed by utilizing a washing protocol employing pH 7 citrate–phosphate
buffer solution containing 1% sodium dodecyl sulfate. High-resolution solid-state 13C NMR and WAXD measurements revealed that the SEFs thus isolated are in the noncrystalline state in which the pyranose rings
of the almost parallel cellulose chains appear to be stacked on each other. The respective CH2OH groups of the SEFs adopt the gt conformation instead of the tg conformation found in cellulose I
α
and I
β
crystals, and undergo significantly enhanced molecular motion in the absence of intermolecular hydrogen bonding associated
with these groups. The main chains are also subject to rapid motional fluctuations while maintaining the parallel orientation
of the respective chains, indicating that the SEFs have a liquid crystal-like structure with high molecular mobility. Moreover,
the SEFs crystallize into cellulose I
β
when the FB molecules that may adhere to the surface of the SEFs are removed by extraction with boiling 70 v/v% ethanol and
0.1N NaOH aqueous solution. On the basis of these results, the crystallization of the SEFs into the I
α
and I
β
forms is discussed, including the possible formation of the crystalline-noncrystalline periodic structure in native cellulose. 相似文献
28.
A great number of studies of polyelectrolyte complexes have been carried out by various investigators; most of them concentrated on the reaction between oppositely charged polyelectrolytes [1-3]. The structure and properties of the resultant complexes have been investigated to a lesser extent, and the understanding of this new class of polymer materials is still insufficient. Thus, we have been investigating the sorption of water vapor by the complexes and the morphological changes caused by this sorption [4,5]. 相似文献
29.
V. V. Kaminskii Toshihiro Kuzuya Shinji Hirai S. M. Solov’ev N. V. Sharenkova M. M. Kazanin 《Physics of the Solid State》2012,54(7):1345-1347
The electrical conductivity of SmS polycrystals has been studied in the temperature range 300?C870 K. It has been shown that, at 300 K ?? T ?? 700 K, the concentration of conduction electrons is determined by electron transfer from impurity donor levels, and at T > 700 K, by that from the samarium 4f levels. 相似文献
30.