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1
Phenolic Acid-based Poly(anhydride-esters) as Antioxidant Biomaterials.基于酚酸的聚(酸酐 - 酯)作为抗氧化生物材料
Macromol Biosci. 2016 Feb;16(2):214-22. doi: 10.1002/mabi.201500244. Epub 2015 Oct 1.
2
Ferulic Acid-Based Polymers with Glycol Functionality as a Versatile Platform for Topical Applications.基于阿魏酸的具有二醇官能团的聚合物,作为一种多功能的局部应用平台。
Biomacromolecules. 2015 Sep 14;16(9):2911-9. doi: 10.1021/acs.biomac.5b00824. Epub 2015 Aug 18.
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Natural, semisynthetic and synthetic tyrosinase inhibitors.天然、半合成及合成酪氨酸酶抑制剂。
J Enzyme Inhib Med Chem. 2016;31(1):1-13. doi: 10.3109/14756366.2015.1004058. Epub 2015 Feb 16.
4
Effect of kojic acid-grafted-chitosan oligosaccharides as a novel antibacterial agent on cell membrane of gram-positive and gram-negative bacteria.曲酸接枝壳寡糖作为新型抗菌剂对革兰氏阳性菌和革兰氏阴性菌细胞膜的影响。
J Biosci Bioeng. 2015 Sep;120(3):335-9. doi: 10.1016/j.jbiosc.2015.01.010. Epub 2015 Feb 11.
5
Discovery of highly potent tyrosinase inhibitor, T1, with significant anti-melanogenesis ability by zebrafish in vivo assay and computational molecular modeling.通过斑马鱼体内试验和计算分子建模发现具有显著抗黑色素生成能力的高效酪氨酸酶抑制剂T1。
Sci Rep. 2015 Jan 23;5:7995. doi: 10.1038/srep07995.
6
Novel kojic acid-polymer-based magnetic nanocomposites for medical applications.新型的基于 kojic 酸-聚合物的磁性纳米复合材料,用于医疗应用。
Int J Nanomedicine. 2014;9:351-62. doi: 10.2147/IJN.S53847. Epub 2014 Jan 7.
7
Synthesis, characterization, and antimicrobial activity of kojic acid grafted chitosan oligosaccharide.曲酸接枝壳寡糖的合成、表征及抗菌活性
J Agric Food Chem. 2014 Jan 8;62(1):297-303. doi: 10.1021/jf404026f. Epub 2013 Dec 23.
8
Effect of Linker Structure on Salicylic Acid-Derived Poly(anhydride-esters).连接体结构对水杨酸衍生聚(酸酐-酯)的影响。
Macromolecules. 2005;38(16):6895-6901. doi: 10.1021/ma048051u.
9
Biodegradable coumaric acid-based poly(anhydride-ester) synthesis and subsequent controlled release.可生物降解的香豆酸基聚(酸酐-酯)的合成及随后的控制释放。
Macromol Rapid Commun. 2013 Aug;34(15):1231-6. doi: 10.1002/marc.201300323. Epub 2013 Jul 9.
10
Protein release from dihydroxyacetone-based poly(carbonate ester) matrices.基于二羟丙酮的聚(碳酸酯酯)基质中的蛋白质释放。
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基于生物可降解曲酸的聚合物:用于抑制黑色素生成的生物活性物质的控释

Biodegradable Kojic Acid-Based Polymers: Controlled Delivery of Bioactives for Melanogenesis Inhibition.

作者信息

Faig Jonathan J, Moretti Alysha, Joseph Laurie B, Zhang Yingyue, Nova Mary Joy, Smith Kervin, Uhrich Kathryn E

机构信息

Department of Chemistry and Chemical Biology, ‡Ernest Mario School of Pharmacy, and §Department of Chemical & Biochemical Engineering, Rutgers University , Piscataway, New Jersey 08854, United States.

出版信息

Biomacromolecules. 2017 Feb 13;18(2):363-373. doi: 10.1021/acs.biomac.6b01353. Epub 2017 Jan 26.

DOI:10.1021/acs.biomac.6b01353
PMID:28026947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5810376/
Abstract

Kojic acid (KA) is a naturally occurring fungal metabolite that is utilized as a skin-lightener and antibrowning agent owing to its potent tyrosinase inhibition activity. While efficacious, KA's inclination to undergo pH-mediated, thermal-, and photodegradation reduces its efficacy, necessitating stabilizing vehicles. To minimize degradation, poly(carbonate-esters) and polyesters comprised of KA and natural diacids were prepared via solution polymerization methods. In vitro hydrolytic degradation analyses revealed KA release was drastically influenced by polymer backbone composition (e.g., poly(carbonate-ester) vs polyester), linker molecule (aliphatic vs heteroatom-containing), and release conditions (physiological vs skin). Tyrosinase inhibition assays demonstrated that aliphatic KA dienols, the major degradation product under skin conditions, were more potent then KA itself. All dienols were found to be less toxic than KA at all tested concentrations. Additionally, the most lipophilic dienols were statistically more effective than KA at inhibiting melanin biosynthesis in cells. These KA-based polymer systems deliver KA analogues with improved efficacy and cytocompatible profiles, making them ideal candidates for sustained topical treatments in both medical and personal care products.

摘要

曲酸(KA)是一种天然存在的真菌代谢产物,由于其强大的酪氨酸酶抑制活性,被用作皮肤美白剂和抗褐变剂。虽然有效,但KA易于发生pH介导的、热降解和光降解,这降低了其功效,因此需要稳定的载体。为了尽量减少降解,通过溶液聚合方法制备了由KA和天然二酸组成的聚(碳酸酯-酯)和聚酯。体外水解降解分析表明,KA的释放受到聚合物主链组成(例如,聚(碳酸酯-酯)与聚酯)、连接分子(脂肪族与含杂原子)和释放条件(生理条件与皮肤条件)的显著影响。酪氨酸酶抑制试验表明,脂肪族KA二烯醇是皮肤条件下的主要降解产物,其活性比KA本身更强。在所有测试浓度下,发现所有二烯醇的毒性均低于KA。此外,在抑制细胞中黑色素生物合成方面,最具亲脂性的二烯醇在统计学上比KA更有效。这些基于KA的聚合物系统提供了具有更高功效和细胞相容性的KA类似物,使其成为医疗和个人护理产品中持续局部治疗的理想候选物。