Ginsenoside compound K-based multifunctional liposomes for the treatment of rheumatoid arthritis

The clinical treatment of rheumatoid arthritis (RA) with first-line therapeutic drugs is hindered by the poor solubility, low bioavailability, off-target toxicity, and insufficient accumulation in inflamed joints. Liposomes have been shown to mitigate some of these limitations in drug delivery systems. However, the use of cholesterol to stabilize liposomal structures remains controversial due to its potential association with cardiovascular diseases. Here, we developed a novel liposome based on ginsenoside compound K (CK), which not only serves as an effective therapeutic agent for RA but also replaces cholesterol as a membrane stabilizer to address these challenges. Compared with conventional liposomes, ginsenoside CK Liposomes (CK@Lipo) are excellent nanoparticles, with CK stabilizing the liposomal structure and providing targeting functionality toward inflamed joints. When encapsulated with dexamethasone (Dex), CK@Lipo exhibits a synergistic anti-inflammatory effect, slowing the progression of RA. This study provides a theoretical basis for the future development of multifunctional novel ginsenoside CK@Lipo.

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Publication Details

Journal
Drug Delivery
Published
2025-02-16
DOI
https://doi.org/10.1080/10717544.2025.2464190
Citations
9
Primary Topic
Ginseng Biological Effects and Applications
Type
article
Field-Weighted Citation Impact
7.25

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article

Ginsenoside compound K-based multifunctional liposomes for the treatment of rheumatoid arthritis

Xinchun Xu, Meng Zhang, Jianxin Wang, Ru Zhang et al.
9 citations
Drug Delivery
Ginseng Biological Effects and Applications
7.25
article

Ginsenoside compound K-based multifunctional liposomes for the treatment of rheumatoid arthritis

Xinchun Xu, Meng Zhang, Jianxin Wang, Ru Zhang, Chun‐Bo Feng, Xinnan Jiang
article en
9 citations

Abstract

The clinical treatment of rheumatoid arthritis (RA) with first-line therapeutic drugs is hindered by the poor solubility, low bioavailability, off-target toxicity, and insufficient accumulation in inflamed joints. Liposomes have been shown to mitigate some of these limitations in drug delivery systems. However, the use of cholesterol to stabilize liposomal structures remains controversial due to its potential association with cardiovascular diseases. Here, we developed a novel liposome based on ginsenoside compound K (CK), which not only serves as an effective therapeutic agent for RA but also replaces cholesterol as a membrane stabilizer to address these challenges. Compared with conventional liposomes, ginsenoside CK Liposomes (CK@Lipo) are excellent nanoparticles, with CK stabilizing the liposomal structure and providing targeting functionality toward inflamed joints. When encapsulated with dexamethasone (Dex), CK@Lipo exhibits a synergistic anti-inflammatory effect, slowing the progression of RA. This study provides a theoretical basis for the future development of multifunctional novel ginsenoside CK@Lipo.

Drug DeliveryVol. 32(1)
Guangzhou University of Chinese Medicine (CN), Fudan University (CN), Shanghai Xuhui Central Hospital (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 3%
Ginseng Biological Effects and Applications
7.25
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