Yazdani Ashtiani Sahar, Ahmad Nasrollahi Saman, Naeimifar Atefeh, Nassiri Kashani Aubid, Samadi Aniseh, Yadangi Somayeh, Aboutaleb Ehsan, Abdolmaleki Poorya, Dinarvand Rassoul, Firooz Alireza
Pharmaceutical, Cosmeceutical and Hygienic Formulation Lab, Center for Research & Training in Skin Diseases & Leprosy, Tehran University of Medical Sciences, Tehran, Iran.
Department of Pharmaceutics, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Adv Pharm Bull. 2021 Jan;11(1):104-110. doi: 10.34172/apb.2021.011. Epub 2020 Nov 7.
Vitiligo is a long-term common autoimmune disease in which growing patches of skin lose their color. There is no FDA-approved treatment for vitiligo. However, recent studies have demonstrated an immunosuppressive effect on vitiligo lesions in mouse models by simvastatin. A topical formulation was prepared containing simvastatin-loaded nano lipid carriers (simNLCs) for vitiligo treatment followed by evaluating their physicochemical characteristics and clinical safety. Both the lipid phase and the aqueous phase were heated to 75°C separately, and then simvastatin was dispersed in the lipid phase added to the aqueous phase. The mixture was homogenized for 1 minute, then for Nanostructured Lipid Carriers (NLC) formation, the emulsion was sonicated using a probe sonicator. The simNLCs produced were evaluated for drug entrapment, particle size and morphology, zeta potential, polydispersity index, viscosity, drug content, in vitro drug release, in vivo skin safety test, and long-term stability studies. Dynamic light scattering, transmission electron microscopy and differential scanning calorimetry techniques proved the formation of a stable formulation containing spherical particles with nanoscale size. The drug entrapment efficiency and the drug-loading capacity were determined to be 99.27% and 3.9%, respectively. Human safety results indicated that adding simvastatin to lipid nanoparticles did not cause any changes to skin biophysical parameters. The preparation method of simNLC developed in this study is a suitable method, and the nanoparticles fabricated were safe with acceptable long-term stability and drug entrapment.
白癜风是一种常见的慢性自身免疫性疾病,患病皮肤区域会逐渐脱色。目前尚无美国食品药品监督管理局(FDA)批准的白癜风治疗方法。然而,最近的研究表明,辛伐他汀在小鼠模型中对白癜风皮损具有免疫抑制作用。制备了一种含载辛伐他汀纳米脂质载体(simNLCs)的外用制剂用于白癜风治疗,随后评估其理化特性和临床安全性。分别将脂质相和水相加热至75°C,然后将辛伐他汀分散于脂质相中并加入水相。混合物均质1分钟,然后为形成纳米结构脂质载体(NLC),使用探头式超声仪对乳液进行超声处理。对所制备的simNLCs进行药物包封率、粒径和形态、zeta电位、多分散指数、粘度、药物含量、体外药物释放、体内皮肤安全性测试以及长期稳定性研究。动态光散射、透射电子显微镜和差示扫描量热法技术证明形成了一种含有纳米级球形颗粒的稳定制剂。药物包封率和载药量分别测定为99.27%和3.9%。人体安全性结果表明,向脂质纳米颗粒中添加辛伐他汀不会对皮肤生物物理参数造成任何改变。本研究中开发的simNLC制备方法是一种合适的方法,所制备的纳米颗粒安全,具有可接受的长期稳定性和药物包封率。