TY - JOUR
T1 - Comparative evaluation of erythromycin release and mechanical properties in gelatin, hydrolyzed carrageenan, and carrageenan-maltodextrin hard-shell capsules
AU - Fauzi, Muhammad Al Rizqi Dharma
AU - Pudjiastuti, Pratiwi
AU - Susanti, Tri
AU - Haqiqoh, Syahnur
AU - Wafiroh, Siti
AU - Hendradi, Esti
AU - Mawazi, Saeid Mezail
AU - Haryanto, Riki
AU - Widodo, Riyanto Teguh
N1 - Publisher Copyright:
© Fauzi MARD et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited https://creativecommons.org/licenses/by/4.0/
PY - 2026
Y1 - 2026
N2 - The mechanical behavior, formulation performance, and erythromycin release kinetics of hard-shell capsules prepared from gelatin, hydrolyzed carrageenan (HC), and hydrolyzed carrageenan-maltodextrin (HC-MD) systems were comparatively evaluated. Capsules were produced using a dip-coating method and assessed for weight variation, mechanical strength, degree of swelling, disintegration time, dissolution profile, drug release kinetics, and surface wettability via contact angle measurements. Erythromycin release at pH 1.2, 4.5, and 6.8 followed diffusion- and surface-area-controlled kinetics, consistent with zero-order, first-order, Higuchi, and Hixson-Crowell models. Both HC and HC-MD capsules exhibited faster disintegration, greater swelling, and higher drug release than gelatin capsules, particularly under neutral and basic conditions. The HC-MD formulation demonstrated superior wettability and lower contact angles, which enhanced drug diffusion across the capsule surface.
AB - The mechanical behavior, formulation performance, and erythromycin release kinetics of hard-shell capsules prepared from gelatin, hydrolyzed carrageenan (HC), and hydrolyzed carrageenan-maltodextrin (HC-MD) systems were comparatively evaluated. Capsules were produced using a dip-coating method and assessed for weight variation, mechanical strength, degree of swelling, disintegration time, dissolution profile, drug release kinetics, and surface wettability via contact angle measurements. Erythromycin release at pH 1.2, 4.5, and 6.8 followed diffusion- and surface-area-controlled kinetics, consistent with zero-order, first-order, Higuchi, and Hixson-Crowell models. Both HC and HC-MD capsules exhibited faster disintegration, greater swelling, and higher drug release than gelatin capsules, particularly under neutral and basic conditions. The HC-MD formulation demonstrated superior wettability and lower contact angles, which enhanced drug diffusion across the capsule surface.
KW - carrageenan
KW - erythromycin
KW - good health and well-being
KW - hard-shell capsule
KW - release kinetics
UR - https://www.scopus.com/pages/publications/105028113310
U2 - 10.3897/pharmacia.73.e174090
DO - 10.3897/pharmacia.73.e174090
M3 - Article
AN - SCOPUS:105028113310
SN - 0428-0296
VL - 73
JO - Pharmacia
JF - Pharmacia
M1 - e174090
ER -