溃疡性结肠炎
氨基水杨酸
血红蛋白
体内
粘液
药理学
药品
结肠炎
治疗效果
药物输送
医学
化学
胃肠病学
内科学
生物
疾病
有机化学
生物技术
生态学
作者
Zahra Vaezi,Shaghayegh Baradaran Ghavami,Maryam Farmani,Reza Mahdavian,Hamid Asadzadeh Aghdaei,Hossein Naderi‐Manesh
标识
DOI:10.1016/j.xphs.2024.03.028
摘要
Abstract The oral formulation design for colon-specific drug delivery brings some therapeutic benefits in the ulcerative colitis treatment. We recently reported the specific delivery of hemoglobin nanoparticles-conjugating 5-aminosalicylic acid (5-ASA- HbNPs) to the inflamed site. In the current study, the in vivo evaluation of 5-ASA from its bio-adhesive nanoparticles shows the greatly long residence time of 5-ASA and complete support of the colon as compared with free 5-ASA due to the suitable mucoadhesive property to traverse the mucus layer and accumulate within the mucosa is a vital process. Furthermore, the UC model mice exhibited notably reduced indexes of disease activity; along with decreased ratios of colon weight/length in the group treated with 5-ASA-HbNPs. This group received a one-thousandth of the standard dosage of 5-ASA amount (50 μg/kg). While, a similar result was observed for a considerable quantity of free 5-ASA (50 mg/kg), confirming the therapeutic efficacy of this formulation in vivo. Furthermore, microscopic images of histological sections of the extracted colons demonstrated that the 5-ASA-HbNPs and 5-ASA groups displayed instances of inflammatory damage within the colon. However, in comparison to the control group, the extent of this damage was relatively moderate, suggesting 5-ASA-HbNPs improved therapeutic efficacy with the lower dosage form.
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