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一项关于含抗痤疮后生元的外用洗剂对轻至中度痤疮患者疗效的初步研究。

A pilot study on the efficacy of topical lotion containing anti-acne postbiotic in subjects with mild -to -moderate acne.

作者信息

Cui Hongchang, Guo Chaoqun, Wang Qian, Feng Congrui, Duan Zhi

机构信息

Qingdao Vland Biotech Group Co., Ltd., Qingdao, China.

出版信息

Front Med (Lausanne). 2022 Dec 9;9:1064460. doi: 10.3389/fmed.2022.1064460. eCollection 2022.

DOI:10.3389/fmed.2022.1064460
PMID:36569166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9780477/
Abstract

INTRODUCTION

Acne can compromise facial esthetics and become a mental burden, especially when it occurs in puberty. Skincare cosmetics with anti-acne efficiency is more convenient than other treatment modalities, such as dietary supplements, in certain circumstances. The purpose of this study was to investigate the efficacy of an anti-acne lotion in alleviating acne.

METHODS

In our study, an anti-acne lotion containing ferment lysate produced by VHProbi E15 were applied to subjects with mild -to -moderate acne over 4 weeks. The efficacy was evaluated based on instrumental measurements using Visia-CR and CK-MPA system.

RESULTS AND DISCUSSION

The anti-acne lotion exhibited favorable safety, meeting the stringent criteria for the detection of microbes, heavy metals, toxicity, and irritation. After 2 weeks of treatment, a statistically significant improvement in acne lesions was observed compared to baseline ( < 0.01), and this continued to the end of the study. After 4 weeks of treatment, the transepidermal water loss ( < 0.05) and sebum production ( < 0.05) were significantly decreased in subjects compared to baseline. In addition, the pore/area of interest (AOI) and stratum corneum hydration displayed slightly positive changes throughout treatment. Thus, we conclude that applying topical anti-acne lotion may be safe and confer effective benefits in people with mild -to -moderate acne and represents a promising therapeutic option for acne.

摘要

引言

痤疮会损害面部美观并成为一种心理负担,尤其是在青春期出现时。在某些情况下,具有抗痤疮功效的护肤化妆品比其他治疗方式(如膳食补充剂)更方便。本研究的目的是调查一种抗痤疮乳液在减轻痤疮方面的功效。

方法

在我们的研究中,一种含有VHProbi E15产生的发酵裂解物的抗痤疮乳液被应用于轻度至中度痤疮患者4周。基于使用Visia-CR和CK-MPA系统的仪器测量来评估疗效。

结果与讨论

该抗痤疮乳液表现出良好的安全性,符合微生物、重金属、毒性和刺激性检测的严格标准。治疗2周后,与基线相比,痤疮损伤有统计学意义的改善(<0.01),并且这种改善持续到研究结束。治疗4周后,与基线相比,受试者的经表皮水分流失(<0.05)和皮脂分泌(<0.05)显著降低。此外,在整个治疗过程中,感兴趣的毛孔/区域(AOI)和角质层水合作用显示出轻微的积极变化。因此,我们得出结论,局部应用抗痤疮乳液可能对轻度至中度痤疮患者是安全且有效的,是一种有前景的痤疮治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/5d0e25a530c8/fmed-09-1064460-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/e61aa138049e/fmed-09-1064460-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/a39ec39f2d0a/fmed-09-1064460-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/5d0e25a530c8/fmed-09-1064460-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/e61aa138049e/fmed-09-1064460-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/a39ec39f2d0a/fmed-09-1064460-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/359b/9780477/5d0e25a530c8/fmed-09-1064460-g003.jpg

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