Evidence map›Paper›PMID 42084709›Full record

ReviewMolecular biology reports2026

Multi-modal therapeutic approaches to inflammatory bowel disease: plant-derived compounds, nanoparticle drug delivery systems, and gene-based interventions.

Arooj Komal, Doua Ilyas, Muhammad Usman Khan, Muhammad Khalil Ur Rehman, Tayyaba Hassan, Hina Ayub, Nokhba Naqi, Noor Ullah, Umair Ilyas

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 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

9 authors.

Arooj KomalRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Doua IlyasRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan. doua.ilyas@riphah.edu.pk.
Muhammad Usman KhanDepartment of Pharmacy, Iqra University, H-9/1, Islamabad, Pakistan.
Muhammad Khalil Ur RehmanDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Tayyaba HassanDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Hina AyubDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Nokhba NaqiRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Noor UllahDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Umair IlyasRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic, relapsing inflammatory disorder primarily affecting the gastrointestinal tract. The pathogenesis arises from complex interactions among genetic predisposition, immune dysregulation, and gut microbiota alterations. Recent advances in molecular biology, genomics, and microbiome research have identified novel therapeutic targets, enabling the development of innovative treatment strategies. Natural products derived from plants offer bioactive compounds with anti-inflammatory, antioxidant, and immunomodulatory properties, gaining attention for IBD symptom management. Conventional therapeutic management includes aminosalicylates, immunomodulators, corticosteroids, and biologics; however, 30-50% of patients show inadequate response, and oral drug delivery faces challenges due to gastrointestinal environmental heterogeneity. Recent years have witnessed substantial advances in nanoparticle-based drug delivery systems for IBD, offering improved targeting capabilities, enhanced therapeutic efficacy, and better tolerability through stimuli-responsive platforms (ROS-sensitive, pH-responsive) and active targeting strategies. Nanoparticle-mediated gene therapy, including siRNA, miRNA, and emerging CRISPR-based approaches, represents a paradigm-shifting strategy for modulating aberrant gene expression in IBD. This comprehensive review synthesizes the current understanding of IBD pathophysiology, evaluates both conventional and emerging therapeutic approaches, and provides critical analysis of advanced nanoparticle delivery systems and gene-based therapeutic strategies.

Indexed as

Genetic TherapyInflammatory Bowel DiseasesNanoparticle Drug Delivery SystemAnimalsAnti-Inflammatory AgentsDrug Delivery SystemsHumansNanoparticlesAnti-Inflammatory AgentsNanoparticle Drug Delivery SystemAnti-inflammatoryColon-targeted drugGene therapyInflammatory bowel disease (IBD)NanoparticlesPlant-derived products

Identifiers

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.