pH-sensitive liposomes for colonic co-delivery of mesalazine and curcumin for the treatment of ulcerative colitis

氨基水杨酸 姜黄素 溃疡性结肠炎 药理学 脂质体 药品 抗氧化剂 体内 药物输送 医学 靶向给药 化学 氧化应激 结肠炎 多酚 内科学 疾病 生物化学 生物技术 生物 有机化学
作者
Soumayya Aib,Kashif Iqbal,Nasir Khan,Sidra Khalid,Muhammad Adnan,Syed Muhammad Umair,M. Junaid Dar
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier]
卷期号:72: 103335-103335 被引量:33
标识
DOI:10.1016/j.jddst.2022.103335
摘要

The ineffectiveness of the current management of ulcerative colitis (UC) demands novel pharmaceutical techniques and advance therapeutic strategies to facilitate safe and efficacious treatment of the disease. In this quest, mesalazine (MZ), a 5-aminosalicylate with anti-inflammatory and potent antioxidant activities, along with curcumin (CM), a natural anti-inflammatory and antioxidant polyphenol, were found to produce a synergistic efficacy to efficiently alleviate UC. In the present study, we have formulated pH-sensitive liposomes (LS) containing a low-dose combination of MZ and CM as a potential therapy for UC. It was hypothesized that the synergistic action of the two drugs, pH-dependent colon-specific delivery, and use of LS as a nano-technological drug carrier system could diminish drug-associated side effects, reduce the dose and provide effective treatment strategy for UC. The guinea pig model of UC was used to evaluate the in vivo efficacy of pH sensitive MZ-CM co-loaded LS and found to be more efficacious than single-drug LS or drug solution. Furthermore, both drugs exhibited high antioxidant activity and mitigated the oxidative stress present along UC; resulting in an effective treatment of UC. In conclusion, eudragit-S100 coated MZ-CM liposomes is a promising treatment strategy for the effective oral therapy of UC.
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