4.7 Review

Epigallocatechin Gallate Nanodelivery Systems for Cancer Therapy

期刊

NUTRIENTS
卷 8, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/nu8050307

关键词

green tea; EGCG; cancer; nanotechnology; nanochemoprevention; anti-cancer therapy

资金

  1. European Union (FEDER funds)
  2. National Fund (FCT/MEC) [PT2020 UID/MULTI/04378/2013-POCI/01/0145/FEDER/007728]
  3. National Fund (Fundacao para a Ciencia e Tecnologia) [PT2020 UID/MULTI/04378/2013-POCI/01/0145/FEDER/007728]
  4. National Fund (Ministerio da Educacao e Ciencia) [PT2020 UID/MULTI/04378/2013-POCI/01/0145/FEDER/007728]
  5. FCT (Fundacao para a Ciencia e Tecnologia)
  6. POPH (Programa Operacional Potencial Humano) [SFRH/BPD/99124/2013]
  7. Fundação para a Ciência e a Tecnologia [SFRH/BPD/99124/2013] Funding Source: FCT

向作者/读者索取更多资源

Cancer is one of the leading causes of morbidity and mortality all over the world. Conventional treatments, such as chemotherapy, are generally expensive, highly toxic and lack efficiency. Cancer chemoprevention using phytochemicals is emerging as a promising approach for the treatment of early carcinogenic processes. (-)-Epigallocatechin-3-gallate (EGCG) is the major bioactive constituent in green tea with numerous health benefits including anti-cancer activity, which has been intensively studied. Besides its potential for chemoprevention, EGCG has also been shown to synergize with common anti-cancer agents, which makes it a suitable adjuvant in chemotherapy. However, limitations in terms of stability and bioavailability have hampered its application in clinical settings. Nanotechnology may have an important role in improving the pharmacokinetic and pharmacodynamics of EGCG. Indeed, several studies have already reported the use of nanoparticles as delivery vehicles of EGCG for cancer therapy. The aim of this article is to discuss the EGCG molecule and its associated health benefits, particularly its anti-cancer activity and provide an overview of the studies that have employed nanotechnology strategies to enhance EGCG's properties and potentiate its anti-tumoral activity.

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