Evidence map›Paper›PMID 41680539›Full record

ReviewInflammopharmacology2026

Hydrogel-enabled drug delivery for ulcerative colitis.

Mohit Sharma, Rupa Mazumder, Abhijit Debnath

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammopharmacology, 2026. 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. 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

3 authors.

Mohit SharmaDepartment of Pharmaceutics, Noida Institute of Engineering and Technology (Pharmacy Institute), Knowledge Park-II, Greater Noida, Uttar Pradesh, 201306, India.
Rupa MazumderDepartment of Pharmaceutics, Noida Institute of Engineering and Technology (Pharmacy Institute), Knowledge Park-II, Greater Noida, Uttar Pradesh, 201306, India. rupa_mazumder@rediffmail.com.ORCID http://orcid.org/0000-0002-1888-548X
Abhijit DebnathDepartment of Pharmaceutics, Noida Institute of Engineering and Technology (Pharmacy Institute), Knowledge Park-II, Greater Noida, Uttar Pradesh, 201306, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ulcerative colitis (UC) represents a chronic, relapsing inflammatory condition primarily affecting the colonic and rectal mucosa, presenting substantial challenges to healthcare systems globally. Conventional therapeutic approaches, including aminosalicylates, corticosteroids, immunosuppressants, and biological agents, face significant limitations including premature drug release, systemic toxicities, narrow therapeutic windows, and inadequate colonic accumulation. Hydrogel-based drug delivery systems have emerged as promising platforms for addressing these multifaceted challenges through their unique physicochemical properties, biocompatibility, and versatile functionalization capabilities. This comprehensive review examines the current landscape and future potential of hydrogel-enabled drug delivery for ulcerative colitis therapy, encompassing material design strategies, stimuli-responsive mechanisms, targeting approaches, and therapeutic cargo delivery. Natural polymer-based hydrogels, including polysaccharides and proteins, offer exceptional biocompatibility and intrinsic therapeutic properties, while synthetic and hybrid systems enable precise control over release kinetics and mechanical properties. Stimuli-responsive mechanisms, including pH, enzyme, and redox sensitivity, facilitate site-specific drug release in response to pathophysiological conditions unique to the inflamed colon. Advanced targeting strategies encompass mucoadhesive systems, cell-specific delivery, and inflammation-site accumulation mechanisms. The therapeutic cargo has expanded from traditional small molecules to encompass biologics, living therapeutics, and engineered nanomedicines. Novel formulation technologies, including injectable systems, microencapsulation approaches, and hybrid delivery platforms, demonstrate superior therapeutic efficacy in preclinical models compared to conventional formulations. Clinical translation faces challenges related to scalability, regulatory considerations, and personalized medicine implementation. Future perspectives point toward smart hydrogels with artificial intelligence integration, combination therapies, gut-brain axis targeting, and biomarker-guided precision medicine approaches. The convergence of materials science, biotechnology, and digital health technologies positions hydrogel-based therapeutics at the forefront of inflammatory bowel disease management, promising to transform treatment paradigms and improve outcomes for millions of patients worldwide.

Indexed as

Colitis, UlcerativeDrug Delivery SystemsHydrogelsAnimalsHumansPolymersHydrogelsPolymersColon-targeted therapyHydrogel drug deliveryInflammatory bowel diseaseMucoadhesive systemsStimuli-responsive systemsUlcerative colitis

Identifiers

PMID41680539

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.