Valorizing natural waste materials is crucial for sustainable biomedical innovation. This study explores a nanomedicine approach using waste from shrimp shells, pomegranate peels, and snail mucus to produce mucinstabilized chitosan nanoparticles (CSNPs-M) as delivery systems for Punica granatum peel extract (PgPE). Chitosan was derived from shrimp shells, while mucins from Helix aspersa snail slime served as a bio-stabilizer and crosslinking agent, creating CSNPs-M through an eco-friendly synthesis. Characterization confirmed CSNPs-M are spherical (54–98 nm) with a zeta potential of − 35.5 mV. The encapsulation efficiency is about 79 %, indicating effective loading of the Punica granatum peel extract within the CSNPs-M nanoparticles. Antioxidant capacity, tested by ABTS scavenging activity, showed that CSNPs-M achieved 89 % inhibition, close to free PgPE (93 %), indicating preserved extract activity. CSNPs-M also exhibited antimicrobial activity against several bacteria and fungi. The antiproliferative activity was evaluated by monitoring cell growth after 24, 48, and 72 h of incubation with CSNPs-M in human colon adenocarcinoma cells (Caco-2), showing that CSNPs-M at a 1: 50 dilution significantly reduced cell proliferation (p 〈0,0001) without any cytotoxic effects. This study addresses a critical need for eco-friendly nanocarriers with preserved bioactivity, presenting CSNPsM as a promising platform for delivering therapeutic compounds in biomedical applications.

Djabali, D., Naimi, D., Panzavolta, S., Caliceti, C., Punzo, A., Bramki, A., et al. (2025). Harnessing Helix aspersa mucins as an innovative gelling agent for the synthesis of Punica granatum peel extract-loaded chitosan nanoparticles (CSNPs-M) with enhanced biological properties. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 308, 142152-142164 [10.1016/j.ijbiomac.2025.142152].

Harnessing Helix aspersa mucins as an innovative gelling agent for the synthesis of Punica granatum peel extract-loaded chitosan nanoparticles (CSNPs-M) with enhanced biological properties

Silvia Panzavolta;Cristiana Caliceti;Angela Punzo;Valentina Di Matteo;
2025

Abstract

Valorizing natural waste materials is crucial for sustainable biomedical innovation. This study explores a nanomedicine approach using waste from shrimp shells, pomegranate peels, and snail mucus to produce mucinstabilized chitosan nanoparticles (CSNPs-M) as delivery systems for Punica granatum peel extract (PgPE). Chitosan was derived from shrimp shells, while mucins from Helix aspersa snail slime served as a bio-stabilizer and crosslinking agent, creating CSNPs-M through an eco-friendly synthesis. Characterization confirmed CSNPs-M are spherical (54–98 nm) with a zeta potential of − 35.5 mV. The encapsulation efficiency is about 79 %, indicating effective loading of the Punica granatum peel extract within the CSNPs-M nanoparticles. Antioxidant capacity, tested by ABTS scavenging activity, showed that CSNPs-M achieved 89 % inhibition, close to free PgPE (93 %), indicating preserved extract activity. CSNPs-M also exhibited antimicrobial activity against several bacteria and fungi. The antiproliferative activity was evaluated by monitoring cell growth after 24, 48, and 72 h of incubation with CSNPs-M in human colon adenocarcinoma cells (Caco-2), showing that CSNPs-M at a 1: 50 dilution significantly reduced cell proliferation (p 〈0,0001) without any cytotoxic effects. This study addresses a critical need for eco-friendly nanocarriers with preserved bioactivity, presenting CSNPsM as a promising platform for delivering therapeutic compounds in biomedical applications.
2025
Djabali, D., Naimi, D., Panzavolta, S., Caliceti, C., Punzo, A., Bramki, A., et al. (2025). Harnessing Helix aspersa mucins as an innovative gelling agent for the synthesis of Punica granatum peel extract-loaded chitosan nanoparticles (CSNPs-M) with enhanced biological properties. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 308, 142152-142164 [10.1016/j.ijbiomac.2025.142152].
Djabali, Dounia; Naimi, Dalila; Panzavolta, Silvia; Caliceti, Cristiana; Punzo, Angela; Bramki, Amina; DI MATTEO, Valentina; Bouhadjar, Meroua...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/1011385
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