<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">CDCST</journal-id><journal-title-group><journal-title>China Daily Chemical Science Technology</journal-title></journal-title-group><issn>2997-7096</issn><eissn>2997-710X</eissn><publisher><publisher-name>Art and Technology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.61369/CDCST.2025030007</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>烟酰胺经皮渗透性研究</title><url>https://artdesignp.com/journal/CDCST/2/3/10.61369/CDCST.2025030007</url><author>李和伟,代颖,汪国鹏,魏国志</author><pub-date pub-type="publication-year"><year>2025</year></pub-date><volume>2</volume><issue>3</issue><history><date date-type="pub"><published-time>2025-09-25</published-time></date></history><abstract>评估烟酰胺在皮肤中的渗透能力及其在皮肤内的驻留量，并探讨影响烟酰胺经皮透过皮肤的因素。采用巴马小型猪的离体皮肤作为研究模型，应用Franz扩散池技术来测定烟酰胺在皮肤中的累积驻留量和经皮透过量。通过经皮吸收房室模型预测其在人体面部皮肤中的驻留量-时间曲线，以探究烟酰胺的美白效果。研究表明，供体池的温度、皮肤的种类以及透明质酸的用量对烟酰胺的经皮吸收有显著影响；烟酰胺在皮肤中的驻留量显著低于其在接收液中的浓度；小鼠实验验证了所建立的房室模型能准确预测烟酰胺在皮肤中的驻留量，并预测了烟酰胺在人体面部皮肤中的驻留量-时间曲线。烟酰胺具有较好的经皮吸收性能，并且在皮肤中能保持适当的驻留水平。</abstract><keywords>烟酰胺,皮肤中驻留量,经皮渗透,经皮吸收房室模型</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1]肖伟莉,王雪梅,闫广义, 等.3种水溶性美白剂的渗透性研究[J].安徽大学学报( 自然科学版),2018,42(04):75-81.[2]施昌松,崔凤玲,李光华.烟酰胺在皮肤美白产品中的应用研究[J]. 日用化学品科学,2005(02):25-26+29.[3]李和伟,魏国志,许飞飞.多层非均相制剂技术制备固态花青素面膜及其稳定性评价[J]. 中国美容医学,2023,32(11):76-81.[4]唐泽严,郭学平,温喜明, 等.不同相对分子质量透明质酸对还原型谷胱甘肽透皮吸收的影响[J].中国药科大学学报,2021,52(02):203-210.[5]魏国志,许飞飞,李和伟.不同来源猪皮与重建人类表皮模型对面膜中咖啡因透过性比较研究[J].中南药学,2023,21(08):2095-2100.[6] Mitragotri S, Anissimov YG, Bunge AL, et al. Mathematical models of skin permeability: an overview[J]. Int J Pharmaceut, 2011, 418(1):115-129.[7] Maharao N, Antontsev V, Hou H, et al. Scalable in silico simulation of transdermal drug permeability: Application of BIOiSIM platform[J].Drug design, development and therapy, 2020: 2307-2317.[8] Valentin J. Basic anatomical and physiological data for use in radiological protection: reference values: ICRP Publication 89[J].Annals of the ICRP, 2002, 32(3-4): 1-277.[9] 杨海洋,汪国鹏,杨文宁, 等.黄芩素、槲皮素、高良姜素对黄嘌呤氧化酶靶点占有率的模拟分析[J].中国实验方剂学杂志,2021,27(14):147-154.[10] Kitaoka M, Nguyen TC, Goto M. Water-in-oil microemulsions composed of monoolein enhanced the transdermal delivery of nicotinamide[J]. Int J Cosmetic Sci, 2021, 43(3): 302-310.[11] Stratford MRL, Dennis MF, Hoskin P, et al. Nicotinamide pharmacokinetics in humans: effect of gastric acid inhibition,comparison of rectal vs oral administration and the use of saliva for drug monitoring[J]. Brit J Cancer, 1996, 74(1): 16-21.[12] Petley A, Macklin B, Renwick AG, et al. The pharmacokinetics of nicotinamide in humans and rodents[J]. Diabetes, 1995, 44(2): 152-155.
[13]李和伟,魏国志,许飞飞.多层非均相制剂技术制备固态花青素面膜及其稳定性评价[J]. 中国美容医学,2023,32(11):76-81.[14]方婷欢,蒋晴,唐礼荣.烟酰胺与茶多酚复配对抑制PIG1细胞黑色素的影响[J]. 日用化学工业,2022,52(06):632-637.[15] 帕它木&amp;middot;莫合买提,阿尔孜古丽&amp;middot;吐尔逊,热沙来提&amp;middot;阿不都瓦衣特, 等.烟酰胺对人皮肤黑素细胞黑素转运作用研究[J].环境与健康杂志,2009,26(8):680-683.
[16] Pavlačkov&amp;aacute; J，Egner P，Pola&amp;scaron;kov&amp;aacute; J，et al. Transdermal absorption of active substances from cosmetic vehicles[J]. J CosmetDermatol-us，2019，18（5）：1410-1415.[17]Pan W, Qin M, Zhang G, et al. Combination of hydrotropic nicotinamide with nanoparticles for enhancing tacrolimus percutaneous delivery[J]. Int J Nanomed, 2016: 4037-4050.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
