4.6 Article

Anti-Pyretic, Analgesic, and Anti-Inflammatory Activities of Meloxicam and Curcumin Co-Encapsulated PLGA Nanoparticles in Acute Experimental Models

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METABOLITES
卷 13, 期 8, 页码 -

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MDPI
DOI: 10.3390/metabo13080935

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meloxicam; curcumin; co-encapsulation; pyrexia; nociception; inflammation

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This study evaluated the in vivo effects of meloxicam and curcumin co-encapsulated PLGA nanoparticles in acute models of pyrexia, nociception, and inflammation. The results showed that PLGA encapsulation significantly improved the in vivo activities of both compounds, and co-encapsulation of meloxicam and curcumin enhanced their anti-pyretic, anti-nociceptive, and anti-inflammatory effects in a dose-dependent manner. Therefore, the combination of meloxicam and curcumin in a biodegradable nanocarrier system could provide a promising therapeutic approach for acute conditions.
Herein, we evaluated the in vivo effects of meloxicam and curcumin co-encapsulated PLGA nanoparticles in experimental acute models of pyrexia, nociception, and inflammation. Seven groups (n = 6) were designed for each investigation and pretreated intraperitoneally (i.p.): the control group, meloxicam (4 mg/kg b.w.), curcumin (15 mg/kg b.w.), and equivalent content containing PLGA capped nanoparticles of meloxicam (Mlx-NP) and curcumin (Cur-NP) alone and in combination (Mlx-Cur-NP; at two doses). The results showed that PLGA encapsulation significantly (p <= 0.05) improved the in vivo activities of each compound. Furthermore, co-encapsulation of meloxicam and curcumin potentiated the anti-pyretic effect on yeast-induced pyretic rats, anti-nociceptive effect on nociception induced in rats by formalin and heat, and anti-edematogenic activity in xylene-induced ear edema in rats in a dose-dependent manner. In carrageenan-induced paw inflammation in rats, meloxicam and curcumin co-loading (Mlx-Cur-NP) resulted in significant (p <= 0.05) inhibition of paw inflammation, reduction in TNF- alpha and PGE2 levels, downregulation of expressions of proinflammatory cytokines (TNF- alpha, IL-1 beta, and IL-6), as well as a decrease in histopathological changes and TNF- alpha immunoexpression in paw tissues. Moreover, Mlx-Cur-NP demonstrated noteworthy potentiation in pharmacological effects compared to free compounds and mono-compound-loaded nanoparticles. Thus, the association of meloxicam with curcumin in a biodegradable nanocarrier system could provide a promising anti-pyretic, anti-nociceptive, and anti-inflammatory therapeutic approach for acute conditions.

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