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开发一种基于透明质酸的优化脂质纳米乳剂,共包封两种多酚用于鼻脑递送。

Development of an optimized hyaluronic acid-based lipidic nanoemulsion co-encapsulating two polyphenols for nose to brain delivery.

作者信息

Nasr Maha

机构信息

a Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy , Ain Shams University , Cairo , Egypt.

出版信息

Drug Deliv. 2016 May;23(4):1444-52. doi: 10.3109/10717544.2015.1092619. Epub 2015 Sep 24.

Abstract

The development of mucoadhesive lipidic nanoemulsion based on hyaluronic acid, co-encapsulating two polyphenols (resveratrol and curcumin) for the transnasal treatment of neurodegenerative diseases was attempted in the current manuscript. Nanoemulsions were prepared by the spontaneous emulsification method, and were characterized for their particle size, zeta potential, mucoadhesive strength and morphology. The selected formula was tested for its antioxidant potential, in vitro and ex vivo release of the two polyphenols, safety on nasal mucosa and in vivo quantification of the two drugs in rat brains. Its stability was tested by monitoring the change in particle size, zeta potential, drugs' content and antioxidant potential upon storage for 3 months. The optimized hyaluronic acid based nanoemulsion formula displayed a particle size of 115.2 ± 0.15 and a zeta potential of -23.9 ± 1.7. The formula displayed a spherical morphology and significantly higher mucoadhesive strength compared to its non mucoadhesive counterpart. In addition, the nanoemulsion was able to preserve the antioxidant ability of the two polyphenols and protect them from degradation. Diffusion controlled release of the two drugs was achievable till 6 hours, with an ex vivo flux across sheep nasal mucosa of 2.86 and 2.09 µg/cm(2)hr for resveratrol and curcumin, respectively. Moreover, the mucoadhesive nanoemulsion was safe on nasal mucosa and managed to increase the amounts of the two polypehnols in the brain (about 7 and 9 folds increase in AUC0-7 h for resveratrol and curcumin, respectively). Hyaluronic acid based lipidic nanoemulsion proved itself as a successful carrier enhancing the solubility, stability and brain targetability of polyphenols.

摘要

在当前手稿中,尝试开发基于透明质酸的粘膜粘附脂质纳米乳剂,共包封两种多酚(白藜芦醇和姜黄素)用于神经退行性疾病的经鼻治疗。通过自发乳化法制备纳米乳剂,并对其粒径、zeta电位、粘膜粘附强度和形态进行表征。对所选配方进行了抗氧化潜力、两种多酚的体外和离体释放、鼻粘膜安全性以及大鼠脑中两种药物的体内定量测试。通过监测储存3个月后粒径、zeta电位、药物含量和抗氧化潜力的变化来测试其稳定性。优化后的基于透明质酸的纳米乳剂配方显示粒径为115.2±0.15,zeta电位为-23.9±1.7。该配方呈现球形形态,与非粘膜粘附对应物相比,粘膜粘附强度显著更高。此外,纳米乳剂能够保留两种多酚的抗氧化能力并保护它们不被降解。两种药物的扩散控制释放可持续6小时,白藜芦醇和姜黄素经羊鼻粘膜的离体通量分别为2.86和2.09μg/cm²·h。此外,粘膜粘附纳米乳剂对鼻粘膜安全,并成功增加了脑中两种多酚的含量(白藜芦醇和姜黄素在AUC0-7h分别增加约7倍和9倍)。基于透明质酸的脂质纳米乳剂证明是一种成功的载体,可提高多酚的溶解度、稳定性和脑靶向性。

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