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Updated: Jun 17, 2026

Efficient Isolation of Adipose-derived Stem Cells and Adipocytes from Porcine Adipose Tissue
Published on: May 26, 2026
Efficient Isolation of Adipose-derived Stem Cells and Adipocytes from Porcine Adipose Tissue
Yating Xiao1, Xinyu Zhou1, Xuanzhang Tang1
1State Key Laboratory of Swine and Poultry Breeding Industry, College of Animal Science and Technology, Sichuan Agricultural University.
Abstract:
Adipose-derived stem cells (ADSCs) have emerged as ideal seed cells in regenerative medicine due to their abundant sources, minimally invasive harvesting, multi-lineage differentiation potential, and immunomodulatory properties. Their applications span tissue repair, disease modelling, and cell therapy; however, efficient isolation of high-viability ADSCs remains critical for advancing research and clinical translation. Conventional isolation methods, such as enzymatic digestion combined with mechanical dissociation via pipetting, are limited by lengthy processing times (1-3 h), poor cell viability (often <70%), and substantial batch-to-batch variability, compromising downstream experiments. Here, we present the SoniConvert system (a mechanical wave-based cell separation system), which combines mechanical wave and enzymatic digestion to address these challenges. The system integrates a microprocessor-based control unit that regulates mechanical wave-mediated dissociation via digital feedback, together with a tissue-specific loosening reagent optimized for adipose tissue (5-15 min incubation). This approach enables rapid conversion of tissue to a single-cell suspension, with mechanical dissociation completed in 3-9 s. The system offers three advantages: (1) ultra-fast processing, with the core isolation process-from enzymatic digestion to initial cell fraction separation-completed in approximately 30 min (>90% reduction compared to conventional methods); (2) high viability preservation, with trypan blue staining confirming cell viability of 80-95%, exceeding traditional protocols; and (3) broad compatibility, as the resulting single-cell suspensions meet requirements for primary cell culture, flow cytometry, cytotoxicity assays, and adipose organoid construction. By reducing processing time, enhancing cell integrity, and limiting variability, this system provides a practical platform for adipose-related research.

