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. 2025 Mar 22;26(7):2885.
doi: 10.3390/ijms26072885.

Synthesis, Characterization, and Preliminary Analysis of Squid Pen Trypsin Hydrolysates and Chitosan Microcapsules

Affiliations

Synthesis, Characterization, and Preliminary Analysis of Squid Pen Trypsin Hydrolysates and Chitosan Microcapsules

Ruimin Li et al. Int J Mol Sci. .

Abstract

Squid pen (SP) was found to contain 64.41% protein and 26.03% chitin. The amino acid composition revealed that Met was the most abundant amino acid in SP, with a concentration of 13.67 g/100 g. To enhance the stability and bioavailability of SP hydrolysates, microcapsules were developed using ultrasonic emulsification techniques with SP trypsin hydrolysates (SPTH) and SP β-chitosan (SPC). The optimal preparation conditions involved using a 2% concentration of SPC, a 4 mg/mL concentration of SPTH, a core-to-wall ratio (v/v) of 1:3 for SPTH/SPC, and subjecting them to ultrasonic treatment for 20 min. These microcapsules had a loading capacity of 58.95% for SPTH under these conditions. The successful encapsulation of SPTH in the SPC complex to form SPC-SPTH microcapsules was confirmed by FTIR, XRD, DSC, and SEM, exhibiting good thermal stability, small particle size, and high encapsulation efficiency. In vitro digestion studies demonstrated a release of 15.61% in simulated gastric fluid and 69.32% in intestinal fluid, achieving targeted release in the intestines. The digested products exhibited superior antioxidant activity compared to free SPTH digests, suggesting that microencapsulation effectively preserves SPTH bioactivity. This study enhances the bioavailability of SPTH and offers a promising delivery system for natural compounds with low bioavailability and stability.

Keywords: antioxidant activity; microcapsules; squid pen trypsin hydrolysates; structural characterization; β-chitosan.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Release profiles of SPTH-SPC microcapsules.
Figure 2
Figure 2
SEM of SPTH-SPC microcapsules at different magnifications. (a) 20,000×; (b) 10,000×; (c) 5000×; (d) 2000×.
Figure 3
Figure 3
FTIR of SPC, SPTH, and SPTH-SPC microcapsules.
Figure 4
Figure 4
XRD of SPC, SPTH, and SPTH-SPC microcapsules.
Figure 5
Figure 5
DSC of SPC, SPTH, and SPTH-SPC microcapsules.
Figure 6
Figure 6
Particle size and ζ-potential of SPC, SPTH, and SPTH-SPC microcapsules: (a) Particle size; (b) ζ-potential.
Figure 7
Figure 7
Antioxidant activity of SPTH-SPC microcapsules before and after digestion. DPPH· represents DPPH· radical scavenging activity, ·OH represents hydroxyl radical scavenging activity, ABTS·+ represents ABTS·+ scavenging activity, O2·− represents O2·− scavenging activity, R represents reducing power, Fe2+ represents chelating activity of ferrous ions, T represents total antioxidant activity. The lowercase letters represent significant differences (p < 0.05) in the activity of SPC-SPTH microcapsules before and after simulated gastric and intestinal digestion in vitro.

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