ArticleScientific reports2026
In vitro release kinetics and in vivo plasma exposure of green tea polyphenols and caffeine from iron oxide chitosan nanoparticles.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Medicinal Value ofInternational journal of molecular sciences · 2026Review
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Authors and funding
6 authors.
Funding
Abstract
Green tea polyphenols (GTPP) are known for their antioxidant and anticancer activities but suffer from low bioavailability due to instability in the gastrointestinal environment. This study aimed to enhance the oral delivery of GTPP by encapsulating epicatechin, epigallocatechin gallate (EGCG), catechin, gallic acid, theaflavin, and caffeine into iron oxide chitosan nanoparticles (IOCHNP). Using high performance liquid chromatography (HPLC), the release of GTPP was evaluated in vitro and in vivo in both simulated intestinal media and rat's plasma. GTPP-IOCHNP efficiently encapsulates GTPP, achieving an encapsulation efficiency of 90.9% for catechin and 83.3% for theaflavin. Additionally, less than 8% of GTPP is released in simulated gastric fluid (SGF), while its more readily released in simulated intestinal fluid (SIF) is enhanced, reaching 70% for caffeine. The release of gallic acid and epicatechin followed Higuchi kinetics, catechin followed Korsmeyer-Peppas, and caffeine followed Weibull model, indicating diverse mechanisms of release. The in vivo results demonstrated that GTPP loaded GTPP-IOCHNP significantly enhanced the absorption of GTPP compared to GTPP administered alone (p < 0.05). The bioavailability of EGCG, epicatechin, catechin, gallic acid and theaflavin was improved by approximately 8.5-, 6.5-, 4.8-, 5- and 3.5- fold respectively when delivered using GTPP-IOCHNP as a carrier. These findings highlight the potential of IOCHNP as an efficient oral delivery platform for tea polyphenols.
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Registered trials
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