Evidence mapPaperPMID 40722243Full record

SynthesisJournal of Zhejiang University. Science. B2025

EGCG as a therapeutic agent: a systematic review of recent advances and challenges in nanocarrier strategies.

Chee Ning Wong, Yang Mooi Lim, Kai Bin Liew, Yik-Ling Chew, Ang-Lim Chua, Siew-Keah Lee

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of Zhejiang University. Science. B, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chee Ning WongM. Kandiah Faculty of M edicine and Health Sciences, Universiti Tunku Abdul Rahman, 43000 Kajang, Selangor, Malaysia.
Yang Mooi LimM. Kandiah Faculty of M edicine and Health Sciences, Universiti Tunku Abdul Rahman, 43000 Kajang, Selangor, Malaysia.
Kai Bin LiewFaculty of Pharmacy, University of Cyberjaya, 63000 Cyberjaya, Selangor, Malaysia.
Yik-Ling ChewFaculty of Pharmaceutical Sciences, UCSI University, 56000 Kuala Lumpur, Malaysia.
Ang-Lim ChuaFaculty of Medicine, Universiti Teknologi MARA, 47000 Sungai Buloh, Selangor, Malaysia.
Siew-Keah LeeM. Kandiah Faculty of M edicine and Health Sciences, Universiti Tunku Abdul Rahman, 43000 Kajang, Selangor, Malaysia. leesiewkeah@utar.edu.my.

Funding

the Ministry of Higher Education (MOHE), Malaysia, through the Fundamental Research Grant Scheme FRGS/1/2022/SKK10/UTAR/02/1the Universiti Tunku Abdul Rahman, Malaysia, through UTAR-Research Fund IPSR/RMC/UTARRF/2024-C1/L04
6 · The paper itself

Abstract

Epigallocatechin-3-gallate (EGCG), a bioactive polyphenol abundant in green tea, has garnered significant attention for its diverse therapeutic applications, ranging from antioxidant and anti-inflammatory effects to potential anticancer properties. Despite its immense promise, the practical utilization of EGCG in therapeutic settings as a medication has been hampered by inherent limitations of this drug, including poor bioavailability, instability, and rapid degradation. This review comprehensively explores the current challenges associated with the application of EGCG and evaluates the potential of nanoparticle-based formulations in addressing these limitations. Nanoparticles, with their unique physicochemical properties, offer a platform for the enhanced stability, bioavailability, and targeted delivery of EGCG. Various nanoparticle strategies, including polymeric nanoparticle, micelle, lipid-based nanocarrier, metal nanoparticle, and silica nanoparticle, are currently employed to enhance EGCG stability and pharmacological activity. This review concludes that the particle sizes of most of these formulated nanocarriers fall within 300 nm and their encapsulation efficiency ranges from 51% to 97%. Notably, the pharmacological activities of EGCG-loaded nanoparticles, such as antioxidative, anti-inflammatory, anticancer, and antimicrobial effects, are significantly enhanced compared to those of free EGCG. By critically analyzing the existing literature and highlighting recent advancements, this article provides valuable insights into the promising prospects of nanoparticle-mediated EGCG formulations, paving the way for the development of more effective and clinically viable therapeutic strategies.

Indexed as

CatechinNanoparticle Drug Delivery SystemAnimalsAnti-Inflammatory AgentsAntineoplastic AgentsAntioxidantsBiological AvailabilityHumansMicellesParticle SizeAnti-Inflammatory AgentsAntineoplastic AgentsAntioxidantsCatechinepigallocatechin gallateMicellesNanoparticle Drug Delivery SystemBiological activityEpigallocatechin-3-gallate (EGCG)NanocarrierNanoformulationNanoparticleNanosystemStability

Identifiers

PMID40722243
PMCPMC12303791

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.