The impact of particle size of nanostructured lipid carriers on follicular drug delivery: A comprehensive analysis of mouse and human hair follicle penetration

IF 2.2 4区 工程技术 Q3 PHARMACOLOGY & PHARMACY
Bioimpacts Pub Date : 2024-03-04 DOI:10.34172/bi.2024.30243
Saman Heydari, Mohammad Barzegar-Jalali, Mostafa Heydari, Afsaneh Radmehr, A. C. Paiva-Santos, M. Kouhsoltani, Hamed Hamishehkar
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Abstract

Introduction: Follicular delivery is one of the targeted drug delivery methods aiming to target the hair follicles. The accumulation and retention time of targeted drugs is enhanced when nanoparticles are used as drug carriers. Particle size is one of the important factors affecting the penetration and accumulation of particles in the hair follicles, and there is a controversy in different studies for the best particle size for follicular delivery. Mouse models are mostly used in clinical trials for dermal, transdermal, and follicular delivery studies. Also, it is essential to investigate the reliability of the results between human studies and mouse models. Methods: Curcumin-loaded nanostructured lipid carriers (NLCs), as a fluorescent agent, with three different particle size ranges were prepared using the hot homogenization method and applied topically on the mouse and human study groups. Biopsies were taken from applied areas on different days after using the formulation. The histopathology studies were done on the skin biopsies of both groups using confocal laser scanning microscopy (CLSM). We compared the confocal laser scanning microscope pictures of different groups, in terms of penetration and retention time of nanoparticles in human and mouse hair follicles. Results: The best particle size in both models was the 400 nm group but the penetration and accumulation of particles in human and mouse hair follicles were totally different even for the 400 nm group. In human studies, 400 nm particles showed good accumulation after seven days; this result can help to increase the formulation using intervals. Conclusion: The best particle size for human and mouse follicular drug delivery is around 400 nm and although mouse models are not completely suitable for follicular delivery studies, they can be used in some conditions as experimental models.
纳米结构脂质载体的粒径对毛囊给药的影响对小鼠和人类毛囊渗透性的综合分析
简介毛囊给药是以毛囊为靶点的靶向给药方法之一。当使用纳米颗粒作为药物载体时,靶向药物的蓄积和保留时间会得到延长。颗粒大小是影响颗粒在毛囊中渗透和蓄积的重要因素之一,不同研究对毛囊给药的最佳颗粒大小存在争议。小鼠模型大多用于皮肤、透皮和毛囊给药研究的临床试验。此外,研究人体研究与小鼠模型之间结果的可靠性也很重要。研究方法采用热均质法制备了三种不同粒径范围的姜黄素负载纳米结构脂质载体(NLCs)作为荧光剂,并将其局部涂抹在小鼠和人类研究组中。在使用制剂后的不同天数从涂抹部位提取活组织切片。使用激光共聚焦扫描显微镜(CLSM)对两组的皮肤活检组织进行病理学研究。我们从纳米颗粒在人和小鼠毛囊中的渗透和滞留时间方面比较了不同组的激光共聚焦扫描显微镜照片。结果显示两种模型的最佳粒径都是 400 nm 组,但即使是 400 nm 组,颗粒在人和小鼠毛囊中的穿透和蓄积也完全不同。在人体研究中,400 nm 颗粒在七天后显示出良好的蓄积性;这一结果有助于增加配方的使用间隔。结论虽然小鼠模型并不完全适合毛囊给药研究,但在某些情况下可以用作实验模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioimpacts
Bioimpacts Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.80
自引率
7.70%
发文量
36
审稿时长
5 weeks
期刊介绍: BioImpacts (BI) is a peer-reviewed multidisciplinary international journal, covering original research articles, reviews, commentaries, hypotheses, methodologies, and visions/reflections dealing with all aspects of biological and biomedical researches at molecular, cellular, functional and translational dimensions.
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