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用于三肽-3局部递送的微乳液和纳米乳液:从实验设计到对面部皮肤的抗皮脂功效

Microemulsions and Nanoemulsions for Topical Delivery of Tripeptide-3: From Design of Experiment to Anti-Sebum Efficacy on Facial Skin.

作者信息

Magrode Nontachai, Poomanee Worrapan, Kiattisin Kanokwan, Ampasavate Chadarat

机构信息

Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.

Center for Excellence in Pharmaceutical Nanotechnology, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Pharmaceutics. 2024 Apr 19;16(4):554. doi: 10.3390/pharmaceutics16040554.


DOI:10.3390/pharmaceutics16040554
PMID:38675215
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11053593/
Abstract

The targeted delivery of a hydrophilic Tripeptide-3 to the skin using microemulsions or nanoemulsions for facial oil reduction was the focus of this study. The impact factors affecting oil/water transparent dispersion formation, such as the surfactant system, HLB value, and co-solvent, were identified through the water titration method and pseudoternary phase diagram plots. The interfacial tension between caprylic/capric triglyceride (CCT oil) and water was significantly reduced by the surfactant/co-surfactant combination (S) of Cremophore RH40 and a double-tails co-surfactant, polyglycerol-3-diisostearate, at an HLB of 13 together with a water-to-co-solvent (PG) ratio of 1:1. A two-level full factorial design of experiment (FFD-DoE) emphasized the independent variables of the HLB value, co-solvent, and CCT oil contents affecting the optimal compositions for micro- or nanoemulsion formation. The low-energy spontaneous emulsification of the optimized combination at a low S content (10%) yielded the translucent oil-in-water Tripeptide-3 nanoemulsions with an internal droplet size of 25.7 ± 1.20 nm, a narrow polydispersity index of 0.237 ± 0.129, and 70.6 ± 0.58% transmittance. The in vitro skin permeation study revealed a significantly higher skin penetration and retention of the Tripeptide-3 nanoemulsions compared to the high surfactant microemulsions and coarse emulsions. Skin irritation and oil control efficacy were evaluated in healthy volunteers before and after product application for 28 days. The obtained nanoemulsions not only decreased sebum production but also enhanced skin moisture levels. In conclusion, the meticulously designed nanoemulsions, incorporating suitable excipients, show a promising delivery system for hydrophilic peptides to control sebum overproduction in oily facial skin.

摘要

本研究的重点是使用微乳液或纳米乳液将亲水性三肽 -3 靶向递送至皮肤以减少面部油脂。通过水滴定法和伪三元相图绘制确定了影响油/水透明分散体形成的影响因素,如表面活性剂体系、HLB 值和助溶剂。在 HLB 为 13 且水与助溶剂(丙二醇)比例为 1:1 时,聚氧乙烯氢化蓖麻油 RH40 和双尾助表面活性剂聚甘油 -3 - 二异硬脂酸酯的表面活性剂/助表面活性剂组合(S)显著降低了辛酸/癸酸甘油三酯(CCT 油)与水之间的界面张力。两级全因子实验设计(FFD - DoE)强调了影响微乳液或纳米乳液形成最佳组成的 HLB 值、助溶剂和 CCT 油含量的自变量。在低 S 含量(10%)下优化组合的低能自发乳化产生了内部液滴尺寸为 25.7 ± 1.20 nm、多分散指数窄为 0.237 ± 0.129 且透光率为 70.6 ± 0.58% 的半透明水包油型三肽 -3 纳米乳液。体外皮肤渗透研究表明,与高表面活性剂微乳液和粗乳液相比,三肽 -3 纳米乳液的皮肤渗透率和保留率显著更高。在健康志愿者身上应用产品前后进行了 28 天的皮肤刺激性和控油功效评估。所获得的纳米乳液不仅减少了皮脂分泌,还提高了皮肤水分含量。总之,精心设计的纳米乳液,结合合适的辅料,显示出一种有前景的亲水性肽递送系统,可控制油性面部皮肤的皮脂过度分泌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/80ff1e97a186/pharmaceutics-16-00554-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/96014843e109/pharmaceutics-16-00554-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/ebcbe7b4ac07/pharmaceutics-16-00554-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/0e69f73bddbe/pharmaceutics-16-00554-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/db6d5970932c/pharmaceutics-16-00554-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/de864a784b9b/pharmaceutics-16-00554-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/814ae0a164f0/pharmaceutics-16-00554-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/e6a69b58cd70/pharmaceutics-16-00554-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/32ba911261bf/pharmaceutics-16-00554-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/80ff1e97a186/pharmaceutics-16-00554-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/96014843e109/pharmaceutics-16-00554-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/ebcbe7b4ac07/pharmaceutics-16-00554-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/0e69f73bddbe/pharmaceutics-16-00554-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/db6d5970932c/pharmaceutics-16-00554-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/de864a784b9b/pharmaceutics-16-00554-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/814ae0a164f0/pharmaceutics-16-00554-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/e6a69b58cd70/pharmaceutics-16-00554-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/32ba911261bf/pharmaceutics-16-00554-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0df/11053593/80ff1e97a186/pharmaceutics-16-00554-g009.jpg

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