Loading...
Welcome to China Surfactant Detergent & Cosmetics, Today is

Table of Content

    22 November 2025, Volume 55 Issue 11 Previous Issue    Next Issue
    Invited paper
    Nuclear magnetic resonance studies of G-quadruplex
    Zeyi Wang, Shuli Dong
    2025, 55 (11):  1361-1377.  doi: 10.3969/j.issn.2097-2806.2025.11.001
    Abstract ( 75 )   HTML ( 17 )   PDF (3256KB) ( 59 )  

    G-quadruplexes, which are unique nucleic acid secondary structures formed by the folding of guanine-rich DNA or RNA, are closely related to essential biological activities. They exhibit extensive application prospects owing to their abundant binding sites and distinct physicochemical properties. Therefore, G-quadruplexes have attracted widespread attention in recent decades. Nuclear magnetic resonance (NMR) technology is an ideal tool for characterizing molecular structures and plays a crucial role in exploring the self-assembly process of G-quadruplexes. In this article, we introduce the basic concepts of NMR, followed by reviewing the applications of NMR in G-quadruplexes. Finally, challenges and prospects of NMR technology in the field of G-quadruplex research are discussed.

    Figures and Tables | References | Related Articles | Metrics
    Preparation and skin-whitening activity evaluation of phenylethyl resorcinol/chitosan Pickering emulsion
    Qiusi Yan, Hui Bi, Wenxin Dong, Aihua Zou
    2025, 55 (11):  1378-1387.  doi: 10.3969/j.issn.2097-2806.2025.11.002
    Abstract ( 96 )   HTML ( 21 )   PDF (1684KB) ( 60 )  

    Chitosan nanoparticles ((212.2±3.2) nm) were synthesized via sol-gel method by adjusting the pH of the chitosan solution. Using polydimethylsiloxane (PDMS) as the oil phase, a chitosan-based Pickering emulsion (CS-PE) was prepared by high-speed shear homogenization, with solid particle mass fraction of 0.4% and water-to-oil volume ratio of 4∶4. Phenylethyl resorcinol (PR) was subsequently loaded into the emulsion to form the PR-loaded CS-PE (PR CS-PE). The encapsulation efficiency and drug loading of PR in PR CS-PE were determined to be 97.2%±0.2% and 2.3%±0.01%, respectively. The radical scavenging rates of PR CS-PE for 2, 2-diphenyl-1-picrylhydrazyl (DPPH) and 2, 2-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) were measured to be 77.4% and 93.8%, respectively, indicative of significant antioxidant activity. The results of Franz diffusion cell test indicated that the PR within the emulsion exhibited sustained release behavior. Furthermore, PR CS-PE could effectively inhibit the melanogenesis in zebrafish models, suggesting notable skin-whitening efficacy. Results of the zebrafish embryonic development and cytotoxicity assay indicated that the PR-loaded chitosan-based Pickering emulsion exhibited lower toxicity compared with free PR. These findings suggest the potential application of the PR/chitosan Pickering emulsion in cosmetics.

    Figures and Tables | References | Related Articles | Metrics
    Basic research
    Synthesis of pH-switchable nonionic polyether surfactant and its potential application in removing phenanthrene from soil
    Lei Dong, Huanjin Zou, Xuefeng Liu
    2025, 55 (11):  1388-1394.  doi: 10.3969/j.issn.2097-2806.2025.11.003
    Abstract ( 51 )   HTML ( 13 )   PDF (1574KB) ( 48 )  

    To achieve the recovery and recycling of eluent from soil washing enhanced by nonionic surfactants, a polyether-type nonionic surfactant C8-DIB-PEG10 with a reversible pH-responsive switch was designed and synthesized. Taking an artificial sample of phenanthrene-contaminated soil as an example, and using the micellar solution of this surfactant as the washing agent, the removal effect on phenanthrene (Phe) in soil, the post-treatment of eluent, and the recovery and recycling of C8-DIB-PEG10 were investigated. The results showed that the critical micelle concentration of C8-DIB-PEG10 at 25 ℃ was approximately 1.01×10-3 mol/L; when pH was adjusted to 3.0 with HCl, C8-DIB-PEG10 lost its surface activity due to the breaking of imine bond, forming PEG10-CHO and octylamine hydrochloride, both of which had good water solubility. When pH was adjusted to 10.0 with NaOH, C8-DIB-PEG10 could be formed again. The removal rate of Phe in soil could reach 99.9%. After C8-DIB-PEG10 was switched to non-surface-active by using HCl, PEG10-CHO and octylamine hydrochloride could be recycled in the aqueous phase. The recovery rate of C8-DIB-PEG10 could reach 96.5%. Over three more cycles of use, no significant abnormal change was observed either in the removal rate of Phe or the recovery rate of C8-DIB-PEG10.

    Figures and Tables | References | Related Articles | Metrics
    Preparation and performance evaluation of sand consolidation and water blocking system for loose sandstone reservoir
    Zhiwei Huang, Yongqian Jian, Mingqiang Zhou, Jinlong Liu
    2025, 55 (11):  1395-1401.  doi: 10.3969/j.issn.2097-2806.2025.11.004
    Abstract ( 57 )   HTML ( 12 )   PDF (4181KB) ( 44 )  

    Sand production and high water content in oil wells are two major challenges that restrict high and stable production in loose sandstone reservoirs. In this paper, nano SiO2, coupling agent triethoxysilane, phenolic resin and n-octanol were used to synthesize the main agent SCA-2. Hexamethylenetetramine and vinyl carbonate were selected to prepare the curing agent YGA-1, which was then compounded with SCA-2 to develop a sand fixation and water plugging system. Firstly, single-factor experiments were conducted to determine the optimal concentrations of SCA-2 and YGA-1, subsequently, the system’s sand fixation and water blocking performance were evaluated. Finally, a pilot test was carried out in the mining site. Experimental results showed that the optimal formula composition of the system was 10% SCA-2+5% YGA-1. The gelation time of the system was 180 minutes and the viscosity after gelation could reach 108.4 mPa·s. When the dosage of the drug system was 0.6 PV, the sand production rate remained below 0.08%. Dual-tube parallel experiments showed that the sand fixation and water plugging system had a water flow channel plugging rate of 87.5%, while the oil flow channel plugging rate was only 11.3%, indicating minimal damage to the oil-bearing reservoir. The field test showed that after the measures taken in Well M of X oilfield, the sand free oil recovery period exceeded 360 days, the water content decreased by 5.0% and the cumulative oil production increased by 7 092 m3. This study provides new ideas for efficient development of loose sandstone reservoirs.

    Figures and Tables | References | Related Articles | Metrics
    Synthesis and properties of phosphobetaine-modified ZnO
    Xiuhua Yan, Lanqin Tang
    2025, 55 (11):  1402-1407.  doi: 10.3969/j.issn.2097-2806.2025.11.005
    Abstract ( 51 )   HTML ( 15 )   PDF (1577KB) ( 40 )  

    To obtain functional ZnO nanoparticles that can be stably dispersed in ethylene glycol, an effective surface modification method was proposed. Using self-made phosphobetaine as the surface modifier, the modified ZnO nanoparticles were synthesized from ZnSO4 and NaOH via one-step method in aqueous solution at low temperature (<100 ℃) and normal pressure. The structural changes between non-modified and modified ZnO nanoparticles were compared by Fourier transform infrared spectroscopy and X-ray diffraction. The microscopic morphology of non-modified and modified ZnO nanoparticles was studied by field emission scanning electron microscopy. The dispersion stability experiments for ZnO nanoparticles were carried out. The results showed that surface modification or capping had no effect on the phase crystallinity of ZnO nanoparticles. When the mass fraction of phosphobetaine was 5% and the reaction temperature was 70 ℃, the product of modified ZnO nanoparticles had relatively small particle size, with an average length of approximately 70 nm, and the contact angle of ethylene glycol thereon was 21°. These modified nanoparticles still had good dispersion stability in ethylene glycol after 30 days.

    Figures and Tables | References | Related Articles | Metrics
    Synthesis and microencapsulation of oleic acid sterol ester liquid crystals for its application in sunscreen formulations
    Xuze Liu, Chang Xu, Liangliang Lin, Hujun Xu
    2025, 55 (11):  1408-1418.  doi: 10.3969/j.issn.2097-2806.2025.11.006
    Abstract ( 57 )   HTML ( 14 )   PDF (2641KB) ( 37 )  

    This study reports the synthesis of oleic acid sterol ester with liquid crystalline properties and its enhanced stability and UV-blocking performance through microencapsulation. Oleic acid sterol ester was synthesized via the esterification of phytosterol and oleic acid, whose structure was characterized using Fourier-transform infrared spectroscopy (FTIR) and mass spectrometry (MS). Its liquid crystalline behavior was confirmed via the polarized optical microscopy (POM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), wide-angle X-ray scattering (WAXS), and small-angle X-ray scattering (SAXS). UV absorption tests were conducted to assess the UV-blocking performance of the oleic acid sterol ester liquid crystals. To improve the stability of its liquid crystalline structure, the oleic acid sterol ester was encapsulated into microcapsules through the emulsion polymerization. SPF measurements were performed on the sunscreen formulations containing liquid crystal microcapsules. The oleic acid sterol ester displayed cholesteric liquid crystalline behavior and strong UVA absorption, which indicates its suitability as a natural UV absorber. Microencapsulation further enhanced its stability and UV-blocking properties. SPF testing showed that the formulations with microcapsules achieved an SPF value of 7.01, which surpasses the nano titanium dioxide (SPF=6.23) and significantly outperform the unencapsulated liquid crystal formulations (SPF=2.65). This study highlights the potential of microencapsulated oleic acid sterol ester as a novel UV absorber in the sunscreen formulations, offers the enhanced stability and effective UV protection, and showcases its application potential in the innovative cosmetic products.

    Figures and Tables | References | Related Articles | Metrics
    To explore the antioxidant mechanism of Hylocereus undatus root based on LC-MS/MS and network pharmacology
    Sha Li, Zumrat Aziz, Jiaqi Pang, Kun Dong
    2025, 55 (11):  1419-1427.  doi: 10.3969/j.issn.2097-2806.2025.11.007
    Abstract ( 53 )   HTML ( 12 )   PDF (2030KB) ( 50 )  

    The study aims to explore the root components of Hylocereus undatus and its potential antioxidant mechanism. Based on liquid chromatography-tandem mass spectrometry (LC-MS/MS), the components of Hylocereus undatus root were identified, and the active components of Hylocereus undatus root were analyzed by TCMSP database. Based on the in vitro efficacy evaluation test, the potential efficacy of the ethanol extract of Hylocereus undatus root was preliminarily screened. Based on Swiss Target prediction, the potential efficacy targets of active ingredients in Hylocereus undatus root were screened. The protein-protein interaction (PPI)network was constructed by Cytoscape and String screening. Metascape database and Cytoscape 3.9.1 software were used for GO and KEGG enrichment analysis, and the active ingredient-potential efficacy target-symptom map of Hylocereus undatus root was constructed. The molecular docking was carried out with Auto Dock software. The results show that 1 041 substances in the root of Hylocereus undatus are identified, and it is found that the substances related to antioxidant efficacy in the root of Hylocereus undatus are abundant, reaching 25.84%. The DPPH·, ABTS·+ and OH· scavenging efficiency of the ethanol extract of pitaya root is equivalent to that of 0.1% Vc. Cytoscape analysis shows that 18 active components such as galangin, kaempferol and quercetin in Hylocereus undatus roots can participate in the antioxidant process. There are 30 potential core targets involved in the antioxidant process. KEGG is enriched into 4 antioxidant-related pathways, involving ErbB signaling pathway, PI3K-Akt signaling pathway, TNF signaling pathway, and Foxo signaling pathway. Molecular docking shows that 18 active components of Hylocereus undatus root have good binding activity with EGFR and ATK1, and some active components have good activity with TNF.

    Figures and Tables | References | Related Articles | Metrics
    Synthesis of open-pored mesoporous silica and its application in cosmetics
    Zhihui Zheng, Minjia Yuan, Wenxing Wang
    2025, 55 (11):  1428-1434.  doi: 10.3969/j.issn.2097-2806.2025.11.008
    Abstract ( 53 )   HTML ( 16 )   PDF (3906KB) ( 37 )  

    An open-pored mesoporous silica (OSMS) was successfully prepared by emulsion method. Its microstructure was analyzed using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and nitrogen adsorption-desorption tests (BET). The results showed that, the OSMS particles were monodisperse, and the particle size was 0.40 μm; the product had open channel structure and uniform mesopore size distribution (pore diameter of 24.4 nm); OSMS had high specific surface area (162 m2/g) and large pore volume (1.12 cm3/g). The results of performance study indicated that, in the oil absorption value test for 10 different oils and fats, OSMS demonstrated superior adsorption performance. Its oil absorption values were 1.3-1.9 times that of porous silica 150H, 3.3-6.3 times that of silicone elastomer KSP-100, and 6.0-7.5 times that of the starch-based TAPIOCA, respectively. Human skin oil-control experiments indicated that OSMS had the features of rapid and long-lasting adsorption, and the oil-control effect was linearly and positively correlated with the dosage (R2>0.95). In vitro SPF value tests showed that OSMS had sun-screening synergistic effect, and just 0.3% (w/%) OSMS could increase the SPF value of a sunscreen. This work might provide experimental support for the application of OSMS as an oil-control raw material and a sun-screening synergist in cosmetics.

    Figures and Tables | References | Related Articles | Metrics
    Study on the polyol extraction process of Platycladus orientalis leaf extract and its effects on human dermal papilla cells
    Xianqi Chen, Timson Chen, Ling Ma, Ya Chen, Zhizhen Li, Guangli Wang, Jing Wang
    2025, 55 (11):  1435-1443.  doi: 10.3969/j.issn.2097-2806.2025.11.009
    Abstract ( 66 )   HTML ( 17 )   PDF (3693KB) ( 42 )  

    Using an aqueous 1,4-butanediol solution as the solvent combined with ultrasonic-assisted extraction, total flavonoids from Platycladus orientalis leaves were extracted. The extraction process was optimized using response surface methodology with the yield of total flavonoids, quercitrin, and myricitrin as the evaluation indicators. The optimized extraction conditions are as follows: 40 wt% 1,4-butanediol, extraction temperature of 60 ℃, extraction time of 60 min, and solid-to-liquid ratio of 1∶10(g∶mL). Under these optimized conditions, the yield of total flavonoids is 50.74 mg/g, while the yields of quercitrin and myricitrin are 3.65 mg/g and 2.10 mg/g, respectively. Compared with water and ethanol extraction, the stability of the extract is significantly improved. Furthermore, the efficacy of the 1,4-butanediol-extracted Platycladus orientalis leaf extract on human dermal papilla cells (HDPCs) was evaluated in comparison with the extracts obtained using traditional solvents (water and ethanol). Cell viability, changes in vascular endothelial growth factor (VEGF) in the cell culture supernatant, as well as the inhibitory effects on intracellular reactive oxygen species (ROS) and the inflammatory factor IL-6 were measured. The results indicate that, compared with the extracts obtained using water or ethanol, the 1,4-butanediol extract more effectively promotes the proliferation of HDPCs and enhances VEGF secretion. It also demonstrates significantly stronger inhibition of ROS and IL-6, suggesting its potential efficacy in promoting hair growth, as well as in scalp antioxidant and anti-inflammatory applications.

    Figures and Tables | References | Related Articles | Metrics
    Development and application
    The protective effect of recombinant human collagen against UV-induced skin photoaging in mice
    Gaiying He, Jinghui Tang, Xuying Liu, Guirong Sun, Yi Wang
    2025, 55 (11):  1444-1451.  doi: 10.3969/j.issn.2097-2806.2025.11.010
    Abstract ( 50 )   HTML ( 9 )   PDF (4028KB) ( 40 )  

    This study investigates the effects of recombinant human collagen (R-HC) on UV-induced photoaging in mouse skin. The photoaging mouse model was established using UVA and UVB irradiation. Changes of skin wrinkles and epidermal thickness were systematically evaluated using the C-Cube multifunctional skin imaging analysis system, optical coherence tomography, and hematoxylin-eosin staining. Collagen fiber alterations were examined using two-photon excitation fluorescence imaging and liquid crystal polarization imaging techniques. Additionally, Gomori aldehyde fuchsin staining and RT-qPCR were employed to assess elastic fiber morphology and extracellular matrix metalloproteinase expression, respectively. The results show that R-HC significantly reduces skin wrinkles, increases stratum corneum and epidermal hydration, and decreases epidermal thickness in photoaged mice. Moreover, R-HC improves collagen fiber content and organization, reduces elastic fiber fragmentation and thickening, and regulates the relative mRNA expression of matrix metalloproteinase-3 and tissue inhibitor of metalloproteinase-1. In conclusion, R-HC mitigates UV-induced skin photoaging and has important application value for the development of products targeting photoaged skin.

    Figures and Tables | References | Related Articles | Metrics
    Study on the effect of recombinant human collagen Ⅲ on anti-skin photoaging
    Fei Liu, Qian Wang, Hui Liu, Suzhen Yang, Tingting Han, Tao Wu
    2025, 55 (11):  1452-1559.  doi: 10.3969/j.issn.2097-2806.2025.11.011
    Abstract ( 60 )   HTML ( 11 )   PDF (2951KB) ( 44 )  

    The aim of this study was to investigate the mechanism of recombinant human collagen Ⅲ (RHC-Ⅲ) on anti-skin photoaging. The blank control group, model control group, positive control group and sample groups were set up in the experiment. Primary human skin cells and ex vivo human skin tissue model were used to detect the changes of photoaging markers in dermal-epidermal junction (DEJ) and dermis by crystal violet staining, enzyme-linked immunosorbent assay (ELISA) and immunofluorescence. The results of the cell experiments show that compared with the blank control group, RHC-Ⅲ significantly increases the adhesion ability of normal human dermal fibroblasts (NHDFs). Compared with the model control group, RHC-Ⅲ significantly decreases the level of ROS, MMPs secretion and increases the activity of CAT. In ex vivo human skin tissue model experiments, compared with the model control group, RHC-Ⅲ significantly increases the contents of COL-Ⅳ, COL-Ⅶ, COL-ⅩⅦ, integrin α6 subunit, COL-Ⅰ, COL-Ⅲ and elastin. The results indicate that the mechanism of RHC-Ⅲ improving skin photoaging is related to promoting NHDFs adhesion, reducing oxidative stress and the degradation of extracellular matrix, improving the expression of DEJ structure-related proteins, and increasing the synthesis of key extracellular matrix proteins in dermis.

    Figures and Tables | References | Related Articles | Metrics
    Study on anti-aging and soothing effects of lily flower peptides
    Peipei Li, Xiaoming Xu, Qiang Zhang, Yangyang Fang, Huiliang Li
    2025, 55 (11):  1460-1467.  doi: 10.3969/j.issn.2097-2806.2025.11.012
    Abstract ( 85 )   HTML ( 16 )   PDF (1709KB) ( 52 )  

    The aim of this study was to investigate the anti-aging and soothing effects of Lanzhou lily flower peptides (LLFPs) generated via enzymatic hydrolysis and microbial fermentation. Comprehensive methodologies including LC-MS/MS analysis, fluorescent probes, ELISA, qRT-PCR, an acetic acid-induced zebrafish model, and human clinical trials were employed to evaluate the related biomarkers across multiple dimensions, alongside chemical component identification. Results demonstrate that LLFPs contain 535 short-chain peptides, with 76.09% exhibiting molecular weights <1 000 Da. The peptides significantly reduce UVB-induced MMP-1 and ROS expression in keratinocytes, promote dermal fibroblast proliferation and collagen secretion, modulate circadian clock genes (CLOCK, BMAL1), alleviate UVB-induced photo-oxidative stress in keratinocytes, and decrease total movement distance in acetic acid-stimulated zebrafish. Clinical trials further validate the anti-aging and soothing efficacy of LLFPs in human subjects. Through integrated in vitro and in vivo verification, this research reveals the dual anti-aging and soothing efficacy of LLFPs, providing a scientific foundation for their application in cosmetic formulations.

    Figures and Tables | References | Related Articles | Metrics
    Reviews
    Research progress in applications of silicone quaternary ammonium surfactants
    Jingru Wang, Xiangji Meng, Yangzhen Zheng, Lifei Zhi, Xiaoming Li, Guoyong Wang, Yan Wang
    2025, 55 (11):  1468-1475.  doi: 10.3969/j.issn.2097-2806.2025.11.013
    Abstract ( 64 )   HTML ( 8 )   PDF (1191KB) ( 45 )  

    Quaternary ammonium surfactants are widely used in various fields typically as efficient fungicides, softeners, and antistatic agents. At present, those quaternary ammonium surfactants with single functions are insufficient to meet people’s needs. Therefore, the researchers have introduced organosilicon groups to quaternary ammonium salts. These surfactants combine the excellent properties of organosilicon compounds and the good antibacterial activity of quaternary ammonium salts. In this review, the application of silicone quaternary ammonium surfactants in antibacterial dyeing of textiles, daily chemicals, dental treatment, civil engineering anticorrosion, cultural relic protection and antibacterial coatings was reviewed. Finally, the development trends of silicone quaternary ammonium surfactants were prospected.

    Figures and Tables | References | Related Articles | Metrics
    Research on the practice and strategy of skincare packaging design under consumer psychological guidance
    Yinghui Wang, Gaojie Zheng, Huadong Liu
    2025, 55 (11):  1476-1485.  doi: 10.3969/j.issn.2097-2806.2025.11.014
    Abstract ( 42 )   HTML ( 11 )   PDF (2618KB) ( 35 )  

    With the development of the social economy and the changes of consumers’ aesthetic concepts, the skincare market has shown a trend towards diversification and individuation. When choosing skin care products, consumers not only focus on the function and effect of the product, but also pay increasing attention to the packaging design and aesthetic experience of the product. First of all, based on consumer psychology theory, this paper establishes the relationship between consumer psychology and the key elements of skin care packaging design, analyzes the differences in psychological needs among different consumer groups, and explores the distinct manifestations of how these needs influence the key aspects of skincare packaging design. Secondly, this paper puts forward the packaging design of skin care products under the guidance of consumer psychology. Through the analysis of skin care packaging design cases, it points out that there are some problems in the current skin care packaging design, such as insufficient sustainability caused by excessive beautification, blurred brand images caused by lack of differentiated design, weak pertinence caused by overload of product information, and lack of personalized design caused by neglect of interactive experience. Finally, this paper puts forward targeted optimization strategies for packaging design, including balancing aesthetics and sustainability to advocate green packaging, strengthening differentiated design to create a distinctive brand image, optimizing product information layout to highlight key content, and strengthening interactive elements to enhance emotional resonance. This paper aims to provide theoretical guidance and practical reference for skin care packaging design, promote design innovation and enhance product market competitiveness.

    Figures and Tables | References | Related Articles | Metrics
    Analytical methods and testing
    Spectroscopic identification of 10 α-hydroxy acid substances in cosmetics
    Jianhua Xiang, Xu Gong, Li Lu, Fang Fang, Youlong Feng, Xinhong Shi
    2025, 55 (11):  1486-1492.  doi: 10.3969/j.issn.2097-2806.2025.11.015
    Abstract ( 55 )   HTML ( 11 )   PDF (1541KB) ( 45 )  

    A chromatographic correlation spectroscopy method was developed for the rapid identification of 10 α-hydroxy acid substances in cosmetics. Spectral data processing and database management were performed using Labsolution software, with chromatographic peaks screened and identified through spectral similarity. The similarity algorithm, spectral preprocessing, spectral similarity threshold, and time window size were examined and optimised. Experimental results indicate that after background compensation and S-G smoothing of spectral data, setting the spectral similarity threshold to 0.99 and the time window size to 2%, and employing the cosine angle method for spectral similarity calculation, enables rapid and accurate screening and identification of the 10 α-hydroxy acid substances in cosmetics. Screening and identification of these 10 α-hydroxy acids in 164 cosmetic batches achieve an accuracy rate ranging from 93.90% to 100.00%, with an average accuracy of 97.80%. This represents an 11.20% improvement over methods relying solely on retention time for peak identification. This method is simple to operate and highly accurate, suitable for the rapid screening and identification of 10 α-hydroxy acid chromatographic peaks in cosmetics via HPLC-DAD. It provides technical support for establishing an HPLC-DAD-UV spectral database of safety-risk substances in cosmetics. This technology can be extended for rapid screening applications in areas such as intelligent chemical identification, detection of illicitly added prohibited substances in traditional Chinese medicines, identification of illegally added chemicals in foodstuffs, and monitoring of food additive misuse.

    Figures and Tables | References | Related Articles | Metrics
    Simultaneous determination of multiple antibacterial components in mouthwash by high performance liquid chromatography
    Lin Cao, Mingwei Liu
    2025, 55 (11):  1493-1500.  doi: 10.3969/j.issn.2097-2806.2025.11.016
    Abstract ( 54 )   HTML ( 9 )   PDF (1082KB) ( 42 )  

    This study developed a high-performance liquid chromatography (HPLC) method for the simultaneous determination of five antibacterial components (chlorhexidine, cetylpyridinium chloride, ethylparaben, sodium methylparaben, and domiphen bromide) in mouthwash. Mouthwash samples were extracted using acetonitrile-0.05 mol/L phosphate buffer (pH 3.8) at a volume ratio of 20∶80. Ultrasonic extraction parameters were set as follows: power of 300 W, extraction time of 20 minutes, temperature of 40 ℃, and solid-to-liquid ratio of 1∶4. An Agilent 1260 HPLC system, equipped with a diode array detector (DAD), was employed using an Agilent ZORBAX Eclipse Plus C18 reversed-phase column (250 mm×4.6 mm, 5 μm). The column temperature was maintained at 30 ℃, with an injection volume of 10 μL, flow rate of 1.0 mL/min, detection wavelength of 260 nm, and total run time of 30 minutes. Methodological validation demonstrates that for intraday precision, the relative standard deviations (RSDs) of the five components range from 2.33% to 4.72%, while interday precision RSDs range from 1.01% to 4.21%. Linear regression analysis reveals that all five components exhibit excellent linearity with the correlation coefficients (r)>0.999 5, the limits of detection (LOD) ranging from 0.09 to 0.18 μg/mL and the limits of quantification (LOQ) ranging from 0.27 to 0.54 μg/mL. Spike recovery experiments indicate that the average recovery rates of the five components range from 96.02% to 104.65%, with the corresponding RSDs of 1.74% to 4.53%. Detection of 20 commercial mouthwash samples show that chlorhexidine is detected only in samples S15 and S19 at the concentrations of 1.25 and 1.27 mg/mL, respectively. Cetylpyridinium chloride is detected in 7 samples with the concentrations ranging from 0.13 to 0.75 mg/mL. Ethylparaben is detected solely in sample S4 at 0.15 mg/mL. Sodium methylparaben is found only in sample S18 at 1.19 mg/mL. Domiphen bromide is detected exclusively in sample S20 at 0.32 mg/mL, and the remaining 9 samples show no detection of the target components. In conclusion, this method enables simultaneous and rapid detection of the five target antibacterial components in commercial mouthwashes.

    Figures and Tables | References | Related Articles | Metrics