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    2025年, 第55卷, 第1期 刊出日期:2025-01-22 上一期    下一期
    特邀专稿
    含硼共聚物:一类环保型润滑油添加剂
    Boron-containing copolymers as environmentally friendly lubricant additives
    薛华, 梁逢春, 杨维利, 贺群, 蔡美荣, 周峰, 卜伟锋
    2025 (1):  1-11.  doi: 10.3969/j.issn.2097-2806.2025.01.001
    摘要 ( 143 )   HTML ( 20 )   PDF(1769KB) ( 53 )  

    随着人们对限制有害排放的日益关注,开发无硫、无磷的绿色润滑油添加剂已变得极为必要。虽然硼基小分子化合物作为绿色润滑油添加剂已被广泛研究,但其大分子类似物却鲜少用于环境友好的润滑油添加剂。本文以甲基丙烯酸硬脂酸酯和异丙烯基硼酸频哪醇酯为原料,通过自由基共聚合成了一系列不同投料比的含硼共聚物(Sn-r-Bm, n=1, m=1/3, 1, 2, 3, 5, 9)。所得的Sn-r-Bm共聚物可均匀分散于基础油PAO-10中,形成胶束状聚集体,其流体动力学直径在9.7~52 nm范围内。SRV-IV振荡往复摩擦试验表明,与PAO-10相比,共聚物基础油分散液的摩擦系数和磨损体积分别降低了62%和97%。此外,S1-r-B1的基础油溶液表现出(850±100) N的优异承载能力。这些优越的润滑性能源于在润滑钢表面形成由Sn-r-Bm、硼氧化物和氧化铁组成的保护摩擦膜。因此,含硼共聚物可以看作是一类新型的不含硫、磷元素的高效减摩抗磨的环保型润滑油大分子添加剂。

    Increasing environmental concerns about limiting harmful emissions has necessitated sulfur-and phosphorus-free green lubricant additives. Although boron-containing compounds have been widely investigated as green lubricant additives, their macromolecular analogs have been rarely considered yet to develop environmentally friendly lubricant additives. In this work, a series of boron-containing copolymers have been synthesized by free-radical copolymerization of stearyl methacrylate and isopropenyl boronic acid pinacol ester with different feeding ratios (Sn-r-Bm, n=1, m=1/3, 1, 2, 3, 5, 9). The resulting copolymers of Sn-r-Bmn=1, m=1/3, 1, 2, 3, 5) are readily dispersed in the PAO-10 base oil and form micelle-like aggregates with hydrodynamic diameters ranging from 9.7 to 52 nm. SRV-IV oscillating reciprocating tribological tests on ball-on-flat steel pairs show that compared with the base oil of PAO-10, the friction coefficients and wear volumes of the base oil solutions of Sn-r-Bm decrease considerably up to 62% and 97%, respectively. Moreover, the base oil solution of S1-r-B1 exhibits an excellent load-bearing capacity of (850±100) N. These superior lubricating properties are due to the formation of protective tribofilms comprising Sn-r-Bm, boron oxide, and iron oxide compounds on the lubricated steel surface. Therefore, the boron-containing copolymers can be regarded as a novel class of environmentally friendly lubricating oil macroadditives for efficient friction and wear reduction without sulfur and phosphorus elements.

    数据和表 | 参考文献 | 相关文章 | 计量指标
    生物润滑用聚合物材料研究进展
    Advances in polymeric materials for bio-lubrication
    侯仕达, 彭平, 刘远康, 颜静, 闫毅
    2025 (1):  12-25.  doi: 10.3969/j.issn.2097-2806.2025.01.002
    摘要 ( 129 )   HTML ( 8 )   PDF(3335KB) ( 66 )  

    生物体不同组织维系正常的生理功能离不开天然润滑剂对组织摩擦界面的润滑作用。当组织界面因各种因素导致润滑功能丧失时,即需要依靠功能性外源润滑材料提供润滑功能。本研究在详细介绍天然润滑剂的种类及生物界面润滑机制的基础上,综述了近年来国内外对于不同组织摩擦界面的润滑策略和聚合物润滑材料构建方面的研究进展。重点总结了用于皮肤保湿润滑、关节软骨润滑、黏膜润滑、抗组织粘连和医用导管润滑等聚合物材料的作用机理、润滑性能和兼具的生物学功能,强调了这些聚合物材料在降低组织摩损和促进受损组织修复方面的独特贡献。此外,还对聚合物润滑材料的功能性优化和应用开发进行了前瞻性展望,希望为聚合物材料在生物组织界面润滑领域的未来发展提供一定的指导作用。

    Natural lubricants play an important role in the functions of living organisms. When the lubrication for tissue interface were lost due to various factors, exogenous lubricant material would be necessary to provide lubrication property. In this review, the types of natural lubricants and the lubrication mechanism at biological interfaces are introduced in detail. The recent research progress on the lubrication strategies for different tissue friction interfaces and on the construction of polymeric lubrication materials are reviewed. Specifically, the conformational relationships, lubrication properties, and additional biological functions of the polymeric materials used for skin moisturizing and lubrication, articular cartilage lubrication, mucosal lubrication, anti-tissue adhesion, as well as medical catheter lubrication are summarized. The unique contributions of these polymeric materials in reducing tissue friction and promoting repair of damaged tissues are emphasized. In addition, the optimization of functionality, and the practical applications of polymeric lubricant materials are prospected, which might provide guidance for the future development of polymeric materials in the field of lubrication at biological tissue interfaces.

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    基础研究
    常用表面活性剂泡沫性能的研究
    Study on the foam properties of common surfactants
    周焱富, 王旭光, 王飞飞
    2025 (1):  26-33.  doi: 10.3969/j.issn.2097-2806.2025.01.003
    摘要 ( 137 )   HTML ( 16 )   PDF(1948KB) ( 77 )  
    选取了10种常用表面活性剂,比较了其水溶液的表面张力,使用DFA100动态泡沫分析仪研究了其泡沫体积、泡沫密度和泡沫稳定性等性质,并通过皮尔逊相关系数来阐明泡沫特性各个指标间的相关性。结果表明:甲基椰油酰基牛磺酸钠具有最优的起泡性;椰油酰谷氨酸二钠和椰油酰氨基丙酸钠的泡沫最绵密;甲基椰油酰基牛磺酸钠和椰油酰谷氨酸二钠的泡沫形态稳定性和泡沫密度稳定性最好,最差的为辛酰/癸酰氨丙基甜菜碱,而泡沫体积稳定性最好的是辛酰/癸酰氨丙基甜菜碱。皮尔逊相关系数分析结果表明:表面活性剂溶液的表面张力越低,产生的泡沫会越绵密;泡沫越丰富,泡沫含液量会越大;初始泡沫密度越大,泡沫体积的坍塌会越快;排液速率越大,泡沫数量的减少会越快。

    In this work, 10 commonly used surfactants were selected. The surface tension of their aqueous solutions was compared, and then the properties such as foam volume, foam density and foam stability were studied by using DFA100 dynamic foam analyzer. Pearson correlation coefficient was used to clarify the correlation between those indexes of foam characteristics. The results showed that, among these 10 surfactants, sodium methyl cocoyl taurate had the best foamability. The foams of disodium cocoyl glutamate and sodium cocoyl alaninate were the densest. The foam morphology stability and foam density stability were the best for sodium methyl cocoyl taurate and disodium cocoyl glutamate, but the worst for capryl/capramidopropyl betaine. However, capryl/capramidopropyl betaine had the best foam volume stability. The results of Pearson correlation coefficient analysis showed that a surfactant solution with lower surface tension was more likely to produce dense foams. The liquid content of foam would be higher if the bubbles were more abundant. The foam volume for the surfactant solution with larger initial foam density was more likely to collapse. The bubble number with higher drainage rate was decreased faster.

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    开发与应用
    甲基甘氨酸二乙酸三钠对几种不同类型表面活性剂应用性能影响的研究
    Study on the effects of trisodium methylglycine diacetate on the application properties of different types of surfactants
    王娜娜, 台秀梅, 耿涛, 张梁, 李赛, 郭凌霄
    2025 (1):  34-40.  doi: 10.3969/j.issn.2097-2806.2025.01.004
    摘要 ( 78 )   HTML ( 15 )   PDF(1884KB) ( 25 )  
    以Cu2+为探针,采用红外光谱法测试了表面活性剂脂肪醇聚氧乙烯醚羧酸钠(AEC-9Na)、十二烷基二苯醚二磺酸钠(2A1)、异构烷基糖苷(IC-06)、脂肪醇聚氧乙烯醚(AEO9)、椰油酰胺基丙基甜菜碱(CAB)、椰油酰胺丙基氧化胺(CAO)与甲基甘氨酸二乙酸三钠(MGDA)对Cu2+的螯合作用,通过透光率考察了6种表面活性剂对MGDA的表观耐盐性和体系稳定性,通过表面张力仪、接触角测量仪及泡沫分析仪研究了MGDA对6种表面活性剂的应用性能的影响。结果表明:绿色螯合剂MGDA对Cu2+具有优异的螯合作用,表面活性剂的加入促进了MGDA对Cu2+的螯合作用;所选择的6种表面活性剂均具有良好的耐盐性能,其中2A1和CAB的耐盐能力最强,分别可以达到50%和30%,且表面活性剂的亲水性越强,耐盐性越好;MGDA的加入对表面活性剂的表面活性影响不大;MGDA的加入提升了表面活性剂的润湿性,在保持表面活性剂浓度不变的条件下,随着MGDA浓度的增加,接触角呈现降低的趋势;MGDA的加入提升了表面活性剂的泡沫性能,起泡时间减小,6种表面活性剂在300 s内均呈现出良好的稳泡性能;采用透光率探究了表面活性剂对MGDA螯合作用的影响,结果表明2A1和CAB对脱除Cu2+的辅助作用最强。

    Using Cu2+ as a probe, the chelation of Cu2+ with trisodium methylglycine diacetate (MGDA) was tested by infrared spectroscopy in presence of different surfactants such as sodium fatty alcohol polyoxyethylene ether carboxylate (AEC-9Na), sodium dodecyl diphenyl ether disulfonate (2A1), iso-alkyl glycoside (IC-06), fatty alcohol polyoxyethylene ether (AEO9), cocamidopropyl betaine (CAB), and cocamidopropyl amine oxide (CAO). The apparent salt tolerance and system stability of these six surfactants in presence of MGDA were evaluated by light transmittance. The effects of MGDA on the application properties of the six surfactants were studied on a surface tensiometer, a contact angle tester and a foam analyzer. The results showed that the addition of surfactants promoted the chelation of MGDA to Cu2+. All these six surfactants had good salt resistance, among which 2A1 and CAB had the strongest salt resistance, which could reach 50% and 30%, respectively. The stronger the hydrophilicity of the surfactant, the better the salt tolerance. The addition of MGDA had sightly good effects on the surface activity of surfactants. The addition of MGDA improved the wetting ability of surfactants. Under the condition of constant surfactant concentration, the contact angle decreased with the increase of MGDA concentration. The addition of MGDA improved the foaming properties of the surfactants, and the foaming was faster. All the six surfactants showed good foam stability within 300 s. The effects of surfactants on MGDA chelation were investigated by light transmittance. The results showed that 2A1 and CAB had the strongest promoting effect on Cu2+ removal.

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    解毒消癥饮改良方的缓解皮肤炎症及机制研究
    Study on relieving skin inflammation and mechanisms of Modified Jiedu Xiaozheng Yin
    章玲, 刘静, 赵炳天, 杨成
    2025 (1):  41-48.  doi: 10.3969/j.issn.2097-2806.2025.01.005
    摘要 ( 63 )   HTML ( 8 )   PDF(1897KB) ( 9 )  

    文章旨在寻求解毒消癥饮改良方(MJXY)的协同抗炎最佳配比,并探究其对脂多糖(LPS)诱导的RAW264.7巨噬细胞的体外抗炎活性及相关机制。以一氧化氮(NO)和2, 2’-联氮-双(3-乙基-苯并噻唑-6-磺酸)二铵盐(ABTS)自由基清除率为指标,对MJXY中不同提取组分的抗炎和抗氧化活性进行评价。依据协同效应得分情况,分别得到最佳ABTS清除(m(白花蛇舌草):m(鹿衔草):m(夏枯草):m(苦参)=20:5:6:6)和NO清除改良方(m(白花蛇舌草):m(鹿衔草):m(夏枯草):m(苦参)=12:12:4:3)。通过体外细胞实验,发现MJXY可以显著降低细胞内的活性氧水平,同时能够抑制细胞炎症因子的分泌。进一步的蛋白印迹实验结果表明MJXY可以通过下调炎症信号通路中JAK2和STAT3蛋白磷酸化水平发挥抗炎作用。综上所述,MJXY具有较好的抗炎效果,并且可以通过干预JAK2/STAT3信号通路起到改善皮肤炎症的效果。

    The aim of this study was to find the best synergistic anti-inflammatory ratio of Modified Jiedu Xiaozheng Yin (MJXY), and to explore its anti-inflammatory effect and related mechanisms through lipopolysaccharide (LPS)-induced RAW264.7 macrophages in vitro. The anti-inflammatory and antioxidant activities of different extracted components in MJXY were evaluated by the scavenging rates of nitric oxide (NO) and 2, 2’-azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS). According to the synergistic effect scores, the best ABTS (mScleromitrion diffusum):mPyrola calliantha):mPrunella vulgaris):mSophora flavescens)=20:5:6:6) and NO scavenging formulation (mScleromitrion diffusum):mPyrola calliantha):mPrunella vulgaris):mSophora flavescens)=12:12:4:3) were obtained. It is found that MJXY can significantly reduce the level of reactive oxygen species in cells, and inhibit the secretion of inflammatory cytokines. Furthermore, western blot experiments show that MJXY can exert anti-inflammatory effects by down-regulating the phosphorylation levels of JAK2 and STAT3 in the inflammatory signaling pathway. In summary, MJXY has a good anti-inflammatory effect and can improve skin inflammation by inhibiting the JAK2/STAT3 signaling pathway.

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    季铵盐阳离子表面活性剂的合成与性能研究
    Study on the synthesis and properties of quaternary ammonium cationic surfactants
    秦恩博, 周磊, 王珏, 陈绘林, 顾雨星, 王元有
    2025 (1):  49-54.  doi: 10.3969/j.issn.2097-2806.2025.01.006
    摘要 ( 99 )   HTML ( 4 )   PDF(1643KB) ( 32 )  
    表面活性剂在农业生产中发挥着重要作用,可以降低表面张力、促进液体渗透、增强吸附力,从而提高农药利用效率。以N, N-二甲基癸胺和脂肪酸为原料,经过季铵化反应及离子交换反应两步法制备了系列季铵盐阳离子表面活性剂NDA-C5~NDA-C8。通过FT-IR、1H NMR以及13C NMR对其结构进行表征分析,并对润湿渗透、铺展、静态表面张力以及动态表面张力性能进行研究。结果表明,系列产物中NDA-C8各项性能最好,当质量分数为0.100%时,静态表面张力低至25.9 mN/m,润湿时间为260 s,同时在超疏水有机玻璃上的铺展面积达到102 mm2。此外,NDA-C8具有优异的动态表面张力性能,0.01 s到1 s范围内,表面张力从53.3 mN/m迅速下降至34.2 mN/m。季铵阳离子本身具有很好的界面活性,并且随着反离子碳链长度的增加,界面处的吸附扩散系数进一步增大,使得各项表面活性性能有所提高。相对于静态表面张力,动态表面张力更能体现实际使用时的情况,并且该系列产品制备工艺简单,原料成本低,所以具有较好的应用前景。

    Surfactants play important roles in agricultural production by reducing surface tension, promoting liquid penetration, and enhancing adsorption, thereby improving the efficiency of pesticide utilization. A series of quaternary ammonium cationic surfactants NDA-C5 to NDA-C8 were prepared by using N, N-dimethyldecylamine and fatty acids as raw materials through quaternization reaction and ion exchange reaction. The structures were characterized by FT-IR, 1H NMR and 13C NMR. The wetting and penetration, spreading, static surface tension, and dynamic surface tension were studied. The results showed that among the series of products, NDA-C8 exhibited the best performance. When the mass fraction of NDA-C8 was 0.100% (w/%), the static surface tension was reduced to 25.9 mN/m, the wetting time was 260 s, and the spreading area on superhydrophobic organic glass reached 102 mm2.In addition, NDA-C8 demonstrated excellent dynamic surface tension performance, with the surface tension rapidly decreasing from 53.3 mN/m to 34.2 mN/m in the range of 0.01 s to 1 s. The quaternary ammonium cation had good interfacial activity, and the adsorption diffusion coefficient at the interface further increased with the increase of the carbon chain length of counterion, so that the surface active properties were improved. In contrast to static surface tension, dynamic surface tension could more accurately reflect the situation in actual use. Furthermore, the preparation process of this series of products was simple, and the cost of raw materials was low, so they had promising application prospects.

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    基于片状ZnO的功效性紫外屏蔽材料的制备及性能研究
    Preparation and properties of effective UV-shielding materials based on flake-shaped ZnO
    孙晓敏, 左士祥, 余瑶瑶, 吴鑫, 蔡悦, 姚超
    2025 (1):  55-62.  doi: 10.3969/j.issn.2097-2806.2025.01.007
    摘要 ( 58 )   HTML ( 9 )   PDF(1730KB) ( 14 )  

    以片状ZnO(F-ZnO)为核体,采用SiO2对其进行表面包覆得到SiO2/F-ZnO (SFZ),然后将原花青素(Pro)负载于SFZ复合物表面,制得Pro/SiO2/F-ZnO (PSFZ)。采用FTIR、XRD、TEM、UV、TGA等技术对所得的样品进行表征。 结果表明:SiO2以非晶态的形式均匀包覆在F-ZnO表面,其适宜包覆量为15%;Pro在SFZ表面形成均匀的膜层,其适宜负载量为20%。采用抗氧化性实验和体外美白实验进行功效性评价,通过在基础配方中应用评价其稳定性。结果表明:PSFZ具有良好的自由基清除能力和抑制酪氨酸酶的能力。防晒指数测试中,PSFZ复合材料比SFZ具有更优异的紫外屏蔽效果。在配方应用中和光照条件下复合材料仍具有较高的稳定性。

    With flaky zinc oxide (F-ZnO) as the core, SiO2 was used to coat the surface of F-ZnO to obtain SiO2 /F-ZnO (SFZ). Then Pro/SiO2 /F-ZnO (PSFZ) was prepared by loading proanthocyanidins (Pro) on SFZ composites. The samples were characterized by FTIR, XRD, TEM, UV and TGA. The results showed that SiO2 uniformly coated on the surface of flake-shaped ZnO particles in amorphous form, and the appropriate coating amount was 15%. Proanthocyanidins formed a uniform layer on the SFZ surface with a suitable loading amount of 20%. The efficacy was evaluated by antioxidant test and in vitro skin-whitening test, and the stability was evaluated by application in the basic formula. The results showed that PSFZ had good free radical scavenging ability and tyrosinase inhibiting ability. In the testing of sun protection indexes, PSFZ composite had better UV-shielding effect than SFZ. The composite still had high stability under the conditions of formulation application and UV irradiation.

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    LC-MS/MS联合网络药理学、分子对接探究草莓叶抗氧化作用靶点及机制
    LC-MS/MS combined with network pharmacology and molecular docking to explore the targets and mechanisms of antioxidant effects of strawberry leaves
    周友良, 路婉杉, 成志伟, 董坤
    2025 (1):  63-74.  doi: 10.3969/j.issn.2097-2806.2025.01.008
    摘要 ( 58 )   HTML ( 6 )   PDF(11303KB) ( 24 )  

    基于LC-MS/MS,联合网络药理学和分子对接探究草莓叶成分发挥抗氧化作用机制。以新鲜草莓叶为试材,采用LC-MS/MS对草莓叶全成分进行检测,共检测到985种化合物。以相对含量(在草莓叶全成分中质量比)大于1%且DL≥0.18为指标,筛选出5种草莓叶活性成分,分别为蔗糖、海藻糖、儿茶素、原花青素B1、灯盏乙素。通过Swiss Target Prediction数据库预测到活性成分的作用靶点共87个,儿茶素未预测到作用靶点;通过Genecards、OMIM、TTD数据库筛选到氧化应激相关靶点共有13 711个;取交集得到草莓叶活性成分抗氧化的潜在靶点共83个。结合STRING数据库进行草莓叶活性成分-抗氧化潜在靶点蛋白互作网络构建,取degree值排名前30的靶点作为草莓叶抗氧化核心靶点,对核心靶点进行GO、KEGG富集分析,GO功能富集分析主要得到蛋白酪氨酸激酶活性、一氧化氮合成酶调节剂活性等条目;KEGG通路富集分析主要得到MAPK、Rap1、PI3K-Akt、Ras、脂质与动脉粥样硬化等通路。通过Cytoscape 3.9.1软件构建草莓叶“活性成分-抗氧化核心靶点-通路”网络并进行分子对接验证,结果显示,原花青素B1、蔗糖、灯盏乙素、海藻糖与SRC、TNF、EGFR均具有较稳定的结合能力。综上所述,草莓叶中的活性成分原花青素B1、蔗糖、灯盏乙素、海藻糖,可能通过SRC、TNF、EGFR等靶点调控MAPK、Rap1、PI3K-Akt、Ras、脂质与动脉粥样硬化等通路实现抗氧化功效,为草莓叶的开发利用提供理论依据。

    This study jointed network pharmacology and molecular docking based on LC-MS/MS to explore the mechanism of strawberry leaf constituents exerting antioxidant effects. A total of 985 compounds were detected in the whole constituents of strawberry leaves by LC-MS/MS using fresh strawberry leaves as test material. Based on the relative content (mass ratio in the whole strawberry leaf constituents) of more than 1% and DL≥0.18, five active ingredients of strawberry leaves are screened out, which are sucrose, trehalose, catechin, procyanidin B1, and scutellarin, respectively. A total of 87 targets of the active ingredients are predicted by Swiss Target Prediction database, and no target is predicted for catechins. A total of 13 711 targets related to oxidative stress are screened by Genecards, OMIM, and TTD databases, and a total of 83 potential antioxidant targets are obtained by taking the intersection to obtain the strawberry leaf active ingredients. Combined with the STRING database, we constructed the protein interaction network of strawberry leaf active ingredient-antioxidant potential targets, and took the targets with the top 30 degree values as the core targets of strawberry leaf antioxidant, and carried out the GO and KEGG enrichment analysis on the core targets, which mainly obtained the entries of protein tyrosine kinase activity and the activity of nitric oxide synthase regulator. The KEGG pathway was also analyzed. KEGG pathway enrichment analysis mainly obtains MAPK, Rap1, PI3K-Akt, Ras, lipid and atherosclerosis pathways. The pathways were analysed by Cytoscape 3.9.1 software to construct the “active ingredient-antioxidant core target-pathway” network of strawberry leaves and carry out molecular docking validation. The results show that procyanidin B1, sucrose, scutellarin, and trehalose have a more stable binding ability with SRC, TNF, and EGFR. In conclusion, the active ingredients of procyanidin B1, sucrose, scutellarin, and trehalose in strawberry leaves may regulate MAPK, Rap1, PI3K-Akt, Ras, lipids and atherosclerosis through SRC, TNF and EGFR to achieve antioxidant efficacy, which provides a theoretical basis for the development and utilisation of strawberry leaves.

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    菜豆多肽的抑菌活性及对趋化因子和炎症因子转录的抑制作用研究
    Study on the antibacterial activity of Phaseolus vulgaris Linn peptide and its inhibitory effect on the transcription of chemokines and inflammatory factors
    辛婷, 李娇娇, 王钊
    2025 (1):  75-83.  doi: 10.3969/j.issn.2097-2806.2025.01.009
    摘要 ( 63 )   HTML ( 4 )   PDF(1272KB) ( 39 )  

    探讨菜豆多肽(Phaseolus vulgaris Linn peptide,PVP)的抑菌活性及其对脂多糖(LPS)诱导的小鼠单核巨噬细胞RAW264.7中趋化因子和炎症因子转录的抑制作用。应用不同质量浓度的菜豆多肽处理金黄色葡萄球菌和大肠杆菌24 h,检测了最小抑菌浓度(MIC)和抑菌圈直径。使用CCK-8试剂盒检测了菜豆多肽对RAW264.7细胞活力的影响。采用RT-qPCR检测RAW264.7细胞中的趋化因子(趋化因子配体2(CCL2)、巨噬细胞炎症蛋白-2(MIP-2)、趋化因子配体5(CCL5))和炎症因子(诱导型一氧化氮合酶(iNOS)、环氧合酶-2(COX-2)、肿瘤坏死因子-α(TNF-α)、白介素-1β(IL-1β)和IL-6)的转录。采用Western blotting检测NF-κB活化。菜豆多肽对金黄色葡萄球菌和大肠杆菌的MIC均为200 μg/mL。与0 μg/mL组相比,10,50,100,200,300,400,500 μg/mL组的金黄色葡萄球菌和大肠杆菌的抑菌圈直径均呈菜豆多肽剂量依赖性升高(P<0.001)。在1~500 μg/mL的质量浓度范围内,菜豆多肽对RAW264.7细胞活力无明显抑制或促进作用(P>0.05)。与LPS组相比,LPS+10,50,100,200,300,400,500 μg/mL PVP组RAW264.7细胞中CCL2、MIP-2、CCL5、iNOS、COX-2、TNF-α、IL-1β和IL-6 mRNA相对水平以及NF-κB p65相对磷酸化水平均呈菜豆多肽剂量依赖性降低(P<0.05)。本研究表明菜豆多肽具有良好的抑菌活性,可有效抑制LPS诱导的RAW264.7细胞中趋化因子和炎症因子的转录。提示菜豆多肽可能是一种具有良好抑菌和抗炎活性的化妆品添加剂,具有潜在的开发价值。

    This study aims to explore the antibacterial activity of Phaseolus vulgaris Linn peptide (PVP) and its inhibitory effect on the transcription of chemokines and inflammatory factors in mouse monocyte macrophages RAW264.7 induced by lipopolysaccharide (LPS). Different mass concentrations of Phaseolus vulgaris Linn peptide were used to treat Staphylococcus aureus and Escherichia coli for 24 hours, and the minimum inhibitory concentration (MIC) and antibacterial circle diameter were detected. Then the CCK-8 kit was used to detect the effect of Phaseolus vulgaris peptide on the viability of RAW264.7 cells. RT-qPCR was used to detect transcription of chemokines (chemokine ligand 2 (CCL2), macrophage inflammatory protein-2 (MIP-2), and chemokine ligand 5 (CCL5)) and inflammatory factors (inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and IL-6). Western blotting was used to detect NF-κB activation. The MIC of Phaseolus vulgaris Linn peptide against Staphylococcus aureus and Escherichia coli is 200 μg/mL. Compared with the 0 μg/mL group, the antibacterial circle diameters of Staphylococcus aureus and Escherichia coli increase in 10, 50, 100, 200, 300, 400, and 500 μg/mL groups in a dose-dependent manner (P<0.001). Within the mass concentration range of 1-500 μg/mL, Phaseolus vulgaris Linn peptide has no significant inhibitory or promotional effect on RAW264.7 cell viability (P>0.05). Compared with the LPS group, CCL2, MIP-2, CCL5, iNOS COX-2, TNF-α, IL-1β and IL-6 mRNA relative levels as well as the relative phosphorylation level of NF-κB p65 in RAW264.7 cells in the LPS+10, 50, 100, 200, 300, 400, 500 μg/mL PVP group are all reduced in a dose-dependent manner (P<0.05). This study shows that Phaseolus vulgaris Linn peptide has good antibacterial properties activity, which can effectively inhibit the transcription of chemokines and inflammatory factors in RAW264.7 cells induced by LPS. This study suggests that Phaseolus vulgaris Linn peptide may be a cosmetic additive with good antibacterial and anti-inflammatory activities and has potential development value.

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    基于细胞自噬的维生素C抗黑素生成作用研究
    Study on the anti-melanogenesis effect of vitamin C based on cellular autophagy
    张帆, 贺东琴, 卞前进, 吴凡, 秦毅, 盘瑶
    2025 (1):  83-88.  doi: 10.3969/j.issn.2097-2806.2025.01.010
    摘要 ( 90 )   HTML ( 10 )   PDF(2540KB) ( 32 )  

    本研究旨在探讨细胞自噬通路对维生素C(VC)抑制小鼠黑素瘤细胞(B16)中黑色素生成的调控作用。采用MTT法检测VC对B16细胞的最大安全剂量,通过加入α-促黑激素(α-MSH)诱导B16细胞的黑色素生成,再使用自噬抑制剂3-甲基腺嘌呤(3-MA)研究细胞自噬在VC的抗黑素生成作用机制。实验结果发现,VC在500 μg/mL及以下质量浓度对B16细胞存活无影响。20和50 μg/mL的VC可显著抑制α-MSH诱导的B16细胞黑色素合成(p<0.01)。与空白组相比,VC可显著诱导B16细胞中自噬相关蛋白LC3-II与p62表达上升,mTOR蛋白表达下降(p<0.05)。为进一步探究自噬对黑色素生成的影响,使用自噬抑制剂3-MA预处理B16细胞,发现3-MA阻断了VC诱导的B16细胞自噬上调,同时逆转VC的抗黑色素生成作用。本研究结果表明VC可通过激活B16细胞的自噬系统抑制黑色素生成。

    The aim of this study was to investigate the role of cellular autophagy pathway in the regulation of melanogenesis in vitamin C (VC)-inhibited mouse melanoma cells (B16). The maximum safe dose of VC on B16 cells was detected by MTT assay, the melanogenesis was induced in B16 cells by adding α-melanotropic hormone (α-MSH), and then the mechanism of cellular autophagy in the anti-melanogenic effect of VC was investigated by using an autophagy inhibitor (3-MA). The results show that VC at 500 μg/mL and below have no effect on the survival of B16 cells. VC at 20 μg/mL and 50 μg/mL significantly inhibit α-MSH-induced melanin synthesis in B16 cells (p<0.01). Compared with the blank group, VC significantly induces the expression of autophagy-related proteins LC3-Ⅱ and p62 in B16 cells, and the expression of mTOR protein decreases (p<0.05). To further investigate the effect of autophagy on melanogenesis, B16 cells are pretreated with the autophagy inhibitor 3-MA, and it is found that 3-MA abolishes VC-induced autophagy up-regulation, as well as the anti-melanogenesis effect in B16 cells. These results suggest that VC can inhibit melanogenesis by activating the autophagy system in B16 melanoma cells.

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    专论与综述
    表皮葡萄球菌应用于化妆品的研究进展
    Research progress of Staphylococcus epidermidis applied in cosmetics
    文霞, 冯静, 刘静霞, 徐健, 陈相孩, 谢小保
    2025 (1):  89-97.  doi: 10.3969/j.issn.2097-2806.2025.01.011
    摘要 ( 83 )   HTML ( 6 )   PDF(1378KB) ( 31 )  

    皮肤微生态系统最大的特点是看似无序实则有条不紊的自我调节功能,为皮肤构筑了内生的免疫系统和外部的战略防线,表皮葡萄球菌是皮肤表面最常见的定殖菌之一,其具有极强的环境适应性和表型多样性,能长期存活于皮肤表面,同时表皮葡萄球菌在改善皮肤状态中具有重要功能如延缓皮肤衰老、保湿、抗紫外线、皮肤屏障修复等。文章介绍了表皮葡萄球菌在皮肤微生物中的角色,以及在功效护肤中的作用,并对表皮葡萄球菌在化妆品中的应用前景进行了分析展望,以期为功效护肤品的开发和应用提供有价值的参考。

    The skin serves as a multifaceted barrier with numerous biological functions, and the presence of skin microbiota is integral to its overall functionality. Increasingly, the bacteria residing on the skin are acknowledged for their positive impact on human health. Staphylococcus epidermidis, the predominant colonizing bacteria on human skin, demonstrates remarkable resilience on normal skin surfaces due to its adept environmental adaptation, surface adhesion capabilities, and its role in maintaining cutaneous homeostasis and immune function. When skin health is compromised, Staphylococcus epidermidis demonstrates beneficial effects by exhibiting anti-inflammatory properties, promoting collagen synthesis, replenishing ceramide levels in the skin through sphingosphydase secretion, enhancing the tight junctions of keratinocytes to maintain skin barrier homeostasis, and interacting with host cells to preserve skin integrity. Furthermore, Staphylococcus epidermidis mitigates UV radiation damage by producing cytokines such as lipoteichoic acid or 6-HAP. Staphylococcus epidermidis and its metabolites have the potential to be utilized topically for skin improvement, either in their natural form or through genetic manipulation to enhance their beneficial properties. Cosmetic companies may explore the integration of these bacteria and their metabolites into skincare formulations to enhance skin health and preserve the skin’s microecological equilibrium, potentially offering personalized skincare solutions utilizing the consumers’ own Staphylococcus epidermidis.

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    分析与检测
    ICP-MS/MS法测定儿童彩妆类化妆品中的7种元素
    Determination of 7 elements in children’s makeup by ICP-MS/MS
    吴莉, 庞庆林, 张妤琳, 耿悦, 陈民辉
    2025 (1):  98-103.  doi: 10.3969/j.issn.2097-2806.2025.01.012
    摘要 ( 73 )   HTML ( 8 )   PDF(1008KB) ( 19 )  

    建立了电感耦合等离子体串联质谱法(ICP-MS/MS)测定儿童彩妆类化妆品中7种元素的含量测定方法。样品经硝酸-氢氟酸的消解酸体系破坏、超级微波消解法进行消解,采用ICP-MS/MS法同时测定儿童彩妆类化妆品中硼(B)、钛(Ti)、锗(Ge)、钼(Mo)、锡(Sn)、锑(Sb)、碲(Te)7种元素的含量,选用铑(Rh)作为内标。分别以霜类、粉类、口红类为基质进行方法学考察,结果表明,所测元素在各自质量浓度范围内线性关系良好,相关系数均大于0.996 7。在2个加标水平下,三种基质的平均回收率范围分别为81.1%~104.6%、84.0%~116.0%、80.8%~113.1%,RSD分别为2.2%~7.5%、0.5%~7.1%、0.8%~7.3%。该方法采用硝酸-氢氟酸体系、超级微波消解法进行样品前处理,应用ICP-MS/MS技术对儿童彩妆类化妆品中元素进行含量测定,解决了不同类型样品尤其是组成复杂、基质干扰大的彩妆类样品在元素检测中的难题,为各类化妆品的样品前处理和元素分析提供了新思路,填补了现有法定标准中尚未建立的7种元素检测方法的空白。

    A method for the determination of 7 elements in children’s makeup by inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) was established. The sample was destroyed by a digestion acid system of nitric acid-hydrofluoric acid and digested by a super microwave digestion method. ICP-MS/MS was used to simultaneously determine the contents of 7 elements in children’s cosmetics, including boron (B), titanium (Ti), germanium (Ge), molybdenum (Mo), tin (Sn), antimony (Sb), and tellurium (Te). Rhodium (Rh) was selected as the internal standard and an internal standard method was used for quantitative analysis. Methodological studies were conducted using cream-based, powder-based and lipstick-based cosmetic as matrices. The results show that 7 elements have good linear relationship within their respective mass concentration ranges, with correlation coefficients greater than 0.996 7. At the two spiked levels, the average recoveries in three matrices are 81.1%-104.6%, 84.0%-116.0%, and 80.8%-113.1%, respectively, and the average relative standard deviations are 2.2%-7.5%, 0.5%-7.1%, and 0.8%-7.3%, respectively. This method uses a digestion acid system of nitric acid-hydrofluoric acid and a super microwave digestion method for sample pretreatment. And ICP-MS/MS technology is applied to determine the contents of elements in children’s cosmetics, solving the problem of element detection in different types of samples, especially those with complex composition and large matrix interference. It provides new ideas for sample pretreatment and element analysis of various cosmetics, filling the gap of 7 elements detection methods that have not yet been established in the existing legal standards.

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    高效液相色谱法测定α-烯基磺酸盐中的磺内酯
    Determination of sultones in α-olefin sulfonate by high performance liquid chromatography
    张红, 姚晨之, 薛伟, 曹圣悌, 公培龙
    2025 (1):  104-109.  doi: 10.3969/j.issn.2097-2806.2025.01.013
    摘要 ( 53 )   HTML ( 2 )   PDF(1214KB) ( 15 )  
    建立了高效液相色谱法测定α-烯基磺酸盐中磺内酯的定量分析方法,并用该方法对市售4批α-烯基磺酸盐样品进行风险监测。样品经水和乙醇溶解,溶解后用石油醚萃取。萃取物溶于正己烷与异丙醇的混合溶液中。采用高效液相色谱法,以正己烷和异丙醇为流动相进行等度洗脱。二者体积比8:2,流速为2.0 mL/min,Inertsil CN-3柱(250 mm×4.6 mm×5 µm)色谱柱分离,进样量为20 µL,柱温为25 ℃。检测器为蒸发光散射检测器。漂移管温度为80 ℃,载气流速为2.0 L/min。外标法定量。结果显示:磺内酯在80~200 μg/mL质量浓度范围内呈良好线性关系,检出限为5.25 μg/mL,相关系数大于0.989,相对标准偏差为1.01% (n=6)。磺内酯的加标回收率为102.82%~108.24%。该方法分离效果好,线性关系好,操作简便,灵敏度高,准确度和重复性好。该方法能快速、准确地测定α-烯基磺酸盐中磺内酯的残留量。

    A method for the determination of sultones in α-olefin sulfonate by high performance liquid chromatography (HPLC) was developed. This method was used to monitor the risk of 4 batches of α-olefin sulfonate samples on the market. The samples were dissolved in water and ethanol, and then extracted with petroleum ether. The extracts were dissolved in the mixed solution of n-hexane and isopropyl alcohol, and the equal degree elution was performed using n-hexane and isopropyl alcohol as the mobile phase by high performance liquid chromatography. The volume ratio of n-hexane to isopropyl alcohol was 8:2.The extracts were separated by Inertsil CN-3 column (250 mm×4.6 mm×5 µm) at the flow rate of 2.0 mL/min. The injection volume was 20 µL and the column temperature was 25 ℃. The detector was the evaporative light scattering detector. The temperature of the drift tube was 80 ℃, and the flow rate of carrier gas was 2.0 L/min. The quantitative method was external standard method. The results show that the mass concentration of sultones in the range of 80-200 μg/mL shows a good linear relationship, and the detection limit is 5.25 μg/mL with the correlation coefficient greater than 0.989. The relative standard deviation is 1.01% (n=6). The recoveries of sultones are 102.82%-108.24%. The method has good separation effect, good linear relationship, simple operation, high sensitivity, and good accuracy and repeatability. The method can quickly and accurately measure the residual amount of sultones in α-olefin sulfonate.

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    UPLC-ESI-Q-TOF/MS法测定化妆品中甲基泼尼松及其9种类似物
    Determination of meprednisone and nine analogues in cosmetics by UPLC-ESI-Q-TOF/MS
    郑佳新, 闵春艳, 鲁辉, 陆林玲, 贾昌平
    2025 (1):  110-116.  doi: 10.3969/j.issn.2097-2806.2025.01.014
    摘要 ( 57 )   HTML ( 1 )   PDF(1138KB) ( 16 )  
    建立了超高效液相色谱-高分辨质谱联用仪(UPLC-ESI-Q-TOF/MS)法同时测定化妆品中甲基泼尼松及其9种类似物的检测方法。样品采用饱和氯化钠分散,乙腈提取,经C8色谱柱分离,以0.1%甲酸水溶液和含0.1%甲酸的50%甲醇乙腈溶液梯度洗脱,在电喷雾离子源正离子模式(ESI+)下,采用全扫描模式进行数据采集,根据保留时间、母离子、子离子进行定性筛查,采用母离子的质谱响应建立含量测定方法。结果表明,10种化合物在相应质量浓度范围内线性关系良好,相关系数均大于0.99;检出限为0.27~1.98 μg/g,平均回收率76.0%~96.4%,RSD为1.9%~5.7%。应用该方法对 20批次样品进行筛查,共有3批检出,1批检出氯倍他索杂质B,1批检出甲基泼尼松和倍他米松杂质E,1批检出地塞米松。该方法操作简便,具有良好的选择性及准确度,能够用于化妆品中糖皮质激素的测定。

    An ultra-high performance liquid chromatography-high resolution mass spectrometry (UPLC-ESI-Q-TOF/MS) method was established for simultaneous determination of meprednisone and its nine analogues in cosmetics. The samples were dispersed in saturated sodium chloride solution and extracted with acetonitrile. The separation was operated on a C8 column using mobile phase consisting of 0.1% aqueous formic acid (A) and 0.1% formic acid-50% methanol/50% acetonitrile (B) in gradient elution. The analysis was performed using a positive electrospray ion source in full scan mode. Confirmatory analysis for target compounds was performed by comparing the retention time, parent ion and daughter ion between the suspected substance and the reference, while quantification was conducted in MS scan mode by external standard method. The results showed that the method had good linearity with the correlation coefficients above 0.99 for the ten compounds. The limits of detection were between 0.27-1.98 μg/g. The average recovery rate was in the range of 76.0%-96.4%, with RSD in the range of 1.9%-5.7%. 3 batches of positive samples were detected among 20 batches of samples, in which Clobetasol impurity B was detected in one batch, meprednisone and betamethasone EP impurity E were found in another batch, and dexamethasone was found in the third batch. This method was simple, selective and accurate, which could be used for determination of glucocorticoids in cosmetics.

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    UPLC-MS/MS法测定化妆品中14种噻嗪类药物
    Determination of 14 thiazides in cosmetics by ultra high performance liquid chromatography-tandem mass spectrometry
    张秋炎, 廖均涛, 梁维维, 黄芳, 吴惠勤, 罗辉泰
    2025 (1):  117-124.  doi: 10.3969/j.issn.2097-2806.2025.01.015
    摘要 ( 59 )   HTML ( 4 )   PDF(1128KB) ( 23 )  

    建立了超高效液相色谱-质谱法(UPLC-MS/MS)测定化妆品中14种非法添加噻嗪类药物的分析方法。化妆品样品经甲醇超声提取,提取液在0.2%甲酸水溶液-甲醇的流动相体系下经Agilent RRHD Eclipse Plus ZorbaxC18(3.0 mm×100 mm,1.8 μm)色谱柱梯度洗脱分离。质谱分析采用电喷雾负离子模式下多反应监测(MRM)方式,基质匹配外标法定量。以水剂、凝胶、乳液、膏霜、粉剂及精油为代表基质,14种噻嗪类药物在各自的质量浓度范围内线性关系良好,相关系数(r2)为0.990 7~0.999 6,检出限为0.004 0~0.100 0 μg/g,定量限为0.008 0~0.400 0 μg/g。低、中、高3个不同质量浓度加标水平下,水剂、凝胶、乳液、膏霜、粉剂及精油样品平均回收率为85.9%~114.4%;相对标准偏差为0.8%~11.8%。该方法前处理高效、灵敏度高、重复性好、定性可靠、定量准确,适用于不同类型化妆品中14种噻嗪类药物的快速定性定量分析。

    A new method for the simultaneous and rapid determination of 14 thiazides in cosmetics by ultra high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The cosmetic samples were dispersed with methanol and ultrasonic extraction, and the filtrate was analyzed by a Agilent RRHD Eclipse Plus Zorbax C18 chromatographic column (3.0 mm×100 mm, 1.8 μm), with 0.2% formic acid aqueous solution and methanol as mobile phases under gradient elution. The condition of mass spectrometry was negative ions scanning with multiple reaction monitor mode (MRM) under the electrospray ionization source. For the representative matrix samples (including water aqua, gel, lotion, cream, powder and essential oil), thiazides tested show the correlation coefficients for linear calibration curves are in the range of 0.990 7-0.999 6 in the corresponding concentration range. The limits of detections (LODs) of 14 thiazides are in the range of 0.004 0-0.100 0 μg/g, and the limits of quantitations (LOQs) are in the range of 0.008 0-0.400 0 μg/g. The recoveries of low, medium and high concentrations ranged 85.9%-114.4%, with the relative standard deviations (n=6) ranged 0.8%-11.8%. The established method is simple, effective, high sensitive, good repeatability, qualitatively reliable, quantitatively accurate, and is suitable for the determination of 14 thiazides in different matrixes of cosmetics.

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    高效液相色谱法同时测定口腔护理牙膏中10种磺胺类物质含量
    Simultaneous determination of 10 sulfonamides in oral care toothpastes by high performance liquid chromatography
    董振花, 王美艳, 路文博, 刘建东, 王子健, 陈超
    2025 (1):  125-130.  doi: 10.3969/j.issn.2097-2806.2025.01.016
    摘要 ( 64 )   HTML ( 4 )   PDF(1076KB) ( 21 )  
    建立了高效液相色谱法(HPLC)同时检测牙膏中10种磺胺类物质的方法。选用0.1%甲酸-甲醇(体积比90:10)作为牙膏样品溶液的提取溶剂,提取方法为20 ℃水浴超声提取20 min。流动相:A为0.1%甲酸,B为甲醇。柱温20 ℃;进样量10 μL,流速1.0 mL/min;检测波长为270 nm。方法学考察结果显示,10种磺胺类物质的精密度RSD范围为0.90%~1.49%,稳定性RSD范围为0.61%~1.42%,重复性RSD范围为0.94%~1.42%,所有RSD均<2.0%。10种磺胺类物质在1~100 mg/L质量浓度范围内呈良好的线性关系,相关系数为0.999 1~0.999 8。10种磺胺类物质的平均回收率范围为91.99%~110.82%,RSD为0.93%~2.03%。应用本方法检测了20种牙膏中10种磺胺类物质的含量,均未检出。本研究建立的HPLC同时测定10种磺胺类物质的方法具有良好的精密度、稳定性、重复性和准确性,适用于检测牙膏中磺胺类物质。

    A method for simultaneous determination of 10 sulfonamides in the toothpaste by high performance liquid chromatography (HPLC) was established. 0.1% formic acid aqueous solution-methanol (volume ratio of 90:10) was used as the extraction solvent for the toothpaste sample solution, and the extraction method was ultrasonic extraction for 20 min in a 20 ℃ water bath. The HPLC conditions were as follows: The mobile phase: A was 0.1% formic acid aqueous solution, and B was methanol. The column temperature was 20 ℃; the injection volume was 10 μL, and the flow rate was 1.0 mL/min; the detection wavelength was 270 nm. The results of methodological investigation showed that the precision RSD of the 10 sulfonamides ranged from 0.90% to 1.49%, the stability RSD ranged from 0.61% to 1.42%, and the repeatability RSD ranged from 0.94% to 1.42%, and all RSDs were<2.0%. The 10 sulfonamides showed good linear relationship in the mass concentration range of 1-100 mg/L, with the correlation coefficients of 0.999 1-0.999 8. The average recovery rate of the 10 sulfonamides ranged from 91.99% to 110.82%, and the RSD ranged from 0.93% to 2.03%. This detection method was used to detect the content of the 10 sulfonamides in 20 toothpastes, and none of the 10 sulfonamides were detected in these 20 toothpastes. The HPLC method established in this work for simultaneous determination of 10 sulfonamides had good precision, stability, repeatability and accuracy, which was suitable for the detection of sulfonamides in toothpastes.

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