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lactam相关的网络例句

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与 lactam 相关的网络例句 [注:此内容来源于网络,仅供参考]

The antibodies in plasma were also detected by indirect antiglobulin test. The result showed that levels of WBC,TB,DB,Glu and reticulocyte in six patients treated with β-lactam antibiotics were raised remarkably. DAT was strongly positive,but no RBC antibodies were detected in the plasma by IAT. The binding of red cells by monocytes or lymphocytes was great,and the hemolysis of red cells by alexin not appeared. After stopping above-mentioned β-lactam antibiotic administration,patient's WBC,TB,DB,and Glu levels returned to normal values.

结果发现:6例患者的临床治疗的药物都属于β内酰胺类;住院期间患者的WBC、TB、DB、Glu的检测结果出现异常,红细胞的DAT试验结果均为阳性,IAT试验结果均为阴性;将DAT阳性的红细胞进行补体结合实验时,结果为阴性;细胞涂片见部分红细胞表面有颗粒状物质附着,细胞培养见部分红细胞被白细胞识别、黏附;改用其它抗生素后,患者的上述化验指标恢复到正常值范围内,DAT试验结果转为阴性。

The result showed that levels of WBC,TB,DB,Glu and reticulocyte in six patients treated with β-lactam antibiotics were raised remarkably. DAT was strongly positive,but no RBC antibodies were detected in the plasma by IAT. The binding of red cells by monocytes or lymphocytes was great,and the hemolysis of red cells by alexin not appeared. After stopping above-mentioned β-lactam antibiotic administration,patient's WBC,TB,DB,and Glu levels returned to normal values.

结果发现:6例患者的临床治疗的药物都属于β内酰胺类;住院期间患者的WBC、TB、DB、Glu的检测结果出现异常,红细胞的DAT试验结果均为阳性,IAT试验结果均为阴性;将DAT阳性的红细胞进行补体结合实验时,结果为阴性;细胞涂片见部分红细胞表面有颗粒状物质附着,细胞培养见部分红细胞被白细胞识别、黏附;改用其它抗生素后,患者的上述化验指标恢复到正常值范围内,DAT试验结果转为阴性。

Modification of the side chain radical of β-lactam class antibiotic is a possible effective way,while the mother nuclide maintain the activity, but the different side chain radical alternating the drug tolerance of bacterium.

改造β-内酰胺类抗生素的侧链,不同侧链改变了细菌的耐药性,而其母核仍保持抗菌活性,这可能是克服抗生素使用剂量不断增大的一条有效途径。

Lactam was gained by the Staudinger reaction of imine and olefineketone in the presence of N-heterocyclic carbene catalyst.

以N-杂环卡宾催化剂1催化亚胺与烯酮之间的Staudinger反应,得到相应的β-内酰胺。

The study was purposed to evaluate synergistic effect of β-lactam antibiotics in drug-induced hemolysis.

本研究的目的是初步探讨β内酰胺类药物诱导患者溶血性贫血的机理。

Objective To learn about the clinical characteristics and the drug resistance of Klebsiella Pneumoniae inducing extensive spectrum β lactam.

目的 了解肺炎克雷伯杆菌肺部感染的临床特征,研究该菌产超广谱β内酰胺酶的耐药特点。

In different regions of the world, monotherapy with a -lactam antimicrobial is common.

在世界不同的区域,单一的β-内酰胺类抗生素治疗比较普遍。

The synthetic process of a novel β-lactam antibiotic, Faropenem, was studied in this paper.

本文是关于新型β-内酰胺类抗生素法罗培南合成及工艺的研究。

The Staudinger reaction is one of the most important methods in synthesis of, 8-lactams. 3-(Thiophen-2-yl)-β-lactam is one class of important β-lactam derivatives.

Staudinger反应是合成β-内酰胺类化合物最重要的方法之一。3-(噻吩-2-基)井内酰胺是一类重要的β-内酰胺类衍生物。

85 And 119486/79. They are a novel type of antibiotic having both the wide antibacterial spectrum and high safety of penicillin and cephem antibiotics belonging to beta -lactam antibiotics, as well as the potent antibacterial activity and high beta -lactamase stability of carbapenem antibiotics.Sodium-(5R, 6S)-6-[-1-hydroxyethyl]-7-oxo-3- [-2-tetrahydrofuryl]-4-thia-1-azabicyclo [3.2.0] hept-2-ene-2-carboxylate 5/2 hydrate (faropenem sodium, hereinafter referred to as compound 1) is currently used as an oral drug for various infectious diseases and is reported to show potent antibacterial activity against not only methicillin-sensitive Staphylococcus aureus, Streptococcus pyrogenes and Streptococcus pneumoniae but also gram-positive bacteria for which conventional beta -lactam drugs have proved ineffective such as penicillin-resistant pneumococci, oral staphylococci and enterococci, also showing a wide antibacterial spectrum covering gram-negative bacteria such as Haemophilus influenzae and anaerobic bacteria such as the genus Bacteroides, which activity is due to its novel skeleton penem ring (Kagaku Ryoho no Ryoiki The Field of Chemotherapy, Vol.

他们是一种新型的抗生素都具有广泛的抗菌谱和高度的安全青霉素和cephem抗生素,属于β-内酰胺类抗生素,以及作为强大的抗菌活性和高β-内酰胺酶稳定的碳青霉烯类antibiotics.sodium -( 5 R , 6 S )-6 -[ - 1 -羟乙基] - 7 -氧- 3 - [ - 2 - t etrahydrofuryl] - 4 -硫杂- 1 -氮杂双环[ 3 。2.0]庚- 2 -节能- 2 -羧酸5 / 2水合物(法罗培南钠,以下简称为化合物1 )是目前用来作为口服药物,为各种传染病和报道,以显示强大的抗菌活性,不仅对甲氧敏感的金黄色葡萄球菌,链球菌pyrogenes和肺炎链球菌,但也克阳性菌为常规β-内酰胺类药物已证明无效,如青霉素耐药pneumococci ,口腔葡萄球菌和肠球菌,也显示出广泛的抗菌谱,包括革兰阴性菌如流感嗜血杆菌和厌氧菌如属杆菌,这活动是由于其新颖的骨架青霉烯环((化学ryoho没有ryoiki领域的化疗),第13卷,第10号,第74-80 , 1997年)。

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