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认识胃肠道的生物学屏障和病理生理学特征,用于设计和应用纳米药物。

Recognizing the biological barriers and pathophysiological characteristics of the gastrointestinal tract for the design and application of nanotherapeutics.

机构信息

Department of Chemistry, College of Basic Medicine, Army Medical University (Third Military Medical University), Chongqing, China.

Department of Gastroenterology, Southwest Hospital, Army Medical University (Third Military Medical University), Chongqing, China.

出版信息

Drug Deliv. 2024 Dec;31(1):2415580. doi: 10.1080/10717544.2024.2415580. Epub 2024 Oct 15.


DOI:10.1080/10717544.2024.2415580
PMID:39404464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11485891/
Abstract

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 infection and inflammatory bowel disease, were selected to investigate the application of nanotherapeutics for GIT disease treatment.

摘要

胃肠道(GIT)是一个重要且复杂的系统,人类通过它来消化食物和吸收营养。GIT 容易受到疾病的影响,这些疾病可能会给人类带来不适甚至死亡。胃肠道疾病的治疗方法面临着多种生物屏障,这大大降低了治疗药物的疗效。了解 GIT 的生物屏障和病理生理学特征可能有助于设计创新的治疗方法。具有特殊靶向和控制治疗释放特性的纳米疗法已被广泛用于胃肠道疾病的治疗。本文综述了胃肠道的生物屏障和病理生理学特征,这可能有助于设计用于胃肠道疾病治疗的有前途的纳米疗法。此外,还选择了上消化道和下消化道的几种典型疾病,如 感染和炎症性肠病,来研究纳米疗法在胃肠道疾病治疗中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/1a58c1d1ec1a/IDRD_A_2415580_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/46ff1c3863d5/IDRD_A_2415580_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/58d067f2a1f5/IDRD_A_2415580_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/cd9add49d6da/IDRD_A_2415580_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/0f03e1207927/IDRD_A_2415580_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/1a58c1d1ec1a/IDRD_A_2415580_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/46ff1c3863d5/IDRD_A_2415580_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/58d067f2a1f5/IDRD_A_2415580_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/cd9add49d6da/IDRD_A_2415580_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/0f03e1207927/IDRD_A_2415580_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8678/11485891/1a58c1d1ec1a/IDRD_A_2415580_F0005_C.jpg

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本文引用的文献

[1]
Recent progress on engineered micro/nanomaterials mediated modulation of gut microbiota for treating inflammatory bowel disease.

J Control Release. 2024-6

[2]
Biomimetic Nano-Drug Delivery System: An Emerging Platform for Promoting Tumor Treatment.

Int J Nanomedicine. 2024

[3]
Paneth cell-derived iNOS is required to maintain homeostasis in the intestinal stem cell niche.

J Transl Med. 2023-11-25

[4]
Delivery Strategies of Probiotics from Nano- and Microparticles: Trends in the Treatment of Inflammatory Bowel Disease-An Overview.

Pharmaceutics. 2023-11-8

[5]
Virofree Associates with the Modulation of Gut Microbiomes and Alleviation of DSS-Induced IBD Symptoms in Mice.

ACS Omega. 2023-10-13

[6]
Plant-based green synthesis of nanoparticles as an effective and safe treatment for gastric ulcer.

Inflammopharmacology. 2023-12

[7]
Cyclosporine A-Encapsulated pH/ROS Dual-Responsive Nanoformulations for the Targeted Treatment of Colitis in Mice.

ACS Biomater Sci Eng. 2023-10-9

[8]
Nano-enabled colorectal cancer therapy.

J Control Release. 2023-10

[9]
Chondroitin sulfate functionalized palmitic acid and cysteine cografted-quaternized chitosan for CD44 and gut microbiota dual-targeted delivery of curcumin.

Mater Today Bio. 2023-3-24

[10]
Hyaluronic acid modified oral drug delivery system with mucoadhesiveness and macrophage-targeting for colitis treatment.

Carbohydr Polym. 2023-8-1

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