Comparative Efficiency of Physical and Physicochemical Microencapsulation of some Medicinal Substances

Article Preview

Abstract:

Microencapsulation of drugs is used for a long time to improve their properties. It was carried out a comparative assessment of the physical and physicochemical methods of microencapsulation on the example of some drugs. The spray drying method was selected from the physical methods. Physicochemical method based on simple coacervation was implemented by changing the solvent. A study and comparison of the properties of the products were obtained by UV and IR spectroscopy, liquid chromatography, electron microscopy. It was carried out a comparative assessment of the release profile of the active substance from microcapsules obtained by various methods. Using the example of furacilin microcapsules has been shown an increase in the biological activity of substances encapsulated in water-soluble polymers. The particle size distribution was determined by analyzing their trajectories. The main advantages and disadvantages of the two investigated encapsulation methods are outlined.

You might also be interested in these eBooks

Info:

* - Corresponding Author

[1] V Suganya, V Anuradha Microencapsulation and Nanoencapsulation: A Review International, Journal of Pharmaceutical and Clinical Research. 9(3) (2017) 233-239.

Google Scholar

[2] Stepanova E.F. et al., Microcapsules: Prospects for Use in Modern Pharmaceutical Practice, Fundamental Research, Pyatigorsk. 3-4 (2014) 766 – 769.

Google Scholar

[3] N. Venkata Naga Jyothi, et al., Microencapsulation techniques, factors influencing encapsulation efficiency, Journal of Microencapsulation. 27(3) (2010) 187–197.

DOI: 10.3109/02652040903131301

Google Scholar

[4] Elena V. Grekhnyova, Tatyana N. Kudryavtseva, Ilona B. Kometiani, Yuriy O. Velyaev Microcapsulation of Furacilin as a Method of Creating New Medicinal Forms, Possessing with Increased Biological Accessibility and Prolongable Effect // Asian Journal of Pharmaceutics Vol 11, Issue 04, (2017).

Google Scholar

[5] Mustafin R.I. Comparative physicochemical and pharmaceutical research of polycomplex carriers based on EUDRAGIT® EPO AND EUDRAGIT® L 100-55 copolymers, Basic research. 12–6 (2014) 1231-1236.

Google Scholar

[6] Raghavendra C. Mundargi, Vidhya Rangaswamy, and Tejraj M. Aminabhavi. pH-Sensitive oral insulin delivery systems using Eudragit microspheres, Drug Development and Industrial Pharmacy. 37(8) (2011) 977–985.

DOI: 10.3109/03639045.2011.552908

Google Scholar

[7] Y. Georgieva, et al.Taste masking of enalapril maleate by microencapsulation in Eudragit EPO® microparticles, Pharmazie 75 (2020) 61-69.

Google Scholar

[8] Alekseev A.A., Bobrovnikov A.E., Terekhova R.P., Krutikov M.G. Microbiological assessment of the effectiveness of modern antimicrobial drugs for local treatment of burn wounds // Combustiology 4(37) (2009). URL: http://combustiolog.ru/journal/mikrobiologicheskaya-otsenka-e-ffektivnosti-sovremenny-hantimikrobny-h-preparatov-dlya-mestnogo-lecheniya-ozhogovy-h-ran (date of the application: 15.02.2021).

Google Scholar

[9] Gulyakin I.D., Oborotova N.A., Pechennikov V.M. Solubilization of hydrophobic anticancer drugs (review), Chemical-Pharmaceutical Journal 48(3) (2014) 46-50.

DOI: 10.1007/s11094-014-1078-7

Google Scholar