Characterization, in vitro dissolution and release kinetics of salicylamide in capsule shells made from κ-carrageenan-hydroxypropyl methylcellulose

This study aimed to characterize, in vitro dissolution, and evaluate the release kinetics of salicylamide in capsule shells made from κ-carrageenan-HPMC. The capsule shell was prepared using the dipping method with CRG: HPMC (1:1, 1:2, 1:3) ratio, supplemented with sorbitol and antifoam silicone emulsion. Characterization was conducted using FTIR, SEM-EDX mapping, AFM, hardness, and swelling degree experiments. The results indicated that the optimal capsule shells were obtained at a CRG: HPMC ratio of 1:2, with a hardness of 7.04 N and a swelling degree of 299.79 % at 15 mins. FTIR analysis revealed the wavenumber of sulfate groups, and SEM-EDX mapping indicated evenly distributed elemental composition. AFM analysis of capsules showed that the surface texture was rough. The disintegration times at different pH levels were 55, 53, and 24 min at pH 1.2; 4.5 and 6.8, respectively. The in vitro dissolution test showed salicylamide release of 6.40, 8.51, and 11.51 % in 120 min at pH 1.2, 4.5, and 6.8, respectively. The release kinetics followed a zero-order model at pH 1.2 and 6.8 and the Ritger-Peppas model at pH 4.5. The CRG-HPMC/sorbitol capsule shells exhibited good physicochemical characteristics with a controlled drug release profile and thereby supporting SDGs 3 and 14.

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Publication Details

Journal
International Journal of Biological Macromolecules
Published
2025-09-08
DOI
https://doi.org/10.1016/j.ijbiomac.2025.147539
Citations
1
Primary Topic
Enzyme Production and Characterization
Type
article
Field-Weighted Citation Impact
1.23
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article

Characterization, in vitro dissolution and release kinetics of salicylamide in capsule shells made from κ-carrageenan-hydroxypropyl methylcellulose

Esti Hendradi, Tri Susanti, Pratiwi Pudjiastuti, Siti Wafiroh et al.
1 citations
International Journal of Biological Macromolecules
Enzyme Production and Characterization
1.23
article

Characterization, in vitro dissolution and release kinetics of salicylamide in capsule shells made from κ-carrageenan-hydroxypropyl methylcellulose

Esti Hendradi, Tri Susanti, Pratiwi Pudjiastuti, Siti Wafiroh, Muhammad Yasin, Oktavia Eka Puspita, Riyanto Teguh Widodo, Syahnur Haqiqoh
article en
1 citations

Abstract

This study aimed to characterize, in vitro dissolution, and evaluate the release kinetics of salicylamide in capsule shells made from κ-carrageenan-HPMC. The capsule shell was prepared using the dipping method with CRG: HPMC (1:1, 1:2, 1:3) ratio, supplemented with sorbitol and antifoam silicone emulsion. Characterization was conducted using FTIR, SEM-EDX mapping, AFM, hardness, and swelling degree experiments. The results indicated that the optimal capsule shells were obtained at a CRG: HPMC ratio of 1:2, with a hardness of 7.04 N and a swelling degree of 299.79 % at 15 mins. FTIR analysis revealed the wavenumber of sulfate groups, and SEM-EDX mapping indicated evenly distributed elemental composition. AFM analysis of capsules showed that the surface texture was rough. The disintegration times at different pH levels were 55, 53, and 24 min at pH 1.2; 4.5 and 6.8, respectively. The in vitro dissolution test showed salicylamide release of 6.40, 8.51, and 11.51 % in 120 min at pH 1.2, 4.5, and 6.8, respectively. The release kinetics followed a zero-order model at pH 1.2 and 6.8 and the Ritger-Peppas model at pH 4.5. The CRG-HPMC/sorbitol capsule shells exhibited good physicochemical characteristics with a controlled drug release profile and thereby supporting SDGs 3 and 14.

International Journal of Biological MacromoleculesVol. 328(Pt 1)
University of Brawijaya (ID), Universitas Airlangga (ID), University of Malaya (MY)
Openalex Percentile: Top 18%
Enzyme Production and Characterization
1.23
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Characterization, in vitro dissolution and release kinetics of salicylamide in capsule shells made from κ-carrageenan-hydroxypropyl methylcellulose — Esti Hendradi, Tri Susanti, et al. · International Journal of Biological Macromolecules (2025) | TGRS Research Map | TGRS