认识胃肠道的生物屏障和病理生理特点,以设计和应用纳米疗法。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2024-12-01 Epub Date: 2024-10-15 DOI:10.1080/10717544.2024.2415580
Shan Li, Tianyu Wu, Jingfeng Wu, Wensheng Chen, Dinglin Zhang
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引用次数: 0

摘要

胃肠道(GIT)是人类消化食物和吸收营养的一个重要而复杂的系统。胃肠道很容易患病,可能导致人体不适甚至死亡。治疗胃肠道疾病的药物面临着多重生物障碍,这大大降低了药物的疗效。认识 GIT 的生物障碍和病理生理特点有助于设计创新疗法。纳米治疗药物具有特殊的靶向性和可控治疗释放特性,已被广泛用于治疗胃食管疾病。在此,我们对胃食管的生物屏障和病理生理特点进行了全面综述,这可能有助于设计治疗胃食管疾病的纳米疗法。此外,我们还选择了幽门螺杆菌感染和炎症性肠病等几种典型的上消化道和下消化道疾病,研究纳米疗法在消化道疾病治疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recognizing the biological barriers and pathophysiological characteristics of the gastrointestinal tract for the design and application of nanotherapeutics.

The gastrointestinal tract (GIT) is an important and complex system by which humans to digest food and absorb nutrients. The GIT is vulnerable to diseases, which may led to discomfort or even death in humans. Therapeutics for GIT disease treatment face multiple biological barriers, which significantly decrease the efficacy of therapeutics. Recognizing the biological barriers and pathophysiological characteristics of GIT may be helpful to design innovative therapeutics. Nanotherapeutics, which have special targeting and controlled therapeutic release profiles, have been widely used for the treatment of GIT diseases. Herein, we provide a comprehensive review of the biological barrier and pathophysiological characteristics of GIT, which may aid in the design of promising nanotherapeutics for GIT disease treatment. Furthermore, several typical diseases of the upper and lower digestive tracts, such as Helicobacter pylori infection and inflammatory bowel disease, were selected to investigate the application of nanotherapeutics for GIT disease treatment.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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