Molecular mechanisms and enhanced functions of Hibiscus sabdariffa L—nanoliposomes as an emerging therapeutic strategy in UV and galactosamine skin aging-induced model

IF 3.4 Q2 PHARMACOLOGY & PHARMACY Future Journal of Pharmaceutical Sciences Pub Date : 2025-01-06 DOI:10.1186/s43094-024-00756-5
Eptehal Nassar, Mai Rady, Heba Handousa
{"title":"Molecular mechanisms and enhanced functions of Hibiscus sabdariffa L—nanoliposomes as an emerging therapeutic strategy in UV and galactosamine skin aging-induced model","authors":"Eptehal Nassar,&nbsp;Mai Rady,&nbsp;Heba Handousa","doi":"10.1186/s43094-024-00756-5","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Skin aging is a multifactorial disorder that occurs due to extrinsic and intrinsic factors, where a decrease in natural antioxidant defenses and an imbalance between molecular biomarkers occur. The current study aims to develop nanoliposomes for the dermal delivery of <i>Hs</i> and to investigate their effects on skin biomarkers and skin aging.</p><h3>Methods</h3><p>Chemical profiling performed via high-performance liquid chromatography (HPLC)/ESI‒PDA‒MS revealed enrichment in phenolic metabolite contents. <i>Hs-</i>nanolopeosomes were characterized for their mean size, encapsulation efficiency of <i>Hs</i> and ability to penetrate the skin via confocal microscopy. An aged rat model generated via UV and galactosamine injection was evaluated for reduced glutathione (GSH) and malondialdehyde (MDA) levels, in addition to the levels of collagenase and elastase enzymes in the different study groups, which included a healthy control group, an aged group, a prophylactic group, an aged group treated with <i>Hs-</i>nanoliposomes, and a green tea extract-treated group (positive control). Moreover, the Bcl-2/Bax proteins were determined via ELISA, and MMP-1, MMP-2, MMP-9, and TIMP-1 expression was determined via RT‒qPCR in the study groups.</p><h3>Results</h3><p><i>Hs-</i>nanoliposomes (~ 400 nm) proved deep skin localization in confocal images. Compared with the aged group and the green tea extract-treated group, the <i>Hs</i>-liposome-treated group presented elevated reduced glutathione and decreased malondialdehyde levels and inhibited collagenase and elastase enzymes. This treatment also decreased the Bcl-2/Bax ratio and downregulated the expression of MMP-1, MMP-2, and MMP-9. However, upregulation of TIMP-1 expression was detected. The outcomes were confirmed by histopathological assays, which revealed reduced saging and collagen damage in the <i>Hs</i>-nanolipid-treated group.</p><h3>Conclusion</h3><p>The present study proposed a potential antiaging nanobased formulation that can deliver <i>Hs</i> extract deep in the dermis layer to prevent the oxidative stress that leads to aging.</p></div>","PeriodicalId":577,"journal":{"name":"Future Journal of Pharmaceutical Sciences","volume":"11 1","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://fjps.springeropen.com/counter/pdf/10.1186/s43094-024-00756-5","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s43094-024-00756-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Skin aging is a multifactorial disorder that occurs due to extrinsic and intrinsic factors, where a decrease in natural antioxidant defenses and an imbalance between molecular biomarkers occur. The current study aims to develop nanoliposomes for the dermal delivery of Hs and to investigate their effects on skin biomarkers and skin aging.

Methods

Chemical profiling performed via high-performance liquid chromatography (HPLC)/ESI‒PDA‒MS revealed enrichment in phenolic metabolite contents. Hs-nanolopeosomes were characterized for their mean size, encapsulation efficiency of Hs and ability to penetrate the skin via confocal microscopy. An aged rat model generated via UV and galactosamine injection was evaluated for reduced glutathione (GSH) and malondialdehyde (MDA) levels, in addition to the levels of collagenase and elastase enzymes in the different study groups, which included a healthy control group, an aged group, a prophylactic group, an aged group treated with Hs-nanoliposomes, and a green tea extract-treated group (positive control). Moreover, the Bcl-2/Bax proteins were determined via ELISA, and MMP-1, MMP-2, MMP-9, and TIMP-1 expression was determined via RT‒qPCR in the study groups.

Results

Hs-nanoliposomes (~ 400 nm) proved deep skin localization in confocal images. Compared with the aged group and the green tea extract-treated group, the Hs-liposome-treated group presented elevated reduced glutathione and decreased malondialdehyde levels and inhibited collagenase and elastase enzymes. This treatment also decreased the Bcl-2/Bax ratio and downregulated the expression of MMP-1, MMP-2, and MMP-9. However, upregulation of TIMP-1 expression was detected. The outcomes were confirmed by histopathological assays, which revealed reduced saging and collagen damage in the Hs-nanolipid-treated group.

Conclusion

The present study proposed a potential antiaging nanobased formulation that can deliver Hs extract deep in the dermis layer to prevent the oxidative stress that leads to aging.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
木芙蓉l -纳米脂质体在紫外线和半乳糖胺诱导皮肤衰老模型中的分子机制和增强功能
皮肤老化是由外在和内在因素引起的多因素疾病,其中天然抗氧化防御能力下降和分子生物标志物之间的不平衡发生。目前的研究旨在开发用于Hs真皮递送的纳米脂质体,并研究其对皮肤生物标志物和皮肤衰老的影响。方法利用高效液相色谱(HPLC)/ ESI-PDA-MS进行化学分析,发现酚类代谢物含量富集。通过共聚焦显微镜对Hs-纳米体的平均大小、Hs的包封效率和穿透皮肤的能力进行了表征。通过紫外线和半乳糖胺注射生成的衰老大鼠模型,除了胶原酶和弹性酶的水平外,还评估了还原型谷胱甘肽(GSH)和丙二醛(MDA)水平,不同研究组包括健康对照组、衰老组、预防组、hs -纳米脂质体处理组和绿茶提取物处理组(阳性对照)。此外,通过ELISA检测Bcl-2/Bax蛋白,通过RT-qPCR检测研究组中MMP-1、MMP-2、MMP-9和TIMP-1的表达。结果shs -纳米脂质体(~ 400 nm)在共聚焦图像上可定位于皮肤深部。与老年组和绿茶提取物处理组相比,hs脂质体处理组还原性谷胱甘肽升高,丙二醛降低,胶原酶和弹性酶抑制。该处理还降低了Bcl-2/Bax比值,下调了MMP-1、MMP-2和MMP-9的表达。然而,检测到TIMP-1表达上调。组织病理学结果证实,hs -纳米脂处理组的衰老和胶原蛋白损伤减少。结论本研究提出了一种潜在的抗衰老纳米配方,该配方可以将Hs提取物深入真皮层,防止氧化应激导致的衰老。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
期刊最新文献
Application of the quality by design (QbD) approach to the development and validation of analytical methods for the quantification of Lumateperone Tosylate as the bulk drug and capsule dosage form by HPLC Icariin zeinmersomes display enhanced anti-proliferative and pro-apoptotic activities in colon cancer cells Quercetin inhibits steroid-induced hypergluconeogenesis in Saccharomyces cerevisiae Lentinula edodes mycelia extract abrogates chemotherapy-evoked cold and mechanical allodynia in mice Stability indicating RP-UPLC determination of three antiviral agents: emtricitabine, tenofovir, and rilpivirine in combined pharmaceutical dosage form
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1