检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:程燕 颜冬梅[3] 李飞[2] 朱卫丰[1] CHENG Yan;YAN Dong-mei;LI Fei;ZHU Wei-feng(Key Laboratory of Modern Preparation of Chinese Medicine of Jiangxi University of Chinese Medicine,Nanchang 330002,China;Laboratory of Metabolomics and Drug-induced Liver Injury,West China Hospital,Sichuan University,Chengdu 610041,China;Academician Work Station of Jiangxi University of Chinese Medicine,Nanchang 330004,China)
机构地区:[1]江西中医药大学现代中药制剂教育部重点实验室,江西南昌330002 [2]四川大学华西医院代谢组学与药源性肝损伤研究室,四川成都610041 [3]江西中医药大学院士工作站,江西南昌330004
出 处:《中国现代中药》2024年第8期1420-1431,共12页Modern Chinese Medicine
基 金:国家重点研发计划项目(2017YFC1702902)。
摘 要:5-氨基水杨酸(5-ASA)是1种从中药柳树皮中分离提纯得到的天然抗炎活性成分水杨酸的衍生物,别名阿米诺水杨酸、美沙拉嗪,是临床治疗炎症性肠病(IBD)并预防其复发的一线药物。尽管目前莎尔福(Salofalk)、亚沙可(Asacol)和潘他沙(Pentasa)等5-ASA口服结肠靶向制剂已广泛用于IBD的临床治疗,但仍存在在小肠提前释药和受胃肠道生理状态影响显著等制剂缺陷、对克罗恩病和重度溃疡性结肠炎(UC)治疗效果不佳等临床未满足的需求,以及减少UC患者黏膜菌群多样性、长期使用增加用药风险和降低患者服药依从性等问题。开发硅胶纳米粒、水凝胶等新型递药载体,基于pH依赖、时滞控制和菌群/酶触发等多机制结合释药原理设计新型口服结肠靶向制剂从而解决制剂缺陷问题,提高5-ASA疗效和患者服药耐受性、依从性是目前制剂研究的重点。此外,5-ASA口服制剂联合中药保留灌肠、中药口服制剂和注射液等治疗IBD可发挥协同抗炎作用,实现增效减毒目的。对5-ASA口服制剂品种、近年来新型制剂和递药载体的研究进展,以及与中药联用的临床应用和研究现状等进行综述,为5-ASA口服制剂的剂型改造、载体材料研究和临床用药等提供参考。The derivative 5-aminosalicylic acid(5-ASA),also known as amino salicylic acid or mesalazine,is derived from natural anti-inflammatory compound salicylic acid isolated and purified from willow,and is a first-line drug for the treatment and prevention of inflammatory bowel disease(IBD)relapses.Despite the widespread clinical use of oral colon-specific 5-ASA formulations such as Salofalk,Asacol,and Pentasa in the treatment of IBD,several unmet clinical needs and formulation deficiencies persist,including premature drug release in the small intestine,significant influence by gastrointestinal physiological conditions,suboptimal efficacy in treating Crohn's disease(CD)and severe ulcerative colitis(UC),reduced mucosal microbiota diversity in UC patients,increased risk with long-term use,and decreased patient compliance.To address these issues,current research focuses on developing novel drug delivery carriers,such as silica nanoparticles and hydrogels.These carriers are designed based on multi-mechanism drug release principles,including pH-dependence,time-delay control,and microbiota/enzyme-triggered release to improve the efficacy of 5-ASA and to enhance patient tolerance and adherence to treatment.Furthermore,combining oral 5-ASA formulations with traditional Chinese medicine(TCM)therapies,such as retention enemas,oral decoctions,and injections,can synergistically enhance anti-inflammatory effects,achieving the goal of increased efficacy and reduced toxicity.This review covers the progress in the development of various oral 5-ASA formulations,recent advancements in new formulations and drug delivery carriers,and the current status of clinical applications and research on combining 5-ASA with TCM.This study is expected to provide references for the modification of 5-ASA dosage forms,research on carrier materials,and clinical use,ultimately improving treatment outcomes for IBD patients.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7