Table 4.
Summary of fabrication methods and encapsulation of hydrophilic and hydrophobic bioactives by polysaccharide nanogel.
Bioactive encapsulant and encapsulant type | Encapsulation technique | Nanogel composition | Encapsulation efficiency (%) | Loading methods of bioactive ingredient | Reference |
---|---|---|---|---|---|
Curcumin (Hydrophobic) |
Physically crosslinked method | Aminated chitosan, tripolyphosphate, folate acid | 94 | Curcumin was dispersed in an aminated chitosan, folate acid, or tripolyphosphate solution followed by ultrasound treatment. Centrifuged the dispersion and washed the precipitates with acetic acid solution and deionized water to obtain the nanogel. | (X. Sun et al., 2019) |
Curcumin (Hydrophobic) |
Physically crosslinked method | Sodium alginate, CS, calcium chloride | 10–13 | Incorporating curcumin-ethanol stock solution in calcium chloride solution. The solution was added to the sodium alginate aqueous solution, and the CS solution was dropped into the system. | (R. K. Das, Kasoju, & Bora, 2010) |
Curcumin (Hydrophobic) |
Physically crosslinked method | Soybean protein isolate-dextran conjugate (SDC) | 89.1 | SDC was dissolved in water through pH adjustment and thermal treatment. Subsequently, incorporate curcumin ethanolic solution into the system through homogenization. The final curcumin-loaded nanogel is obtained through centrifugation and lyophilization processes. | (Y. X. Sun et al., 2024) |
Resveratrol (Hydrophobic) |
Physically crosslinked method | Trimethyl chitosan | 46–72 | Add RV to TMC aqueous solution. Introduce a TPP, alginate, or a mixed solution of TPP and alginate dropwise into the resultant solution. | (Min et al., 2018) |
Curcumin (Hydrophobic) |
Chemically crosslinked method | Chitosan hydrochloride, carboxymethyl starch | 89–94 | A curcumin-ethanol solution was added to the CHC solution to prepare the Cur-CHC stock solution. CMC solution of carboxyl groups activated by EDC was added into the stock solution to form amide bond and followed by washing and centrifugation to get nanogel. |
(X. M. Li et al., 2019) |
β-Carotene (Hydrophobic) |
Physically crosslinked method | Pectin, 2-hydroxypropyl-β-cyclodextrin (HP-CD) | – | β-Carotene-acetone solution was added to the preheated HP-CD solution with stirring. After evaporating acetone, the resultant solution was dropwise to pectin solution to obtain the final nanoparticle. | (Celitan et al., 2022) |
Riboflavin (Hydrophillic) and quercetin (Hydrophobic) | Physically crosslinked method | Gallic acid modified chitosan (GCS), Ovalbumin (OVA) | 66 (riboflavin) 96 (quercetin) |
Add riboflavin-water or quercetin-ethanol solution to the OVA solution with stirring. Introduce the resultant solution into GCS solution and supplement with calcium chloride solution to obtain nanoparticles. | (L. Li et al., 2022) |
Green coffee extract (Hydrophillic) |
Chemically crosslinked method | Carrageenan, | – | Dissolve Carrageenan in water, then incorporate green coffee extract at varying concentrations. Subsequently, the mixture is combined with glutaraldehyde to form crosslinked networks and purified through dialysis to yield the final nanogel systems. | (Khalaf, Gouda, Taleb, Heakal, & El-Lateef, 2024) |
Blueberry anthocyanins (Hydrophillic) |
Physically crosslinked method | Olive pectin (PC), chitosan (CS) | 92 | ANCs and PC solution were added to CS-acetic acid solution and followed by adjusting pH of this system. |
(C. Xie et al., 2023) |
Oyster peptides (Hydrophillic) |
Physically crosslinked method | Carboxymethyl chitosan, carboxymethyl cellulose | 92.7 | Commence by incorporating oyster peptide solution into carboxymethyl chitosan to form a homogeneous mixture. Subsequently, introduce this mixture into the carboxymethyl cellulose solution. The nanogel was obtained by pH adjustment and thermal treatment | (P. Zhang et al., 2024) |
Blueberry anthocyanins (Hydrophillic) |
Physically crosslinked method | Pectin, lysozyme | 73 | Mix the pectin, lysozyme, and anthocyanin solution with pH 5 in the ice bath, followed by stirring at room temperature to form a nanogel. | (Rosales, da Silva, Lourenço, Hassimotto, & Fabi, 2021) |
Anthocyanins (Hydrophoillic) |
Physically crosslinked method | Chitosan, pectin | 67 | Anthocyanin powder was added to the chitosan solution to form CS-ANC complexes, followed by dropwise pectin solution into the mixture to form nanogel. | (Zhao et al., 2020) |
Cyanidin-3-glucoside (Hydrophillic) |
Physically crosslinked method | Carboxymethyl chitosan (CMC), β-cyclodextrin graft epichlorohydrin (β-CD-EP), CaCl2 | 48 | Combine C3G, β-CD-EP, CMC solution, and CaCl2 solution with carboxymethyl chitosan solution. Stir at 800 rpm for 30 min to form a nanogel. | (J. Sun et al., 2022) |