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1.
Molecules ; 29(2)2024 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-38257324

RESUMEN

Despite advancements in analytical technologies, the complex nature of cosmetic matrices, coupled with the presence of diverse and trace unauthorized additives, hinders the application of these technologies in cosmetics analysis. This not only impedes effective regulation of cosmetics but also leads to the continual infiltration of illegal products into the market, posing serious health risks to consumers. The establishment of cosmetic regulations is often based on extensive scientific experiments, resulting in a certain degree of latency. Therefore, timely advancement in laboratory research is crucial to ensure the timely update and adaptability of regulations. A comprehensive understanding of the composition of cosmetic matrices and their pretreatment technologies is vital for enhancing the efficiency and accuracy of cosmetic detection. Drawing upon the China National Medical Products Administration's 2021 Cosmetic Classification Rules and Classification Catalogue, we streamline the wide array of cosmetics into four principal categories based on the following compositions: emulsified, liquid, powdered, and wax-based cosmetics. In this review, the characteristics, compositional elements, and physicochemical properties inherent to each category, as well as an extensive overview of the evolution of pretreatment methods for different categories, will be explored. Our objective is to provide a clear and comprehensive guide, equipping researchers with profound insights into the core compositions and pretreatment methods of cosmetics, which will in turn advance cosmetic analysis and improve detection and regulatory approaches in the industry.


Asunto(s)
Cosméticos , China , Industrias , Polvos , Tecnología
2.
Zhongguo Zhong Yao Za Zhi ; 47(16): 4292-4304, 2022 Aug.
Artículo en Chino | MEDLINE | ID: mdl-36046855

RESUMEN

Sesquiterpene pyridine alkaloids are important components in Tripterygium plants, possessing a wide range of pharmacological activities, such as anti-inflammation immunosuppression, anti-tumor, anti-virus, and deinsectization, and are of great research value. They are composed of highly oxidized dihydro-ß-furansquiterpene and pyridine dicarboxylic acid through ester bonds. According to the structural characteristics of pyridine dicarboxylic acid fragments, they can be divided into various structural subtypes. Up to now, more than 110 sesquiterpene pyridine alkaloids have been isolated and identified from Tripterygium plants. This study reviewed the structural features and spectral(i.e., UV, IR, MS, and NMR) characteristics of sesquiterpene pyridine alkaloids and summarized the structural elucidation process in detail to provide references for their further research and development.


Asunto(s)
Alcaloides , Medicamentos Herbarios Chinos , Sesquiterpenos , Alcaloides/farmacología , Medicamentos Herbarios Chinos/farmacología , Estructura Molecular , Piridinas/química , Piridinas/farmacología , Tripterygium/química
3.
Zhongguo Zhong Yao Za Zhi ; 44(16): 3368-3373, 2019 Aug.
Artículo en Chino | MEDLINE | ID: mdl-31602897

RESUMEN

Tripterygium wilfordii preparations,with various biological activities such as immunosuppressive,anti-inflammatory and anti-cancer effects,are widely used in the treatment of autoimmune diseases such as rheumatoid arthritis,lupus erythematosus,and nephrotic syndrome. They have definite therapeutic effect,but often cause serious adverse reactions and result in damages to liver,kidney,blood,reproduction,and other systems due to their complex compositions,great toxicity,and narrow margin between the toxic and therapeutic dosages. At present,T. wilfordii preparations produced by different manufacturers exhibit large variations in clinical efficacy and side effects in account of their different chemical compositions and quality fluctuation due to differences in raw materials and production process. However,the existing quality standards are controversial in terms of index components and content limit,which cannot be effectively used for the overall quality control of the preparations. In this paper,the research progress on chemical constituents,quality standard and quality control methods of four T. wilfordii preparations including Tripterygium Tablets,Tripterygium Zongtie Tablets,Tripterygium Shuangceng Tablets and Tripterygium Glycosides Tablets was reviewed,in order to provide ideas and reference for the quality improvement of this type of preparations.


Asunto(s)
Medicamentos Herbarios Chinos/normas , Control de Calidad , Tripterygium/química , Comprimidos
4.
Zhongguo Zhong Yao Za Zhi ; 43(6): 1156-1161, 2018 Mar.
Artículo en Chino | MEDLINE | ID: mdl-29676122

RESUMEN

Ultra-performance liquid chromatography-evaporative light scattering detection (UPLC-ELSD) fingerprint analysis method was established for quality control of Guci tablets. Chromatographic separation was performed on Waters Acquity UPLC BEH C18 column (2.1 mm×100 mm, 1.7 µm) at 30 °C of column temperature. Acetonitrile-0.1% formic acid solution was adopted as mobile phase for gradient elution. The flow rate was set at 0.3 mL·min⁻¹, and the injection volume was 3 µL. Detection was carried out on an ELSD with a nitrogen pressure of 0.28 MPa, drift tube temperature of 60 °C, and gain of 400. A total of 39 batches of samples produced by six manufacturers were measured by using the above method and the data were analyzed by ChemPattern software. The peak present in more than 75% of the samples was defined as a common peak, and 30 common peaks were determined. Among them, 19 peaks were identified by rapid resolution liquid chromatography/tandem mass spectrometry (RRLC-MS/MS) method, 16 of which were confirmed by reference substances. The similarity of the tested samples was 0.47-0.98, suggesting that the quality of the samples from different manufacturers varied greatly. Furthermore, principal component analysis (PCA) and hierarchical analysis (HCA) were performed to clarify the main different components in samples. The results indicated that there might be some feeding problems about Paeoniae Radix Alba, Notoginseng Radix et Rhizoma, and Clematidis Radix et Rhizoma in a few manufacturers. This study provided some evidences for the overall quality control of Guci tablets, as well as its quality standard improvements.


Asunto(s)
Medicamentos Herbarios Chinos/normas , Control de Calidad , Cromatografía Líquida de Alta Presión , Comprimidos , Espectrometría de Masas en Tándem
5.
Molecules ; 22(6)2017 May 23.
Artículo en Inglés | MEDLINE | ID: mdl-28545244

RESUMEN

Two new phloroglucinols, lysidisides X and Y (1 and 2), and two known compounds, 2-(2-methylbutyryl)phloroglucinol 1-O-ß-d-glucopyranoside (3) and (E)-resveratrol 3-(6″-galloyl)-O-ß-d-glucopyranoside (4), have been isolated from the roots of Lysidice rhodostegia. The structures of 1 and 2 were elucidated primarily by NMR experiments. Their absolute configurations were deduced via circular dichroism (CD) data and electronic circular dichroism (ECD) calculations. Compounds 1 and 2 exhibited significant antioxidative activities with IC50 values of 12.0 and 11.8 µM, respectively.


Asunto(s)
Antioxidantes/química , Fabaceae/química , Floroglucinol/química , Raíces de Plantas/química , Espectroscopía de Resonancia Magnética , Estructura Molecular
6.
Bull Entomol Res ; 104(1): 12-8, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23651539

RESUMEN

The intensity of pupal diapause in the cotton bollworm, Helicoverpa armigera (Hübner) was investigated under both laboratory and natural conditions. By transferring diapausing pupae induced under LD 11:13, LD 12:12 and LD 13:11 at 20, 22 and 25 °C to 25 °C combined with LD 15:9 to terminate diapause the rearing day length of 11 h evoked greater intensity of diapause than did 12 and 13 h at 25 °C; whereas the rearing temperature of 25 °C evoked more intense diapause than did 20 and 22 °C under LD 11:13. By transferring diapausing pupae induced under LD 12:12 at 20 and 22 °C to six temperatures of 18, 20, 22, 25, 28 and 31 °C combined with LD 15:9 to terminate diapause, the duration of diapause was significantly shortened from 146 days at 18 °C to 24 days at 31 °C, showing that high temperatures significantly accelerate diapause development. Furthermore, the duration of diapause was significantly longer at the rearing temperature of 22 °C than that at 20 °C when the diapause-terminating temperatures were 20 and 22 °C. Chilling at 5 °C did not shorten the duration of diapause but lengthened it when chilling period was included. However, chilling plays an important role in synchronizing adult emergence. Rearing temperature of 22 °C also evoked more intense diapause than did 20 °C in most chilling treatments. When the overwintering pupae were transferred at different times from natural temperatures to 25 °C, it was found that the earlier the transfer took place, the earlier the adults emerged when the time spent under natural conditions was included. However, cool temperatures before March showed an enhanced effect on diapause development at 20 °C, suggesting that the high diapause-terminating temperature can offset the effect of chilling on diapause development. The result of diapause termination under natural conditions suggests that the developmental threshold for post-diapause development in H. armigera should be around 17.5 °C.


Asunto(s)
Diapausa de Insecto/fisiología , Mariposas Nocturnas/fisiología , Fotoperiodo , Temperatura , Análisis de Varianza , Animales , Pupa/fisiología , Factores de Tiempo
7.
Steroids ; 77(5): 375-81, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22212302

RESUMEN

Six new cardenolides, periforosides D-E (1-2), periforgenin C (3) and periforosides F-H (4-6), as well as 10 previously identified cardenolides (7-16) were isolated from the ethanol extract of the stems of Periploca forrestii. The structures of the new compounds were determined using extensive spectroscopic analyses including HRESI-MS, 1D and 2D NMR data. Evaluation of the cytotoxic activity of all the isolated compounds in five different human cancer cell lines indicated that compounds 2-6, 8, 9 and 12-16 have potent activity.


Asunto(s)
Cardenólidos/farmacología , Periploca/química , Fitosteroles/farmacología , Tallos de la Planta/química , Cardenólidos/química , Cardenólidos/aislamiento & purificación , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Doxorrubicina , Etanol/química , Humanos , Concentración 50 Inhibidora , Espectroscopía de Resonancia Magnética , Estructura Molecular , Fitosteroles/química , Fitosteroles/aislamiento & purificación
8.
Phytochemistry ; 72(1): 115-25, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21112063

RESUMEN

Eleven prenylated C(6)-C(3) compounds, illioliganpyranone A (1), illioliganfunone A-D (2-5), and illioliganone D-I (6-11), together with five known prenylated C(6)-C(3) compounds (12-16), were isolated from roots of Illicium oligandrum. The structures of 1-11 were elucidated by spectroscopic methods including 1D and 2D NMR, HRESIMS, and CD experiments. Possible biosynthetic pathways to compounds 1-16 derived from a common precursor of 5-allylbenzene-1,2,4-triol were postulated. All compounds were evaluated for cytotoxic activities against five human cancer cell lines (HCT-8, Bel-7402, BGC-823, A549 and A2780). Compound 15 exhibited significant cytotoxicity against HCT-8, BGC-823, A549, and A2780 cell lines with IC(50) values of 0.30-2.57 µM. Compound 16 showed moderate selective cytotoxicity against sensitive A2780 cells with IC(50) value of 1.38 µM.


Asunto(s)
Antineoplásicos Fitogénicos/aislamiento & purificación , Benzodioxoles/aislamiento & purificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Illicium/química , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Benzodioxoles/química , Benzodioxoles/farmacología , Ensayos de Selección de Medicamentos Antitumorales , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Humanos , Concentración 50 Inhibidora , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Raíces de Plantas/química , Prenilación
9.
J Asian Nat Prod Res ; 12(6): 516-21, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20552492

RESUMEN

Two new compounds, lysidiside S (1) and 7-O-(+)-peltogynol-beta-d-glucopyranoside (2), together with six known phenolic glycosides (3-8) were isolated from the bark of Lysidice brevicalyx Wei. The structures of these compounds were characterized by chemical and spectroscopic methods. The antioxidant activities of compounds 1-8 were evaluated, and compound 3 exhibited remarkable antioxidant activity at concentrations of 10(-4), 10(-5), and 10(-6) mol/l.


Asunto(s)
Antioxidantes/aislamiento & purificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Fabaceae/química , Glicósidos/aislamiento & purificación , Fenoles/aislamiento & purificación , Antioxidantes/química , Antioxidantes/farmacología , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Glicósidos/química , Glicósidos/farmacología , Microsomas Hepáticos/efectos de los fármacos , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Fenoles/química , Fenoles/farmacología , Corteza de la Planta/química , Vitamina E/farmacología
10.
Org Lett ; 12(10): 2390-3, 2010 May 21.
Artículo en Inglés | MEDLINE | ID: mdl-20420380

RESUMEN

Three new phloroglucinols, named lysidicins F-H (1-3), were isolated from the roots of Lysidice rhodostegia. These compounds have a unprecedented benzyl benzo[b]furo[3,2-d]furan skeleton, and lysidicin F (1) is the first example of natural product with trans-fused furan rings. Their structures were established on the basis of extensive spectroscopic analysis, and the absolute configurations of them were determined by computational methods. A possible biosynthetic pathway for 1-3 was also postulated.


Asunto(s)
Antioxidantes/aislamiento & purificación , Fabaceae/química , Floroglucinol/análogos & derivados , Antioxidantes/química , Simulación por Computador , Modelos Químicos , Conformación Molecular , Floroglucinol/síntesis química , Floroglucinol/química , Floroglucinol/aislamiento & purificación , Raíces de Plantas/química , Estereoisomerismo
11.
J Insect Physiol ; 55(11): 1039-43, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19643107

RESUMEN

It is generally accepted that in most insects adults are sexually immature when they initiate migration and that migratory behaviour terminates with the onset of sexual maturation. However, a few studies examining the mating status of field collected moths have suggested that sexually mature individuals may continue migrating, but in these cases it was impossible to completely eliminate the possibility that the mated females captured came from local, non-migrant populations. In this study we examined the ovarian development of Mythimna separata females captured using a vertical pointing searchlight trap on Beihuang Island in the Bohai Gulf, China, a site >40km from land. Moths were collected from May to October from 2003 to 2008 in order to test the hypothesis that the onset of sexual maturation resulted in the termination of migratory behaviour. While females at the end of the summer had little ovarian development and were unmated, a significant proportion of those migrating northward in the early summer had developed ovaries and often had at least one spermatophore. Given that theses insects were captured while flying up to 500m above sea level, at a site with no local populations, the findings would not support the hypothesis and suggest that both ovarian development and mating may occur during migration.


Asunto(s)
Migración Animal , Mariposas Nocturnas/fisiología , Animales , China , Femenino , Masculino , Mariposas Nocturnas/crecimiento & desarrollo , Ovario/crecimiento & desarrollo , Conducta Sexual Animal , Maduración Sexual
12.
J Insect Physiol ; 55(5): 488-93, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19183558

RESUMEN

Photoperiodic control of diapause induction was systematically investigated in the cabbage butterfly, Pieris melete, which enters summer and winter diapause as a pupa. Summer and winter diapause are induced principally by short and long scotophases, respectively; the intermediate scotophases (11-12 h) permit pupae to develop without diapause. Photoperiodic responses under 24-h light-dark cycles at 16.9, 18, 20 and 22 degrees C showed that the hibernation response was temperature compensated, whereas aestivation response was strongly temperature-dependent. The incidence of diapause for both aestivation and hibernation showed a decline at the ultra-short and ultra-long scotophases. Experiments using non-24-h light-dark cycles showed that the length of the scotophase played an essential role in the determination of diapause. The highest photosensitivity differed under hibernation and aestivation conditions. With a 3 x LD 12:12 interruption, a maximal inhibition of aestivation occurred in the L3/2 stage, and of hibernation it occurred in the L4/0 stage. A long-night of LD 10:14 induced hibernation diapause but inhibited aestivation diapause and, conversely, a short-night of LD 14:10 inhibited hibernation diapause but induced aestivation diapause. With a 1-h light pulse at LD 11:13, a maximal inhibition of hibernation occurred 3 h before lights-on (late scotophase), whereas, with a 1-h light pulse at LD 12.5:11.5, a maximal induction of aestivation occurred 2-3 h after the onset of darkness (early scotophase). Nanda-Hamner and Bünsow experiments failed to reveal the involvement of a circadian system, suggesting that the photoperiodic time measurement for diapause induction in this butterfly resembles an hourglass-like timer or a damped circadian oscillator.


Asunto(s)
Mariposas Diurnas/crecimiento & desarrollo , Animales , Relojes Biológicos/efectos de la radiación , Brassica , Mariposas Diurnas/fisiología , Mariposas Diurnas/efectos de la radiación , Femenino , Luz , Masculino , Metamorfosis Biológica , Fotoperiodo
13.
J Asian Nat Prod Res ; 11(12): 1056-61, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20183276

RESUMEN

Two new prenylated C(6)-C(3) compounds, 4-epi-illicinone E-12-shikimate (1) and 3-hydroxyillifunone B (2), together with five known prenylated C(6)-C(3) compounds (3-7), were isolated from the fruits of Illicium simonsii. Their structures were elucidated on the basis of extensive spectroscopic methods, including 1D and 2D NMR, CD spectra, and ESI-MS analysis.


Asunto(s)
Medicamentos Herbarios Chinos/aislamiento & purificación , Illicium/química , Ácido Shikímico/análogos & derivados , Ácido Shikímico/aislamiento & purificación , Medicamentos Herbarios Chinos/química , Frutas/química , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Ácido Shikímico/química
14.
Environ Entomol ; 37(3): 774-81, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18559184

RESUMEN

The autumn migration of Mythimna separata (Walker) (Lepidoptera: Noctuidae) across the Bohai Sea was observed with a scanning entomological radar and a searchlight trap at Beihuang, an island located in the center of the Bohai Gulf of northern China, in 2003-2006. During the autumn migration, M. separata flew at the altitudes of 50-500 m, with a displacement speed of 4-12 m/s, toward the southwest. Variations of area density of the radar targets and of catches in the searchlight trap through the night indicated that the flight duration of M. separata was approximately 10 h. Based on these observations, M. separata that originated in northeastern China (i.e., Liaoning, Jilin, and Heilongjiang provinces and part of the Inner Mongolia autonomous region) could immigrate into eastcentral China and subsequently to southern China (i.e., Fujian, Guangdong, and Guangxi provinces) within a week for overwintering.


Asunto(s)
Migración Animal , Mariposas Nocturnas/fisiología , Animales , China , Femenino , Vuelo Animal , Luz , Masculino , Océanos y Mares , Orientación , Radar , Estaciones del Año
15.
J Asian Nat Prod Res ; 9(3-5): 471-7, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17701568

RESUMEN

Two new compounds, lysidicin D (1) and lysidicin E (2), were isolated from the roots of Lysidice rhodostegia. Their structures were elucidated by means of spectroscopic methods. Among them compound 1 showed potent anti-oxidant activity on in vitro.


Asunto(s)
Antioxidantes/aislamiento & purificación , Fabaceae/química , Fenantrenos/aislamiento & purificación , Floroglucinol/análogos & derivados , Raíces de Plantas/química , Antioxidantes/química , Antioxidantes/farmacología , Fenantrenos/química , Fenantrenos/farmacología , Floroglucinol/química , Floroglucinol/aislamiento & purificación , Floroglucinol/farmacología
16.
Org Lett ; 8(11): 2269-72, 2006 May 25.
Artículo en Inglés | MEDLINE | ID: mdl-16706503

RESUMEN

[structure: see text] Three novel phloroglucinol derivatives of lysidicins A-C (1-3) have been isolated from the roots of Lysidice rhodostegia and structures were elucidated by comprehensive NMR and MS spectroscopic analysis. 1 and 2 possess spirocyclic benzodihydrofuran skeleton. Their relative stereochemistries were assigned by NOE or NOESY experiment. A plausible pathway for the biosynthesis of 1-3 from 4 and a ketose derivative was postulated.


Asunto(s)
Fabaceae/química , Floroglucinol , Plantas Medicinales/química , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Floroglucinol/análogos & derivados , Floroglucinol/química , Floroglucinol/aislamiento & purificación , Raíces de Plantas/química
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