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Open AccessDOI: 10.1007/s40843-025-3646-1Original Research

Microcrystallization-Gelation Enabled Mechanocompatible and Antibacterial Hydrogels for Cartilage Repair

Beijing University of Chemical Technology

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Microcrystallization-Gelation Enabled Mechanocompatible and Antibacterial Hydrogels for Cartilage Repair
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Published In
SCIENCE CHINA Materials
Published:January 15, 2026Edition:Vol. 69, Issue 4 • pp. 100-112Citation:Tailong Shi et al. (2026), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料

Key Takeaways & Executive Findings

  • • • The optimal hydrogel formulation achieves a compressive modulus of 0.2 MPa and tensile strength of 2.2 MPa, matching human cartilage mechanical benchmarks, enabling load-bearing support in joint defects. • • The hydrogel withstands 50,000 compression cycles without structural failure, indicating fatigue resistance critical for long-term in vivo performance under cyclic joint loading. • • Incorporation of gentamicin confers antibacterial activity, addressing infection risks in cartilage repair, while nano-hydroxyapatite promotes osteogenesis for osteochondral integration. • • The material exhibits excellent flowability pre-crosslinking, allowing minimally invasive injection and adaptation to irregular defect geometries, a key advantage over pre-formed implants.

Abstract

Repairing cartilage defects requires biomaterials with mechanical properties similar to native cartilage. However, balancing these properties with biodegradability remains a major challenge. In this study, a degradable antibacterial hydrogel with promising mechanical characteristics was developed for personalized cartilage defect repair. The hydrogel was synthesized using chitosan and gelatin via microcrystallization and gelation, combined with chemical crosslinking facilitated by epichlorohydrin. This method significantly enhanced the mechanical properties of the material, with compressive modulus of the optimal group reaching 0.2 MPa and tensile strength reaching 2.2 MPa, which are comparable to those of human cartilage. The hydrogel maintained its integrity after 50000 compression cycles. With excellent flowability prior to crosslinking, it can adapt to complex cartilage defects. The inclusion of gentamicin provides antibacterial properties, while nano-hydroxyapatite promotes osteogenesis. This hydrogel, with its multiple crosslinking mechanisms, balances mechanical strength, biodegradability, and adaptability, offering a promising solution for repairing infected cartilage defects.

1. Introduction

Cartilage defects, often arising from trauma or osteoarthritis, present a clinical challenge due to the tissue's avascular nature, which severely limits self-repair. Current surgical interventions, including autologous chondrocyte implantation and microfracture, show declining success rates of 25-50% within a decade and require recovery periods exceeding 12 months, particularly in patients aged 40-50. Hydrogels offer a promising scaffold platform due to their biocompatibility and tunable properties, yet their clinical translation is hampered by a fundamental trade-off: high mechanical strength often compromises biodegradability, and vice versa. This dichotomy restricts their utility in load-bearing cartilage applications where both initial mechanical integrity and eventual resorption are required for tissue regeneration.

The present work addresses this bottleneck by employing a dual crosslinking strategy combining microcrystallization and chemical crosslinking of natural polymers, chitosan and gelatin. This approach synergistically enhances mechanical properties—achieving compressive modulus of 0.2 MPa and tensile strength of 2.2 MPa—while maintaining biodegradability. The incorporation of gentamicin and nano-hydroxyapatite further imparts antibacterial and osteogenic functionalities, respectively, targeting infected and osteochondral defects. This multifunctional hydrogel, with its injectable pre-crosslinked state, offers a personalized, minimally invasive solution that balances mechanical robustness, degradability, and bioactivity, potentially overcoming the limitations of existing cartilage repair materials.

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Cite This Research Paper
Tailong Shi, Yan-Hua Xiong, Cheng Shen, Zongpeng Xiu, Lujiao Zhang, Ruonan Wu, Yang Li, Shun Duan, Tan Guo, Fu-Jian Xu (2026). Microcrystallization-Gelation Enabled Mechanocompatible and Antibacterial Hydrogels for Cartilage Repair. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-025-3646-1
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Frequently Asked Questions

What is the degradation profile of the hydrogel under physiological conditions, and how does it correlate with tissue regeneration kinetics?

The abstract does not provide specific degradation rates or times. However, the hydrogel is designed to be degradable, with the balance between mechanical strength and biodegradability achieved via multiple crosslinking mechanisms. Further in vitro and in vivo degradation studies would be required to quantify mass loss over time and match it with cartilage repair rates.

How does the compressive modulus of 0.2 MPa and tensile strength of 2.2 MPa compare to native human cartilage, and what are the implications for load-bearing applications?

These values are stated to be comparable to human cartilage, which typically has a compressive modulus in the range of 0.1-2 MPa and tensile strength of 1-10 MPa depending on zone and testing conditions. Achieving these benchmarks suggests the hydrogel can withstand physiological joint loads, but long-term fatigue and wear under dynamic loading require further validation.

What is the mechanism of antibacterial action of gentamicin in the hydrogel, and does it affect the mechanical properties or cytocompatibility?

Gentamicin is an aminoglycoside antibiotic that inhibits bacterial protein synthesis. Its inclusion likely provides local antibacterial activity against common pathogens. The abstract does not specify the concentration or release kinetics, nor its impact on mechanical properties or cell viability. These aspects would need to be evaluated to ensure no adverse effects on chondrocyte function.

How does the microcrystallization-gelation process affect the injectability and in situ gelation time, and what are the optimal injection parameters for clinical use?

The hydrogel exhibits excellent flowability prior to crosslinking, allowing adaptation to complex defects. The gelation time and injection parameters (e.g., needle gauge, temperature) are not detailed. For clinical translation, it is crucial to determine the working time and gelation kinetics to ensure proper handling and defect filling.

What is the in vivo degradation and biocompatibility profile of the hydrogel, particularly regarding the release of degradation byproducts and inflammatory response?

The abstract does not provide in vivo data. Chitosan and gelatin are generally biocompatible and biodegradable, but the crosslinker epichlorohydrin may raise toxicity concerns. In vivo studies are necessary to assess local and systemic toxicity, degradation byproducts, and the host immune response to ensure safety and efficacy.

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