Evidence map›Paper›PMID 40611758›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2025

Soft Extrudable Dendritic Particles with Nanostructured Tendrils for Local Adhesion and Drug Release to Bladder Cancers.

Jin Gyun Lee, Joseph Petraccione, Katherine A Trese, Alex C Hughes, Taylor R Ausec, Maren Salzmann-Sullivan, Lih-Jen Su, Matthew T Kim, Sangchul Roh, Andrew P Goodwin and 3 more

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  6. Review
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

13 authors.

Jin Gyun LeeDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.ORCID https://orcid.org/0000-0002-5708-2284
Joseph PetraccioneDivision of Medical Oncology, Department of Internal Medicine, University of Colorado Anschutz Medical Campus, 12801 East 17th Avenue 8122, Aurora, CO, 80045, USA.
Katherine A TreseDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.
Alex C HughesDivision of Medical Oncology, Department of Internal Medicine, University of Colorado Anschutz Medical Campus, 12801 East 17th Avenue 8122, Aurora, CO, 80045, USA.ORCID https://orcid.org/0000-0001-6083-5884
Taylor R AusecDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.
Maren Salzmann-SullivanDivision of Medical Oncology, Department of Internal Medicine, University of Colorado Anschutz Medical Campus, 12801 East 17th Avenue 8122, Aurora, CO, 80045, USA.
Lih-Jen SuDivision of Medical Oncology, Department of Internal Medicine, University of Colorado Anschutz Medical Campus, 12801 East 17th Avenue 8122, Aurora, CO, 80045, USA.
Matthew T KimDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.
Sangchul RohSchool of Chemical Engineering, Chonnam National University, 77, Yongbong-ro, Buk-gu, Gwangju, 61186, Republic of Korea.ORCID https://orcid.org/0000-0003-3268-6214
Andrew P GoodwinDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.ORCID https://orcid.org/0000-0002-7284-4005
Frances Xiuyan FengDepartment of Pathology, University of Colorado Anschutz Medical Campus, 13001 E 17th Pl, Aurora, CO, 80045, USA.ORCID https://orcid.org/0009-0008-6813-0027
Thomas W FlaigDivision of Medical Oncology, Department of Internal Medicine, University of Colorado Anschutz Medical Campus, 12801 East 17th Avenue 8122, Aurora, CO, 80045, USA.ORCID https://orcid.org/0000-0001-6145-9040
C Wyatt ShieldsDepartment of Chemical and Biological Engineering, University of Colorado Boulder, 3415 Colorado Ave, Boulder, CO, 80303, USA.ORCID https://orcid.org/0000-0003-4138-8462

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Adoptive Macrophage Transfers for Nanoparticle DeliveryR35GM147455 · NIGMS · UNIVERSITY OF COLORADO · PI Charles Wyatt Shields IV · 2022 to 2026
$2.0M
Multi-Modal Optical/ microCT system for Colorado Animal Imaging ResourceS10OD027023 · OD · UNIVERSITY OF COLORADO DENVER · PI SERKOVA, NATALIE J. · 2020 to 2020
$733k
Macrophage-Mediated Delivery of Acoustically Propelled Nanoparticles for Sensitizing Immunologically Cold TumorsR21CA267608 · NCI · UNIVERSITY OF COLORADO · PI GOODWIN, ANDREW P, SHIELDS IV, CHARLES WYATT · 2022 to 2023
$381k
National Cancer Institute grant supported to the University of Colorado Cancer Center P30CA046934National Institutes of Health SIFAR S10 shared instrumentation grant S10OD027023NCI NIH HHS P30 CA046934NCI NIH HHS R21 CA267608NIGMS NIH HHS R35 GM147455NIH HHS R21CA267608NIH HHS S10 OD027023
6 · The paper itself

Abstract

Bladder cancer is a leading cause of cancer-related mortality, yet current intravesical drug delivery methods often suffer from poor retention times in the bladder. Gecko feet-like nanomaterials offer the potential to overcome this challenge, however, conventional methods to fabricate high surface area nanomaterials for drug delivery involve complex and expensive manufacturing processes. In this work, a simple fluid flow templating method is reported for manufacturing soft dendritic particles (SDPs) composed of poly(lactic-co-glycolic acid) (PLGA) with a chitosan coating for enhanced adhesion to epithelial tissues via van der Waals interactions. The biodegradable SDPs encapsulate chemotherapeutic agents and are administered using an alginate hydrogel, enabling precise deposition by extrusion for sustained drug release. The results demonstrate that SDPs adhere to mouse and human cancer cells for several days. The SDPs effectively encapsulate and release several clinically utilized chemotherapeutic drugs such as gemcitabine, docetaxel, and methotrexate, exhibiting superior cancer cell killing in vitro. In murine models, gemcitabine-loaded SDPs instilled into tumor-bearing bladders elicited stronger CD45+ immune cell responses than control groups while maintaining minimal toxicity. This work presents a simple, biomimetic drug delivery platform with prolonged retention and controlled drug release, offering a versatile approach for enhancing therapeutic delivery in epithelial cancer models.

Indexed as

DendrimersDrug CarriersNanostructuresUrinary Bladder NeoplasmsAnimalsAntineoplastic AgentsCell Line, TumorChitosanDeoxycytidineDocetaxelDrug LiberationFemaleGemcitabineHumansHydrogelsMethotrexateAntineoplastic AgentsChitosanDendrimersDeoxycytidineDocetaxelDrug CarriersGemcitabineHydrogelsMethotrexatePolylactic Acid-Polyglycolic Acid Copolymerbladder cancersdendritic particlesdrug deliverystructural adhesion

Identifiers

PMID40611758
PMCPMC12233162

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Registered trials

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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.