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聚己内酯基填充剂联合糖皮质激素用于真皮填充剂的安全性和有效性评估:一项临床前研究。

Evaluation of Safety and Efficacy of Polycaprolactone-Based Fillers Combined with Glucocorticoid in Dermal Fillers: A Preclinical Investigation.

作者信息

Cui Hengqing, Zhang Jun, Zhang Ziqi, Qi Lili, Tan Linlin, Cui Haiyan

机构信息

Department of Plastic and Cosmetic Surgery, Tongji Hospital, School of Medicine, Tongji University, Shanghai, 200092, China.

Institute of Aesthetic Plastic Surgery and Medicine, School of Medicine, Tongji University, Shanghai, 200065, China.

出版信息

Aesthetic Plast Surg. 2025 Aug 18. doi: 10.1007/s00266-025-05155-6.

Abstract

BACKGROUND

Polycaprolactone (PCL) fillers are widely used for facial rejuvenation due to their biodegradability and collagen-stimulating effects. However, PCL injections can trigger inflammation, leading to nodules and swelling. This study evaluated whether co-administration of dexamethasone and triamcinolone (PCL+D+T) mitigates inflammation while preserving collagen formation.

METHODS

Cytotoxicity and apoptosis of PCL+D+T were assessed in fibroblast cells using MTT and Annexin V-FITC/PI assays. Sprague-Dawley rats received PCL injections alone or with corticosteroids. Local inflammation was analyzed via flow cytometry (CD86/CD206) and ELISA (CXCL-1, IL-1β, IL-10, TNF-α). Histology and transmission electron microscopy (TEM) evaluated collagen deposition and fiber structure.

RESULTS

PCL injection increased pro-inflammatory cytokines and M1 macrophages, indicating acute inflammation. Co-treatment with dexamethasone and triamcinolone reduced inflammatory markers without impairing collagen deposition, as evidenced by similar dermal thickness, collagen area fraction, and fiber diameter across groups.

CONCLUSIONS

Dexamethasone and triamcinolone effectively suppress PCL-induced acute inflammation while maintaining collagen-stimulating properties. This approach may enhance PCL filler safety and efficacy, warranting further clinical investigation.

NO LEVEL ASSIGNED

This journal requires that authors assign a level of evidence to each submission to which Evidence-Based Medicine rankings are applicable. This excludes Review Articles, Book Reviews, and manuscripts that concern Basic Science, Animal Studies, Cadaver Studies, and Experimental Studies. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .

摘要

背景

聚己内酯(PCL)填充剂因其生物可降解性和刺激胶原蛋白生成的作用而被广泛用于面部年轻化治疗。然而,PCL注射可能引发炎症,导致结节和肿胀。本研究评估了地塞米松和曲安奈德联合使用(PCL+D+T)是否能减轻炎症,同时保留胶原蛋白的形成。

方法

使用MTT和Annexin V-FITC/PI检测法评估PCL+D+T在成纤维细胞中的细胞毒性和凋亡情况。将Sprague-Dawley大鼠单独注射PCL或与皮质类固醇联合注射。通过流式细胞术(CD86/CD206)和酶联免疫吸附测定(ELISA)(CXCL-1、IL-1β、IL-10、TNF-α)分析局部炎症。组织学和透射电子显微镜(TEM)评估胶原蛋白沉积和纤维结构。

结果

PCL注射增加了促炎细胞因子和M1巨噬细胞,表明存在急性炎症。地塞米松和曲安奈德联合治疗降低了炎症标志物,同时不影响胶原蛋白沉积,各组间真皮厚度、胶原蛋白面积分数和纤维直径相似即证明了这一点。

结论

地塞米松和曲安奈德可有效抑制PCL诱导的急性炎症,同时保持刺激胶原蛋白生成的特性。这种方法可能会提高PCL填充剂的安全性和有效性,值得进一步进行临床研究。

未指定证据水平

本期刊要求作者为每篇适用循证医学排名的投稿指定证据水平。这排除了综述文章、书评以及涉及基础科学、动物研究、尸体研究和实验研究的手稿。有关这些循证医学评级的完整描述,请参阅目录或作者在线指南www.springer.com/00266

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