Abstract

Introduction . Saturated polymer microspheres represent one of the leading developments in the field of chemoembolization. Due to the complicated multi-stage production in the Russian market, mainly foreign manufacturers of these products are represented, which may indicate the relevance of studying this topic. Aim . The aim of the work was to develop a technological scheme for the production of polymer microspheres and a description of critical control points of production. Materials and methods . The study of the intermediate product was carried out using a Levenhuk D320L microscope (Levenhuk Inc, USA). Analysis of production control points was carried out by the HACCP (Hazard analysis and critical control points) method. Results and discussion . As a result of the study, the main technological stages of the production of microspheres, which are a copolymer of vinyl alcohol and sodium acrylate, have been identified and described. For each technological stage, control critical points are determined with an indication of the controlled parameters and control methods. The photographs of the intermediate product at intermediate stages are shown. Conclusion . A technological scheme for the production of microspheres has been developed. The analysis of critical control points of the stages of the main production process is carried out. Identified irreversible critical points of production.

Highlights

  • Saturated polymer microspheres represent one of the leading developments in the field of chemoembolization

  • Due to the complicated multi-stage production in the Russian market, mainly foreign manufacturers of these products are represented, which may indicate the relevance of studying this topic

  • The aim of the work was to develop a technological scheme for the production of polymer microspheres and a description of critical control points of production

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Summary

Conclusion

The analysis of critical control points of the stages of the main production process is carried out. Процедура с использованием данных препаратов позволяет поддерживать достаточно высокие концентрации химиопрепарата в опухоли, но лекарственное средство удерживается носителем непродолжительное время (до нескольких часов), кроме того, такие препараты не способны вызывать длительную или необратимую эмболизацию сосудов и нередко тяжело переносятся пациентами, вызывая сильные боли [1, 5]. Данный вид эмболического материала позволяет доставить препарат к опухоли, произвести окклюзию сосудов и обеспечить продолжительное контролируемое высвобождение препарата при минимальном выбросе в системный кровоток [6]. По сравнению с масляными эмболическими материалами полимерные микросферы способны высвобождать лекарственное средство в течение длительного времени (не менее месяца), вместе с этим обеспечивая полное прекращение кровоснабжения злокачественного новообразования [1, 3, 4, 7]. Цель настоящего исследования – разработка технологической схемы производства полимерных микросфер и описание критических контрольных точек производства

МАТЕРИАЛЫ И МЕТОДЫ
РЕЗУЛЬТАТЫ И ОБСУЖДЕНИЕ
Апирогенность Apyrogenicity
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