# In Vivo Evaluation of the Anti-Skin-Ageing Bioactivity of a Recombinant Dual Humanised Collagen and Poly-L-Lactic Acid

**Authors:** Mingjie Tong, Xin Zhou, Jiongni Zhong, Dengjian Qu, Wei Chen, Chun Chen, Yiting Wang, Yaoping Liu, Shaochuan Li, Yuan Xiao, Ning Wang, Chaowan Guo, Qiuling Xie, Sheng Xiong

PMC · DOI: 10.3390/bioengineering12050510 · Bioengineering · 2025-05-12

## TL;DR

A new collagen-based material called DuCol was tested in rats and shown to improve skin regeneration and reduce aging effects more effectively than existing treatments.

## Contribution

The study introduces a novel recombinant humanised collagen (DuCol) with superior early-phase anti-aging effects compared to poly-L-lactic acid.

## Key findings

- DuCol significantly increased dermal thickness by 23.4% compared to poly-L-lactic acid (PLLA) at 90 days.
- DuCol activated the TGF-β/Smad3 pathway, enhancing COL1A1 expression and collagen deposition.
- A combination of DuCol and PLLA (P&C) achieved a 31.7% thicker collagen matrix than monotherapy groups.

## Abstract

This study introduces a novel recombinant humanised collagen (DuCol) developed through codon optimisation and prokaryotic soluble expression, exhibiting exceptional biocompatibility and bioactivity. Structural integrity was confirmed via RP-HPLC, SEM, and CD spectroscopy. In vitro evaluations revealed DuCol’s dose-dependent enhancement of NIH-3T3 fibroblast proliferation, adhesion, and migration. In a D-galactose-induced ageing rat model, subcutaneous implantation of DuCol showcased time-dependent anti-ageing effects. Early-stage intervention (30 days post-injection) markedly upregulated COL1A1 expression through the TGF-β/Smad3 pathway activation, outperforming poly-l-lactic acid (PLLA) in collagen deposition. Histological analysis revealed 23.4% greater dermal thickness in DuCol-treated groups compared to PLLA at 90 days. While PLLA exhibited sustained collagen stimulation beyond 90 days, DuCol exhibited superior early-phase efficacy (p < 0.001) with comparable safety profiles (no inflammatory response observed through 180-day monitoring). The combinatorial PLLA/DuCol (P&C) formulation synergistically enhanced dermal regeneration, achieving a 31.7% thicker collagen matrix than monotherapy groups. These results underscore the potential of DuCol as a novel implantable filler material for skin repair and regeneration.

## Linked entities

- **Genes:** COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277]
- **Proteins:** TGFB1 (transforming growth factor beta 1), SMAD3 (SMAD family member 3)
- **Chemicals:** D-galactose (PubChem CID 206)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Smad3 (SMAD family member 3) [NCBI Gene 25631] {aka Madh3, Smad 3, mad3}, Col1a1 (collagen type I alpha 1 chain) [NCBI Gene 29393] {aka COLIA1}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** D-galactose (MESH:D005690), PLLA (MESH:C033616), DuCol (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** NIH-3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12109386/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12109386/full.md

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Source: https://tomesphere.com/paper/PMC12109386