Evidence map›Paper›PMID 39493006›Full record

ArticleInternational journal of pharmaceutics: X2024

Multifunctional poloxamer-based thermo-responsive hydrogel loaded with human lactoferricin niosomes:

Sirikwan Sangboonruang, Natthawat Semakul, Kiattikhun Manokruang, Nuttawut Khammata, Kanyaluck Jantakee, Katanchalee Mai-Ngam, Satrawut Charoenla, Phadungkiat Khamnoi, Kanokwan Saengsawang, Usanee Wattananandkul and 2 more

Abstract read
In one paragraph

Article in International journal of pharmaceutics: X, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

12 authors.

Sirikwan SangboonruangDivision of Clinical Microbiology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Natthawat SemakulDepartment of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
Kiattikhun ManokruangDepartment of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
Nuttawut KhammataDepartment of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
Kanyaluck JantakeeDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.
Katanchalee Mai-NgamNational Metal and Materials Technology Center, National Science and Technology Development Agency, Pathumthani 12120, Thailand.
Satrawut CharoenlaNational Metal and Materials Technology Center, National Science and Technology Development Agency, Pathumthani 12120, Thailand.
Phadungkiat KhamnoiDiagnostic Laboratory, Maharaj Nakorn Chiang Mai Hospital, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Kanokwan SaengsawangDepartment of Medical Technology, Lampang Hospital, Lampang 52000, Thailand.
Usanee WattananandkulDivision of Clinical Microbiology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Sorasak IntorasootDivision of Clinical Microbiology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Khajornsak TragoolpuaDivision of Clinical Microbiology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic wound infections are attributed to delayed tissue repair, which remains a major clinical challenge in long-term health care. Particularly, infections with antibiotic resistance have more serious effects on health, often resulting in unsuccessful treatments. Thus, antimicrobial peptide (AMP)-based therapy holds promise as a potential therapeutic approach to overcoming drug resistance. Conventional wound dressing is a passive strategy for wound care that is not capable of eradicating pathogens and promoting tissue repair. In this study, we aim to construct an advanced wound dressing; a thermo-responsive hydrogel incorporated with lactoferricin (Lfcin) niosome (Lfcin-Nio/hydrogel) for bacterial pathogen treatment. The Lfcin-loaded niosome (Lfcin-Nio) has a particle size of 396.91 ± 20.96 nm, 0.38 ± 0.01 of PdI, -10.5 ± 0.3 mV of ζ potential, and 72.30 ± 7.05 % Lfcin entrapment efficiency. Lfcin-Nio exhibited broad antibacterial activity on both drug-susceptible and drug-resistant strains, and also on bacteria residing in the biofilm matrix. The Lfcin-Nio/hydrogel was fabricated from 0.5 %

Indexed as

Anti-bacterial activityAnti-inflammationLfcin-NioThermo-responsive hydrogelWound healing

Identifiers

PMID39493006
PMCPMC11530604

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.