BackgroundLow-molecular-weight chitosan oligosaccharide (LMCOS), a chitosan degradation product, is water-soluble and easily absorbable, rendering it a popular biomaterial to study. However, its effect on bone remodelling remains unknown. Therefore, we evaluated the effect of LMCOS on lipopolysaccharide (LPS)-induced bone resorption in mice.MethodsSix-week-old male C57BL/6 mice (n = five per group) were randomly divided into five groups: PBS, LPS, LPS + 0.005% LMCOS, LPS + 0.05% LMCOS, and LPS + 0.5% LMCOS. Then, the corresponding reagents (300 μL) were injected into the skull of the mice. To induce bone resorption, LPS was administered at 10 mg/kg per injection. The mice were injected three times a week with PBS alone or LPS without or with LMCOS and sacrificed 2 weeks later. The skull was removed for micro-computed tomography, haematoxylin-eosin staining, and tartrate-resistant acid phosphatase staining. The area of bone damage and osteoclast formation were evaluated and recorded.ResultsLMCOS treatment during LPS-induced skull resorption led to a notable reduction in the area of bone destruction; we observed a dose-dependent decrease in the area of bone destruction and number of osteoclasts with increasing LMCOS concentration.ConclusionsOur findings showed that LMCOS could inhibit skull bone damage induced by LPS in mice, further research to investigate its therapeutic potential for treating osteolytic diseases is required.
Temperature-sensitive calcium alginate-based microspheres were prepared in two steps. Firstly, free-radical polymerization of temperature-sensitive N-vinylcaprolactam monomer was performed in aqueous solution of sodium alginate, yielding a mixed aqueous solution bearing temperature-sensitivity composed of poly(N-vinylcaprolactam), sodium alginate-graft- poly(N-vinylcaprolactam) and sodium alginate. Then temperature-sensitive composite microspheres were prepared by inverse emulsification-crosslinking using the as-prepared solution as water phase, n-hexane as oil phase, Span-85 and Tween-85 as emulsifiers and calcium chloride as crosslinker respectively. The morphology and temperature-sensitivity of the composite microspheres were investigated by scanning electron microscope and turbidity method respectively. The controlled release behavior of the microspheres towards temperature was investigated preliminarily using berberine as a model drug.
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