# Nanoemulsion based on natural components enables oral liver-targeting delivery of Schizandrol B to enhance liver regeneration after hepatectomy in hepatocellular carcinoma

**Authors:** Yi Chen, Jinzhuan Xu, Jing Huang, Huizhou He, Zhimei Cheng, Zhengli Zhou, Man Zhang, Yuanxing Huang, Cao Huang, Jianqing Peng, Shuai Zhang, Runbin Sun, Zipeng Gong

PMC · DOI: 10.1093/rb/rbag019 · Regenerative Biomaterials · 2026-02-13

## TL;DR

A new nanoemulsion improves oral delivery of a compound that helps regenerate the liver after surgery for liver cancer.

## Contribution

A natural-component nanoemulsion enhances SCHB bioavailability and liver targeting for improved liver regeneration.

## Key findings

- The nanoemulsion achieved 2.03-fold higher oral bioavailability compared to free SCHB.
- The nanoemulsion showed 7.64-fold greater liver accumulation than free SCHB.
- The nanoemulsion accelerated liver regeneration in HCC models via STAT3/YAP activation and bile acid normalization.

## Abstract

Hepatocellular carcinoma (HCC) remains a major cause of cancer-related mortality worldwide, with partial hepatectomy (PHx) serving as the primary curative treatment. Schizandrol B (SCHB) has demonstrated significant efficacy in promoting liver regeneration and restoring hepatic function following PHx. However, the clinical application of SCHB faces two critical challenges: poor oral bioavailability and inadequate liver-specific targeting. Here, this study developed a nanoemulsion based on natural components named SCHB@SPC/Gal-BSA/DHA. It effectively overcame the limitations of SCHB by synergizing Gal-BSA-mediated liver-specific targeting and DHA-enhanced intestinal absorption, achieving prolonged gastrointestinal tract retention, 2.03-fold higher oral bioavailability and 7.64-fold greater liver accumulation compared to free SCHB. In both 70% PHx and in situ PHx in HCC models, the nanoemulsion robustly accelerated liver regeneration, evidenced by upregulated proliferation markers via STAT3/YAP activation and normalized bile acids metabolism, ultimately restoring liver mass faster than control. This study demonstrates that the dual-targeted nanoemulsion effectively overcomes the key limitations of SCHB by combining enhanced intestinal absorption with liver-specific targeting. The developed nanoemulsion system not only improves drug delivery efficiency but also significantly promotes liver regeneration after PHx, offering a promising therapeutic approach for postoperative recovery in HCC patients while establishing a platform for future liver-targeted oral drug delivery systems.

Graphical Abstract

## Linked entities

- **Proteins:** STAT3 (signal transducer and activator of transcription 3), YAP1 (Yes1 associated transcriptional regulator)
- **Chemicals:** Schizandrol B (PubChem CID 3001662), DHA (PubChem CID 15608515)
- **Diseases:** Hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}
- **Diseases:** cancer (MESH:D009369), HCC (MESH:D006528)
- **Chemicals:** bile acids (MESH:D001647), SCHB (MESH:C033585), SCHB@SPC (-), DHA (MESH:C027493)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12988586/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12988586/full.md

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Source: https://tomesphere.com/paper/PMC12988586