



Knee osteoarthritis (OA) is a common and often painful condition that affects millions of people worldwide. It can make simple activities—like walking or climbing stairs—difficult and uncomfortable. Traditional treatments , such as corticosteroid or hyaluronic acid injections , typically offer only short-term relief and often require repeated procedures. In recent years, polyacrylamide hydrogel (PAAG) has emerged as a promising new option. This article explores the unique chemistry behind PAAG and how its innovative design helps it stay in the knee joint longer, providing lasting cushioning and pain relief.
Knee OA happens when the cartilage that cushions your joints gradually wears away, leading to pain, stiffness, and limited movement. This can make daily life challenging. Most current treatments focus on managing symptoms: corticosteroid injections help reduce inflammation, and hyaluronic acid injections aim to lubricate the joint. However, these solutions are often temporary, with relief typically lasting only a few weeks to months. Frequent injections also increase the risk of side effects like joint irritation . These limitations highlight the need for longer-lasting, safer alternatives—this is where PAAG stands out.
PAAG is unique thanks to its advanced polymer-matrix design. It’s a gel composed of millions of tiny, interconnected chains of polyacrylamide , all suspended in sterile water. This forms a stable, jelly-like substance that closely mimics the natural cushioning in healthy cartilage . Unlike some other injectable gels that the body gradually absorbs, PAAG is non-degradable. This means it stays inside the joint, providing steady support and cushioning without the need for frequent top-ups. The product, known commercially as Arthrosamid , acts as a soft, elastic cushion—reducing friction and protecting the joint from further damage.
PAAG’s long-lasting effects come from its remarkable chemical stability and physical resilience. Because it does not break down or get absorbed, PAAG remains in the joint space for months—or even longer. This allows it to serve as a mechanical cushion, absorbing shocks and reducing the pressure on damaged cartilage . PAAG is also viscoelastic, which means it acts like both a liquid and a solid: it can stretch and compress with the movement of the knee, then return to its original shape. This mimics the natural behavior of healthy joint fluid , offering immediate pain relief and ongoing joint lubrication for smoother movement. Patients often experience longer-lasting symptom relief, meaning fewer injections and more consistent comfort over time.
Clinical studies highlight PAAG’s impressive real-world benefits. For example, recent research has shown that PAAG can significantly improve knee OA symptoms for up to 24 months after injection, particularly in certain groups such as older adults and those with less advanced OA or without diabetes. Many patients report meaningful improvement in pain and mobility, as measured by standard outcome tools. This evidence suggests that PAAG’s innovative polymer-matrix technology offers not just theoretical advantages, but real, lasting enhancements in quality of life for people living with knee OA .
In summary, PAAG’s novel design—a non-degradable, cross-linked polyacrylamide gel with viscoelastic properties—sets the stage for longer-term relief from knee osteoarthritis . By staying stable within the joint and providing continuous cushioning and lubrication, PAAG offers an effective alternative to traditional treatments that may fall short. This deeper understanding of PAAG’s chemistry opens new possibilities for managing OA and improving patient care. As research and technology evolve, PAAG stands out as a valuable option, offering hope for longer-lasting relief and improved mobility for those facing knee osteoarthritis.
Gao, H. C. K., Akhtar, M., Creedon, C., Nar, Ö. O., Verma, T., & Lee, P. Y. F. (2025). Polyacrylamide hydrogel injections in knee osteoarthritis: A PROMs-based 24 month cohort study. Journal of Clinical Orthopaedics and Trauma. https://doi.org/10.1016/j.jcot.2025.103136
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