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pH-Responsive Carrier-Free Polyphenol Nanoparticles Assembled by Oxidative Polymerization with Enhanced Stability and Antioxidant Activity for Improved Bioaccessibility.
Liu, Danni; Chen, Xiangyu; Yi, Zeng; Tong, Qiulan; Ma, Lei; Tan, Yunfei; Cao, Xiaoyu; Li, Xudong.
Afiliação
  • Liu D; National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, PR China.
  • Chen X; College of Biomedical Engineering, Sichuan University, Chengdu 610064, PR China.
  • Yi Z; National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, PR China.
  • Tong Q; College of Biomedical Engineering, Sichuan University, Chengdu 610064, PR China.
  • Ma L; National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, PR China.
  • Tan Y; College of Biomedical Engineering, Sichuan University, Chengdu 610064, PR China.
  • Cao X; National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, PR China.
  • Li X; College of Biomedical Engineering, Sichuan University, Chengdu 610064, PR China.
ACS Appl Bio Mater ; 7(3): 1763-1777, 2024 03 18.
Article em En | MEDLINE | ID: mdl-38377541
ABSTRACT
Encapsulation of plant polyphenols with micro-/nano-carriers for enhanced bioavailability has been well documented, but the preparation of these carriers and subsequent loading of polyphenols is a multiple process, which is generally complicated with potentially unexpected negative effects on the bioactivity of the polyphenols. Here, we reported a convenient method to assemble carrier-free polyphenol nanoparticles (NPs) based on oxidative coupling polymerization. The effectiveness was assessed with five different polyphenols including pyrocatechol (PY), catechin (CA), epigallocatechin gallate (EGCG), tannic acid (TA), and proanthocyanidin (PC). The structural characteristics of these assembled nanoparticles (PY NPs, CA NPs, EG NPs, TA NPs, and PC NPs) were systematically analyzed with dynamic light scattering (DLS), transmission electron microscopy (TEM), UV-visible spectroscopy, and Fourier transform infrared spectroscopy (FTIR). All NPs were colloidally stable with varying NaCl concentrations from 0 to 300 mM, were acid-resistant and alkali-intolerant, and were suitable for oral administration. An array of antioxidant assays further confirmed the superior antioxidant capabilities of NPs over Trolox and polyphenol monomers, indicating that the oxidative polymerization of polyphenols did not compromise the polyphenol activity of NPs. The in vitro simulated digestion studies validated that these responsive NPs were actually gastrointestinal pH-responsive and applicable to the gastrointestinal physiological environment. The bioaccessibility assessments by using a static in vitro digestion model revealed that better results were achieved with NPs than polyphenol monomers, with TA NPs showing about 1.5-fold higher bioaccessibility than other polyphenol nanoparticles. The present study with five polyphenols demonstrated that the oxidative polymerization of polyphenols provides an effective platform to assemble various carrier-free NPs with enhanced antioxidant activity, favorable stability, and improved bioaccessibility, which could be used promisingly as a functional food ingredient in food matrices or as oral drug delivery candidates for helping to manage human health or treating various gastrointestinal disorders in both the pharmaceutical and nutritional fields.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas / Antioxidantes Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas / Antioxidantes Idioma: En Ano de publicação: 2024 Tipo de documento: Article