Chromatographic purification of bovine testicular hyaluronidase
- Authors: Melnikova I.V1, Yashtubaeva A.D1, Glazova N.V1
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Affiliations:
- St. Petersburg State Chemical-Pharmaceutical University
- Issue: Vol 22, No 4 (2019)
- Pages: 29-34
- Section: Articles
- URL: https://journals.eco-vector.com/1560-9596/article/view/112628
- DOI: https://doi.org/10.29296/25877313-2019-04-05
- ID: 112628
Cite item
Abstract
Hyaluronidase is an enzyme that breaks down the acidic mucopolysaccharides which are the basis of connective tissue. Integration and analysis of the literature data of different authors, that presented in the article [1], and comparative analysis of the properties of hyaluronidase from different sources, that was carried out at the Department of Biotechnology SPCPU [2], showed that hyaluroni-dases isolated from various sources possess different physicochemical characteristics such as molecular weight, the range of enzymatic activities, stability etc. Therefore, the choice of raw materials determines the approaches to hyaluronidase isolation and purification. In this investigation the bovine testes were chosen as a raw material, since currently only this raw material is used to produce hyaluroni-dase on an industrial scale. Studies of ion exchange sorption of hyaluronidase from the bovine testes showed that the enzyme is selectively sorbed on macroporous sulfocationite KU-23 [3, 4]. The use of this chromatographic method made it possible to replace the unsustainable conventional method of isolating hyaluronidase using organic solvents. However, ionite KU-23 is currently commercially unavailable, that's why the selection of modern sorbent for the isolation and purification of hyaluronidase is a crucial task. The aim of this investigation was to develop a chromatographic procedure of hyaluronidase purification from test solution with the use of modern macroporous sorbents. Materials and methods. The object of research - hyaluronidase in active pharmaceutical ingredient «Lidaza», which is manufactured by «Samson-Med". The object of research is a test solution of hyaluronidase with a protein concentration 10 mg / ml and pH 4.0-4.5. Methods: method for determination of protein with the use of biuret reagent [5]; method for determination of hyaluronidase activity in solution [6]; method for preparation of sorbents [7, 8]; method of chromatographic procedure under static and dynamic condition. Conclusion. The study of chromatographic purification of hyaluronidase under static and dynamic conditions with the use of macroporous sorbents revealed that the optimal sorbent is Nuvia™ S (Bio-Rad Laboratories, Inc). That sorbent provides for the maximum of the protein and hyaluronidase activity yield. Hereafter Nuvia™ S can be used for isolation and purification of hyaluronidase from the orchic extract. New technology can replace conventional technology that uses organic solvents.
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About the authors
I. V Melnikova
St. Petersburg State Chemical-Pharmaceutical University
Email: yana.melnikova@pharminnotech.com
Post-graduate Student, Department of Biotechnology
A. D Yashtubaeva
St. Petersburg State Chemical-Pharmaceutical UniversityMaster Student, Department of Biotechnology
N. V Glazova
St. Petersburg State Chemical-Pharmaceutical UniversityPh.D. (Chem.), Associate Professor, Department of Biotechnology
References
- Мельникова Я.В., Глазова Н.В. Свойства и биологическая роль гиалуронидаз из различных источников сырья // Сб. материалов VIII Всеросс. науч. конф. студентов и аспирантов с международным участием «Молодая Фармация - потенциал будущего», Санкт-Петербург, 23.04.18-24.04.18. СПб.: СПХФУ. 2018. С. 259-263.
- Заинкова Н.В. Получение и сравнительный анализ свойств гиалуронидаз из различных источников: Автореф. дис.. канд. биол. наук: 03.00.04. СПб. 1998. 142 с
- Игонина Л.М. Хроматографическое выделение и изучение свойств фермента гиалуронидазы из семенников крупного рогатого скота: Автореф. дис. канд. хим. наук: 03.00.04. СПб. 1996. 134 с.
- Igonina L.M., Glazova N.V., El'kin G.E., Zainkova N. V. Sorption of hyaluronidase to macroporous sorbents // Applied Biochemistry and Microbiology. 1998. V. 34. № 5. 442-445.
- Государственная Фармакопея XIII. Т. 1. М.: ФЭМБ. 2015. 1469 с.
- Патент № 2417097 (РФ). Фармацевтическая композиция, содержащая гиалуронидазу и липосомы для наружного применения / В.Л. Багирова, Н.В. Глазова, М.Д. Дулькис, В.Н. Иванов. 27.04.11.
- ГОСТ 20298-74. Смолы ионообменные. Катиониты. Технические условия (с Изменениями № 1-5). М.: Издательство стандартов. 1991. 13 с.
- UNOsphere™ S and Q, Macro-Prep®, Nuvia™ S and Q High-Capacity Ion Exchange Media Instruction manual. BioRad Laboratories Inc.
- Патент № 2658605 (РФ). Способ получения гиалурони-дазы из семенников крупного рогатого скота / Н.В. Глазова, А.М. Элиханов, О.В. Чайка, Я.В. Мельникова, О.Г. Дудник. 21.06.18.