Multifunctional nanoparticles encapsulating methotrexate and curcumin for holistic management of rheumatoid arthritis: in-vitro and pre-clinical assessment.

IF 2.4 4区 医学 Q3 CHEMISTRY, MEDICINAL Drug Development and Industrial Pharmacy Pub Date : 2023-08-01 DOI:10.1080/03639045.2023.2245057
Ayesha Syed, Preeti Karwa, Kusum Devi Vemula, Salwa
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引用次数: 1

Abstract

Purpose: Bovine serum albumin (BSA) nanoparticles (BSA-MTX-CUR-NPs) encapsulating methotrexate (MTX) and curcumin (CUR) was developed with an aim to co-deliver the drugs at the inflamed joint so as to maximize the therapeutic efficacy and alleviate toxic side effects associated with MTX.

Methods: Nanoparticle albumin-bound technology was used to formulate nanoparticles, followed by characterization for its particle size, polydispersity index, encapsulation efficiency, zeta potential, surface morphology, in-vitro drug release and drug release kinetics. Further, we investigated the pharmacokinetics and pharmacodynamics of the developed nanoparticles in the adjuvant-induced arthritis model.

Results: BSA-MTX-CUR-NPs exhibited particle size of 163.05 ± 1.708 nm, polydispersity index of 0.195 ± 0.0024 and % encapsulation efficiency of 68.23 ± 0.640% for MTX and 75.71 ± 0.216% for CUR with controlled release pattern for both the drugs. The scanning electron microscopy revealed nanoparticles exhibited a spherical shape. DSC study confirmed the absence of incompatibility between the drugs and the excipients. Half-life and area under the curve were significantly higher for MTX in the nanoparticulate form in comparison to free MTX. Pharmacodynamic studies revealed that BSA-MTX-CUR-NPs possessed better disease-modifying effects in comparison to free MTX.

Conclusion: Hence, it can be concluded that albumin nanoparticles constitute a viable method for delivering MTX and CUR to inflamed joints simultaneously, because of the strong affinity of albumin and enhanced permeability and retention effect at the inflamed joint. This combinational therapy of MTX & CUR in nanoparticulate form has the potential for the holistic management of rheumatoid arthritis.

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多功能纳米颗粒包封甲氨蝶呤和姜黄素对类风湿关节炎的整体管理:体外和临床前评估。
目的:研制包膜甲氨蝶呤(MTX)和姜黄素(CUR)的牛血清白蛋白(BSA)纳米颗粒(BSA-MTX-CUR- nps),目的是在炎症关节处共同递送药物,以最大限度地提高治疗效果并减轻MTX相关的毒副作用。方法:采用纳米颗粒白蛋白结合技术制备纳米颗粒,对其粒径、多分散指数、包封效率、zeta电位、表面形貌、体外释药及释药动力学进行表征。此外,我们研究了开发的纳米颗粒在佐剂诱导的关节炎模型中的药代动力学和药效学。结果:BSA-MTX-CUR-NPs的粒径为163.05±1.708 nm,多分散指数为0.195±0.0024,包封率为68.23±0.640%,CUR为75.71±0.216%,两种药物均呈控释模式。扫描电镜显示纳米颗粒呈球形。DSC研究证实了药物与辅料之间不存在不相容性。与游离MTX相比,纳米粒形式的MTX的半衰期和曲线下面积明显更高。药效学研究显示,与游离MTX相比,BSA-MTX-CUR-NPs具有更好的疾病改善作用。结论:白蛋白纳米颗粒具有较强的亲和力,增强了炎症关节的渗透性和滞留性,因此可以认为白蛋白纳米颗粒是同时向炎症关节递送MTX和CUR的可行方法。这种纳米颗粒形式的MTX和CUR的联合治疗具有全面治疗类风湿性关节炎的潜力。
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来源期刊
CiteScore
6.80
自引率
0.00%
发文量
82
审稿时长
4.5 months
期刊介绍: The aim of Drug Development and Industrial Pharmacy is to publish novel, original, peer-reviewed research manuscripts within relevant topics and research methods related to pharmaceutical research and development, and industrial pharmacy. Research papers must be hypothesis driven and emphasize innovative breakthrough topics in pharmaceutics and drug delivery. The journal will also consider timely critical review papers.
期刊最新文献
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