Evidence map›Paper›PMID 42875418›Full record

ArticleNature communications2026

On-demand design of controlled-release systems using an expert-mimic AI framework.

Ying Qin, Rushuang Zhou, Yali Ming, Bohao Li, Yuning Hu, Donglin Sui, Jingxuan Liu, Hang Wang, Guanghui Ma, Yuedong Yang and 2 more

Abstract read
In one paragraph

Article in Nature communications, 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

12 authors.

Ying Qin *Department of Data Science, City University of Hong Kong, Hong Kong, PR China.
Rushuang Zhou *Department of Biomedical Engineering, City University of Hong Kong, Hong Kong, PR China.
Yali Ming *State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China.
Bohao Li *School of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, PR China.ORCID http://orcid.org/0009-0004-0627-806X
Yuning HuHuili Pharmaceutical Co., Ltd., Suzhou, PR China.
Donglin SuiState Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China.
Jingxuan LiuState Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China.
Hang WangHuili Pharmaceutical Co., Ltd., Suzhou, PR China.
Guanghui MaState Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China.ORCID http://orcid.org/0000-0001-9154-5556
Yuedong YangSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, PR China. yangyd25@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-6782-2813
Yining DongDepartment of Data Science, City University of Hong Kong, Hong Kong, PR China. yining.dong@cityu.edu.hk.
Yufei XiaState Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China. yfxia@ipe.ac.cn.ORCID http://orcid.org/0000-0003-1215-6128

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Navigating a vast formulation-preparation design space that is highly sensitive to perturbations makes trial-and-error approaches inefficient and costly for diverse clinical needs. Here, we introduce an expert-mimic AI framework called E-MAF that integrates a process-aware surrogate with an optimized genetic algorithm to emulate coarse-to-fine reasoning, autonomously generating lab-ready designs tailored to desired release profiles. We show that E-MAF delivers on-demand release and shortens design cycles from 6-12 months to approximately 1 hour. We demonstrate that in vitro release, in vivo pharmacokinetics and therapeutic effects match or surpass commercial benchmarks across 7 active pharmaceutical ingredients. We show that E-MAF also enables release profiles that are hard to achieve by conventional approaches, exemplified by ≤2% risperidone burst within 1 h and near-zero-order release over ~28 days in vivo. These results demonstrate E-MAF's potential to accelerate polymeric controlled-release system development and drug-delivery industrialization.

Indexed as

Delayed-Action PreparationsDrug Delivery SystemsAlgorithmsAnimalsBulk DrugsDrug LiberationGenetic AlgorithmsHumansPolymersRisperidoneBulk DrugsDelayed-Action PreparationsPolymersRisperidone

Identifiers

PMID42875418
PMCPMC13669340

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.