Simões S I, Delgado T C, Lopes R M, Jesus S, Ferreira A A, Morais J A, Cruz M E M, Corvo M L, Martins M B F
Unidade de Novas Formas de Agentes Bioactivos, Departamento de Biotecnologia, Instituto Nacional de Engenharia, Tecnologia e Inovação, Edifício F, Estrada do Paço do Lumiar, 22 1649-038 Lisboa, Portugal.
J Control Release. 2005 Mar 21;103(2):419-34. doi: 10.1016/j.jconrel.2004.12.008. Epub 2005 Jan 15.
The aim of this study was firstly to refine a rat model of arthritis, the adjuvant arthritis (AA) model, by studying the time course of the disease, introducing new evaluation methods such as haematological and biochemical parameters in order to identify the main stages of the disease. An optimisation of treatment schedule and evaluation criteria was developed. This refinement provided novel non-invasive anti-inflammatory treatment of the AA with SOD by using mixed lipid vesicles specially developed for transdermal delivery, Transfersomes (Tfs), this being the second major aim. The time course of AA includes a first stage: 1 day after the disease induction, the induced paw volume more than doubled and the paw circumference increased by approx. 50%. Two weeks later, another stage occurred where the disease shifted from the local arthritis form towards polyarthritis: an additional increase of volume and circumference of the induced and non-induced paws, occurred. The animals also started to loose weight around day 14 after the disease induction. Radiographic observable lesions increased correspondingly. Treatment of animals, started at day 1 after induction, by epicutaneous application of SOD-Tfs showed that 1 mg SOD/kg body weight is more efficient than 0.66 mg SOD /kg body weight. As a positive control, SOD liposomes intravenously injected were used for comparison and confirmed the biological efficiency of epicutaneously applied SOD in Tfs. SOD solution and empty Tfs epicutaneously applied exerted no effect. In addition, epicutaneous application of SOD-Tfs used prophylactically was able to suppress the induced rat paw oedema. Radiographic images showed less joint lesions in SOD-Tfs treated animals in comparison with control and placebo treated rats. It was shown for the first time that SOD incorporated into Tfs and applied onto a skin area not necessarily close to the inflamed tissue is able to promote non-invasive treatment of induced arthritis.
本研究的目的首先是通过研究疾病的时间进程来优化大鼠关节炎模型——佐剂性关节炎(AA)模型,引入血液学和生化参数等新的评估方法,以确定疾病的主要阶段。并制定了治疗方案和评估标准的优化方法。这种优化实现了第二个主要目标,即通过使用专门为经皮递送开发的混合脂质囊泡——传递体(Tfs),对AA进行新型非侵入性抗炎治疗。AA的时间进程包括第一阶段:疾病诱导后1天,诱导爪体积增加一倍多,爪周长增加约50%。两周后,出现另一个阶段,疾病从局部关节炎形式转变为多关节炎:诱导爪和未诱导爪的体积和周长进一步增加。动物在疾病诱导后约第14天也开始体重减轻。X线可见病变相应增加。在诱导后第1天开始对动物进行经皮应用SOD-Tfs治疗,结果显示1mg SOD/kg体重比0.66mg SOD/kg体重更有效。作为阳性对照,静脉注射SOD脂质体用于比较,并证实了经皮应用于Tfs中的SOD的生物学有效性。经皮应用SOD溶液和空Tfs没有效果。此外,预防性经皮应用SOD-Tfs能够抑制诱导的大鼠爪水肿。X线图像显示,与对照和安慰剂处理的大鼠相比,SOD-Tfs处理的动物关节病变更少。首次表明,掺入Tfs并应用于不一定靠近炎症组织的皮肤区域的SOD能够促进诱导性关节炎的非侵入性治疗。