Evidence map›Paper›PMID 41218704›Full record

ArticleJournal of advanced research2026

Fucose-tobramycin sponge-like microparticles to treat pulmonary Pseudomonas aeruginosa infections in a lectin-competitive approach.

Yuzhen Jin, Jun Chen, Cenfeng Liu, Wenhao Wang, Yue Zhou, Kaiqing Zhang, Xiaolu Xiao, Guixiang Chen, Xuejuan Zhang, Zhengwei Huang and 2 more

Abstract read
In one paragraph

Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

Yuzhen JinState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: jyz18279923520@163.com.
Jun ChenState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: 18806030836@163.com.
Cenfeng LiuState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: lcfeng2021@163.com.
Wenhao WangSchool of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China. Electronic address: whwang97@yeah.net.
Yue ZhouState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: zhouyue42626@163.com.
Kaiqing ZhangState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: zkz1998@stu.jnu.edu.cn.
Xiaolu XiaoState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: m19152049598@163.com.
Guixiang ChenState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: 19200528516@163.com.
Xuejuan ZhangState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: zhanghongdou0223@126.com.
Zhengwei HuangState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: huangzhengw@jnu.edu.cn.
Chuanbin WuState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China; Jiangmen Wuyi Hospital of Traditional Chinese Medicine, Affiliated Jiangmen Traditional Chinese Medicine Hospital of Jinan University, Jiangmen 529031 Guangdong Province, China. Electronic address: chuanbinwu@jnu.edu.cn.
Ying HuangState Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, College of Pharmacy, Jinan University, Guangzhou 511443, China. Electronic address: huangy2007@jnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe high incidence of pulmonary infections caused by multidrug-resistant bacteria such as Pseudomonas aeruginosa (PA) poses significant treatment challenges. Dry powder inhaler (DPIs) are an effective treatment method, delivering antibiotics directly to lung lesions. However, DPIs face two main issues: abnormal respiratory variability causes inadequate pulmonary deposition and PA's biofilms hinder antibiotic access.

objectivesA sponge-like dry powder based on the lectin-competitive strategy was developed with tobramycin (TOB) to solve the crucial issue.

methodsLectin-affinity sugars were screened using isothermal titration calorimetry. Sponge-like TOB-Formulation were then developed with the selected sugar as a carrier via spray freeze-drying. The formulation with the highest lung delivery efficiency was identified with a next-generation impactor and validated in a rat model of chronic pulmonary infection.

resultsFucose was used as a carrier to develop sponge-like TOB- Formulation by spray freeze-drying technology with spherical low-density and nanoporous particles, making them suitable for patient's inspiratory mode and improving lung deposition. Among them, the F

conclusionThis tobramycin spongy-like dry powder, identified as high lectin affinity and excellent respiratory variability tolerance, holds significant promise for the treatment of pulmonary infections.

Indexed as

Anti-Bacterial AgentsFucoseLectinsPseudomonas aeruginosaPseudomonas InfectionsTobramycinAdministration, InhalationAnimalsBiofilmsDry Powder InhalersLungMaleRatsAnti-Bacterial AgentsFucoseLectinsTobramycinAbnormal respiratory variabilityBiofilmsDry powder inhalerLectin affinity sugarPulmonary infections

Identifiers

PMID41218704
PMCPMC13453960

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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.