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Development of voltage gated transdermal drug delivery platform to impose synergistic enhancement in skin permeation using electroporation and gold nanoparticle

机译:电压门控透皮给药平台的开发,以利用电穿孔和金纳米颗粒增强皮肤渗透的协同作用

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摘要

Owing to poor skin permeability, the transdermal (TRD) drug delivery at the required therapeutic rate still remains an arduous task. In the present investigation, a novel TRD enhancement strategy was introduced using the synergistic effect of gold nanoparticle (GNP) and skin electroporation. Diclofenac sodium (DS) was selected as a model drug. An electro-sensitive patch was constructed using skin adhesive matrix, polyvinyl alcohol/poly(dimethyl siloxane)-g-polyacrylate. GNP/ carbon nanotube nanocomposite (GNP-CNT) was incorporated into the matrix with GNP and CNT to enhance skin permeability and electrical conductivity, respectively. Varying the concentration of GNP-CNT, alters the thermomechanical properties, water vapor permeability (WVP), drug encapsulation efficiency (DEE) and drug release profile, building a possibility to fine-tune the properties of the device. The membrane constructed with 1.5% GNP-CNT displayed the highest DEE and thermomechanical properties. The TRD DS release study was performed in rat skin at different GNP-CNT contents and variable conditions of applied voltage. Incorporating GNP-CNT enhanced the DS permeation profile with the best performance exhibited by device containing 1.5% nanofillers at an applied bias of 10.0 V. Electroporation in conjugation with GNP remarkably destroys the stratum comeum (SC) barrier by disparate mechanisms involving the breakdown of multilamellar lipid system, generation of new aqueous pathway and thermal effect. Furthermore, the dramatic disruption of lipid barriers generated by applied voltage was efficiently stabilized by GNP in addition to the transient and reversible openings created by them. Finally the safety of the device was confirmed by cell viability assay and environmental stability test. The developed skin permeation approach may open new avenues in TRD drug delivery.
机译:由于不良的皮肤渗透性,以所需的治疗速率进行透皮(TRD)药物递送仍然是艰巨的任务。在本研究中,利用金纳米颗粒(GNP)和皮肤电穿孔的协同效应,引入了一种新的TRD增强策略。选择双氯芬酸钠(DS)作为模型药物。使用皮肤粘合剂基质聚乙烯醇/聚(二甲基硅氧烷)-g-聚丙烯酸酯构建电敏贴剂。将GNP /碳纳米管纳米复合材料(GNP-CNT)与GNP和CNT掺入基质中,分别增强皮肤渗透性和导电性。改变GNP-CNT的浓度会改变热机械性能,水蒸气透过率(WVP),药物封装效率(DEE)和药物释放曲线,从而有可能微调设备的性能。用1.5%GNP-CNT制成的膜表现出最高的DEE和热机械性能。 TRD DS释放研究是在大鼠皮肤中不同GNP-CNT含量和施加电压的可变条件下进行的。掺入GNP-CNT可以增强DS的渗透性能,在10.0 V的施加偏压下,含1.5%纳米填料的装置表现出最佳的性能。与GNP结合的电穿孔可通过涉及多层分解的不同机制显着破坏角质层(SC)屏障。脂质系统,新的水通道的产生和热效应。此外,除了由它们产生的瞬时和可逆开口外,GNP还有效地稳定了由施加电压产生的脂质屏障的显着破坏。最后,通过细胞活力测定和环境稳定性测试确认了该装置的安全性。发达的皮肤渗透方法可能为TRD药物输送开辟新途径。

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  • 来源
    《Materials science & engineering》 |2019年第9期|437-446|共10页
  • 作者

    Anirudhan T. S.; Nair Syam S.;

  • 作者单位

    Univ Kerala, Sch Phys & Math Sci, Dept Chem, Trivandrum 695581, Kerala, India;

    Univ Kerala, Sch Phys & Math Sci, Dept Chem, Trivandrum 695581, Kerala, India;

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  • 入库时间 2022-08-18 04:19:16

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