Evidence mapPaperPMID 41869409Full record

ReviewInternational journal of nanomedicine2026

Recent Advances in Nanoscale Sprayable Hydrogels for Cancer Management: Nanoparticle-Loaded Formulations for Therapy and Prevention.

Jae Min Lee, Su Jeong Kang, Moon Sup Yoon, Min Jeong Jo, Myeong Kyun Yoo, So Yeon Park, Sunghyun Bong, Jonghyuk Kim, Seonmin Park, Yeseung Lee and 5 more

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Jae Min Lee *College of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Su Jeong Kang *College of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Moon Sup YoonCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Min Jeong JoDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, 66047, USA.
Myeong Kyun YooCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
So Yeon ParkCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Sunghyun BongCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.ORCID 0009-0003-7985-477X
Jonghyuk KimCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Seonmin ParkCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Yeseung LeeCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Yuseon ShinCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Hye Jin LeeCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Jin-Seok KimDrug Information Research Institute (DIRI), College of Pharmacy, Sookmyung Women's University, Seoul, 04310, Republic of Korea.
Chun-Woong ParkCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.
Dae Hwan ShinCollege of Pharmacy, Chungbuk National University, Cheongju, Chungcheongbuk-do, 28160, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sprayable hydrogels represent an emerging class of nanoscale, localized drug delivery systems in oncology, offering rapid in situ gelation, strong tissue adhesion, and minimally invasive administration. Recent advances have integrated nanotechnology into sprayable hydrogel formulations to enhance therapeutic efficacy at tumor sites through various strategies, including nanoemulsions, nanocomposites, nanoparticle-loaded matrices, nanovaccines, and nanosprays. Across preclinical models, these platforms have demonstrated quantitative improvements, including up to 70-95% reductions in residual tumor burden, 2-5-fold increases in intratumoral drug retention, and survival extensions ranging from 30% to over 60% compared with free-drug controls. These platforms have demonstrated the ability to eliminate residual tumor cells, activate antitumor immunity, and prevent recurrence at surgical margins or mucosal interfaces. Therapeutic modalities include the controlled release of chemotherapeutics, immune checkpoint inhibitors, and metabolic or oxidative regulators, all delivered within nanostructured hydrogel matrices. Several systems also reported over 80% suppression of local recurrence at surgical margins and significant potentiation of immune activation markers such as CD8⁺ T-cell infiltration and dendritic cell maturation. Nanoscale sprayable hydrogels have shown promise across diverse clinical applications, including peritoneal carcinomatosis, superficial skin tumors, and premalignant mucosal lesions. The hydrogels themselves comprise a wide range of nanostructured materials, such as thermosensitive polymers, self-gelling powders, supramolecular assemblies, and nanoparticle-laden scaffolds, that enable precise spatial and temporal control of drug delivery. In this review, we categorize these systems based on cancer type, underlying mechanisms of action, and therapeutic goals (treatment vs prevention). By integrating nanotechnology, immunotherapy, and tissue-responsive design, nanoscale sprayable hydrogels represent a modular and adaptable platform for personalized cancer care, with compatibility across surgical, endoscopic, and topical administration routes. However, despite these advances, the clinical translation of sprayable hydrogels remains limited by challenges such as sterilization constraints, device-material compatibility issues, storage and handling stability, and regulatory hurdles, all of which must be systematically addressed to enable widespread clinical adoption.

Indexed as

Antineoplastic AgentsDrug Delivery SystemsHydrogelsNanoparticlesNeoplasmsAnimalsHumansNanomedicineAntineoplastic AgentsHydrogelscancer immunotherapylocalized drug deliverypostoperative cancer therapyprecancerous lesion preventionsprayable hydrogel

Identifiers

PMID41869409
PMCPMC13005149

What Socratic holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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 Socratic graph.