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1.
J Asian Nat Prod Res ; 26(3): 302-312, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37312516

RESUMO

Three new quinolizidine alkaloids (1 - 3), including one new naturally isoflavone and cytisine polymer (3), along with 6 known ones were isolated from the ethanol extract of Sophora tonkinensis Gagnep. Their structures were elucidated by comprehensive spectroscopic data analysis (IR, UV, HRESIMS, 1D and 2D NMR), combined with ECD calculations. The antifungal activity against Phytophythora capsica, Botrytis cinerea, Gibberella zeae, and Alternaria alternata of the compounds was evaluated in a mycelial inhibition assay. Biological tests indicated that compound 3 exhibited strong antifungal activity against P. capsica with EC50 values of 17.7 µg/ml.


Assuntos
Alcaloides , Sophora , Alcaloides Quinolizidínicos , Sophora/química , Antifúngicos/farmacologia , Raízes de Plantas/química , Alcaloides/química , Estrutura Molecular
2.
J Asian Nat Prod Res ; 25(2): 163-170, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-35675145

RESUMO

Two new isoflavones (1 and 2), as well as eight known ones were isolated from the roots of Sophora tonkinensis Gagnep. Compound 1 represents an unprecedented polymerization pattern constructed by isoflavone and cytisine. Their structures were elucidated by comprehensive spectroscopic data analysis, combined with ECD calculations. Compound 1 displayed significant anti-tobacco mosaic virus (TMV) activity compared with the positive control ningnanmycin. Moreover, compound 6 exhibited potent α-glucosidase inhibitory activity with IC50 value of 47.4 mg/L.


Assuntos
Alcaloides , Isoflavonas , Sophora , Isoflavonas/farmacologia , Sophora/química , Raízes de Plantas/química , Alcaloides/química , Quinolizinas/análise
3.
J Org Chem ; 87(17): 11309-11318, 2022 09 02.
Artigo em Inglês | MEDLINE | ID: mdl-35981284

RESUMO

Six novel Maillard reaction products (MRPs) (1-6) were isolated from the processed Thermopsis lanceolata R. Br. seed extract, along with one biogenetically related intermediate (7). Compounds 1-4 possessed three rare dimerization patterns constructed by cytisine, whereas compounds 5 and 6 represented the first example of the addition products of cytisine and 5,6-dihydroxy-4-hexanolide. Their structures were elucidated by comprehensive spectroscopic data analysis and quantum chemistry calculations including GIAO 13C{1H} NMR and ECD calculation, combined with single-crystal X-ray diffraction analysis. Biologically, compound 3 displayed significant anti-tobacco mosaic virus activity compared with the positive control ningnanmycin.


Assuntos
Vírus do Mosaico do Tabaco , Antivirais/química , Produtos Finais de Glicação Avançada , Extratos Vegetais/química
4.
J Asian Nat Prod Res ; 24(12): 1141-1149, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34984943

RESUMO

Two new (1 and 2) cytisine-type alkaloids that were chemically inseparable isomers (present in a 1:1 ratio) were identified from the seeds of Thermopsis lanceolata R. Br. Their structures were elucidated by comprehensive spectroscopic data analysis (IR, UV, NMR, HRESIMS) and ECD calculation. Compound 1 displayed significant anti-tobacco mosaic virus (TMV) activity, while compounds 1 and 2 displayed moderate insecticidal activities against Aphis fabae with LC50 value of 43.15 and 46.47 mg/L, respectively.


Assuntos
Alcaloides , Fabaceae , Estrutura Molecular , Quinolizinas/farmacologia , Alcaloides/farmacologia , Alcaloides/química , Azocinas , Sementes , Antivirais/química
5.
J Asian Nat Prod Res ; 23(7): 644-651, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33583289

RESUMO

Two new compounds, including one new arylbenzofuran (1) and one new pterocarpanoid (2), along with nine known ones, were isolated from the seeds of Sophora tonkinensis. The structures of the new compounds were elucidated based on a comprehensive spectroscopic data analysis. Compounds 2 and 3 exhibited good anti-tobacco mosaic virus (TMV) activities with the protective inhibition rate of 69.62% and 68.72% respectively, at concentration of 100 µg/ml.


Assuntos
Sophora , Vírus do Mosaico do Tabaco , Antivirais/farmacologia , Estrutura Molecular , Sementes
6.
Small ; 11(42): 5675-86, 2015 Nov 11.
Artigo em Inglês | MEDLINE | ID: mdl-26366746

RESUMO

To overcome traditional barriers in optical imaging and microscopy, optoacoustic-imaging has been changed to combine the accuracy of spectroscopy with the depth resolution of ultrasound, achieving a novel modality with powerful in vivo imaging. However, magnetic resonance imaging provides better spatial and anatomical resolution. Thus, a single hybrid nanoprobe that allows for simultaneous multimodal imaging is significant not only for cutting edge research in imaging science, but also for accurate clinical diagnosis. A core-shell-structured coordination polymer composite microsphere has been designed for in vivo multimodality imaging. It consists of a Fe3 O4 nanocluster core, a carbon sandwiched layer, and a carbocyanine-Gd(III) (Cy-Gd(III) ) coordination polymer outer shell (Fe3 O4 @C@Cy-Gd(III) ). Folic acid-conjugated poly(ethylene glycol) chains are embedded within the coordination polymer shell to achieve extended circulation and targeted delivery of probe particles in vivo. Control of Fe3 O4 core grain sizes results in optimal r2 relaxivity (224.5 × 10(-3) m(-1) s(-1) ) for T2 -weighted magnetic resonance imaging. Cy-Gd(III) coordination polymers are also regulated to obtain a maximum 25.1% of Cy ligands and 5.2% of Gd(III) ions for near-infrared fluorescence and T1 -weighted magnetic resonance imaging, respectively. The results demonstrate their impressive abilities for targeted, multimodal, and reliable imaging.


Assuntos
Gadolínio/química , Imageamento por Ressonância Magnética/métodos , Nanopartículas de Magnetita/química , Imagem Multimodal/métodos , Neoplasias/diagnóstico , Técnicas Fotoacústicas/métodos , Polímeros/química , Animais , Carbono/química , Células Cultivadas , Óxido Ferroso-Férrico/química , Células HeLa , Humanos , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Nus , Microesferas , Neoplasias/patologia , Imagem Óptica/métodos
7.
J Agric Food Chem ; 72(9): 5047-5061, 2024 Mar 06.
Artigo em Inglês | MEDLINE | ID: mdl-38394631

RESUMO

As part of our ongoing investigation of natural bioactive substances from the genus Thermopsis of the tribe Fabaceae for agricultural protection, the chemical constituents of the herb Thermopsis lupinoides were systematically investigated, which led to the isolation of 39 quinolizidine alkaloids (QAs) (1-39), including 14 new QAs (1-14) and 14 isoflavones (40-53). Their structures were elucidated through comprehensive spectroscopic data analysis (IR, UV, NMR, HRESIMS), ECD calculations, and X-ray crystallography. The antitomato spotted wilt virus (TSWV) and antifungal (against Botrytis cinerea, Gibberella zeae, Phytophythora capsica, and Alternaria alternata) and insecticidal (against Aphis fabae and Tetranychus urticae) activities of the isolated compounds were screened using the lesion counting method, mycelial inhibition assay, and spray method, respectively. The bioassay results showed that 34 exhibited excellent protective activity against TSWV, with an EC50 value of 36.04 µg/mL, which was better than that of the positive control, ningnanmycin (86.03 µg/mL). The preliminary mechanistic exploration illustrated that 34 induced systemic acquired resistance in the host plant by acting on the salicylic acid signaling pathway. Moreover, 1 showed significant antifungal activity against B. cinerea (EC50 value of 20.83 µg/mL), while 2 exhibited good insecticidal activity against A. fabae (LC50 value of 24.97 µg/mL). This research is promising for the invention of novel pesticides from QAs with high efficiency and satisfactory ecological compatibility.


Assuntos
Fabaceae , Fungicidas Industriais , Inseticidas , Antifúngicos/farmacologia , Antifúngicos/química , Fungicidas Industriais/farmacologia , Fungicidas Industriais/química , Alcaloides Quinolizidínicos , Inseticidas/farmacologia , Inseticidas/química , Antivirais/farmacologia , Relação Estrutura-Atividade
8.
J Agric Food Chem ; 72(14): 8225-8236, 2024 Apr 10.
Artigo em Inglês | MEDLINE | ID: mdl-38557068

RESUMO

As a continuous flow investigation of novel pesticides from natural quinolizidine alkaloids, the chemical compositions of the seeds of Sophora alopecuroides were thoroughly researched. Fifteen new aloperine-type alkaloids (1-15) as well as six known aloperine-type alkaloids (16-21) were obtained from the extract of S. alopecuroides. The structures of 1-21 were confirmed via HRESIMS, NMR, UV, IR, ECD calculations, and X-ray diffraction. The antiviral activities of 1-21 against tobacco mosaic virus (TMV) were detected following the improved method of half-leaf. Compared with ningnanmycin (protective: 69.7% and curative: 64.3%), 15 exhibited excellent protective (71.7%) and curative (64.6%) activities against TMV. Further biological studies illustrated that 15 significantly inhibited the transcription of the TMV-CP gene and increased the activities of polyphenol oxidase (PPO), peroxidase (POD), superoxide dismutase (SOD), and phenylalanine ammonia-lyase (PAL). The antifungal activities of 1-21 against Phytophythora capsica, Botrytis cinerea, Alternaria alternata, and Gibberella zeae were screened according to a mycelial inhibition test. Compound 13 displayed excellent antifungal activity against B. cinerea (EC50: 7.38 µg/mL). Moreover, in vitro antifungal mechanism studies displayed that 13 causes accumulation of reactive oxygen species and finally leads to mycelia cell membrane damage and cell death in vitro.


Assuntos
Alcaloides , Quinolizidinas , Sophora , Vírus do Mosaico do Tabaco , Antifúngicos , Sophora/química , Alcaloides/química , Antivirais/farmacologia , Antivirais/química , Sementes/química
9.
Nat Prod Res ; 37(6): 967-973, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35848408

RESUMO

Sorghum (Sorghum bicolor L.) is the fifth largest crop in the world and has potential health benefits, but vast quantities of sorghum roots are discarded after harvest. Based on the previous antiplatelet aggregation for this species, two new multi-substituted 3H-indole alkaloids sorghumine A (1) and sorghumine B (2), together with 14 known compounds (3-16), were found from the water extract of sorghum roots. Compounds 1-2 were identified by analyzing their spectroscopic data and physic and chemical properties, and the absolute configuration was further determined by electronic circular dichroism (ECD) analysis and calculations. 1-2, 4, 6-8 and 13-15 showed significant inhibition of platelet aggregation induced by adenosine diphosphate. 2-4, 6-9 and 11 showed significant inhibition of platelet aggregation induced by collagen. 4-6, 8, 10-11 and 16 showed significant inhibition on platelet aggregation induced by thrombin. Furthermore, molecular docking showed that active compounds can bind to P2Y12 and COX-1 receptors in platelet.


Assuntos
Sorghum , Simulação de Acoplamento Molecular , Plaquetas , Agregação Plaquetária , Inibidores da Agregação Plaquetária/farmacologia
10.
J Agric Food Chem ; 71(10): 4394-4407, 2023 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-36854107

RESUMO

As a continuation of our research on the development of pesticide active quinolizidine alkaloids (QAs) from the family Fabaceae, the chemical constituents of the root of Sophora tonkinensis Gagnep. were systematically investigated. Seventeen new matrine-type alkaloids (1-17), including one new naturally occurring compound (17), along with 20 known ones were isolated from the EtOH extract of S. tonkinensis. Notably, compound 5 possessed an unprecedented 6/6/5/4/6/6 hexacyclic system. Their structures were confirmed via comprehensive spectroscopic data analysis (IR, UV, NMR, HRESIMS), ECD calculation, and X-ray crystallography. Biological tests indicated that compounds 1, 4, 10, 12, 13, and 30 displayed significant anti-tomato spotted wilt virus (TSWV) activities compared with the positive control ningnanmycin. Moreover, compound 12 strongly inhibited the expression of the TSWV N, NSs, and NSm genes and TSWV NSs protein in plant host. Furthermore, compounds 4, 10, 12, 20, and 22 exhibited moderate insecticidal activities against TSWV thrip vector (Frankliniella occidentalis).


Assuntos
Sophora , Tospovirus , Matrinas/química , Matrinas/farmacologia , Tospovirus/efeitos dos fármacos , Antivirais/química , Antivirais/farmacologia , Espectrofotometria , Cristalografia por Raios X , Ativação Viral/efeitos dos fármacos , Animais , Inseticidas/química , Inseticidas/farmacologia , Proteínas não Estruturais Virais/genética , Modelos Moleculares , Estrutura Molecular , Raízes de Plantas
11.
J Agric Food Chem ; 70(29): 9214-9226, 2022 Jul 27.
Artigo em Inglês | MEDLINE | ID: mdl-35849433

RESUMO

As part of our ongoing investigation of pesticide active quinolizidine alkaloids (QAs) from the family Fabaceae, the chemical constituents of the seeds of Thermopsis lanceolata R. Br. were systematically investigated. Bioassay-guided fractionation and purification of the crude extract led to the isolation of seventeen new QAs (1-17), including three new naturally occurring compounds (15-17), along with 15 known compounds (18-32). Their structures were elucidated by comprehensive spectroscopic data analysis (IR, UV, NMR, and HRESIMS) and quantum chemistry calculations (13C NMR and ECD). The antitomato spotted wilt virus activities and insecticidal activities against Aphis fabae, Nilaparvata lugens (Stal), and Tetranychus urticae of compounds 1-32 were screened using the lesion counting method, spray method, and rice-stem dipping method, respectively. Biological tests indicated that compounds 6, 9, 10, and 18 displayed significant anti-TSWV activities compared with the positive control ningnanmycin. Compounds 3, 4, and 5 showed better insecticidal activities against A. fabae with LC50 values of 10.07, 12.07, and 6.56 mg/L, respectively. Moreover, compounds 5, 18, and 24 exhibited moderate insecticidal activities against N. lugens (Stal) with LC50 values of 37.91, 53.44, and 31.21 mg/L, respectively. Furthermore, compounds 9 and 10 exhibited moderate insecticidal activities against T. urticae.


Assuntos
Alcaloides , Afídeos , Fabaceae , Inseticidas , Quinolizidinas , Alcaloides/análise , Alcaloides/farmacologia , Animais , Inseticidas/química , Quinolizidinas/farmacologia , Sementes/química
12.
Fitoterapia ; 158: 105140, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35122885

RESUMO

Seven undescribed thermopsine-based alkaloids (1-7), including one undescribed biogenetically related intermediate (7), were isolated from the seeds of Thermopsis lanceolata R. Br. Compound 1 possessed a 6/6-6 tricyclic skeleton, while compounds 2-6 represented three rare dimerization patterns constructed by quinolizidine alkaloids. Their structures were elucidated by comprehensive spectroscopic data analysis as well as ECD calculations. Biologically, compound 6 displayed significant anti-Tomato spotted wilt virus (TSWV) activity compared with the positive control ningnanmycin. Moreover, compound 1 exhibited good insecticidal activity against Aphis fabae with LC50 value of 25.2 mg/L.


Assuntos
Alcaloides , Inseticidas , Alcaloides/química , Antivirais/química , Antivirais/farmacologia , Inseticidas/química , Inseticidas/farmacologia , Estrutura Molecular , Sementes/química
13.
Fitoterapia ; 143: 104572, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32224153

RESUMO

Three new tuberostemoamide-type alkaloids, stemtuberolines A-C (1-3), four new stenine-type alkaloids, stemtuberolines D-G (4-7), together with five known Stemona alkaloids (8-12), were isolated from the roots of Stemona tuberosa. Their structures were elucidated on the basis of comprehensive spectroscopic data analysis. Stemtuberoline C (3) exhibited significant anti-TMV activity with an inhibition rate of 60.48% at the concentration of 50 µg/mL, while that of ningnamycin, the positive control, was 52.89%.


Assuntos
Alcaloides/farmacologia , Antivirais/farmacologia , Stemonaceae/química , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Alcaloides/isolamento & purificação , Antivirais/isolamento & purificação , China , Estrutura Molecular , Compostos Fitoquímicos/isolamento & purificação , Compostos Fitoquímicos/farmacologia , Doenças das Plantas/prevenção & controle , Doenças das Plantas/virologia , Raízes de Plantas/química , Nicotiana/virologia
14.
J Agric Food Chem ; 68(50): 15015-15026, 2020 Dec 16.
Artigo em Inglês | MEDLINE | ID: mdl-33285067

RESUMO

The discovery of novel, effective, and botanical pesticides is one of the main strategies for modern plant protection and insect pest control. During the search for novel botanical pesticides from natural sources, the seeds of Sophora tonkinensis were systematically investigated to obtain 11 new matrine-type alkaloids (1-11), including one novel matrine-type alkaloid featuring an unprecedented 5/6/6/6 tetracyclic skeleton (1), along with 16 known compounds (12-27). Their structures were elucidated by comprehensive spectroscopic data analysis (IR, UV, NMR, and HRESIMS), ECD calculations, and single-crystal X-ray diffraction. The anti-tobacco mosaic virus (TMV) activity and insecticidal activities against Aphis fabae and Tetranychus urticae of the compounds were also respectively screened using the half-leaf method and spray method. Biological tests indicated that compounds 2, 4, 6, and 26 displayed significant anti-TMV biological activities compared with the positive control ningnanmycin. Compounds 7, 17, and 26 presented moderate activities against A. fabae with LC50 values of 38.29, 18.63, and 23.74 mg/L, respectively. Moreover, compounds 13 and 26 exhibited weak activities against T. urticae.


Assuntos
Alcaloides/farmacologia , Antivirais/farmacologia , Inseticidas/farmacologia , Extratos Vegetais/farmacologia , Quinolizidinas/farmacologia , Sophora/química , Alcaloides/química , Animais , Antivirais/química , Insetos/efeitos dos fármacos , Insetos/crescimento & desenvolvimento , Inseticidas/química , Extratos Vegetais/química , Quinolizidinas/química , Sementes/química , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Vírus do Mosaico do Tabaco/crescimento & desenvolvimento
15.
Phytochemistry ; 167: 112111, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31491684

RESUMO

A C20-diterpenoid alkaloid with an unprecedented carbon skeleton, acoapetaludine A, together with ten undescribed aconitine-type C19-diterpenoid alkaloids, acoapetaludines B-K, were isolated from the whole plants of Aconitum apetalum (Huth) B. Fedtsch. (Ranunculaceae). The structures were elucidated based on a comprehensive spectroscopic data analysis. The absolute configuration of acoapetaludine A was determined by quantum ECD calculation. Acoapetaludines D and E exhibited weak anti-Helicobacter pylori activity at a minimum inhibitory concentration (MIC) of 100 and 50 µg/mL, respectively.


Assuntos
Aconitum/química , Alcaloides/química , Alcaloides/farmacologia , Antibacterianos/química , Antibacterianos/farmacologia , Diterpenos/química , Helicobacter pylori/efeitos dos fármacos , Testes de Sensibilidade Microbiana , Modelos Moleculares , Conformação Molecular
16.
Chem Commun (Camb) ; 51(10): 1908-10, 2015 Feb 04.
Artigo em Inglês | MEDLINE | ID: mdl-25531983

RESUMO

Porous magnetic supraparticles (p-MSPs) with surface area up to 285.4 m(2) g(-1) have been fabricated by a one-step etching method, which is 4 times greater than the unetched counterpart. They exhibit significantly better biodegradability than their counterpart in both mimicked physiological buffer solution and the cellular environment of HeLa cells.


Assuntos
Fenômenos Magnéticos , Nanopartículas/química , Nanopartículas/metabolismo , Soluções Tampão , Microambiente Celular/fisiologia , Células HeLa , Humanos , Microscopia Eletrônica de Transmissão , Estrutura Molecular , Porosidade
17.
ACS Appl Mater Interfaces ; 7(8): 4969-78, 2015 Mar 04.
Artigo em Inglês | MEDLINE | ID: mdl-25674936

RESUMO

A hydrid microsphere Fe3O4@carbon@poly(In(III)-carboxylate) consisting of a cluster of Fe3O4 nanoparticles as the core, a carbon layer as the inner shell and a porous In(III)-carboxylate coordination polymer as the outer shell was prepared and applied as a recyclable catalyst for the cycloaddition reaction of CO2 and epoxides. Construction of this hybrid microsphere was achieved in the two steps, including (1) the one-pot solvothermal synthesis of Fe3O4@C particles with the abundant carboxylic groups on the carbon surface and (2) the subsequent growth of the outer shell polymers based on the precipitation coordination polymerization. Imidazolium-substituted Salen ligands were synthesized and chelated with the In(III) ions using the terminal carboxylic groups. The coordination polymer shell was formed on the Fe3O4@C particles, and the structures including shell thickness, surface area and porosity could be varied by tuning the feeding ratios of the In(III) ions and the ligands. The optimal structure of the coordination polymers showed a shell thickness of ca. 45 nm with ∼5 nm of mesopore, 174.7 m(2)/g of surface area and 0.2175 cm(3)/g of pore volume. In light of gas uptake capability, catalytic activity and magnetic susceptibility, cycloaddition of CO2 with a series of epoxides were studied by using Al-complexed Fe3O4@C@In(III)-[IL-Salen] microspheres. The results validated that the self-supporting catalytic layer with high surface area was of remarkable advantages, which were attributed from great increment of effective active sites and combination of nucleophilic/electrophilic synergistic property and CO2 uptake capability. Therefore, these hybrid microspheres provided excellent catalytic activity, prominent selectivity to cyclic carbonates and outstanding recyclability with the assistance of an applied magnetic field.

18.
Di Yi Jun Yi Da Xue Xue Bao ; 23(9): 902-4, 2003 Sep.
Artigo em Zh | MEDLINE | ID: mdl-13129714

RESUMO

After the almost nation-wide outbreak of SARS this year, all the health administration agencies have made attempt to analyze the origin of the epidemic and draw lessons from the measures taken against it, hoping to be better able to cope with such potential public health threats. For effectively preventing and timely controlling drinking water pollution accident so as to ensure the sanitation of life drinking water, it is of great importance to prepare emergency counterplan beforehand against such accident. In this article the author proposes the emergency counterplan against urban drinking water pollution on the basis of established laws and regulations of the state and Beijing municipality.


Assuntos
Poluição da Água/prevenção & controle , Abastecimento de Água , Emergências , Humanos , Saúde Pública , Saneamento
19.
Di Yi Jun Yi Da Xue Xue Bao ; 23(9): 895-8, 2003 Sep.
Artigo em Zh | MEDLINE | ID: mdl-13129712

RESUMO

OBJECTIVE: To achieve expression of recombinant human endostatin (rhES) in a highly efficient foreign gene expression system, the yeast strain Pichia pastoris, and to evaluate the inhibitory effect of rhES on the growth of nude mouse pulmonary adenocarcinoma cells. METHODS AND RESULTS: The rhES gene was efficiently expressed in the yeast strain, and heparin affinity chromatography yielded highly purified endostatin identified by Western blotting, which proved to significantly inhibit the growth of the ECV-304 cells in vitro and also the growth of the lung adenocarcinoma Astc-a-1 in nude mice. CONCLUSIONS: The rhES gene can be expressed in Pichia pastoris, and has the ability to restrain the growth of ECV-304 cells and lung adenocarcinoma Astc-a-1 in nude mice, showing important potentials for future clinical applications.


Assuntos
Adenocarcinoma/tratamento farmacológico , Endostatinas/biossíntese , Neoplasias Pulmonares/tratamento farmacológico , Pichia/genética , Adenocarcinoma/patologia , Animais , Linhagem Celular Tumoral , Endostatinas/isolamento & purificação , Endostatinas/uso terapêutico , Humanos , Neoplasias Pulmonares/patologia , Masculino , Camundongos , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/uso terapêutico
20.
J Colloid Interface Sci ; 389(1): 10-5, 2013 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-22975398

RESUMO

Mesoporous magnetic Co-NPs(nanoparticles)/carbon nanocomposites were synthesized by carbonization of polyacrylonitrile (PAN) microspheres entrapped with cobalt salt for the first time. The structure and morphology of the porous magnetic nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), and N(2) adsorption-desorption technique. The nanocomposites possess very high saturation magnetization (Ms is up to ~133 emu/g), near-zero remanence, and very low coercivity (Hc is down to ~0.023 KOe). Meanwhile, the nanocomposites have mesoporous structure with average pore size of 4 nm and high specific surface area of 232 m(2)/g, which can be tuned by changing the carbonization conditions. Using methyl orange (MO) as model pollutant in water, the mesoporous magnetic nanocomposites showed good adsorption capacity of 380 mg/g, and the absorbed MO could be easily released in ethanol. The mesoporous nanocomposites were facile separated from solution under external magnetic force, and over 85% adsorption capacity for MO could be retained after five adsorption/desorption cycles.

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