Evidence map›Paper›PMID 42514923›Full record

ReviewPharmaceutics2026

Artificial Intelligence-Driven Nanomedicine: From Drug Formulation and Nanocarrier Design to Clinical Translation.

Abdulrahman A Alsaqabi, Abdulaziz A Almoutairi, Faisal Alnehari, Abdulaziz N Alanazi, Rema Aldugiem, Yara Alsaeed, Sarah Alotaibi

Abstract readReview
In one paragraph

Review in Pharmaceutics, 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

7 authors.

Abdulrahman A AlsaqabiDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.ORCID 0009-0001-4764-0203
Abdulaziz A AlmoutairiDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.ORCID 0009-0000-5989-2355
Faisal AlnehariDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.
Abdulaziz N AlanaziDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.ORCID 0009-0005-1087-5999
Rema AldugiemDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.
Yara AlsaeedDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.
Sarah AlotaibiDepartment of Pharmaceutical Sciences, College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The integration of artificial intelligence (AI) and machine learning (ML) is fundamentally transforming pharmaceutical sciences, shifting drug formulation and nanocarrier design from traditional empirical approaches toward predictive, data-driven methodologies. By enabling the analysis of large, complex datasets, AI technologies are accelerating decision-making, improving formulation efficiency, and supporting the development of more effective therapeutic systems. Despite these advances, the successful clinical translation of advanced nanomedicines, including polymeric nanoparticles and mRNA-lipid nanoparticle platforms, remains limited by challenges such as biological barriers, highly sensitive formulation parameters, scalability issues, and the limited interpretability of many computational models. This review provides a comprehensive overview of AI applications throughout the pharmaceutical development lifecycle. It explores how classical machine learning algorithms and deep learning architectures optimize conventional dosage forms, enhance formulation development, and enable the rational design of targeted nanocarriers. Particular emphasis is placed on predicting critical quality attributes, encapsulation efficiency, physicochemical properties, drug-release behavior, therapeutic efficacy, and early-stage nanotoxicity. Furthermore, we critically assess the regulatory considerations, manufacturing constraints, data quality issues, and tumor microenvironment heterogeneity that continue to impede bench-to-clinic translation. Ultimately, overcoming these challenges requires moving beyond isolated algorithmic optimization toward an integrated framework that combines computational intelligence, robust experimental validation, and continuous clinical feedback. Such a synergistic approach is expected to drive the next generation of precision nanomedicine and facilitate the safe and effective translation of AI-enabled pharmaceutical innovations into clinical practice.

Indexed as

artificial intelligenceclinical translationdrug deliverymachine learningnanocarriersnanomedicine

Identifiers

PMID42514923
PMCPMC13414497

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.