Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors

Objectives. The introduction of digital tools for the development of medicines, intelligent management systems, and quality control is stipulated not only by modern requirements for the chemical and pharmaceutical industry but also by strict regulatory requirements for manufactured products. This pr...

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Main Authors: V. F. Kornyushko, O. M. Nikolaeva, A. V. Panov, R. R. Biglov, A. S. Kuznetsov
Format: Article
Language:Russian
Published: MIREA - Russian Technological University 2021-07-01
Series:Тонкие химические технологии
Subjects:
Online Access:https://www.finechem-mirea.ru/jour/article/view/1713
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spelling doaj-81abe9010bd5430c8509cf9dc65ae8a82021-07-28T13:24:03ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752021-07-0116325226610.32362/2410-6593-2021-16-3-252-2661641Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactorsV. F. Kornyushko0O. M. Nikolaeva1A. V. Panov2R. R. Biglov3A. S. Kuznetsov4MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)MIREA – Russian Technological University (M.V. Lomonosov Institute of Fine Chemical Technologies)Objectives. The introduction of digital tools for the development of medicines, intelligent management systems, and quality control is stipulated not only by modern requirements for the chemical and pharmaceutical industry but also by strict regulatory requirements for manufactured products. This principle ensures the release of a quality product on the first attempt. The aim of this study is to develop information support for the intelligent quality management system for the production of active pharmaceutical substances (APSs) for medicines using a fundamentally new technology: continuous synthesis in flow microreactors. To develop the necessary information support, we developed appropriate systemic, informational, and mathematical models; algorithms for the online management of the experiment; and techniques and algorithms to qualitatively assess whether the product meets official regulatory documents.Methods. System analysis techniques, information and mathematical modeling techniques with multireference regression models, and online optimization using the Hook–Jeevs algorithm (a method of expert evaluation based on the concordance factor) were used to solve the problems formulated.Results. To manage the quality of the process of continuous APS synthesis in the flow microreactor, we developed theoretic multiple system models that were designed to build the digital information environment for the process of experimental research. We developed algorithms for mathematical modeling and optimization of the control process based on multiresponse regression models and an online optimization algorithm that allows the process to be managed step by step, taking into account the limitations. Our results show that the degree of conversion is higher in reactions that contain bromodiphenylmethan.Conclusions. Based on mathematical modeling method algorithms for the quality control of the process of continuous APS synthesis on a fundamentally new microreactor system, Qmix were developed. The applicability of the proposed methods and algorithms in the production of the drug diphenhydramine from chlorobenzohydrol and bromobenzohydrol as initial substances was proven by an experimental study. The built models were statistically adequate and valid.https://www.finechem-mirea.ru/jour/article/view/1713continuous synthesis in flow microreactorsactive pharmaceutical substancetheoretic multiple system modelsmulticell regression modelsonline optimizationhook–jeeves methodexpert evaluationconcordance factordiphenhydramine drug
collection DOAJ
language Russian
format Article
sources DOAJ
author V. F. Kornyushko
O. M. Nikolaeva
A. V. Panov
R. R. Biglov
A. S. Kuznetsov
spellingShingle V. F. Kornyushko
O. M. Nikolaeva
A. V. Panov
R. R. Biglov
A. S. Kuznetsov
Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
Тонкие химические технологии
continuous synthesis in flow microreactors
active pharmaceutical substance
theoretic multiple system models
multicell regression models
online optimization
hook–jeeves method
expert evaluation
concordance factor
diphenhydramine drug
author_facet V. F. Kornyushko
O. M. Nikolaeva
A. V. Panov
R. R. Biglov
A. S. Kuznetsov
author_sort V. F. Kornyushko
title Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
title_short Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
title_full Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
title_fullStr Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
title_full_unstemmed Quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
title_sort quality management of the chemical-technological process for continuous synthesis of pharmaceutical substances of medicinal compounds in flow microreactors
publisher MIREA - Russian Technological University
series Тонкие химические технологии
issn 2410-6593
2686-7575
publishDate 2021-07-01
description Objectives. The introduction of digital tools for the development of medicines, intelligent management systems, and quality control is stipulated not only by modern requirements for the chemical and pharmaceutical industry but also by strict regulatory requirements for manufactured products. This principle ensures the release of a quality product on the first attempt. The aim of this study is to develop information support for the intelligent quality management system for the production of active pharmaceutical substances (APSs) for medicines using a fundamentally new technology: continuous synthesis in flow microreactors. To develop the necessary information support, we developed appropriate systemic, informational, and mathematical models; algorithms for the online management of the experiment; and techniques and algorithms to qualitatively assess whether the product meets official regulatory documents.Methods. System analysis techniques, information and mathematical modeling techniques with multireference regression models, and online optimization using the Hook–Jeevs algorithm (a method of expert evaluation based on the concordance factor) were used to solve the problems formulated.Results. To manage the quality of the process of continuous APS synthesis in the flow microreactor, we developed theoretic multiple system models that were designed to build the digital information environment for the process of experimental research. We developed algorithms for mathematical modeling and optimization of the control process based on multiresponse regression models and an online optimization algorithm that allows the process to be managed step by step, taking into account the limitations. Our results show that the degree of conversion is higher in reactions that contain bromodiphenylmethan.Conclusions. Based on mathematical modeling method algorithms for the quality control of the process of continuous APS synthesis on a fundamentally new microreactor system, Qmix were developed. The applicability of the proposed methods and algorithms in the production of the drug diphenhydramine from chlorobenzohydrol and bromobenzohydrol as initial substances was proven by an experimental study. The built models were statistically adequate and valid.
topic continuous synthesis in flow microreactors
active pharmaceutical substance
theoretic multiple system models
multicell regression models
online optimization
hook–jeeves method
expert evaluation
concordance factor
diphenhydramine drug
url https://www.finechem-mirea.ru/jour/article/view/1713
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AT avpanov qualitymanagementofthechemicaltechnologicalprocessforcontinuoussynthesisofpharmaceuticalsubstancesofmedicinalcompoundsinflowmicroreactors
AT rrbiglov qualitymanagementofthechemicaltechnologicalprocessforcontinuoussynthesisofpharmaceuticalsubstancesofmedicinalcompoundsinflowmicroreactors
AT askuznetsov qualitymanagementofthechemicaltechnologicalprocessforcontinuoussynthesisofpharmaceuticalsubstancesofmedicinalcompoundsinflowmicroreactors
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