首页> 外文期刊>Drug Design, Development and Therapy >Electroporation-enhanced transdermal diclofenac sodium delivery into the knee joint in a rat model of acute arthritis
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Electroporation-enhanced transdermal diclofenac sodium delivery into the knee joint in a rat model of acute arthritis

机译:在急性关节炎大鼠模型中,电穿孔增强的经皮双氯芬酸钠经皮递送至膝关节

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Purpose: Since electroporation (EP) can increase the permeability of biological membranes, we hypothesized that it offers an opportunity to enhance the transdermal delivery of drugs for intra-articular indications. Our aim was to compare the anti-inflammatory and analgesic efficacy of EP-combined topical administration of diclofenac sodium hydrogel (50 mg mL-1 in 230 μL volume) with that of an equivalent dose of oral (75 mg kg-1) and simple topical administration. Methods: Arthritis was induced with the injection of 2% λ-carrageenan and 4% kaolin into the right knee joints of male Sprague Dawley rats. EP was applied for 8 min with 900 V high-voltage pulses for 5 ms followed by a 20 ms break. Drug penetration into the synovial fluid and plasma was detected by high-performance liquid chromatography. Leukocyte–endothelial interactions were visualized by intravital videomicroscopy on the internal surface of the synovium. Inflammation-induced thermal and mechanical hyperalgesia reactions, knee joint edema, and inflammatory enzyme activities were assessed at 24 and 48 h after arthritis induction. Results: EP significantly increased the plasma level of diclofenac as compared with the topical controls 10 min after the 2% λ-carrageenan and 4% kaolin injection. Increased leukocyte–endothelial interactions were accompanied by joint inflammation, which was significantly reduced by oral and EP diclofenac (by 45% and by 30%, respectively) and only slightly ameliorated by simple topical diclofenac treatment (by 18%). The arthritis-related secondary hyperalgesic reactions were significantly ameliorated by oral and EP-enhanced topical diclofenac treatments. The knee cross-section area (which increased by 35%) was also reduced with both approaches. However, simple topical application did not influence the development of joint edema and secondary hyperalgesia. Conclusion: The study provides evidence for the first time of the potent anti-inflammatory and analgesic effects of EP-enhanced topical diclofenac during arthritis. The therapeutic benefit provided by EP is comparable with that of oral diclofenac; EP is a useful alternative to conventional routes of administration.
机译:目的:由于电穿孔(EP)可以增加生物膜的通透性,因此我们假设它为增强关节内适应症药物的透皮递送提供了机会。我们的目的是比较EP联合局部用双氯芬酸钠水凝胶(50 mg mL -1 ,剂量为230μL)与同等剂量口服(75)的抗炎和镇痛效果。 mg kg -1 )和简单的局部给药。方法:在雄性Sprague Dawley大鼠的右膝关节中注射2%λ角叉菜胶和4%高岭土诱发关节炎。使用900 V高压脉冲施加EP 8分钟,持续5 ms,然后中断20 ms。通过高效液相色谱检测药物渗透到滑液和血浆中。通过滑膜内表面的活体视频显微镜观察白细胞与内皮的相互作用。在关节炎诱发后24和48小时评估炎症引起的热和机械痛觉过敏反应,膝关节水肿和炎性酶活性。结果:与2%λ角叉菜胶和4%高岭土注射后的局部对照相比,EP显着增加了双氯芬酸的血浆水平。白细胞与内皮的相互作用增加伴随着关节发炎,口服和双氯芬酸显着降低了关节发炎率(分别降低了45%和30%),而简单的局部双氯芬酸治疗则仅有轻微的改善(降低了18%)。口服和EP增强的局部双氯芬酸治疗可显着改善关节炎相关的继发性痛觉过敏反应。两种方法均减小了膝盖的横截面积(增加了35%)。然而,简单的局部应用并不影响关节水肿和继发性痛觉过敏的发展。结论:该研究首次证明了EP增强的局部双氯芬酸在关节炎中有效的抗炎和镇痛作用。 EP提供的治疗效果与口服双氯芬酸相当。 EP是常规给药途径的有用替代物。

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