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1.
Food Res Int ; 188: 114393, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38823852

RÉSUMÉ

After successfully addressing to mitigate bitterness of naringin through construction Pickering emulsion using pea protein (PP) and naringin (NG) in our previous study, we now probed thermal stability, antioxidant efficacy, and bioavailability. FTIR analysis and UV-vis spectroscopy indicated predominant interactions between PP and NG were hydrogen and hydrophobic bonds. TGA and DSC analyses demonstrated that PP-NG complexes exhibited superior heat-resistance compared to pure PP and NG. Thermal stability assessments indicated a significant retention of NG in the PP-NG Pickering emulsion than the control NG across varied temperatures (4 °C, 25 °C, 37 °C, and 65 °C). Moreover, the antioxidant activity of PP-NG emulsion was dependent on the concentration of NG, as evidenced by DPPH and ABTS free radicals scavenging abilities, ferric reducing power, and lipid peroxidation resistance. Additionally, PP-NG Pickering emulsion exhibited substantially high bioavailability (92.01 ± 3.91%). These results suggest a promising avenue for the application of NG with improved characteristics.


Sujet(s)
Antioxydants , Biodisponibilité , Émulsions , Flavanones , Protéines de pois , Flavanones/composition chimique , Antioxydants/composition chimique , Protéines de pois/composition chimique , Température élevée , Spectroscopie infrarouge à transformée de Fourier , Peroxydation lipidique/effets des médicaments et des substances chimiques , Pisum sativum/composition chimique
2.
Eur J Med Chem ; 268: 116233, 2024 Mar 15.
Article de Anglais | MEDLINE | ID: mdl-38408390

RÉSUMÉ

Antibody-drug conjugates (ADCs) have arisen as a promising class of biotherapeutics for targeted cancer treatment, combining the specificity of monoclonal antibodies with the cytotoxicity of small-molecule drugs. The choice of an appropriate payload is crucial for the success development of ADCs, as it determines the therapeutic efficacy and safety profile. This review focuses on payloads derived from natural products, including cytotoxic agents, DNA-damaging agents, and immunomodulators. These offer several advantages such as diverse chemical structures, unique mechanism of actions, and potential for improved therapeutic index. Challenges and opportunities associated with their development were highlighted. This review underscores the significance of natural product payloads in the elaboration of ADCs, which serves as a valuable resource for researchers involved in developing and optimizing next-generation ADCs for cancer treatment.


Sujet(s)
Antinéoplasiques , Produits biologiques , Immunoconjugués , Tumeurs , Humains , Immunoconjugués/pharmacologie , Immunoconjugués/usage thérapeutique , Immunoconjugués/composition chimique , Antinéoplasiques/pharmacologie , Antinéoplasiques/usage thérapeutique , Antinéoplasiques/composition chimique , Produits biologiques/composition chimique , Anticorps monoclonaux/pharmacologie , Anticorps monoclonaux/usage thérapeutique , Anticorps monoclonaux/composition chimique , Cytotoxines/usage thérapeutique , Tumeurs/traitement médicamenteux
3.
Food Funct ; 14(7): 3230-3241, 2023 Apr 03.
Article de Anglais | MEDLINE | ID: mdl-36938848

RÉSUMÉ

An unacceptable bitter taste limits the application of luteolin in healthier food systems. In this study, a bitterness-masking assessment was performed on whey protein isolate-coated liposomes loaded with luteolin (WPI-coated liposomes) using an electronic tongue and human sensory test. The physical properties of the WPI-coated colloidal nanocarrier were characterized by zeta potential, average diameter, distribution, and morphology analyses. The results indicated that WPI-coated nanocarrier systems exhibited a uniformly dispersed distribution and spherical morphology. After the comparison of the bitterness value, the bitterness-reducing effect of 5% WPI-coated liposomes was the most significant and reduced the bitterness of luteolin by 75%. Raman spectroscopy and X-ray diffraction analysis demonstrated that the decoration of WPI on the liposomes reduced the free motion of lipid molecules. This promoted the ordering at the polar headgroup area and hydrophobic core of the lipid bilayer, which explained why luteolin-loaded liposomes (uncoated liposomes) and WPI-coated liposomes could reduce the bitterness of luteolin from the perspective of bitter molecular groups. Combined with the Raman spectral data, the bilayer rigidity of 5% WPI-coated liposomes was positively responsive to the stabilization of uncoated liposomes against storage and resistance ability against surfactants. It was proven that the emergence of the surface modification of the WPI coating enhanced the stability of uncoated liposomes. These results may contribute to the use of WPI-coated liposomes as prospective candidates for effective delivery of the bioactive bitter substance in nutraceuticals and functional foods.


Sujet(s)
Liposomes , Goût , Humains , Protéines de lactosérum/composition chimique , Lutéoline , Interactions hydrophobes et hydrophiles
4.
Food Chem ; 409: 135270, 2023 May 30.
Article de Anglais | MEDLINE | ID: mdl-36580701

RÉSUMÉ

Nanoliposome is an effective delivery system for polyphenols, whereas it always suffers from low electrostatic stability and oxidation of lipid membranes. Here, different charged anionic polysaccharides including carrageenan (-62.67 ± 1.85 mV), trehalose (-20.73 ± 1.42 mV), and pectin (-4.47 ± 0.38 mV) were used as coating material to improve the stability of nanoliposomes. Results showed that carrageenan coating greatly inhibited aggregation and fusion of nanoliposome. The coating of the higher charged polysaccharides produced the more hydrogen bonds and made the inner chains of lipid molecules more compact, thus improving the rigidity of the membrane and thermal stability. In addition, the polysaccharide coating effectively reduced the lateral diffusion within the membrane and the propagation rate of oxidation reaction. The aim of this study is to investigate the effect of anionic polysaccharides with different charges on coated nanoliposomes, provide reference for the delivery of quercetin.


Sujet(s)
Polyosides , Quercétine , Carragénane/composition chimique , Polyosides/composition chimique , Pectine/composition chimique , Lipides
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