Evidence map›Paper›PMID 38549081›Full record

ArticleJournal of nanobiotechnology2024

Minocycline-loaded nHAP/PLGA microspheres for prevention of injury-related corneal angiogenesis.

Zitong Li, Wenpeng Huang, Ming Zhang, Yan Huo, Feifei Li, Lele Song, Sitong Wu, Qi Yang, Xiaoming Li, Jianjun Zhang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
8.1field-weighted citation impact, top 2% of its field
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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Tumor-Targeted Delivery Therapy Based on PLGA Nanoparticles.Journal of functional biomaterials · 2026
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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

13 authors at 4 institutions in 1 country.

Zitong Li *Department of Ophthalmology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Wenpeng Huang *Department of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Ming Zhang *Department of Pathology, Peking University International Hospital, Beijing, China.
Yan Huo *Department of Ophthalmology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Feifei LiBeijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, People's Republic of China.
Lele SongDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Sitong WuDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Qi YangDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Xiaoming LiBeijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, People's Republic of China.
Jianjun ZhangBeijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, People's Republic of China. zhangjj@mail.buct.edu.cn.
Liu YangDepartment of Ophthalmology, Peking University First Hospital, Beijing, 100034, People's Republic of China. liu_yang@bjmu.edu.cn.
Jianchen HaoDepartment of Ophthalmology, Peking University First Hospital, Beijing, 100034, People's Republic of China. haojianchen@bjmu.edu.cn.
Lei KangDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China. kanglei@bjmu.edu.cn.
Peking University · CNPeking University First Hospital · CNBeijing University of Chemical Technology · CNPeking University International Hospital · CN

Funding

Beijing Municipal Science & Technology Commission Z221100007422027Beijing Science Foundation for Distinguished Young Scholars JQ21025National High Level Hospital Clinical Research Funding(Interdisciplinary Research Project of Peking University First Hospital) 2023IR17National High Level Hospital Clinical Research Funding (Youth clinical research project of Peking University First Hospital) 2022CR101National Natural Science Foundation of China 82171970
6 · The paper itself

Abstract

backgroundCorneal neovascularization (CoNV) threatens vision by disrupting corneal avascularity, however, current treatments, including pharmacotherapy and surgery, are hindered by limitations in efficacy and adverse effects. Minocycline, known for its anti-inflammatory properties, could suppress CoNV but faces challenges in effective delivery due to the cornea's unique structure. Therefore, in this study a novel drug delivery system using minocycline-loaded nano-hydroxyapatite/poly (lactic-co-glycolic acid) (nHAP/PLGA) nanoparticles was developed to improve treatment outcomes for CoNV.

resultsUltra-small nHAP was synthesized using high gravity technology, then encapsulated in PLGA by a double emulsion method to form nHAP/PLGA microspheres, attenuating the acidic by-products of PLGA degradation. The MINO@PLGA nanocomplex, featuring sustained release and permeation properties, demonstrated an efficient delivery system for minocycline that significantly inhibited the CoNV area in an alkali-burn model without exhibiting apparent cytotoxicity. On day 14, the in vivo microscope examination and ex vivo CD31 staining corroborated the inhibition of neovascularization, with the significantly smaller CoNV area (29.40% ± 6.55%) in the MINO@PLGA Tid group (three times daily) than that of the control group (86.81% ± 15.71%), the MINO group (72.42% ± 30.15%), and the PLGA group (86.87% ± 14.94%) (p < 0.05). Fluorescein sodium staining show MINO@PLGA treatments, administered once daily (Qd) and three times daily (Tid) demonstrated rapid corneal epithelial healing while the Alkali injury group and the DEX group showed longer healing times (p < 0.05). Additionally, compared to the control group, treatments with dexamethasone, MINO, and MINO@PLGA were associated with an increased expression of TGF-β as evidenced by immunofluorescence, while the levels of pro-inflammatory cytokines IL-1β and TNF-α demonstrated a significant decrease following alkali burn. Safety evaluations, including assessments of renal and hepatic biomarkers, along with H&E staining of major organs, revealed no significant cytotoxicity of the MINO@PLGA nanocomplex in vivo.

conclusionsThe novel MINO@PLGA nanocomplex, comprising minocycline-loaded nHAP/PLGA microspheres, has shown a substantial capacity for preventing CoNV. This study confirms the complex's ability to downregulate inflammatory pathways, significantly reducing CoNV with minimal cytotoxicity and high biosafety in vivo. Given these findings, MINO@PLGA stands as a highly promising candidate for ocular conditions characterized by CoNV.

Indexed as

Corneal NeovascularizationMinocyclineAlkaliesAngiogenesisHumansMicrospheresAlkaliesMinocyclineControlled drug releaseCorneal neovascularizationMinocyclinenHAP/PLGA microspheresOcular inflammation

Identifiers

PMID38549081
PMCPMC10979583
OpenAlexW4393258695

What OpenQuestion 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 OpenQuestion graph.