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首页> 外文期刊>International Journal of Nanomedicine >Methotrexate-Loaded Nanostructured Lipid Carrier Gel Alleviates Imiquimod-Induced Psoriasis by Moderating Inflammation: Formulation, Optimization, Characterization, In-Vitro and In-Vivo Studies
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Methotrexate-Loaded Nanostructured Lipid Carrier Gel Alleviates Imiquimod-Induced Psoriasis by Moderating Inflammation: Formulation, Optimization, Characterization, In-Vitro and In-Vivo Studies

机译:甲氨蝶呤负载纳米结构脂质载体凝胶通过调节炎症来缓解咪喹莫德诱导的牛皮癣:制剂,优化,表征,体外和体内研究

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Introduction: Methotrexate exhibits poor cutaneous bioavailability and systemic side effects on topical administration, so there is an unmet need for a novel carrier and its optimized therapy. Methotrexate-loaded nanostructured lipid carriers (MTXNLCs) were formulated and characterized to determine in vitro drug release and evaluate the role of MTXNLC gel in the topical treatment of psoriasis. Methods: A solvent diffusion technique was employed to prepare MTXNLCs, which was optimized using 3sup2/sup full factorial designs. The mean diameter and surface morphology of MTXNLCs was evaluated. The crystallinity of lyophilized MTXNLCs was characterized by differential scanning calorimetry (DSC) and powder X-ray diffraction (XRD). MTXNLCs were integrated in 1% w/w Carbopol 934 P gel base, and in vitro skin deposition studies in human cadaver skin (HCS) were carried out. Results: The optimized MTXNLCs were rod-shaped, with an average particle size of 253 ± 8.65 nm, a zeta potential of ? 26.4± 0.86 mV, and EE of 54.00± 1.49%. DSC and XRD data confirmed the formation of NLCs. Significantly higher deposition of MTX was found in HCS from MTXNLC gel (71.52 ± 1.13%) as compared to MTX plain gel (38.48± 0.96%). In vivo studies demonstrated significant improvement in therapeutic response and reduction in local side effects with MTXNLCs-loaded gel in the topical treatment of psoriasis. Anti-psoriatic efficacy of MTXNLCs 100 ug/cmsup2/sup compared with plain MTX gel was evaluated using imiquimod (IMQ)-induced psoriasis in BALB/c mice. The topical application of MTXNLCs to the mouse ear resulted in a significant reduction of psoriatic area and severity index, oxidative stress, inflammatory cytokines like TNF-α, IL-1β, and IL-6 and IMQ-induced histopathological alterations in mouse ear samples. Conclusion: Developed formulation of MTXNLC gel demonstrated better anti-psoriatic activity and also displayed prolonged and sustained release effect, which shows that it can be a promising alternative to existing MTX formulation for the treatment of psoriasis.
机译:简介:甲氨蝶呤对外用管理的皮肤生物利用度和系统副作用差,因此对新型载体的未满足并有所优化。配制甲氨蝶呤纳米结构脂质载体(MTXNLC),并表征以体外药物释放,并评估MTXNLC凝胶在牛皮癣局部治疗中的作用。方法:采用溶剂扩散技术制备MTXNLC,其使用3 2 全部造型设计进行了优化。评估MTXNLC的平均直径和表面形态。通过差示扫描量热法(DSC)和粉末X射线衍射(XRD)的特征在于冻干MTXNLC的结晶度。 MTXNLCS集成在1%W / W Carbopol 934 P凝胶基础中,进行人尸体皮肤(HCS)的体外皮肤沉积研究。结果:优化的MTXNLC是杆状,平均粒度为253±8.65nm,Zeta电位为? 26.4±0.86 mV,EE为54.00±1.49%。 DSC和XRD数据确认了NLC的形成。与MTX平原凝胶相比,在MTXNLC凝胶的HCS中发现MTX的显着较高沉积MTX(71.52±1.13%)(38.48±0.96%)。体内研究表明,治疗响应和局部副作用的显着改善,在牛皮癣的局部治疗中,用MTXNLCS加载的凝胶降低。使用咪唑(IMQ)在Balb / C小鼠中诱导牛皮癣,评价与普通MTX凝胶相比的MTXNLCs 100ug / cm 2 的抗银效效应。 MTXNLCS对小鼠耳的局部施用导致银屑病区域和严重程度指数的显着降低,氧化应激,炎性细胞因子等TNF-α,IL-1β和IL-6和IMQ诱导的小鼠耳朵样品的组织病理学改变。结论:MTXNLC凝胶的开发配方显示出更好的抗银屑病活性,并且还显示出长期和持续的释放效果,表明它可以是现有MTX制剂治疗牛皮癣的有希望的替代品。

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