SELECTION OF A METHOD FOR STERILIZATION OF NANOSTRUCTURED BIOMATERIAL BASED ON BACTERIAL CELLULOSE

Authors

DOI:

https://doi.org/10.26577/bb20251057
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Keywords:

BC/HAp/MXene, nanocomposite, sterilization methods, cold plasma, ethylene oxide, supercritical CO₂

Abstract

Nanocomposites based on bacterial cellulose (BC), hydroxyapatite (HAp), and MXene represent a promising class of biomaterials for regenerative medicine and photothermal technologies due to their combination of biocompatibility, mechanical stability, electrical conductivity, and strong infrared absorption capability. However, the high sensitivity of MXene phases and the cellulose matrix to physicochemical impacts requires careful selection of sterilization approaches that provide sterility without substantial loss of key functional properties. This study presents a comparative evaluation of nine sterilization methods – autoclaving, dry heat, ethylene oxide treatment, γ-irradiation, electron beam (E-beam) irradiation, ultraviolet irradiation, ozonation, supercritical CO₂ treatment, and cold plasma – applied to BC/HAp/MXene nanocomposites. Sterility was assessed by direct plating on nutrient media; sterilization efficiency was calculated based on microbial growth. Complete sterility was achieved for all methods except UV (50%) and CO₂ treatment (90%). The effects of sterilization on material structure and properties were analyzed using SEM imaging, porosity measurement, mechanical testing, electrical conductivity assessment, and photothermal activity evaluation. Thermal treatment and ozonation caused the most pronounced structural damage and reduction in mechanical strength. Radiation-based methods induced moderate changes, whereas ethylene oxide, supercritical CO₂, and cold plasma treatment resulted in minimal morphological degradation. Cold plasma and EtO preserved up to 94–98% of the initial conductivity and photothermal response, while thermal treatment led to significant loss of functional performance due to thermo-oxidative degradation of MXene. Comprehensive analysis demonstrated that cold plasma and ethylene oxide provide the best balance between sterility and preservation of structural–functional properties of BC/HAp/MXene nanocomposites. These methods are the most promising for preparing such materials for biomedical applications.

Author Biographies

I.S. Savitskaya, 1Al-Farabi Kazakh National University, Almaty, Kazakhstan

Savitskaya Irina Stanislavovna – Doctor of Biological Sciences, Professor, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: irasava_2006@mail.ru )

D.Kh. Shokatayeva, Al-Farabi Kazakh National University, Almaty, Kazakhstan

Shokatayeva Dina Khabdulmanatovna – PhD, Senior Lecturer, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: shokatayeva.dina@kaznu.kz)

I.I. Abashidze, ТОО «Клиника AMD», Алматы, Казахстан

Shokatayeva Dina Khabdulmanatovna – PhD, Senior Lecturer, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: shokatayeva.dina@kaznu.kz)

A.B. Talipova, Al-Farabi Kazakh National University, Almaty, Kazakhstan

Talipova Aizhan Berikovna – PhD student, Senior Lecturer, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: talipova.aizhan@gmail.com).

S.D. Zhantlessova, Al-Farabi Kazakh National University, Almaty, Kazakhstan

Zhantlessova Sirina Duissenovna – PhD, Senior Lecturer, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: sirina.zhantlessova@mail.ru).

Zh. Khamitkyzy, Al-Farabi Kazakh National University, Almaty, Kazakhstan

Khamitkyzy Zhazira – PhD student, Department of Biotechnology, Al-Farabi Kazakh National University (Almaty, Kazakhstan; e-mail: bailovazhazira@gmail.com).

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How to Cite

Savitskaya, I. ., Shokatayeva, D. ., Abashidze, I. ., Talipova, A. ., Zhantlessova, S. ., & Khamitkyzy, Z. (2025). SELECTION OF A METHOD FOR STERILIZATION OF NANOSTRUCTURED BIOMATERIAL BASED ON BACTERIAL CELLULOSE . Experimental Biology, 105(4), 78–90. https://doi.org/10.26577/bb20251057