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负载薯蓣皂苷元的壳聚糖可生物降解纳米颗粒通过调节炎症和氧化应激生物标志物改善佐剂诱导的关节炎、疼痛和周围神经病变。

Diosgenin loaded-chitosan biodegradable nanoparticles ameliorate adjuvant-induced arthritis, pain, and peripheral neuropathy through moderation of inflammatory and oxidative stress biomarkers.

作者信息

Tahir Maria, Saleem Ammara, Akhtar Muhammad Furqan

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Faisalabad 38000, Pakistan.

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Faisalabad 38000, Pakistan.

出版信息

Int J Biol Macromol. 2025 Feb;290:138926. doi: 10.1016/j.ijbiomac.2024.138926. Epub 2024 Dec 18.

Abstract

This research work was designed to develop efficient Diosgenin (DGN) loaded biodegradable nanoparticles (DGN-NPs) for treating rheumatoid arthritis. The DGN-NPs were synthesized by ionic-gelation method using chitosan as a biodegradable polymer and in-vitro release study was performed followed by kinetics study. DGN-NPs had an average size of 290 nm, zeta potential of +11.5 mV with 72 % entrapment efficiency, and PDI of 0.398. XRD analysis of DGN-NPs indicated the crystallographic nature while SEM analysis showed the spherical morphology and smooth surface. The release of DGN from NPs occurred by diffusion and erosion mechanism. The anti-arthritic potential of DGN-NPs was investigated by injecting 0.1 ml Complete Freund's adjuvant in the left hind paw of Wistar rats on day 1 while oral therapy with DGN 15 mg/kg, and DGN-NPs at 5, 10, and 15 mg/kg was carried daily. Methotrexate (1 mg/kg) served as standard and was started on day 8 and continued till the 28th day by oral route. The DGN-NPs notably (p < 0.05-0.0001) reduced paw edema, pain, arthritic scoring, and improved body weight in contrast to DGN and standard therapy. The oxidative stress biomarkers were restored by GDN-NPs in the liver and sciatic nerve homogenates along with restoration of altered blood parameters as compared to disease control. The level of serotonin and nor-adrenaline in sciatic nerve homogenates was also profoundly elevated in DGN-NPs-treated arthritic rats. Treatment with DGN-NPs significantly (p < 0.01-0.0001) downregulated NF-κβ, IL-6, IL-1β, COX-2, and TNF-α while upregulated IL-4 in contrast to disease control which resulted in the improvement of the histological lesions in ankle joints and sciatic nerve. It can be inferred from the current study that DGN-NPs especially at 15 mg/kg exhibited notable anti-arthritic, and analgesic activity in contrast to DGN. Moreover, DGN-NPs are also effective against peripheral neuropathy.

摘要

本研究旨在开发用于治疗类风湿性关节炎的高效负载薯蓣皂苷元(DGN)的可生物降解纳米颗粒(DGN-NPs)。采用离子凝胶法,以壳聚糖作为可生物降解聚合物合成了DGN-NPs,并进行了体外释放研究及动力学研究。DGN-NPs的平均粒径为290 nm,zeta电位为+11.5 mV,包封率为72%,多分散指数(PDI)为0.398。DGN-NPs的X射线衍射(XRD)分析表明其具有晶体性质,扫描电子显微镜(SEM)分析显示其呈球形形态且表面光滑。DGN从纳米颗粒中的释放通过扩散和侵蚀机制进行。通过在第1天向Wistar大鼠的左后爪注射0.1 ml完全弗氏佐剂来研究DGN-NPs的抗关节炎潜力,同时每日口服给予15 mg/kg的DGN以及5、10和15 mg/kg的DGN-NPs。甲氨蝶呤(1 mg/kg)作为标准药物,于第8天开始口服给药并持续至第28天。与DGN和标准疗法相比,DGN-NPs显著(p < 0.05 - 0.0001)减轻了爪部水肿、疼痛、关节炎评分,并改善了体重。与疾病对照组相比,GDN-NPs使肝脏和坐骨神经匀浆中的氧化应激生物标志物恢复正常,同时使改变的血液参数也恢复正常。在经DGN-NPs治疗的关节炎大鼠中,坐骨神经匀浆中血清素和去甲肾上腺素水平也显著升高。与疾病对照组相比,DGN-NPs治疗显著(p < 0.01 - 0.0001)下调了核因子κB(NF-κβ)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)、环氧化酶-2(COX-2)和肿瘤坏死因子-α(TNF-α),同时上调了白细胞介素-4(IL-4),这导致踝关节和坐骨神经的组织学损伤得到改善。从当前研究可以推断,与DGN相比,DGN-NPs尤其是15 mg/kg剂量时表现出显著的抗关节炎和镇痛活性。此外,DGN-NPs对外周神经病变也有效。

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