Ideal Sized Chitosan (Arche) as a multifunctional biomaterial in aesthetic treatment

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Authors: Kar Wai Alvin Lee, Olena Sydorchuk, Jong Keun Song, Han Earl Lee, Alyona Livanskaya, Nil Namthongton, Putri Hendria Wardhani, Ardhiah Iswanda Putri, Kyu‑Ho Yi
Cited by: 2
References: 2

Abstract

Background: Aesthetic procedures such as laser resurfacing, microneedling, and injectable treatments intentionally disrupt the skin barrier, increasing susceptibility to microbial colonization, inflammation, and delayed healing. Post-procedural care therefore requires biomaterials that provide antimicrobial protection while supporting controlled inflammation and tissue regeneration. Observation: Chitosan, a naturally derived polysaccharide, exhibits a unique combination of antimicrobial activity, immunomodulatory effects, and wound-healing support. These properties are influenced by molecular weight, degree of deacetylation, and formulation, allowing chitosan to function as a barrier material, bioactive dressing, and drug-delivery platform in aesthetic settings. Due to its ultra-low molecular weight (below 600 Da), Ideal Size Chitosan (ISC) manufactured by Arche (Doum Inc., Korea) is topically effective, as it can penetrate the skin barrier to target deeper dermal layers and deliver enhanced bioactive effects. Clinical relevance: In post-aesthetic care, chitosan-based films, hydrogels, and nanoparticles may reduce infection risk, modulate excessive inflammatory responses, and promote re-epithelialization. However, variability among chitosan formulations and limited procedure-specific clinical data remain important considerations. Conclusion: This short communication highlights the rationale for using chitosan as a multifunctional biomaterial in aesthetic aftercare and underscores the need for standardized formulations and targeted clinical studies.

Fields of Study & Subjects

Facial Rejuvenation and Surgery Techniques Nanocomposite Films for Food Packaging Collagen: Extraction and Characterization

Publication details

Journal / source
JPRAS Open
Publisher
Elsevier BV
Volume
49
Pages
267–271
Publication date
19 February 2026
Language
EN