Background: Prevention of surgical site infection and wound dehiscence are imperative and also challenging in clinical practice. This study examines the healing response of laparotomy wounds following application of silver nanoparticles. Materials and Methods: Dermal fibroblasts were exposed to incremential doses of silver nanoparticles and its effect on collagen synthesis and cytotoxicity was assessed. Laparotomy surgery was performed on rabbits and the operation site was treated topically either with silver nanoparticle once, or once daily for 14 days or with vehicle. Healing response and local tissue reaction was evaluated clinically by histopathology and scanning electron microscopy (SEM); microbial load on the operation site was assessed. Clinical tests and histopathology were performed to assess systemic toxicity. Results: Silver nanoparticles increased collagen expression from dermal fibroblasts and longer time exposure increased caspase 3 expression and produced cyotoxic effect with an IC 50 of 0.16 mg/mL. Daily treatment of operation sites resulted in increased collagen deposition and improved wound healing, microbial load was reduced. Although a sub dermal edema was evident in histopatho logy, SEM showed normal architecture of cells with infiltration of lymphocytes. There was no systemic toxicity.
Present investigation focuses on development and detailed characterization of a new Mg alloy sample (BM) with and without coating of hydroxyapatite (BMH) and bioactive glass (BMG) by air plasma spray method. After detailed mechano-physico-chemical characterization of powders and coated samples, electrochemical corrosion and SBF immersion tests were carried out. Detailed in vitro characterizations for cell viability were undertaken using MG-63 cell line followed by in vivo tests in rabbit model for studying bone healing up to 60 days. Starting current density increases from BM to BMH to BMG indicating highest resistance towards corrosion in case of BMG samples, however BMH also showed highest icorr value suggesting slowest rate of corrosion than BM and BMG samples. Dissolution of calcium ion in case of BMH and BMG control formation of apatite phases on surface. Ca2+ ions of coatings and from SBF solution underwent reduction reaction simultaneously with conversion of Mg to MgCl2 releasing OH− in the solution, which increases pH. Viability and propagation of human osteoblast-like cells was verified using confocal microscopy observations and from expression of bone specific genes. Alkaline phosphatase assay and ARS staining indicate cell proliferation and production of neo-osseous tissue matrix. In vivo, based on histology of heart, kidney and liver, and immune response of IL-2, IL-6 and TNFα, all the materials show no adverse effects in body system. The bone creation was observed to be more for BMH. Although both BMH and BMG show rays of possibilities in early new bone formation and tough bone–implant bonding at interface as compared to bare Mg alloy, however, BMG showed better well-sprayed coating covering on substrate and resistance against corrosion prior implanting in vivo. Also, better apatite formation on this sample makes it more favourable implant.
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