Janakiraman Kumar, Krishnaswami Venkateshwaran, Rajendran Vijaya, Natesan Subramanian, Kandasamy Ruckmani
National Facility for Drug Development for Academia, Pharmaceutical and Allied Industries (NFDD), Centre for Excellence in Nanobio Translational REsearch (CENTRE), Department of Pharmaceutical Technology, University College of Engineering, Anna University, BIT Campus, Tiruchirappalli 620 024, Tamil Nadu, India.
Mater Today Commun. 2018 Dec;17:200-213. doi: 10.1016/j.mtcomm.2018.09.011. Epub 2018 Sep 15.
Rheumatoid arthritis (RA) is the most common complex multifactorial joint related autoimmune inflammatory disease with unknown etiology accomplished with increased cardiovascular risks. RA is characterized by the clinical findings of synovial inflammation, autoantibody production, and cartilage/bone destruction, cardiovascular, pulmonary and skeletal disorders. Pro-inflammatory cytokines such as IL-1, IL-6, IL-8, and IL-10 were responsible for the induction of inflammation in RA patients. Drawbacks such as poor efficacy, higher doses, frequent administration, low responsiveness, and higher cost and serious side effects were associated with the conventional dosage forms for RA treatment. Nanomedicines were recently gaining more interest towards the treatment of RA, and researchers were also focusing towards the development of various anti-inflammatory drug loaded nanoformulations with an aid to both actively/passively targeting the inflamed site to afford an effective treatment regimen for RA. Alterations in the surface area and nanoscale size of the nanoformulations elicit beneficial physical and chemical properties for better pharmacological activities. These drug loaded nanoformulations may enhances the solubility of poorly water soluble drugs, improves the bioavailability, affords targetability and may improve the therapeutic activity. In this regimen, the present review focus towards the novel nanoparticulate formulations (nanoparticles, nanoemulsions, solid lipid nanoparticles, nanomicelles, and nanocapsules) utilized for the treatment of RA. The recent advancements such as siRNA, peptide and targeted based nanoparticulate systems for RA treatment were also discussed. Special emphasis was provided regarding the pathophysiology, prevalence and symptoms towards the development of RA.
类风湿性关节炎(RA)是最常见的复杂多因素关节相关自身免疫性炎症疾病,病因不明,且伴有心血管风险增加。RA的特征在于滑膜炎症、自身抗体产生以及软骨/骨破坏、心血管、肺部和骨骼疾病等临床症状。促炎细胞因子如白细胞介素-1(IL-1)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)和白细胞介素-10(IL-10)是导致RA患者炎症的原因。RA治疗的传统剂型存在疗效不佳、剂量高、给药频繁、反应性低、成本高以及严重副作用等缺点。纳米药物最近在RA治疗方面越来越受到关注,研究人员也在致力于开发各种载有抗炎药物的纳米制剂,以主动/被动靶向炎症部位,为RA提供有效的治疗方案。纳米制剂表面积和纳米级尺寸的改变引发了有益的物理和化学性质,以实现更好的药理活性。这些载药纳米制剂可以提高难溶性药物的溶解度,提高生物利用度,实现靶向性,并可能改善治疗活性。在本综述中,重点关注用于治疗RA的新型纳米颗粒制剂(纳米颗粒、纳米乳液、固体脂质纳米颗粒、纳米胶束和纳米胶囊)。还讨论了用于RA治疗的小干扰RNA(siRNA)、肽和基于靶向的纳米颗粒系统等最新进展。特别强调了RA发病机制、患病率和症状等方面。