Evidence map›Paper›PMID 40183273›Full record

ReviewCurrent drug delivery2026

Precision Drug Delivery to the Liver: A Nanoparticle Approach.

Krishna Yadav, Ajazuddin, Mukesh Sharma, Kushagra Nagori, Parag Jain, Sunita Minz, Manju Rawat Singh, Deependra Singh, Madhulika Pradhan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current drug delivery, 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. 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

9 authors.

Krishna YadavRungta College of Pharmaceutical Sciences and Research, Kohka, Bhilai 490024, India.
AjazuddinRungta College of Pharmaceutical Sciences and Research, Kohka, Bhilai 490024, India.
Mukesh SharmaRungta College of Pharmaceutical Sciences and Research, Kohka, Bhilai 490024, India.
Kushagra NagoriRungta College of Pharmaceutical Sciences and Research, Kohka, Bhilai 490024, India.
Parag JainRungta College of Pharmaceutical Sciences and Research, Kohka, Bhilai 490024, India.
Sunita MinzDepartment of Pharmacy, Indira Gandhi National Tribal University, Amarkantak, India.
Manju Rawat SinghUniversity Institute of Pharmacy, Pandit Ravishankar Shukla University, Raipur, Chhattisgarh 492010, India.
Deependra SinghUniversity Institute of Pharmacy, Pandit Ravishankar Shukla University, Raipur, Chhattisgarh 492010, India.
Madhulika PradhanGracious College of Pharmacy, Abhanpur, Affiliated to Chhattisgarh Swami Vivekanand Technical University, Bhilai, Chhattisgarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global burden of Chronic Liver Diseases (CLDs) is escalating, with increasing prevalence and mortality. Various conditions ranging from fibrosis, cirrhosis, and hepatocellular carcinoma are associated with conditions such as toxin accumulation, viral infections, and metabolic derangements. In this already difficult context, the emergence of metabolic dysfunction-associated steatotic liver disease and steatohepatitis complicated the picture even further. While there has been much advancement in medical research, there is currently no standard cure; hence, the best treatment options are limited, providing a rising need for new therapeutic approaches. Nanoparticle drug delivery systems represent a promising avenue, providing targeted delivery and enhanced therapeutic effectiveness. Nanosystems can protect therapeutic agents from degradation, evade rapid clearance mechanisms, and target drugs directly to a specific hepatic cell type. However, the complex architecture of the liver presents challenges for these therapies, including the need to precisely target individual cells and retain the stability of nanoparticles within the hepatic microenvironment. This review presents recent advances in nanoparticle and targeted ligands-based technologies. These technologies help to navigate barriers associated with similar therapies. As these challenges are addressed, nanotechnological advancements could potentially lead to a major revolution in the treatment of CLDs, paving the way for improved management strategies and providing new hope for affected individuals worldwide.

Indexed as

Drug Delivery SystemsLiverLiver DiseasesNanoparticle Drug Delivery SystemNanoparticlesAnimalsHumansNanoparticle Drug Delivery SystemChronic liver diseasescirrhosisclinical translation.fibrosisinflammationmetabolic dysfunction-associated steatotic liver diseasenanoparticle drug deliverynanoparticles

Identifiers

PMID40183273

What Socratic 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 Socratic graph.