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Dendritic polyglycerol and N-isopropylacrylamide based thermoresponsive nanogels as smart carriers for controlled delivery of drugs through the hair follicle

机译:树突状聚甘油和基于N-异丙丙烯酰胺的热响应纳米凝胶作为智能载体,用于通过毛囊控制药物的智能载体

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摘要

Nanoparticles with a size of several hundred nanometers can effectively penetrate into the hair follicles and may serve as depots for controlled drug delivery. However, they can neither overcome the hair follicle barrier to reach the viable cells nor release the loaded drug adequately. On the other hand, small drug molecules cannot penetrate deep into the hair follicles. Thus, the most efficient way for drug delivery through the follicular route is to employ nanoparticles that can release the drug close to the target structure upon exposure to some external or internal stimuli. Accordingly, 100-700 nm sized thermoresponsive nanogels with a phase transition temperature of 32-37 degrees C were synthesized by the precipitation polymerization technique using N-isopropylacrylamide as a monomer, acrylated dendritic polyglycerol as a crosslinker, VA-044 as an initiator, and sodium dodecyl sulphate as a stabilizer. The follicular penetration of the indodicarbocyanine (IDCC) labeled nanogels into the hair follicles and the release of coumarin 6, which was loaded as a model drug, in the hair follicles were assessed ex vivo using porcine ear skin. Confocal laser scanning microscopy (CLSM) enabled independent tracking of the nanogels and the loaded dye, although it is not as precise and accurate as standard analytical methods. The results showed that, unlike smaller nanogels (<100 nm), medium and larger sized nanogels (300-500 nm) penetrated effectively into the hair follicles with penetration depths proportional to the nanogel size. The release of the loaded dye in the hair follicles increased significantly when the investigation on penetration was carried out above the cloud point temperature of the nanogels. The follicular penetration of the nanogels from the colloidal dispersion and a 2.5% hydroxyethyl cellulose gel was not significantly different.
机译:数百纳米大小的纳米颗粒可以有效地渗透到毛囊中,并可以用作可控制药物输送的库。但是,他们既不能克服毛囊屏障,无法到达活细胞,也不能充分释放荷载药物。另一方面,小药物分子无法深入毛囊。因此,通过滤泡途径输送药物的最有效方法是使用纳米颗粒,可在暴露于某些外部或内部刺激的情况下释放接近靶结构的药物。因此,通过使用N-异丙基酰胺作为单体,通过降水聚合技术合成100-700 nm尺寸的热响应纳米凝胶,其相过渡温度为32-37摄氏度,由降水聚合技术合成,丙烯酸化的树枝状聚甘油作为交叉链接,VA-044和发行剂,并将十二烷基硫酸钠作为稳定剂。卵泡的卵泡渗透(IDCC)标记纳米凝胶到毛囊中,并使用猪耳朵皮肤评估了毛囊中的香豆素6的释放,并在毛囊中释放了毛细血管。共聚焦激光扫描显微镜(CLSM)启用了纳米凝胶和负载染料的独立跟踪,尽管它不像标准分析方法那么精确和准确。结果表明,与较小的纳米凝胶(<100 nm)不同,中等大小的纳米凝胶(300-500 nm)有效地渗透到毛囊中,其穿透深度与纳米凝胶大小成正比。当对穿透性的研究在纳米凝胶的云点温度上方进行时,毛囊中负载的染料的释放显着增加。纳米凝胶从胶体分散液和2.5%羟基乙基纤维素凝胶中的卵泡穿透没有显着差异。

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