Evidence map›Paper›PMID 41624071›Full record

ArticleRegenerative engineering and translational medicine2025

Niclosamide-Loaded Polyanhydride Nanoparticles to Combat Gemcitabine Resistance in Pancreatic Cancer.

Brianna M White, Venugopal Gunda, Susheel Kumar Nethi, Nagabhishek Sirpu Natesh, Adam S Mullis, Mariaelena Roman Sotelo, Jeffrey North, Chris Destache, Balaji Narasimhan, Surinder K Batra and 2 more

Abstract read
In one paragraph

Article in Regenerative engineering and translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Brianna M WhiteDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa USA.
Venugopal GundaDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE USA.
Susheel Kumar Nethi *Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa USA.
Nagabhishek Sirpu Natesh *Department of Veterinary Medicine and Surgery, University of Missouri, Columbia, MO USA.
Adam S MullisDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa USA.
Mariaelena Roman SoteloDepartment of Pharmacy Sciences, Creighton University, Omaha, NE USA.
Jeffrey NorthDepartment of Pharmacy Sciences, Creighton University, Omaha, NE USA.
Chris DestacheDepartment of Pharmacy Practice, Creighton University, Omaha, NE USA.
Balaji NarasimhanDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa USA.
Surinder K BatraDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE USA.
Surya K MallapragadaDepartment of Chemical and Biological Engineering, Iowa State University, Ames, Iowa USA.ORCID 0000-0002-9482-7273
Satyanarayana RachaganiDepartment of Veterinary Medicine and Surgery, University of Missouri, Columbia, MO USA.

Funding

Targeting tumor and its microenvironment using nanotherapeutics for pancreatic cancerR01CA247763 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RACHAGANI, SATYANARAYANA · 2020 to 2024
$1.9M
NCI NIH HHS R01 CA247763
6 · The paper itself

Abstract

Purpose: Pancreatic cancer (PC) is a highly lethal malignancy and lacks effective treatments. Current chemotherapies, including gemcitabine (Gem) in combination treatment regimens, produce dose-limiting toxicity, drug resistance, and ultimately limited improvement in the overall survival of PC patients. Niclosamide (Nic), a clinically safe FDA-approved anthelmintic drug has been shown to have anti-cancer properties; however, its limited bioavailability makes Nic largely ineffective as a therapeutic agent. To address this challenge, we have developed a novel combination therapy of Gem with the repurposed drug, Nic, loaded in biodegradable polyanhydride nanoparticles (NicNp), as an effective treatment option for PC. Methods: We synthesized and characterized NicNp in vitro and evaluated their biodistribution and efficacy in xenograft and syngeneic pancreatic tumor models in mice. Results: The biodistribution study indicated that NicNp accumulated in high concentrations in the pancreatic tumors of the mice with C Conclusions: This study demonstrates the potential for effective repurposing Nic via nanoformulations in combination with Gem to improve PC treatment efficacy. Lay summary: Pancreatic cancer (PC) ranks among the most lethal types of cancer, with largely ineffective current treatments and toxic side effects in patients. Niclosamide is an FDA-approved anti-parasitic drug with minimal side effects, that has shown some anti-cancer properties. However, it is not effectively absorbed in the body. We produced polymer nanoparticles to deliver niclosamide effectively to treat pancreatic tumors in mice in combination with the chemotherapeutic gemcitabine. This combination treatment led to PC tumor reduction and increased the survival, demonstrating that niclosamide encapsulated in nanoparticles in combination with gemcitabine has the potential to be a more effective treatment for PC. Graphical Abstract: Supplementary Information: The online version contains supplementary material available at 10.1007/s40883-025-00394-0.

Indexed as

BiodegradableDrug deliveryNanoparticlesNiclosamidePancreatic cancer

Identifiers

PMID41624071
PMCPMC12852149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.