离子交换色谱法回收克拉维酸的动力学研究。

M Barboza, R M Almeida, C O Hokka
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引用次数: 25

摘要

Clavulanic acid (CA)是一种由链霉菌clavuligerus产生的β -内酰胺酶抑制剂。目前,CA与阿莫西林的联合使用是对β -内酰胺酶敏感的β -内酰胺类抗生素与这些酶的抑制剂一起使用的最成功的例子。Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acid Clavulanic acidAmberlite IRA 400是一种强阴离子交换树脂,对CA具有很高的吸附能力(Mayer et al. 1997)。这种树脂可以用氯化钠(氯循环)预处理,选择性地去除那些能够取代树脂中的氯的阴离子,或者用氢氧化钠(羟基循环)去除所有种类的阴离子。为了确定离子交换树脂回收CA的最佳操作条件,并建立该分离过程的模型,采用Amberlite IRA 400在氯循环中进行了批量实验。这些实验在一个200毫升的搅拌槽中进行,在两种不同的初始溶液pH, 6.2和4.0;吸附阶段温度保持在10℃和20℃,解吸阶段温度保持在30℃。在这些批处理结果的基础上,可以对分离过程进行建模,包括吸附动力学、平衡数据和传质限制。
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Kinetic studies of clavulanic acid recovery by ion exchange chromatography.

Clavulanic acid (CA) is a beta-lactamase inhibitor produced by strains of Streptomyces clavuligerus. Nowadays, the combination of CA with amoxycillin is the most successful example of the use of a beta-lactam antibiotic sensitive to beta-lactamases together with an inhibitor of these enzymes. Clavulanic acid is purified from fermentation broth by a series of steps consisting mainly of two-phase separation processes such as liquid-liquid extraction, adsorption or ion-exchange chromatography, among others. Amberlite IRA 400, a strong anion-exchange resin, has a very high adsorption capacity for CA (Mayer et al. 1997). This resin can be pre-treated with NaCl (chloride cycle), to remove selectively only those anions, which are able to displace chloride from the resin or with NaOH (hydroxyl cycle), to remove all species of anions. In order to decide the best operating conditions for CA recovery by ion-exchange resins and then to construct a model of this separation process, batch experiments were conducted using Amberlite IRA 400 in the chloride cycle. These runs were carried out in a 200 ml stirred tank, at two different initial solution pH, 6.2 and 4.0; the temperature was maintained at 10 degrees C and 20 degrees C during adsorption and 30 degrees C during the desorption step. It was possible, on the basis of these batch results, to model the separation process, including the adsorption kinetics, equilibrium data and mass transfer limitations.

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