Surface coating nanoarchitectonics for optimizing cytocompatibility and antimicrobial activity: The impact of hyaluronic acid positioning as the outermost layer.
Neto GLB., Quinalia TRB., de Almeida DA., Madruga LYC., Souza PR., Popat KC.
Laboratory Study on Face & Skin, published in Int J Biol Macromol (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- Int J Biol Macromol (2025)
- Country
- Netherlands
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 39818370
- DOI
- 10.1016/j.ijbiomac.2025.139908
- Citations
- 1
Abstract (original English)
Polyelectrolyte multilayers (PEMs) based on hyaluronic acid (HA) and poly (diallyldimethylammonium chloride) (PDDA) were deposited on oxidized polystyrene (PS ox ) via the layer-by-layer (LbL) method. The X-ray photoelectron spectroscopy (XPS) confirmed the PEM deposition on PS ox , and atomic force microscopy (AFM) indicated that the surface roughness of PS also increased after PEM deposition. The PEMs significantly enhanced PS wettability, reducing the contact angle from 73° on PS to 24° on PDDA-terminated (PDDA/HA) 2.5 PEM (2.5 bilayers, 5 layers) and 36° on HA-terminated (PDDA/HA) 3 PEM (3 bilayers, 6 layers). The HA-terminated (PDDA/HA)₃ PEM demonstrated antimicrobial activity. Compared to uncoated PS surfaces, this PEM reduced the surface coverage of viable P. aeruginosa cells from 36.5 % to 3.7 % and S. aureus cells from 13.3 % to 2.5 % on uncoated PS surfaces. The antimicrobial assay following the JIS Z 2801-2010 standard demonstrated that the PDDA-terminated (PDDA/HA) 2.5 PEM inhibited S. aureus growth by 48 %, compared to 32 % inhibition by the HA-terminated (PDDA/HA) 3 PEM relative to the uncoated and non-oxidized polystyrene (PS) surface (control). HA-terminated PEM demonstrated lesser antimicrobial activity than PDDA-terminated PEM. However, both PEMs were cytocompatible against erythrocytes and human adipose-derived stem cells (ADSCs), indicating their potential f
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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