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Multivariate calibration methods applied to the monitoring of the enzymatic synthesis of amipicilin

机译:多元校正方法应用于氨苄青霉素酶促合成的监测

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摘要

An integrated semi-continuous rector, with simultaneous crystallization of the antibiotic, is the most promising alternative for the enzymatic synthesis of semi-synthetic penicillins. Closed-loop optimization of the reactor operation requires the measurement of its state variables. An efficient method for on-line monitoring of these variables, i.e., the species concentrations, which is consistent with the dynamics of the process, is presented here. Multivariate calibration has been used to reduce times of analysis in multicomponent systems, and this is the approach of this work. Three multivariate calibration methods are compared for prediction of the concentrations of the components present in the enzymatic synthesis of ampicillin. UV spectra and their first-order derivatives were used as input data for the models. Results showed that all methods (SPA, PCR and PLS) had similar performances for this system. The use of first-order derivatives of the spectra did not improve substantially the performance of the methods. Bench assays of synthesis of ampicillin using immobilized penicillin G acylase (PGA) as catalyst were carried out to validate the methodology. Its results were compared with HPLC analyses. The technique showed to be very accurate for monitoring the concentrations of ampicillin (desired product) and 6-aminopenicillanic acid (6-APA, most expensive substrate), with precision similar to those obtained by HPLC. Prior information of the initial reactor state may be used to improve the estimation of less sensitive components (phenylglycine methyl ester, PGME and phenylglycine, PG). Modifications on the biocatalyst must be made in order to use the proposed automatic sampler when crystallization of products occurs.
机译:半合成青霉素的酶促合成是一种最有希望的替代方法,同时使抗生素同时结晶。反应堆运行的闭环优化需要测量其状态变量。本文介绍了一种在线监控这些变量(即物种浓度)的有效方法,该方法与过程的动态过程一致。多变量校准已被用来减少多组分系统中的分析时间,这就是这项工作的方法。比较了三种多元校正方法,以预测氨苄青霉素酶促合成中存在的组分的浓度。 UV光谱及其一阶导数用作模型的输入数据。结果表明,该方法的所有方法(SPA,PCR和PLS)都具有相似的性能。光谱的一阶导数的使用基本上没有改善方法的性能。进行了以固定化青霉素G酰基转移酶(PGA)为催化剂的氨苄西林合成的台式测定,以验证该方法。将其结果与HPLC分析进行比较。该技术对监测氨苄西林(所需产品)和6-氨基青霉酸(6-APA,最昂贵的底物)的浓度非常准确,其精密度与HPLC相似。初始反应器状态的先验信息可用于改善对较不敏感组分(苯基甘氨酸甲酯,PGME和苯基甘氨酸,PG)的估计。为了在出现产品结晶时使用建议的自动进样器,必须对生物催化剂进行修改。

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