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From micro to macro, nanotechnology demystifies acute pancreatitis: a new generation of treatment options emerges.

作者信息

Du Wei, Wang Xinyue, Zhou Yuyan, Wu Wencheng, Huang Haojie, Jin Zhendong

机构信息

Department of Gastroenterology, Shanghai Institute of Pancreatic Diseases, National Key Laboratory of Immunity and Inflammation, Changhai Hospital, Naval Medical University, Shanghai, 200433, China.

Central Laboratory, Department of Medical Ultrasound, Sichuan Provincial People's Hospital, Sichuan Academy of Medical Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan, 610072, China.

出版信息

J Nanobiotechnology. 2025 Jan 29;23(1):57. doi: 10.1186/s12951-025-03106-6.


DOI:10.1186/s12951-025-03106-6
PMID:39881355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11776322/
Abstract

Acute pancreatitis (AP) is a disease characterized by an acute inflammatory response in the pancreas. This is caused by the abnormal activation of pancreatic enzymes by a variety of etiologic factors, which results in a localized inflammatory response. The symptoms of this disease include abdominal pain, nausea and vomiting and fever. These symptoms are induced by a hyperinflammatory response and oxidative stress. In recent years, research has focused on developing anti-inflammatory and antioxidative therapies for the treatment of acute pancreatitis (AP). However, there are still limitations to this approach, including poor drug stability, low bioavailability and a short half-life. The advent of nanotechnology has opened up a novel avenue for the management of acute pancreatitis (AP). Nanomaterials can serve as an efficacious vehicle for conventional pharmaceuticals, enhancing their targeting ability, improving bioavailability and prolonging their half-life. Moreover, they can also exert a direct therapeutic effect. This review begins by introducing the general situation of acute pancreatitis (AP). It then discusses the pathogenesis of acute pancreatitis (AP) and the current status of treatment. Finally, it considers the literature related to the treatment of acute pancreatitis (AP) by nanomaterials. The objective of this study is to provide a comprehensive review of the existing literature on the use of nanomaterials in the treatment of acute pancreatitis (AP). In particular, the changes in inflammatory markers and therapeutic outcomes following the administration of nanomaterials are examined. This is done with the intention of offering insights that can inform subsequent research and facilitate the clinical application of nanomaterials in the management of acute pancreatitis (AP).

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/5877d7e6a79e/12951_2025_3106_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/5491c3554b15/12951_2025_3106_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/286eba750de6/12951_2025_3106_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/d47105d7eadc/12951_2025_3106_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/7bc53ddc259c/12951_2025_3106_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/a3245f271e80/12951_2025_3106_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/a988a6474d6f/12951_2025_3106_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/c056df0c8f13/12951_2025_3106_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/5877d7e6a79e/12951_2025_3106_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/5491c3554b15/12951_2025_3106_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/286eba750de6/12951_2025_3106_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/d47105d7eadc/12951_2025_3106_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/7bc53ddc259c/12951_2025_3106_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/a3245f271e80/12951_2025_3106_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/a988a6474d6f/12951_2025_3106_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/c056df0c8f13/12951_2025_3106_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11776322/5877d7e6a79e/12951_2025_3106_Fig8_HTML.jpg

相似文献

[1]
From micro to macro, nanotechnology demystifies acute pancreatitis: a new generation of treatment options emerges.

J Nanobiotechnology. 2025-1-29

[2]
Research Progress of Antioxidant Nanomaterials for Acute Pancreatitis.

Molecules. 2022-10-25

[3]
Antioxidative phytoceuticals to ameliorate pancreatitis in animal models: an answer from nature.

World J Gastroenterol. 2014-11-28

[4]
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Biomed Pharmacother. 2021-5

[5]
Methane-rich saline alleviates cerulein-induced acute pancreatitis by inhibiting inflammatory response, oxidative stress and pancreatic apoptosis in mice.

Int Immunopharmacol. 2017-7-29

[6]
Microenvironment of pancreatic inflammation: calling for nanotechnology for diagnosis and treatment.

J Nanobiotechnology. 2023-11-23

[7]
Prussian blue nanozyme-mediated nanoscavenger ameliorates acute pancreatitis via inhibiting TLRs/NF-κB signaling pathway.

Theranostics. 2021

[8]
Elucidating the role of oxidative stress in the therapeutic effect of rutin on experimental acute pancreatitis.

Free Radic Res. 2016-12

[9]
Therapeutic effects of ellagic acid on L-arginin ınduced acute pancreatitis.

Acta Cir Bras. 2016-6

[10]
Calycosin alleviates cerulein-induced acute pancreatitis by inhibiting the inflammatory response and oxidative stress via the p38 MAPK and NF-κB signal pathways in mice.

Biomed Pharmacother. 2018-6-8

本文引用的文献

[1]
Nanotechnology in healthcare, and its safety and environmental risks.

J Nanobiotechnology. 2024-11-15

[2]
Deletion of the WD40 domain of ATG16L1 exacerbates acute pancreatitis, abolishes LAP-like non-canonical autophagy and slows trypsin degradation.

Autophagy. 2025-1

[3]
Trehalose attenuates testicular aging by activating autophagy and improving mitochondrial quality.

Andrology. 2025-5

[4]
Is Copper Still Safe for Us? What Do We Know and What Are the Latest Literature Statements?

Curr Issues Mol Biol. 2024-8-2

[5]
Therapeutic use of fisetin and pirfenidone combination in bleomycin-induced pulmonary fibrosis in adult male albino rats.

Naunyn Schmiedebergs Arch Pharmacol. 2025-2

[6]
A comprehensive view on the fisetin impact on colorectal cancer in animal models: Focusing on cellular and molecular mechanisms.

Animal Model Exp Med. 2024-10

[7]
Hyaluronic Acid-Coated Nanoliposomes as Delivery Systems for Fisetin: Stability, Membrane Fluidity, and Bioavailability.

Foods. 2024-7-29

[8]
SEC16A Variants Predispose to Chronic Pancreatitis by Impairing ER-to-Golgi Transport and Inducing ER Stress.

Adv Sci (Weinh). 2024-10

[9]
VMP1: a multifaceted regulator of cellular homeostasis with implications in disease pathology.

Front Cell Dev Biol. 2024-7-19

[10]
Biomimetic Trypsin-Responsive Structure-Bridged Mesoporous Organosilica Nanomedicine for Precise Treatment of Acute Pancreatitis.

ACS Nano. 2024-7-23

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