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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles <t>(QPNPs).</t> ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).
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( A ) Particle size and PDI of quinoa peptide nanoparticles (QPNPs). ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).

Journal: Foods

Article Title: Development and Characterization of Quinoa Peptide Nanoparticles as Carriers for Bioactive Food Ingredient Encapsulation

doi: 10.3390/foods15091589

Figure Lengend Snippet: ( A ) Particle size and PDI of quinoa peptide nanoparticles (QPNPs). ( B ) Zeta potentials of QPNPs. ( C ) Transmission electron microscopy (TEM) images of QPNPs, scale bar: 100 nm. Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively. Different letters on columns mean significantly different ( p < 0.05).

Article Snippet: The morphologies of QPNPs and CAPE-loaded QPNPs (CAPE-QPNPs) were observed using a transmission electron microscope (JEM-2100, JEOL Ltd., Tokyo, Japan) according to a previously reported method [ ] with some modifications.

Techniques: Transmission Assay, Electron Microscopy

( A ) Surface tension of quinoa peptide nanoparticles (QPNPs). ( B ) Fourier transform infrared spectroscopy (FT-IR) of QPNPs. ( C ) Effect of different denaturants on the particle size of QPNPs, 1: deionized water; 2: SDS; 3: DTT; 4: Urea; 5: SDS + DTT; 6: DTT + Urea; 7: SDS + Urea; 8: SDS + DTT +Urea. Different letters on columns mean significantly different ( p < 0.05). Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively.

Journal: Foods

Article Title: Development and Characterization of Quinoa Peptide Nanoparticles as Carriers for Bioactive Food Ingredient Encapsulation

doi: 10.3390/foods15091589

Figure Lengend Snippet: ( A ) Surface tension of quinoa peptide nanoparticles (QPNPs). ( B ) Fourier transform infrared spectroscopy (FT-IR) of QPNPs. ( C ) Effect of different denaturants on the particle size of QPNPs, 1: deionized water; 2: SDS; 3: DTT; 4: Urea; 5: SDS + DTT; 6: DTT + Urea; 7: SDS + Urea; 8: SDS + DTT +Urea. Different letters on columns mean significantly different ( p < 0.05). Chy-QPNPs, Try-QPNPs, and Alc-QPNPs refer to QPNPs prepared by controllable enzymolysis of α-chymotrypsin, trypsin, and Alcalase 2.4L, respectively.

Article Snippet: The morphologies of QPNPs and CAPE-loaded QPNPs (CAPE-QPNPs) were observed using a transmission electron microscope (JEM-2100, JEOL Ltd., Tokyo, Japan) according to a previously reported method [ ] with some modifications.

Techniques: Fourier Transform Infrared Spectroscopy, Spectroscopy

( A ) Particle size distribution of CAPE-loaded QPNPs (CAPE-QPNPs) (Inset: TEM images of CAPE-QPNPs), the different colors represent three independent replicate experiments. ( B ) Fourier transform infrared spectroscopy (FT-IR) of CAPE, QPNPs, and CAPE-QPNPs. ( C ) Secondary structure proportion of QPNPs and CAPE-QPNPs, * p < 0.05, ** p < 0.01.

Journal: Foods

Article Title: Development and Characterization of Quinoa Peptide Nanoparticles as Carriers for Bioactive Food Ingredient Encapsulation

doi: 10.3390/foods15091589

Figure Lengend Snippet: ( A ) Particle size distribution of CAPE-loaded QPNPs (CAPE-QPNPs) (Inset: TEM images of CAPE-QPNPs), the different colors represent three independent replicate experiments. ( B ) Fourier transform infrared spectroscopy (FT-IR) of CAPE, QPNPs, and CAPE-QPNPs. ( C ) Secondary structure proportion of QPNPs and CAPE-QPNPs, * p < 0.05, ** p < 0.01.

Article Snippet: The morphologies of QPNPs and CAPE-loaded QPNPs (CAPE-QPNPs) were observed using a transmission electron microscope (JEM-2100, JEOL Ltd., Tokyo, Japan) according to a previously reported method [ ] with some modifications.

Techniques: Fourier Transform Infrared Spectroscopy, Spectroscopy

( A ) Effect of temperatures on the remaining amount of CAPE in CAPE-loaded QPNPs (CAPE-QPNPs), * p < 0.05, ** p < 0.01, *** p < 0.001. ( B ) Effect of irradiation on the remaining amount of CAPE in CAPE-QPNPs. ( C ) Effect of storage time on the particle size of CAPE-QPNPs at 4 °C and 25 °C. ( D ) Effect of storage time on the remaining amount of CAPE in CAPE-QPNPs at 4 °C and 25 °C.

Journal: Foods

Article Title: Development and Characterization of Quinoa Peptide Nanoparticles as Carriers for Bioactive Food Ingredient Encapsulation

doi: 10.3390/foods15091589

Figure Lengend Snippet: ( A ) Effect of temperatures on the remaining amount of CAPE in CAPE-loaded QPNPs (CAPE-QPNPs), * p < 0.05, ** p < 0.01, *** p < 0.001. ( B ) Effect of irradiation on the remaining amount of CAPE in CAPE-QPNPs. ( C ) Effect of storage time on the particle size of CAPE-QPNPs at 4 °C and 25 °C. ( D ) Effect of storage time on the remaining amount of CAPE in CAPE-QPNPs at 4 °C and 25 °C.

Article Snippet: The morphologies of QPNPs and CAPE-loaded QPNPs (CAPE-QPNPs) were observed using a transmission electron microscope (JEM-2100, JEOL Ltd., Tokyo, Japan) according to a previously reported method [ ] with some modifications.

Techniques: Irradiation

In vitro release profile of CAPE-loaded QPNPs (CAPE-QPNPs) in simulated gastric fluid (SGF) and intestinal fluid (SIF). The dotted lines indicate the transition from SGF to SIF and the end of the intestinal digestion phase, respectively.

Journal: Foods

Article Title: Development and Characterization of Quinoa Peptide Nanoparticles as Carriers for Bioactive Food Ingredient Encapsulation

doi: 10.3390/foods15091589

Figure Lengend Snippet: In vitro release profile of CAPE-loaded QPNPs (CAPE-QPNPs) in simulated gastric fluid (SGF) and intestinal fluid (SIF). The dotted lines indicate the transition from SGF to SIF and the end of the intestinal digestion phase, respectively.

Article Snippet: The morphologies of QPNPs and CAPE-loaded QPNPs (CAPE-QPNPs) were observed using a transmission electron microscope (JEM-2100, JEOL Ltd., Tokyo, Japan) according to a previously reported method [ ] with some modifications.

Techniques: In Vitro