Evidence map›Paper›PMID 42587338›Full record

ArticleAdvanced healthcare materials2026

A Self-Adaptive Programming Strategy Enables Local Microenvironment Modulation and Temporal Immunomodulation for Diabetic Infected Bone Regeneration.

Xiaoyang Ding, Zhiqiang Song, Jing Li, Mingjin Zhang, Liang Lyu, Yi Yu, Jiayi Liu, Qirui Wang, Chenyi Xiong, Baodong Hao and 4 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 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

14 authors.

Xiaoyang DingDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.ORCID https://orcid.org/0009-0005-0454-2215
Zhiqiang SongBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinses Academy of Sciences, Beijing, China.
Jing LiDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Mingjin ZhangDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Liang LyuDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.ORCID https://orcid.org/0000-0002-2681-8092
Yi YuDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Jiayi LiuDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Qirui WangDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Chenyi XiongDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Baodong HaoDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Ting ZhangDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Tingting YuDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Xing WangBeijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinses Academy of Sciences, Beijing, China.ORCID https://orcid.org/0000-0003-3926-1999
Dawei LiuDepartment of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.ORCID https://orcid.org/0000-0002-7625-4600

Funding

Beijing Physician Scientist Training Project BJPSTP-2025-01Key R&D Plan of Ningxia Hui Autonomous Region 2020BCG01001National Key R&D Program of China 2022YFA1206100National Natural Science Foundation of China 52373123National Natural Science Foundation of China 52573186National Natural Science Foundation of China 82271009National Natural Science Foundation of China 82571132
6 · The paper itself

Abstract

The repair of diabetic bone defects remains challenging due to disrupted bone immune homeostasis and increased susceptibility to infection. Under hyperglycemic conditions, the immune microenvironment fails to switch between the pro-inflammatory environment required for pathogen clearance and the anti-inflammatory environment for osteogenesis. Here, a glucose-responsive hydrogel (PEG-ZnO-sita) is developed by integrating zinc oxide (ZnO) and sitagliptin into a network formed by dopamine-modified tetra-armed poly(ethylene glycol) succinimidyl glutarate (DA-PEG-SG) and phenylboronic acid-modified gelatin (PBA-Gel). PEG-ZnO-sita, enabled by amidation, phenylboronic ester bonds, and metal-catechol coordination, confers rapid gelation, injectability, mechanical stability, self-healing, and robust tissue adhesion, adapting to the local complexity at the bone defect. In a diabetic microenvironment, the rapid breakage of boronate ester bonds triggers the early burst release of Zn

Indexed as

Bone RegenerationCellular MicroenvironmentDiabetes Mellitus, ExperimentalImmunomodulationAnimalsHumansHydrogelsMiceOsteogenesisPolyethylene GlycolsRAW 264.7 CellsSitagliptin PhosphateHydrogelsPolyethylene GlycolsSitagliptin Phosphatediabetic infected bone defectsmicroenvironment modulationsmart hydrogeltemporal immunomodulation

Identifiers

PMID42587338
PMCPMC13568870

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.