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Updated: Sep 29, 2026

Clinical Protocol of Producing Adipose Tissue-Derived Stromal Vascular Fraction for Potential Cartilage Regeneration
Published on: September 29, 2018
Injection-free piperine-loaded hyaluronic acid-modified proposomes rejuvenate cartilage deterioration in
Passant M Elhalmoushy1, Soha M El-Masry2, Haidy Abbas2
1Department of Pharmaceutics & Pharmaceutical Technology, Faculty of Pharmacy, Pharos University in Alexandria, Alexandria, Egypt; Department of Pharmaceutics, Faculty of Pharmacy, Damanhour University, Damanhour, Egypt.
Abstract:
Osteoarthritis (OA) is a degenerative disorder impacting individuals' quality of life. The current medications fail to halt the disease's progression or attain long-term safety and efficacy. Piperine (PIP) is a natural chondroprotective agent, acting via its anti-inflammatory and antioxidant effects. However, it suffers from poor solubility that limits its pharmacological activity. Herein, a novel PIP-loaded hyaluronic acid-modified proposomes (PIP-HAPs) was investigated for the first time by integrating the penetration-enhancing effects of both proposomes nanovesicles and hyaluronic acid as a non-invasive transdermal treatment for OA. The optimized PIP-HAPs showed a particle size 108 ± 3.71 nm, zeta potential -31.9 ± 0.62 mV, and an entrapment efficiency 92.3% ± 0.64, with a sustained drug release over 48 h. The ex vivo permeability test exhibited a remarkable enhancement in PIP-HAPs' transdermal permeability relative to the conventional gel. Also, confocal laser microscopy photographs revealed the deepest penetration into the articular cartilage in the PIP-HAPs treated group. A comprehensive preclinical study using a mono-iodoacetate (MIA)-induced osteoarthritis rat model demonstrated that PIP-HAPs exhibited the most significant anti-arthritic efficacy, mitigating OA progression. Conclusively, PIP-HAPs are a novel, nanodermatological approach that demonstrates a significant antinociceptive effect, preserves the articular cartilage structure, and restores joint mobility, thereby offering a promising non-invasive treatment for OA.

