Nayak Tapas R, Wang Hao, Pant Aakansha, Zheng Minrui, Junginger Hans, Goh Wei Jiang, Lee Choon Keong, Zou Shui, Alonso Sylvie, Czarny Bertrand, Storm Gert, Sow Chorng Haur, Lee Chengkuo, Pastorin Giorgia
Department of Pharmacy, National University of Singapore, Singapore 117583, Singapore.
Department of Electrical Engineering, National University of Singapore, Singapore 117583, Singapore.
Nanomaterials (Basel). 2017 Jun 15;7(6):147. doi: 10.3390/nano7060147.
Intradermal delivery of antigens for vaccination is a very attractive approach since the skin provides a rich network of antigen presenting cells, which aid in stimulating an immune response. Numerous intradermal techniques have been developed to enhance penetration across the skin. However, these methods are invasive and/or affect the skin integrity. Hence, our group has devised zinc oxide (ZnO) nano-rods for non-destructive drug delivery. Chemical vapour deposition was used to fabricate aligned nano-rods on ZnO pre-coated silicon chips. The nano-rods' length and diameter were found to depend on the temperature, time, quality of sputtered silicon chips, etc. Vertically aligned ZnO nano-rods with lengths of 30-35 µm and diameters of 200-300 nm were selected for in vitro human skin permeation studies using Franz cells with Albumin-fluorescein isothiocyanate (FITC) absorbed on the nano-rods. Fluorescence and confocal studies on the skin samples showed FITC penetration through the skin along the channels formed by the nano-rods. Bradford protein assay on the collected fluid samples indicated a significant quantity of Albumin-FITC in the first 12 h. Low antibody titres were observed with immunisation on Balb/c mice with ovalbumin (OVA) antigen coated on the nano-rod chips. Nonetheless, due to the reduced dimensions of the nano-rods, our device offers the additional advantage of excluding the simultaneous entrance of microbial pathogens. Taken together, these results showed that ZnO nano-rods hold the potential for a safe, non-invasive, and painless intradermal drug delivery.
通过皮内注射抗原进行疫苗接种是一种非常有吸引力的方法,因为皮肤拥有丰富的抗原呈递细胞网络,有助于刺激免疫反应。为了增强药物穿透皮肤的能力,人们已经开发了许多皮内注射技术。然而,这些方法具有侵入性和/或会影响皮肤完整性。因此,我们团队设计了氧化锌(ZnO)纳米棒用于无损药物递送。采用化学气相沉积法在预涂有ZnO的硅芯片上制备排列整齐的纳米棒。发现纳米棒的长度和直径取决于温度、时间、溅射硅芯片的质量等因素。选择长度为30 - 35 µm、直径为200 - 300 nm的垂直排列的ZnO纳米棒,使用Franz扩散池进行体外人皮肤渗透研究,纳米棒上吸附有白蛋白 - 异硫氰酸荧光素(FITC)。对皮肤样本的荧光和共聚焦研究表明,FITC沿着纳米棒形成的通道穿透皮肤。对收集的液体样本进行Bradford蛋白测定表明,在前12小时内有大量的白蛋白 - FITC。用涂有卵清蛋白(OVA)抗原的纳米棒芯片对Balb/c小鼠进行免疫接种时,观察到抗体滴度较低。尽管如此,由于纳米棒尺寸减小,我们的装置还具有排除微生物病原体同时进入的额外优势。综上所述,这些结果表明ZnO纳米棒具有实现安全、无创和无痛皮内药物递送的潜力。