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Novel simulated moving bed processes for antibiotics purification.

机译:用于抗生素纯化的新型模拟移动床工艺。

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Purification is an important process in pharmaceutical production. Maximizing yield while maintaining required purity is paramount to reducing purification costs, but this goal is difficult to achieve when the product and its impurities are very similar. Crystallization is often used is this case, but results in a substantial loss of yield. This research develops a simulated moving bed chromatography (SMB) process for purifying an important antibiotic, Clarithromycin (6-o-methyl erythromycin), from a similar impurity, 6,11-o-methyl erythromycin, using a systematic design approach. First, appropriate adsorbent and mobile phase combinations (adsorption systems) are found from preliminary experiments. A series of single-column chromatography experiments are then used to estimate the adsorption and mass transfer parameters.; Second, a design method for four-zone SMB processes that have non-linear adsorption isotherms and significant mass transfer effects was developed in this research. This method provides the highest throughput and the lowest solvent consumption for the isocratic four-zone SMB process. Rate model simulations confirm that the design method can guarantee high purity and yield. It is demonstrated that this design method can be applied to both Langmuir and Bi-Langmuir adsorption isotherm behavior. Because most real adsorption systems have these properties, this is an important development. This method is especially important when selectivity is low and cost minimization is of great importance.; A five-zone SMB process is a novel development of this research that improves upon the typical four-zone SMB process by substantially reducing solvent consumption. The non-linear, non-ideal design equations developed for four-zone SMB processes are modified to determine optimal operating conditions for the five-zone SMB process. This process is tested using a series of lab-scale SMB experiments. These lab-scale SMB experiments are also used to validate the design method and intrinsic parameters.; These intrinsic parameters are used to develop plant-scale designs of a four-zone SMB process and a five-zone SMB process using the most promising adsorptions systems. From these plant-scale designs, cost estimations are used to determine the most cost-efficient process for removal of 6,11. In addition, further processes are proposed for removing the remaining impurities.
机译:纯化是药物生产中的重要过程。在保持所需纯度的同时使产率最大化对于降低纯化成本至关重要,但是当产品及其杂质非常相似时,很难实现此目标。在这种情况下,经常使用结晶,但会导致产量大幅下降。这项研究开发了一种模拟移动床色谱(SMB)工艺,使用系统设计方法从相似的杂质6,11-o-甲基红霉素中纯化了重要的抗生素克拉霉素(6-o-甲基红霉素)。首先,从初步实验中可以找到合适的吸附剂和流动相的组合(吸附系统)。然后,使用一系列单柱色谱实验估算吸附和传质参数。第二,研究了具有非线性吸附等温线和显着传质效果的四区SMB工艺的设计方法。该方法为等度四区SMB工艺提供了最高的通量和最低的溶剂消耗。速率模型仿真证明该设计方法可以保证高纯度和高产率。结果表明,该设计方法可同时应用于Langmuir和Bi-Langmuir吸附等温线行为。因为大多数实际的吸附系统都具有这些特性,所以这是一个重要的发展。当选择性低且成本最小化非常重要时,此方法尤为重要。五区SMB工艺是这项研究的一项新进展,通过显着减少溶剂消耗,对典型的四区SMB工艺进行了改进。修改了为四区域SMB过程开发的非线性,非理想设计方程,以确定五区域SMB过程的最佳运行条件。使用一系列实验室规模的SMB实验测试了此过程。这些实验室规模的SMB实验也用于验证设计方法和固有参数。这些内在参数用于开发使用最有前途的吸附系统的四区SMB工艺和五区SMB工艺的工厂规模设计。从这些工厂规模的设计中,成本估算用于确定去除6,11的最具成本效益的过程。另外,提出了进一步的方法以去除残留的杂质。

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