药理学
化学
体内
粘液
药物输送
髓过氧化物酶
氨基水杨酸
离体
血红蛋白
IC50型
体外
生物化学
医学
炎症
免疫学
生物
有机化学
生物技术
生态学
作者
Zahra Vaezi,Hamid Asadzadeh Aghdaei,Mosslim Sedghi,Reza Mahdavian,Maryam Molakarimi,Naimeh Hashemi,Hossein Naderi‐Manesh
标识
DOI:10.1016/j.ijpharm.2022.121531
摘要
A colonic drug delivery system was developed to specifically deliver 5-aminosalicylic acid (5-ASA) to the inflamed site by conjugating with hemoglobin nanoparticles (HbNPs). The 5-ASA-HbNPs (eight 5-ASA molecules per Hb molecule) with the size of 220 nm and zeta potential of -14.6 mV is a tailored nanoparticle able to pass through the mucus layer. The 5-ASA-HbNPs do not undergo chemical and enzymatic hydrolysis in the simulated gastrointestinal fluids over 6 h. Significantly higher cellular uptakes and prolonged release was seen for the 5-ASA-HbNPs in Caco-2 cells, compared to free 5-ASA over 72 h. In addition, 5-ASA-HbNPs revealed similar therapeutic effectiveness with free 5-ASA against tumor necrosis factor and showed less inhibitory concentration (IC50) for myeloperoxidase enzyme activity. In vivo imaging of mouse demonstrated the localization of drug in the descending colon after oral administration and about 15% of the administered dose was recovered as 5-ASA from urine in 6 h. The use of these nanoparticles with the mucus adhesion properties and permeability to intestinal epithelial cells can be a good candidate with potential application in the colonic drug delivery field.
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