Evidence map›Paper›PMID 41737492›Full record

ReviewRSC advances2026

Formulation approaches for colon-specific drug delivery: conventional to nanocarrier systems.

Ashish Sriram Mishra, Bhavna Ghosh, Sivakumar Ponnurengam Malliappan, Gouranga Dutta, Manimaran Vasanthan

Abstract readReview
In one paragraph

Review in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

5 authors.

Ashish Sriram MishraDepartment of Pharmaceutical Quality Assurance, SRM College of Pharmacy, SRM Institute of Science and Technology Kattankulathur Chengalpattu 603203 Tamil Nadu India manimarv@srmist.edu.in.
Bhavna GhoshDepartment of Pharmaceutical Analysis, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan Bhubaneswar Odisha India.
Sivakumar Ponnurengam MalliappanSchool of Medicine and Pharmacy, Institute of Research and Development, Duy Tan University Da Nang Vietnam.
Gouranga DuttaDepartment of Pharmaceutics, Bharat Technology Uluberia Howrah India.
Manimaran VasanthanDepartment of Pharmaceutical Quality Assurance, SRM College of Pharmacy, SRM Institute of Science and Technology Kattankulathur Chengalpattu 603203 Tamil Nadu India manimarv@srmist.edu.in.ORCID https://orcid.org/0009-0002-0617-9745

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of colon-targeted drug delivery systems (CDDS) has gained increasing attention due to their potential to improve therapeutic outcomes for diseases such as inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), colorectal cancer, and other colonic disorders. Targeted delivery to the colon offers the advantages of site-specific action, reduced systemic side effects, and improved patient compliance. However, several physiological barriers, such as variable pH, microbial metabolism, enzymatic degradation, and transit time, pose significant formulation challenges. This review provides a comprehensive overview of conventional and advanced formulation strategies for colon-targeted drug delivery. Various approaches, including pH-responsive systems, time-dependent delivery, microbially triggered systems, prodrug strategies, pressure-controlled devices, and nanotechnology-based delivery platforms, are critically discussed. Additionally, the emerging role of natural polysaccharide-based systems and innovative hybrid formulations is highlighted. Comparative analysis of different strategies is presented to guide future formulation design. Advancements in nanotechnology and biomaterials offer promising opportunities to overcome existing challenges and enable precise and efficient colon-targeted drug delivery. Further research is warranted to translate these innovative systems into clinically viable therapies with improved efficacy and patient outcomes.

Identifiers

PMID41737492
PMCPMC12928187

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.