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Therapeutic effects of iontophoresis with gold nanoparticles in the repair of traumatic muscle injury. | LitMetric

AI Article Synopsis

  • - This study examined how gold nanoparticles (GNPs) combined with iontophoresis treatment can aid recovery in rat models with muscle injuries.
  • - A total of 50 Wistar rats were divided into five groups to assess various treatments, including a control, injury alone, and different combinations with GNPs and microcurrent therapy.
  • - Results indicated that rats treated with both GNPs and microcurrent showed reduced inflammation, less oxidative stress, and better pain management, suggesting that this combination accelerates recovery in injured muscle.

Article Abstract

Studies have shown the benefits of gold nanoparticles (GNPs) in muscle and epithelial injury models. In physiotherapy, the use of the microcurrent apparatus is associated with certain drugs (Iontophoresis) to increase the topical penetration and to associate the effects of both therapies. Therefore, the objective of this study was to investigate the effects of iontophoresis along with GNPs in the skeletal muscle of rats exposed to a traumatic muscle injury. We utilised 50 Wistar rats randomly divided in to five experimental groups ( = 10): Control group (CG); Muscle injury group (MI); MI + GNPs (20 nm, 30 mg kg); MI + Microcurrent (300 μA); and MI + Microcurrent + GNPs. The treatment was performed daily for 7 days, with the first session starting at 24 h after the muscle injury. The animals were sacrificed and the gastrocnemius muscle was surgically removedand stored for the proper evaluations. The group that received iontophoresis with GNPs showed significant differences in inflammation and oxidative stress parameters and in the histopathological evaluation showed preserved morphology. In addition, we observed an improvement in the locomotor response and pain symptoms of these animals. These results suggest that the association of boththerapies accelerates the inflammatory response of the injured limb.

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Source
http://dx.doi.org/10.1080/1061186X.2019.1652617DOI Listing

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