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Delivery of small molecules through intact and compromised skin.

机译:通过完好无损的皮肤输送小分子。

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摘要

The topical route provides localized delivery for many skin diseases. The objective of this study was to determine the feasibility of intradermal delivery of a novel lipophilic molecule, PTTC, as a potential psoriasis therapy. Microneedles were utilized to bypass the stratum corneum and achieve delivery to the viable epidermis. In vitro cell culture techniques were used to assess the skin irritation potential of PTTC and a psoriatic cell culture was dosed to determine efficacy by measurement of IL-6. The results show PTTC delivery could be achieved with use of microneedles, and the molecule was found to be non-irritant and efficacious in downregulating IL-6 in psoriatic skin. As many topical products are intended for skin diseases with damaged barrier, in vitro models simulating compromised skin were investigated, using diclofenac diethylamine as a model compound. Human cadaver skin treated with delipidization solvent, insertion of microneedles, or tape stripping was used as models to simulate damaged skin. Permeation studies were carried out on Franz diffusion cells using a lipophilic and hydrophilic vehicle for comparison. The results show delivery is greater with a hydrophilic vehicle across and correlates with degree of barrier impairment. In addition to simulating compromised skin, clinical usage of topical products can also be mimicked in vitro. A gel was rubbed into human cadaver skin, applied multiple times a day, and varying strengths were tested to determine effect on delivery. Diclofenac permeation was found to be concentration dependent, and significantly increased with multiple applications. The transdermal delivery route can bypass first pass metabolism. However, permeation is limited to small, moderately lipophilic compounds. Active techniques, such as microneedles or iontophoresis, can enhance the delivery of charged molecules that may not permeate well passively. Glycopyrrolate is a quaternary amine with an inherent positive charge. Each of these techniques was applied to a drug solution and permeation studies were performed on Franz cells. The results indicate iontophoresis alone enhanced delivery, and no synergism was observed for combination of both techniques. In conclusion, in vitro methods of Franz cells and cell culture models are powerful tools to determine drug delivery into and across skin.
机译:局部途径可为许多皮肤疾病提供局部递送。这项研究的目的是确定一种新型亲脂分子PTTC皮内递送作为潜在的牛皮癣治疗方法的可行性。利用微针绕过角质层并实现向活表皮的递送。使用体外细胞培养技术评估PTTC对皮肤的刺激潜力,并通过测量IL-6剂量对银屑病细胞培养进行剂量测定,以确定疗效。结果表明,使用微针可以实现PTTC的递送,并且发现该分子对银屑病皮肤中IL-6的下调无刺激性和有效作用。由于许多局部产品旨在用于屏障受损的皮肤疾病,因此使用双氯芬酸二乙胺作为模型化合物,研究了模拟受损皮肤的体外模型。用去脂溶剂处理过的人体尸体皮肤,插入微针或剥离胶带作为模拟受损皮肤的模型。使用亲脂性和亲水性媒​​介物对Franz扩散池进行渗透研究,以进行比较。结果表明,在亲水性载体上的传递更大,并且与屏障损害的程度相关。除了模拟受损的皮肤外,局部产品的临床用法也可以在体外进行模拟。将凝胶涂在人的尸体皮肤上,每天使用多次,并测试各种强度以确定对分娩的影响。发现双氯芬酸渗透是浓度依赖性的,并且随着多次施用而显着增加。透皮递送途径可以绕过首过代谢。但是,渗透仅限于小的,中等亲脂性化合物。诸如微针或离子电渗疗法之类的主动技术可以增强带电分子的传递,而带电分子可能无法很好地被动渗透。格隆溴铵是具有固有正电荷的季胺。这些技术中的每一种都应用于药物溶液,并且在Franz细胞上进行了渗透研究。结果表明,仅离子电渗疗法可增强递送,并且两种技术的组合均未观察到协同作用。总之,Franz细胞的体外方法和细胞培养模型是确定药物在皮肤内和皮肤中传递的有力工具。

著录项

  • 作者

    Gujjar, Meera.;

  • 作者单位

    Mercer University.;

  • 授予单位 Mercer University.;
  • 学科 Pharmaceutical sciences.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 91 p.
  • 总页数 91
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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