Evidence map›Paper›PMID 41384079›Full record

ReviewRSC advances2025

Nanoliposome-based drug delivery systems for the treatment of diabetes mellitus: a review.

Muhammad Umar, Tauqir A Sherazi, Muhammad Talha, Mohamed Fawzy Ramadan, Ahmed Ezzat Ahmed, Ramadan Taha, Syed Ali Raza Naqvi

Abstract readReview
In one paragraph

Review in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
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

7 authors.

Muhammad UmarDepartment of Chemistry, Government College University Faisalabad Faisalabad-38000 Pakistan draliraza@gcuf.edu.pk.
Tauqir A SheraziDepartment of Chemistry, COMSATS University Islamabad Abbottabad Campus Abbottabad Pakistan.ORCID https://orcid.org/0000-0003-4690-7700
Muhammad TalhaDepartment of Chemistry, Government College University Faisalabad Faisalabad-38000 Pakistan draliraza@gcuf.edu.pk.
Mohamed Fawzy RamadanDepartment of Clinical Nutrition, Faculty of Applied Medical Sciences, Umm Al-Qura University Makkah Saudi Arabia mfhassanien@uqu.edu.sa.
Ahmed Ezzat AhmedDepartment of Biology, College of Science, King Khalid University P.O. Box 9004 61414 Abha Saudi Arabia.
Ramadan TahaDepartment of Biology, College of Science, King Khalid University P.O. Box 9004 61414 Abha Saudi Arabia.
Syed Ali Raza NaqviDepartment of Chemistry, Government College University Faisalabad Faisalabad-38000 Pakistan draliraza@gcuf.edu.pk.ORCID https://orcid.org/0000-0002-2172-9066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes mellitus (DM) is one of the leading world health complications, with chronic hyperglycemia that is due to a lack of insulin production or insulin action. Although many pharmacological agents are available, the current treatment modality is hampered by low bioavailability, rapid drug clearance, frequent dosing, and adverse effects. Such difficulties have been especially pronounced in the treatment of type 1 and type 2 diabetes, where long-term glycemic control that does not undermine patient compliance has been hard to reach. Nanotechnology has become one of the most revolutionary tools in drug delivery to achieve targeted, sustained, and more effective therapeutic outcomes in the past few years. Nanoliposomes are nanoscale vesicles formed from lipid bilayers and have exhibited remarkable potential due to their biocompatibility, ability to host both hydrophilic and lipophilic drugs, and controlled release. Nanoliposomes have the potential of improving solubility of drugs, protect therapeutic agents against enzyme activities, and produce a controlled drug release, which offers a new possibility in the treatment of diabetes. In addition to glucose-lowering, targeted liposomal treatment approaches combat major complications, such as cardiomyopathy, nephropathy, and retinopathy, through increased myocardial protection, renal resilience, and ocular drug exposure. This review provides a thorough overview of the progress, formulation methods, and therapeutic value of nanoliposomal-based delivery systems targeting antidiabetic drugs. It also focuses on the recent trend in research, the challenges of clinical translation, and the future of nanoliposomes as a paradigm-altering platform in the treatment of diabetes mellitus.

Identifiers

PMID41384079
PMCPMC12690642

What OpenQuestion holds

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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.