# D-Penicillamine/Dihydroquercetin Dual-Loaded Metal–Organic Framework as a Microenvironment Copper Regulator for Enhancing the Therapeutic Efficacy of Polyphenolic Antioxidant in Alzheimer’s Disease

**Authors:** Xuhan Wu, Gang Huang, Licong Chen, Yiling Xie, Qi Ding, Enpeng Xi, Yun Zhao, Nan Gao

PMC · DOI: 10.3390/molecules31010111 · Molecules · 2025-12-28

## TL;DR

A new treatment approach for Alzheimer's disease uses a compound that regulates copper and boosts antioxidant effects in the brain.

## Contribution

A dual-loaded metal-organic framework regulates copper microenvironment to enhance antioxidant therapy for Alzheimer’s.

## Key findings

- DD@MOF improved spatial learning and memory deficits in a 5 × FAD mouse model.
- D-penicillamine released faster than dihydroquercetin, enabling copper regulation.
- The system prevents metal ion interference with polyphenolic antioxidants.

## Abstract

Polyphenols like dihydroquercetin, rutin, and rifampicin show promise for Alzheimer’s disease (AD) therapy due to their ability to inhibit amyloid-β (Aβ) aggregation and reduce reactive oxygen species (ROS), garnering significant recent interest. However, their efficacy is substantially diminished because excess metal ions present in amyloid plaques can chelate these compounds. Therefore, reshaping the metal microenvironment in the patient’s brain is particularly important for the therapeutic effect of AD. To address the above issues, we have constructed a composite system formed by NH2-MIL-101(Fe) (MOF), dihydroquercetin (DHQ), and D-penicillamine (D-pen). Due to the lack of π-π interaction and the low adsorption energy between D-pen/MOF, the release order and speed of D-pen was much faster than DHQ, thus achieving metal microenvironment regulation and ensuring the therapeutic effect of DHQ. In a 5 × FAD transgenic mouse model, DD@MOF treated and improved spatial learning and memory deficits. Therefore, the DD@MOF based on polyphenolic compounds provides a potential research direction for intervention in Alzheimer’s disease through chelating copper ions and antioxidant properties.

## Linked entities

- **Chemicals:** dihydroquercetin (PubChem CID 471), D-penicillamine (PubChem CID 5852), rutin (PubChem CID 5280805), rifampicin (PubChem CID 135398735)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** AD (MESH:D000544), learning and memory deficits (MESH:D007859)
- **Chemicals:** DHQ (MESH:C003377), rutin (MESH:D012431), Metal (MESH:D008670), Fe (MESH:D007501), D-Penicillamine (MESH:D010396), MOF (MESH:C037042), ROS (MESH:D017382), FAD (MESH:D005182), DD@MOF (-), rifampicin (MESH:D012293), Copper (MESH:D003300), Polyphenols (MESH:D059808)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12787126/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12787126/full.md

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Source: https://tomesphere.com/paper/PMC12787126