Evidence map›Paper›PMID 41098428›Full record

ArticlePlastic and reconstructive surgery. Global open2025

Evaluation of Hyaluronic Acid Filler Injections in Mice Over 28 Days: A Controlled In Vivo Study.

Woonji E Jang, Jung Im No, Chung Lee, Yeojin Kim, TaeHyeob Kim, Jiyoung Lee

Abstract read
In one paragraph

Article in Plastic and reconstructive surgery. Global open, 2025. 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

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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

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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

6 authors.

Woonji E JangFrom the Aesthetic Medical Team, LG Chem, Ltd., Seoul, Republic of Korea.
Jung Im NoFrom the Aesthetic Medical Team, LG Chem, Ltd., Seoul, Republic of Korea.
Chung LeeBio-Technology Team, Drug Development, LG Chem, Ltd., Seoul, Republic of Korea.
Yeojin KimBio-Technology Team, Drug Development, LG Chem, Ltd., Seoul, Republic of Korea.
TaeHyeob KimBio-Technology Team, Drug Development, LG Chem, Ltd., Seoul, Republic of Korea.
Jiyoung LeeFrom the Aesthetic Medical Team, LG Chem, Ltd., Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Initial and early swelling post injection of hyaluronic acid (HA) filler are considered to affect outcomes and complications in patients; however, the contribution of HA filler type to swelling postinjection remains undetermined. Here, initial and early swelling post injection of HA fillers manufactured via different crosslinking technologies was evaluated in mice. Methods: Mice received injections of HA fillers or controls: High Concentration Equalized (HICE), Stabilized High Concentration Equalized (S-HICE), High molecular Ideal, VYCROSS, NASHA, HICE control, non-HICE control, or no HA control. Initial and early swelling were evaluated via magnetic resonance imaging and collagen deposition via histological evaluation over 28 days. Results: Mice (N = 65) were allocated to 13 groups (per group, n = 5) to receive subcutaneous injections of HA filler or control. Maximum swelling in descending order was High molecular Ideal, 290%; non-HICE control, 256%; VYCROSS 1, 249%; S-HICE 2, 248%; S-HICE 1, 238%; S-HICE 3, 226%; VYCROSS 2, 210%; HICE 1, 203%; HICE 2, 184%; NASHA 1, 174%; HICE control, 159%; NASHA 2, 148%; and no HA control, 100.0%. The mean (SD) collagen area in the residual substance ranged from 2525 (3612) µm Conclusions: HA fillers manufactured via different crosslinking technologies may lead to different levels of initial and early swelling and collagen stimulation over 28 days.

Identifiers

PMID41098428
PMCPMC12520210

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