Effect of particle size on release of solid dispersed particles during the "Dissolution" test

Introduction. The use of the solid disperse systems method to increase the solubility of lipophilic active pharmaceutical ingredients is industrially applicable using different technologies, but the influence of particle size on the dissolution of these systems, depending on the method, is not suffi...

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Main Authors: S. A. Zolotov, A. V. Panov
Format: Article
Language:Russian
Published: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2025-06-01
Series:Разработка и регистрация лекарственных средств
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Online Access:https://www.pharmjournal.ru/jour/article/view/2098
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author S. A. Zolotov
A. V. Panov
author_facet S. A. Zolotov
A. V. Panov
author_sort S. A. Zolotov
collection DOAJ
description Introduction. The use of the solid disperse systems method to increase the solubility of lipophilic active pharmaceutical ingredients is industrially applicable using different technologies, but the influence of particle size on the dissolution of these systems, depending on the method, is not sufficiently reflected in the literature.Aim. To study the influence of the particle size of amorphous solid disperse systems "darunavir-water-soluble polymer" obtained by solvent removal and hot melt extrusion on the dissolution of Darunavir in the biological pH range of 1.2; 4.5 and 6.8.Materials and methods. Amorphous solid disperse systems were obtained in two ways: solvent removal and hot melt extrusion. Amorphism was determined by X-ray powder diffraction and electron microscopy. The efficiency of disperse systems was compared based on the results of the "Dissolution" test of powders mechanically ground to the same particle size in the biological pH range. The concentration of Darunavir in solution was determined using high-performance liquid chromatography with diode array detection.Results and discussion. The best result was shown by a solid dispersion system based on the Eudragit® E PO polymer with a particle size D90 of less than 10 μm. The increase in the concentration of Darunavir relative to the crystalline form corresponding to Darunavir ethanolate was 324, 2485, and 740%, respectively, in dissolution media with pH 1.2; 4.5, and 6.8.Conclusions. Methods for obtaining solid dispersion systems, such as solvent removal and hot melt extrusion with the same particle size, do not affect the concentration of the Darunavir API in solution in the biological pH range during the Dissolution test.
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spelling doaj-art-037843877e2d47409f69e718f447e1c92025-08-20T03:19:31ZrusLLC Center of Pharmaceutical Analytics (LLC «CPHA»)Разработка и регистрация лекарственных средств2305-20662658-50492025-06-0114214915510.33380/2305-2066-2025-14-2-20551363Effect of particle size on release of solid dispersed particles during the "Dissolution" testS. A. Zolotov0A. V. Panov1Limited Liability Company "AMEDART"MIREA – Russian Technological UniversityIntroduction. The use of the solid disperse systems method to increase the solubility of lipophilic active pharmaceutical ingredients is industrially applicable using different technologies, but the influence of particle size on the dissolution of these systems, depending on the method, is not sufficiently reflected in the literature.Aim. To study the influence of the particle size of amorphous solid disperse systems "darunavir-water-soluble polymer" obtained by solvent removal and hot melt extrusion on the dissolution of Darunavir in the biological pH range of 1.2; 4.5 and 6.8.Materials and methods. Amorphous solid disperse systems were obtained in two ways: solvent removal and hot melt extrusion. Amorphism was determined by X-ray powder diffraction and electron microscopy. The efficiency of disperse systems was compared based on the results of the "Dissolution" test of powders mechanically ground to the same particle size in the biological pH range. The concentration of Darunavir in solution was determined using high-performance liquid chromatography with diode array detection.Results and discussion. The best result was shown by a solid dispersion system based on the Eudragit® E PO polymer with a particle size D90 of less than 10 μm. The increase in the concentration of Darunavir relative to the crystalline form corresponding to Darunavir ethanolate was 324, 2485, and 740%, respectively, in dissolution media with pH 1.2; 4.5, and 6.8.Conclusions. Methods for obtaining solid dispersion systems, such as solvent removal and hot melt extrusion with the same particle size, do not affect the concentration of the Darunavir API in solution in the biological pH range during the Dissolution test.https://www.pharmjournal.ru/jour/article/view/2098darunavirsolid dispersionsdissolution testamorphousnessmicroscopy
spellingShingle S. A. Zolotov
A. V. Panov
Effect of particle size on release of solid dispersed particles during the "Dissolution" test
Разработка и регистрация лекарственных средств
darunavir
solid dispersions
dissolution test
amorphousness
microscopy
title Effect of particle size on release of solid dispersed particles during the "Dissolution" test
title_full Effect of particle size on release of solid dispersed particles during the "Dissolution" test
title_fullStr Effect of particle size on release of solid dispersed particles during the "Dissolution" test
title_full_unstemmed Effect of particle size on release of solid dispersed particles during the "Dissolution" test
title_short Effect of particle size on release of solid dispersed particles during the "Dissolution" test
title_sort effect of particle size on release of solid dispersed particles during the dissolution test
topic darunavir
solid dispersions
dissolution test
amorphousness
microscopy
url https://www.pharmjournal.ru/jour/article/view/2098
work_keys_str_mv AT sazolotov effectofparticlesizeonreleaseofsoliddispersedparticlesduringthedissolutiontest
AT avpanov effectofparticlesizeonreleaseofsoliddispersedparticlesduringthedissolutiontest