Nabila Fahmida Habib, Islam Rashedul, Yamin Li, Yoshirou Kawaguchi, Wakabayashi Rie, Kamiya Noriho, Moniruzzaman Muhammad, Goto Masahiro
Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Advanced Transdermal Drug Delivery System Center, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
ACS Biomater Sci Eng. 2025 Jan 13;11(1):402-414. doi: 10.1021/acsbiomaterials.4c02000. Epub 2024 Dec 17.
Transdermal insulin delivery is a promising method for diabetes management, providing the potential for controlled, sustained release and prolonged insulin effectiveness. However, the large molecular weight of insulin hinders its passive absorption through the stratum corneum (SC) of the skin, and high doses of insulin are required, which limits the commercial viability. We developed ethosome (ET) and -ethosome (TET) nanovesicle formulations containing a biocompatible lipid-based ionic liquid, [EDMPC][Lin], dissolved in 35% ethanol. TET formulations were obtained by adding isopropyl myristate (IPM), Tween-80, or Span-20 as surfactants to ET formulations. Dynamic light scattering, ζ-potential, transmission electron microscopy, and confocal laser scanning microscopy studies revealed that the nanovesicles had a stable particle size. The formulations remained stable at 4 °C for more than 3 months. ET and TET formulations containing IPM (TET1) significantly ( < 0.0001) enhanced the transdermal penetration of FITC-tagged insulin (FITC-Ins) in both mouse and pig skin, compared with that of the control FITC-Ins solution and other TET formulations, by altering the molecular structure of the SC layer. These nanovesicles were found to be biocompatible and nonirritants (cell viability >80%) in the and studies on three-dimensional (3D) artificial human skin and a diabetic mouse model, respectively. The ET and TET1 formulations were applied to the skin of diabetic mice at an insulin dosage of 30 IU/kg. The nanovesicle formulations significantly reduced blood glucose levels (BGLs) compared with the initial high BGL value (>150 mg/dL). The nanovesicle-treated mice maintained low BGLs for over 15 h, as opposed to only 2 h in the injection group. The ET and TET1 formulations reduced the BGLs by 62 and 34%, respectively, of the initial value. These ET and TET1 formulations have a high potential for use in commercial transdermal insulin patches, enhancing comfort and adherence in diabetes treatment.
经皮胰岛素递送是一种很有前景的糖尿病管理方法,具有可控、持续释放和延长胰岛素疗效的潜力。然而,胰岛素的大分子质量阻碍了其通过皮肤角质层(SC)的被动吸收,需要高剂量的胰岛素,这限制了其商业可行性。我们开发了包含溶解在35%乙醇中的生物相容性脂质基离子液体[EDMPC][Lin]的乙醇脂质体(ET)和转乙醇脂质体(TET)纳米囊泡制剂。通过向ET制剂中添加肉豆蔻酸异丙酯(IPM)、吐温80或司盘20作为表面活性剂来获得TET制剂。动态光散射、ζ电位、透射电子显微镜和共聚焦激光扫描显微镜研究表明,纳米囊泡具有稳定的粒径。这些制剂在4℃下保持稳定超过3个月。与对照FITC-胰岛素溶液和其他TET制剂相比,含有IPM的ET和TET制剂(TET1)通过改变SC层的分子结构,显著(<0.0001)增强了FITC标记的胰岛素(FITC-Ins)在小鼠和猪皮肤中的透皮渗透。分别在三维(3D)人工人皮肤和糖尿病小鼠模型的研究中发现,这些纳米囊泡具有生物相容性且无刺激性(细胞活力>80%)。将ET和TET1制剂以30 IU/kg的胰岛素剂量应用于糖尿病小鼠的皮肤。与初始高血糖水平(>150 mg/dL)相比,纳米囊泡制剂显著降低了血糖水平(BGLs)。纳米囊泡处理的小鼠将低血糖水平维持超过15小时,而注射组仅维持2小时。ET和TET1制剂分别将血糖水平降低了初始值的62%和34%。这些ET和TET1制剂在商业经皮胰岛素贴剂中具有很高的应用潜力,可提高糖尿病治疗的舒适度和依从性。