Hemoglobin bio-adhesive nanoparticles as a colon-specific delivery system for sustained release of 5-aminosalicylic acid in the effective treatment of inflammatory bowel disease

被引:15
作者
Vaezi, Zahra [1 ,2 ]
Aghdaei, Hamid Asadzadeh [2 ]
Sedghi, Mosslim [3 ]
Mahdavian, Reza [3 ]
Molakarimi, Maryam [4 ]
Hashemi, Naimeh [5 ]
Naderi-Manesh, Hossein [1 ,3 ]
机构
[1] Tarbiat Modares Univ, Fac Interdisciplinary Sci & Technol, Dept Bioact Cpds, Tehran 14115154, Iran
[2] Shahid Beheshti Univ Med Sci, Basic & Mol Epidemiol Gastrointestinal Disorders, Res Inst Gastroenterol & Liver Dis, POB 1985717411, Tehran, Iran
[3] Tarbiat Modares Univ, Fac Biol Sci, Dept Biophys, Tehran 14115154, Iran
[4] Tarbiat Modares Univ, Fac Biol Sci, Dept Biochem, Tehran 14115154, Iran
[5] AUVA, Ludwig Boltzmann Inst Traumatol, Res Ctr, Donaueschingenstr 13, A-1200 Vienna, Austria
关键词
Hemoglobin nanoparticles; Oral administration; Colon-specific delivery; Myeloperoxidase; Mucus adhesion; Ulcerative colitis; TARGETED DRUG-DELIVERY; 5-AMINO SALICYLIC-ACID; BOVINE SERUM-ALBUMIN; KAPPA-B; THERAPY; MYELOPEROXIDASE; CARRIERS; MICROPARTICULATE; NANOCARRIERS; ENHANCEMENT;
D O I
10.1016/j.ijpharm.2022.121531
中图分类号
R9 [药学];
学科分类号
1007 ;
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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页数:11
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