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February 26, 2026Gels0 citationsOpen Access

Migration and Chondrogenesis of Cells from Minced Nasal Cartilage in Type I Collagen Hydrogel: A Workflow for One-Step Engineering of Injectable Grafts

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AGAlexander GenschUniversity of BaselADAtharva DamleUniversity of BaselOSOrhan SonsözUniversity of Basel

Key Points

  • The aim is to determine the feasibility of using nasal septal cartilage for cartilage repair through a one-step implantation technique.
  • Evaluated nasal septal cartilage (NSC) obtained from rhinoplasties as a source for cartilage repair.
  • Minced NSC with and without Poloxamer 188 (P188), embedded in collagen I gel, and cultured for 42 days.
  • Used a novel decontamination protocol with antibiotics to maintain cell viability.
  • Assessed the cellular outgrowth and cartilaginous matrix formation through histological analysis.
  • Histological analysis confirmed robust cellular outgrowth and matrix deposition in constructs.
  • Tissues from minced NSC with P188 exhibited greater cartilaginous matrix formation compared to those without P188.
  • NSC fragments in a 1 mL hydrogel showed strong outgrowth and satisfactory matrix formation capable of addressing clinically relevant defect volumes.

Abstract

Articular cartilage (AC) damage heals poorly and can progress to osteoarthritis. Implantation of AC fragments (Minced Cartilage Implantation, MCI) is a promising one-step repair technique but is constrained by the limited availability of healthy AC. In this study, we evaluated the feasibility of MCI using nasal septal cartilage (NSC) as an alternative source of hyaline tissue with strong regenerative capacity. NSC obtained from rhinoplasties was decontaminated using a novel protocol, minced with or without Poloxamer 188 (P188), embedded in collagen I gel (0.5 mL per sample), and cultured for 42 days in platelet-rich plasma (PRP)-supplemented medium. The decontamination procedure with a combination of antibiotics was effective and did not impair cell viability. Histology of the resulting constructs confirmed robust cellular outgrowth and matrix deposition. Tissues produced from NSC and fragmented with P188 contained more cartilaginous matrix than those from NSC fragmented without P188 and those from AC fragmented with P188. NSC fragments embedded in a 1 mL hydrogel, sufficient for clinically relevant defect volumes, also demonstrated strong outgrowth and satisfactory matrix formation. Overall, the developed protocol supports the use of NSC as a viable tissue source in gel-based, injectable MCI grafts for focal cartilage repair.

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Cite This Study

Gensch et al. (2026) studied this question.

synapsesocial.com/papers/699fe40c95ddcd3a253e8397https://doi.org/10.3390/gels12030190
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