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951.
Shigeyama M Ohgaya O Takeuchi H Hino T Kawashima Y 《Chemical & pharmaceutical bulletin》2001,49(2):129-133
We intended to develop a desired ointment base suitable for treatment of bedsores including the proliferation of granulation and epidermis. The main bedsore bacteria detected in our hospital were S. aureus in gram-positive coccus and P. aeruginosa in gram-negative bacillus. As the macrogol ointment (MO) was found to have bactericidal effects on these bacteria, MO was adopted as the base for the objective ointment. To improve the properties of the ointment base such as regulating the humidity of the exudation and controlling the release of antibiotics formulated in the ointment, co-formulating effects of various additives to MO were evaluated. The sustained release function of the ointment base was obtained by adding hydrophilic petrolatum (HP) to MO. However, the resultant ointment was found to have a poor humidity regulating property. On the other hand, MO containing 5% of hydroxypropyl cellulose (HPC) showed both the humidity regulating and the controlled drug releasing properties. It was considered that HPC particles dispersed in the ointment could be swelled by absorbing water to form a gel network. The curd tension meter tests for the ointments prepared with the various polymers showed that the MO-HPC base, which showed the highest sustained drug releasing property, was found to have the highest hardness. This result means that HPC formulated into the base forms the most rigid gel structure to resist the erosion of the ointment and to control the drug release. 相似文献
952.
A. Fukumi I. Endo T. Horiguchi Y. Ishida T. Kondo T. Kuwamoto H. Matsuzaki T. Nakamura T. Takahashi 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1997,42(4):243-249
Systematic study of hyperfine structures, Zeeman and Stark effects in Sm I is performed for the lowest 7G1-6 levels belonging to the configuration 4f 66s6p by atomic-beam laser spectroscopy with fluorescence detection. The hyperfine coupling constants of 7G2-6 levels are determined. From the Zeeman splittings for the 4f 66s 2 7F2-6 ? 4f 66s6p 7G2-6 transitions, g-values are determined for the 7G2.6 levels and the precision is improved by several orders of magnitude. From the Stark splittings for the 7F0-3 ? 7G1-3 transitions, tensor polarizabilities α 2(J) are determined for the upper 7G1-3 levels. Particularly for the 7G1 level (15 650.55 cm?1) which has close-lying opposite-parity level, the isotope dependence of α 2(J) is clearly observed for the first time. 相似文献
953.
The elastic vibrations of spherical nanoparticles have been widely studied by Raman scattering. However, there exist more than one set of selection rules for Raman scattering from these vibrations. For instance, Kanehisa has stated that only torsional modes with angular momentum l = 2 are Raman-active, while Tanaka et al. proposed that spheroidal modes of even l and torsional modes of odd l are Raman-active. These contradict selection rules of Duval which states that only spheroidal modes of l = 0 or 2 are Raman-active. Our present calculations based on a macroscopic model show that all torsional modes have vanishing intensity in the Raman spectrum. 相似文献
954.
Terada Y Misoi R Watanabe N Hornberger M Kreis W 《Chemical & pharmaceutical bulletin》2000,48(3):349-352
Cardenolide glucohydrolase II (CGH II) is a cardenolide-specific glucohydrolase obtained from Digitalis lanata leaves. We investigated the structure-specificity relationship of several cardenolide disaccharides as a substrate for CGH II. Conformation analysis of the substrates was performed using molecular mechanics calculations. The sugar chain conformation of two inert glycosides was significantly different from that of the other glycosides. The other two glycosides, which were weak substrates of CGH II, were suggested to have an intramolecular hydrogen bond between the sugar groups. It was deduced that this hydrogen bond restricts the conformational change of the sugar chain and prevents the glycosides from enzymatic recognition. 相似文献
955.
Ten samples of commercial blue mussels (Mytilus edulis) from Japan were analyzed for domoic acid by an indirect competitive enzyme immunoassay (idc-EIA) based on an anti-domoic acid monoclonal antibody. Domoic acid was found in all samples at low concentrations (0.11-1.81 ng/g mussel tissue). The presence of domoic acid was confirmed by liquid chromatography coupled with immunoaffinity chromatography using an anti-domoic acid monoclonal antibody as ligand. To our knowledge, this is the first reported detection of domoic acid, a causative agent of amnesic shellfish poisoning, in Japanese mussels. 相似文献
956.
玻璃载体表面脱氧核糖核酸的固定及其化学发光检测 总被引:2,自引:0,他引:2
用硅烷化偶联剂把DNA直接共价固定在载玻片表面,将辣根过氧化物酶标记的探针与之进行核酸杂交,杂交后用增强的化学发光检测。方法的检出限为75pg。研究了DNA分子固定在玻璃载体表面的各种条件,并建立了在玻璃载体表面进行核酸杂交的体系,为研究光纤DNA生物传感器打下了基础。 相似文献
957.
The capillary gas chromatographic behaviour of diethylhydrogensilyl (DEHS) ethers and/or diethylsilylene (DES) derivatives of fifty bile acids including 4- and 6-hydroxylated compounds is described. The methylene unit (MU) values of methyl and pentafluorobenzyl esters of bile acids were determined as their trimethylsilyl (TMS), dimethylethylsilyl (DMES) ethers and DEHS-DES derivatives. The differences in methylene unit values between the corresponding TMS ethers and DMES ethers or DEHS-DES derivatives were used for estimating the number and stereochemistry of hydroxyl groups on the steroid nucleus. On treatment with the silylating agent N,O-bis (diethylhydrogensilyl)trifluoroacetamide, bile acids possessing isolated hydroxyl in addition to diaxial trans-glycol groups were easily converted into the DEHS ehters, whereas those having a vicinal glycol group except for the diaxial group were converted into cyclic DES derivatives. The mass spectrometric properties obtained with negative-ion chemical ionization detection are discussed. 相似文献
958.
Effects of monoclonal antibody anti-EGF receptor on human nasopharyngeal carcinoma cell and other tumor cells 总被引:1,自引:0,他引:1
E N Guan T C Zhou J H Wang Y Chen Y X Sun P G Huang W P Tang M L Zhao 《Science in China. Series B, Chemistry, life sciences & earth sciences》1990,33(11):1334-1340
Three anti-EGF receptor MoAbs were used in these studies. Administration of MoAbs 3 and 176 inhibited tumor formation in nude mice by CNE-2, a poorly differentiated nasopharyngeal carcinoma cell line and A431, an epidermoid carcinoma cell line. When the same MoAbs were used in treatment against HeLa, a cervical carcinoma, tumor growth was not affected. The number of EGF receptors and apparent dissociation constants for 125I-EGF on CNE-2 and A431 was 1.3 x 10(5)/cell (Kd 7.7 x 10(-8) mol/L) and 1.4 x 10(6)/cell (Kd 2.4 x 10(-9) mol/L), respectively. Both MoAbs 3 and 176, capable of competing with EGF for receptor binding, showed significant tumor growth inhibition. MoAb 101 was incapable of blocking the binding of EGF to its receptor, and not as effective as MoAbs 3 and 176 in tumor growth inhibition. Our observation is that the MoAb anti-EGF receptor is cytostatic rather than cytocidal, in vitro against CNE-2 and A431. 相似文献
959.
Concentrations of uranium and thorium in some West Malaysian limestones have been determined using neutron activation and delayed neutron analyses. These limestones are mainly calcium carbonates and contain uranium and thorium in concentrations of about a few parts per million. 相似文献
960.
A Kuno Y Sugiyama K Katsuta T Kamitani H Takasugi 《Chemical & pharmaceutical bulletin》1992,40(6):1452-1461
Novel 4-arylpyrimidine derivatives were synthesized by the oxidation of 4-aryl-1,4-dihydropyrimidines, and their effects on anti-anoxic (AA) activity in mice and anti-lipid peroxidation (ALP) activity in rat brain mitochondria were investigated. Among these compounds, ethyl 6-methyl-2-phenyl-4-(4-pyridyl)-5-pyrimidinecarboxylate (4b) has AA activity (10 mg/kg, i.p.) and ethyl 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (4f) has ALP activity (73% inhibition at 10(-5) g/ml). The latter compound (100 mg/kg, i.p.) was also effective on arachidonate-induced cerebral edema in rats with comparable potency to that of vitamin E. 相似文献