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A new polymorph of the drug active pharmaceutical ingredient piracetam (Form VI) has been discovered and characterized by X-ray powder diffraction (PXRD), solid-state Raman, attenuated total reflectance infrared spectroscopy, and differential scanning calorimetry. The PXRD diffractogram of Form VI shows a distinct peak at 24.2° (2θ) that distinguishes it from the previously known polymorphs and solvates. Form VI is metastable with respect to the previously known polymorphs Form II and Form III; in ethanol solution at 288 K, Form VI transforms into Form II within 15 min, while in isopropanol solution Form VI is kinetically stable for at least 6 h. A total of 1200 crystal nucleation induction time experiments of piracetam in ethanol and isopropanol solutions have been conducted, in sets of 40-80 repeat experiments carried out at different temperatures and solute concentrations. Each solution nucleated as a single polymorph, and each set of repeat experiments resulted in different proportions of Form II, Form III, and Form VI, with Form VI dominating at low nucleation temperatures and Form II at higher nucleation temperatures. The induction time data for Form VI at 288 K have been evaluated within the framework of the classical nucleation theory. At equal driving force, nucleation of Form VI is less obstructed in ethanol than in isopropanol, as captured by a lower interfacial energy and higher pre-exponential factor in ethanol. The proportion of Form VI obtained at a comparable driving force increases in the order ethanol < isopropanol.
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To learn the current situation and strengthen the management of national standards for Chinese medicinal materials, we sorted out the relevant national standards. According to incomplete statistics, there are 1 185 kinds of Chinese medicinal materials, including 1 024 kinds of plant medicines, 106 kinds of animal medicines, and 54 kinds of mineral medicines, in addition to ethnic medicinal materials with different functions. The relevant standards include 819 Pharmacopoeia standards, 342 standards issued by the Ministry of Health or National Medicinal Products Administration, 7 standards for new medicinal materials, and 17 standards for imported medicinal materials. In this paper, the sources of standards as well as the distribution of families and genera and the distribution of medicinal parts of medicinal materials are analyzed. The suggestions are as follows:(1)to improve the coordination among different national standards of Chinese medicinal materials;(2)to improve the standardization and controllability of relevant standards;(3)to revise the issued standards for Chinese medicinal materials(including Tibetan, Uygur, and Mongolian medicinal materials).
Assuntos
Medicamentos de Ervas Chinesas , Plantas Medicinais , Animais , Povo Asiático , China , Humanos , Medicina Tradicional Chinesa , Padrões de ReferênciaRESUMO
To learn the current situation and strengthen the management of national standards for Chinese medicinal materials, we sorted out the relevant national standards. According to incomplete statistics, there are 1 185 kinds of Chinese medicinal materials, including 1 024 kinds of plant medicines, 106 kinds of animal medicines, and 54 kinds of mineral medicines, in addition to ethnic medicinal materials with different functions. The relevant standards include 819 Pharmacopoeia standards, 342 standards issued by the Ministry of Health or National Medicinal Products Administration, 7 standards for new medicinal materials, and 17 standards for imported medicinal materials. In this paper, the sources of standards as well as the distribution of families and genera and the distribution of medicinal parts of medicinal materials are analyzed. The suggestions are as follows:(1)to improve the coordination among different national standards of Chinese medicinal materials;(2)to improve the standardization and controllability of relevant standards;(3)to revise the issued standards for Chinese medicinal materials(including Tibetan, Uygur, and Mongolian medicinal materials).
Assuntos
Animais , Humanos , Povo Asiático , China , Medicamentos de Ervas Chinesas , Medicina Tradicional Chinesa , Plantas Medicinais , Padrões de ReferênciaRESUMO
The solid-liquid solubility of two polymorphs of the title compound has been measured in n-propanol over the temperature range (278 K-303 K) by an isothermal, gravimetric method and a low heating rate polythermal method. Due to marked differences in the settling behavior of crystals of the two polymorphs in the investigated solvent, it is found that the low heating rate polythermal method gives the overall best performance for this particular system. Systematic slurry conversion experiments show that FII is the stable polymorph over the investigated temperature range (268 K-308 K). Solubility data for both polymorphs is well correlated, and has been extrapolated to the melting point, by a previously proposed semi-empirical regression model based on solid-phase calorimetric data. The system exhibits a marked positive deviation from Raoult's law, with solute activity coefficients at equilibrium decreasing with increasing temperature.
Assuntos
1-Propanol , Tolbutamida , Varredura Diferencial de Calorimetria , Cristalização , Solubilidade , TermodinâmicaRESUMO
The solubility of butamben has been measured gravimetrically in pure methanol, 1-propanol, 2-propanol, 1-butanol, and toluene over the temperature range 268-298 K. Polymorph transition and melting temperatures, associated enthalpy changes, and the heat capacity of the solid forms and the supercooled melt have been measured by differential scanning calorimetry. Based on extrapolated calorimetric data, the Gibbs energy, enthalpy and entropy of fusion, and the activity of solid butamben (the ideal solubility) have been calculated from below ambient temperature up to the melting point. Activity coefficients of butamben at equilibrium in the different solvents have been estimated from solubility data and the activity of the solid, revealing that all investigated systems exhibit positive deviation from Raoult's law. Solubility data are well correlated by a semiempirical regression model. On a mass basis, the solubility is clearly higher in methanol than in the other solvents, but mole fraction solubilities are very similar across all 5 solvents. The 2 known polymorphs are enantiotropically related, and the transition point is located at 283 K. Polymorph interconversions occur within 0.3 K of the transition point even in the solid state, and the 2 forms exhibit strong similarities in investigated properties.
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Benzocaína/análogos & derivados , Solventes/química , 2-Propanol/química , Benzocaína/química , Varredura Diferencial de Calorimetria/métodos , Cristalização/métodos , Temperatura Alta , Metanol/química , Solubilidade , Temperatura , Termodinâmica , Temperatura de Transição , Difração de Raios X/métodosRESUMO
Herein we report a one-step method to prepare high internal water-phase double emulsions (W/O/W) via catastrophic phase inversion of water-in-oil high internal phase emulsions (W/O HIPEs) stabilized solely by 12-acryloxy-9-octadecenoic acid (AOA) through increasing the content of water phase. This is the first time for double emulsions to be stabilized solely by a single small molecular surfactant, which are usually costabilized by both hydrophilic and hydrophobic surfactants. After neutralized with ammonia, AOA is confirmed to be capable of stabilizing both W/O emulsions and O/W emulsions, which may account for its unique ability to stabilize double emulsions. The effects of different conditions (including changing the concentrations of AOA and salt (NaCl), pH value, the polarity of oils, the addition interval of water and stirring rate, etc.) on the formation and the stability of double emulsions as well as the inversion point have been investigated by using optical microscopy and conductivity monitoring. Finally, porous polymer microspheres with high interconnection (polyHIPE microspheres) were fabricated by γ-ray initiated polymerization of the as-prepared double emulsions composed of different monomers (styrene, or n-butyl acrylate, or methyl methacrylate), which have been confirmed by scanning electron microscopy. Our method is facile and effective for preparing high interconnecting porous polymer microspheres without tedious post-treatment of the products in common emulsion polymerization due to the use of polymerizable surfactant.
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OBJECTIVE: To investigate the chemical constituents in the roots of Angelica nitida. METHODS: The chemical constituents were isolated by silica gel,their structures were identified by spectral analysis. RESULTS: Nine compounds were isolated and identified as isoimperatorin(I), imperatorin(II), cnidilin(III), beta-sitosterol(IV), isopimpinellin(V), phellopterin(VI), neobyakangelicol(VII), (3S)-2,2-dimethyl-3,5-dihydroxy-8-hydroxylmethyl-3,4-dihydro-2H,6H-benzo[1,2-b: 5,4-b'] dipyran-6-one(VIll) and byakangelicin (IX). CONCLUSION: All the compounds are isolated from the plant for the first time.
Assuntos
Angelica/química , Medicamentos de Ervas Chinesas/química , Raízes de Plantas/química , Plantas Medicinais/química , China , Cumarínicos/química , Cumarínicos/isolamento & purificação , Medicamentos de Ervas Chinesas/isolamento & purificação , Furocumarinas/química , Furocumarinas/isolamento & purificação , Espectroscopia de Ressonância Magnética , Estrutura MolecularRESUMO
This study was carried out to evaluate the protective effect of anthocyanins extract of blueberry on trinitrobenzene sulfonic acid (TNBS)-induced inflammatory bowel disease (IBD) model of mice. The study employed female C57BL/6 mice (n = 50), and colitis was induced by intracolonic injection of 0.5 mg of TNBS dissolved in 50% ethanol-phosphate buffered solution. The mice were divided into five groups (n = 10): vehicle, TNBS control and anthocyanins groups that received different doses of anthocyanins extract (10, 20 and 40 mg kg(-1)) daily for 6 days. Both increase in body weight and diarrhea symptoms were monitored each day. After 6 days, the animals were killed, and the following parameters were assessed: colon length, morphological score, histological score and biochemical assay (NO, myeloperoxidase (MPO), interleukin (IL)-12, IL-10, tumor necrosis factor (TNF)-α and interferon (IFN)-γ). The results showed that the anthocyanins extract of blueberry rendered strong protection against TNBS-induced colonic damage at a dosage of 40 mg kg(-1). When compared with the control, anthocyanins extract significantly prevented loss of body weight and ameliorated the scores of diarrhea, morphology and histology. Treatment with anthocyanins extract restored IL-10 excretion, as well as caused reduction in the levels of NO, MPO, IL-12, TNF-α and IFN-γ. Our research revealed the protective effect of anthocyanins extract from blueberry on TNBS-induced experimental colitis in mice, as well as examined whether high levels of dietary blueberries would lower the risk or have protective effects on human IBD, which may require further investigation.
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OBJECTIVE: Compared the difference of the configuration of vegetative organs of medicinal Chrysanthemum in the same habitats but from various original locations and species, in order to provide scientific basis for the study of introduction, differentiation within the species, breeding and genetic diversity. METHODS: The experimental plot were divided into some groups randomly in design and the configuration of vegetative organs were observed, measureed and analysed. RESULTS: The differences of the type and shape of the leaves were obvious. All the Chrysanthemum morifolium cv. 'Gongju' had deep notch long-leaves; Chrysanthemum morifolium cv. 'Boju', Chrysanthemum morifolium cv. 'Chuju', Chrysanthemum morifolium cv. 'Hang bai ju' and Chrysanthemum morifolium cv. 'Hang huang ju' had deep notch correctitude-leaves; Chrysanthemum nakingense and Chrysanthemum indicum had long-leaves; Chrysanthemum indicum had clump-leaves. All the 12 medicinal Dendranthema material had auricle except Chrysanthemum morifolium cv. 'Boju' and Chrysanthemum morifolium cv. 'Chuju'. The young leaves of Chrysanthemum morifolium cv. 'Gongju', Chrysanthemum morifolium cv. 'Gongju' and Chrysanthemum morifolium cv. 'Hang bai ju' did not split and the rest were all splitting. CONCLUSION: The differences of the configuration of vegetative organs were obvious and the Key of Vegetative organs was built.
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Chrysanthemum/anatomia & histologia , Chrysanthemum/classificação , Folhas de Planta/anatomia & histologia , Plantas Medicinais/anatomia & histologia , Biodiversidade , China , Chrysanthemum/crescimento & desenvolvimento , Filogenia , Plantas Medicinais/classificação , Plantas Medicinais/crescimento & desenvolvimento , Especificidade da EspécieRESUMO
OBJECTIVE: To study the chemical constituents in roots of Angelica tianmuensis and A. megaphylla. METHODS: Compounds were isolated by column chromatography with silica gel, their structures were identified by spectral analysis. RESULTS: Another three compounds (ligustilone, 5-methoxyhamaudol, cimifugin) were obtained from the roots of Angelica tianmuensis, and another two compounds (ligustilone, angelol) were obtained from the roots of A. megaphylla. CONCLUSION: All the compounds are isolated in these two plants for the first time, and ligustilone is first found from Angelica L..
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Angelica/química , Cromonas/isolamento & purificação , Cumarínicos/isolamento & purificação , Plantas Medicinais/química , Sesquiterpenos/isolamento & purificação , Angelica/classificação , Cromonas/química , Cumarínicos/química , Estrutura Molecular , Raízes de Plantas/química , Sesquiterpenos/químicaRESUMO
OBJECTIVE: To select the microorganism which can hydrolyze dioscin to diosgenin. METHODS: The microorganism were selected from the surface of rhizome, rhizosphere soil, the inside of the leaves and rhizome of Dioscorea zingiberensis C. H. Wright. Diosgenin was identified by thin-layer chromatography and HPLC. RESULTS: The microorganism which could hydrolyze dioscin from the experiment were identified as Aspergillus sp and Alternaria sp. Characteristics of enzymes production and fermentation technology of Aspergillus No. 1 were also studied primarily. CONCLUSION: The Aspergillus strain No. 1 can secret enzyme to hydrolyze dioscin into diosgenin effectively.
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Alternaria/metabolismo , Aspergillus/metabolismo , Dioscorea/microbiologia , Diosgenina/análogos & derivados , Plantas Medicinais/microbiologia , Alternaria/enzimologia , Alternaria/crescimento & desenvolvimento , Aspergillus/enzimologia , Aspergillus/crescimento & desenvolvimento , Cromatografia Líquida de Alta Pressão , Cromatografia em Camada Fina , Diosgenina/metabolismo , Hidrólise , Rizoma/microbiologiaRESUMO
OBJECTIVE: To isolate a homogeneous polysaccharide RP from RDP (a crude polysaccharide from Dioscorea opposita Thunb.) , and study its preliminary composition and structure. METHODS: RP was obtained with water extraction, alcohol sedimentation, CTAB deprotein, cellulose column and SephadexG-100 column. The purities of RP were identified by SephadexG-200. PC analysis on its acidic hydrolysates was used to determine the sugar components. Sephadex chromatography was used to mensurate its molecular weight. IR was used to analysis RP. RESULTS: RP was homogeneous. IR indicated that RP had beta configurations. The compositon was identified by paper chromatography as glucose, D-mannose, D-galactose. CONCLUSION: The research could provide a theoretical foundation for further development and utilization.
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Dioscoreaceae/química , Plantas Medicinais/química , Polissacarídeos/química , Polissacarídeos/isolamento & purificação , Galactose/análise , Glucose/análise , Manose/análise , Peso Molecular , Tubérculos/química , Espectrofotometria Infravermelho , Espectrofotometria UltravioletaRESUMO
OBJECTIVE: To investigate the chemical constituents from the aerial parts of Breynia fruticosa. METHOD: Various chromatographic techniques were employed for isolation and purification of the constituents. The structures were elucidated by chemical evidence and spectral methods. RESULT: Seven compounds were obtained and identified by spectroscopic methods and compared with authentic samples as aviculin [(+)-isolariciresinol-9'-rhamno-pyranoside], friedelan-3beta-ol, friedelin, arborinone, isoarborinol, 5-hydroxy-7,8,4'-trimethoxy flavone, 2,4-dihydroxy-6-methoxy-3-methyl-acetophenone. CONCLUSION: All compounds were firstly isolated from B. genus, furthermore, aviculin was isolated from Euphorbiaceae for the first time.
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Euphorbiaceae/química , Glicosídeos/isolamento & purificação , Plantas Medicinais/química , Triterpenos/isolamento & purificação , Glicosídeos/química , Componentes Aéreos da Planta/química , Triterpenos/químicaRESUMO
<p><b>OBJECTIVE</b>To investigate the chemical constituents from the aerial parts of Breynia fruticosa.</p><p><b>METHOD</b>Various chromatographic techniques were employed for isolation and purification of the constituents. The structures were elucidated by chemical evidence and spectral methods.</p><p><b>RESULT</b>Seven compounds were obtained and identified by spectroscopic methods and compared with authentic samples as aviculin [(+)-isolariciresinol-9'-rhamno-pyranoside], friedelan-3beta-ol, friedelin, arborinone, isoarborinol, 5-hydroxy-7,8,4'-trimethoxy flavone, 2,4-dihydroxy-6-methoxy-3-methyl-acetophenone.</p><p><b>CONCLUSION</b>All compounds were firstly isolated from B. genus, furthermore, aviculin was isolated from Euphorbiaceae for the first time.</p>