Journal of Chromatography B: Biomedical Sciences and Applications最新文献

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Simultaneous determination of fifteen low-dosed benzodiazepines in human urine by solid-phase extraction and gas chromatography–mass spectrometry 固相萃取-气相色谱-质谱联用法同时测定人尿中15种低剂量苯二氮卓类药物
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00419-4
D Borrey , E Meyer , W Lambert , C Van Peteghem , A.P De Leenheer
{"title":"Simultaneous determination of fifteen low-dosed benzodiazepines in human urine by solid-phase extraction and gas chromatography–mass spectrometry","authors":"D Borrey ,&nbsp;E Meyer ,&nbsp;W Lambert ,&nbsp;C Van Peteghem ,&nbsp;A.P De Leenheer","doi":"10.1016/S0378-4347(01)00419-4","DOIUrl":"10.1016/S0378-4347(01)00419-4","url":null,"abstract":"<div><p>A gas chromatographic–mass spectrometric method was developed for the simultaneous analysis of 15 low-dosed benzodiazepines, both parent compounds and their corresponding metabolites, in human urine. The target compounds are alprazolam, α-hydroxyalprazolam, 4-hydroxyalprazolam, flunitrazepam, 7-aminoflunitrazepam, desmethylflunitrazepam, flurazepam, hydroxyethylflurazepam, nitrogen-desalkylflurazepam, ketazolam, oxazepam, lormetazepam, lorazepam, triazolam and α-hydroxytriazolam. Nitrogen-methylclonazepam is used as the internal standard. The urine sample preparation involves enzymatic hydrolysis of the conjugated metabolites with <em>Helix pomatia</em> β-glucuronidase for 1 h at 56°C followed by solid-phase extraction on a phenyl-type column. The extracted benzodiazepines are subsequently analyzed on a polydimethylsiloxane column using on-column injection to enhance sensitivity. The extraction efficiency exceeded 80% for all compounds except for oxazepam, lorazepam and 4-hydroxyalprazolam which had recoveries of about 60%. The LODs ranged from 13 to 30 ng/ml in the scan mode and from 1.0 to 1.7 ng/ml in the selected ion monitoring (SIM) mode. Linear calibration curves were obtained in the concentration ranges from 50 to 1000 ng/ml in the scan mode and from 5 to 100 ng/ml in the SIM mode. The within-day and day-to-day relative standard deviations at three different concentrations never exceeded 15%.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00419-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80549491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 58
Gas chromatographic–mass spectrometric confirmation of atractyloside in a patient poisoned with Callilepis laureola 气相色谱-质谱联用确证月桂叶中毒患者中含有白术皂苷
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00410-8
J.B Laurens , L.C Bekker , V Steenkamp , M.J Stewart
{"title":"Gas chromatographic–mass spectrometric confirmation of atractyloside in a patient poisoned with Callilepis laureola","authors":"J.B Laurens ,&nbsp;L.C Bekker ,&nbsp;V Steenkamp ,&nbsp;M.J Stewart","doi":"10.1016/S0378-4347(01)00410-8","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00410-8","url":null,"abstract":"<div><p>The South African traditional remedy <em>Impila</em> (<em>Callilepis laureola</em>) contains the mitochondrial toxin atractyloside. The plant is sold widely and continues to lead to fatalities in patients. We describe, for the first time, a simple GC–MS procedure for the identification of atractyloside, which we have applied to the gastric washing from a poisoned patient and to extracts of <em>Impila</em> tuber.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00410-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91741845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 29
Highly sensitive analysis of the antifolate pemetrexed sodium, a new cancer agent, in human plasma and urine by high-performance liquid chromatography 高效液相色谱法分析新型抗癌药物抗叶酸培美曲塞钠在人血浆和尿液中的高灵敏度
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00406-6
Laurent P Rivory, Stephen J Clarke, Michael Boyer, James F Bishop
{"title":"Highly sensitive analysis of the antifolate pemetrexed sodium, a new cancer agent, in human plasma and urine by high-performance liquid chromatography","authors":"Laurent P Rivory,&nbsp;Stephen J Clarke,&nbsp;Michael Boyer,&nbsp;James F Bishop","doi":"10.1016/S0378-4347(01)00406-6","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00406-6","url":null,"abstract":"<div><p>A reversed-phase high-performance liquid chromatography method was developed and validated for the quantitation of pemetrexed (LY231514, ALIMTA) in human urine and plasma. Plasma samples were spiked with the internal standard lometrexol and extracted using Certify II columns. Pemetrexed was assayed in diluted urine by an external calibration method. A C<sub>8</sub> column was used for the separation of analytes with a mobile phase composed of sodium formate buffer and acetonitrile. Between- and within-day precision and accuracy were acceptable down to the limit of quantitation of 5 ng/ml in plasma. This method was used successfully for an investigation of the disposition of pemetrexed in patients receiving 500 mg/m<sup>2</sup> as a 10-min infusion.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00406-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90033156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
Determination of sodium cromoglycate in human plasma by liquid chromatography–mass spectrometry in the turbo ion spray mode 涡流喷雾液相色谱-质谱法测定人血浆中氨基甘氨酸钠
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00420-0
M.L Ozoux , J Girault , J.M Malgouyat , O Pasquier
{"title":"Determination of sodium cromoglycate in human plasma by liquid chromatography–mass spectrometry in the turbo ion spray mode","authors":"M.L Ozoux ,&nbsp;J Girault ,&nbsp;J.M Malgouyat ,&nbsp;O Pasquier","doi":"10.1016/S0378-4347(01)00420-0","DOIUrl":"10.1016/S0378-4347(01)00420-0","url":null,"abstract":"<div><p>A highly sensitivity liquid chromatography–tandem mass spectrometry method has been developed for the quantitation of sodium cromoglycate (SCG) in human plasma. The method was validated over a linear range of 0.100–50.0 ng/ml, using <sup>13</sup>C<sub>4</sub> sodium cromoglycate as the internal standard. Compounds were extracted from 1.0 ml of lithium heparin plasma by methanol elution of C<sub>18</sub> solid-phase extraction cartridges. The dried residue was reconstituted with 100 μl of 0.01 N HCl, and 30 μl was injected onto the LC–MS–MS system. Chromatographic separation was achieved on a C8 (3.5 μm) column with an isocratic mobile phase of methanol–water–0.5 <em>M</em> ammonium acetate (35:64.8:0.2, v/v/v). The analytes were detected with a PE Sciex API 3000 mass spectrometer using turbo ion spray with positive ionization. Ions monitored in the multiple reaction monitoring (MRM) mode were <em>m</em>/<em>z</em> 469.2 (precursor ion) to <em>m</em>/<em>z</em> 245.1 (product ion) for SCG and <em>m</em>/<em>z</em> 473.2 (precursor ion) to <em>m</em>/<em>z</em> 247.1 (product ion) for <sup>13</sup>C<sub>4</sub> SCG (I.S.). The average recoveries of SCG and the I.S. from human plasma were 91 and 87%, respectively. The low limit of quantitation was 0.100 ng/ml. Results from a 4-day validation study demonstrated excellent precision (C.V.% values were between 1.9 and 6.5%) and accuracy (−5.4 to −1.2%) across the calibration range of 0.100–50.0 ng/ml.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00420-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91220981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Retention of bile salts in micellar electrokinetic chromatography: relation of capacity factor to octanol-water partition coefficient and critical micellar concentration. 胶束电动色谱中胆盐的保留:容量因子与辛醇-水分配系数和临界胶束浓度的关系。
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00417-0
S. Lucangioli, C. Carducci, V. Tripodi, E. Kenndler
{"title":"Retention of bile salts in micellar electrokinetic chromatography: relation of capacity factor to octanol-water partition coefficient and critical micellar concentration.","authors":"S. Lucangioli, C. Carducci, V. Tripodi, E. Kenndler","doi":"10.1016/S0378-4347(01)00417-0","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00417-0","url":null,"abstract":"","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87915174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 32
Author Index Vol. 765 作者索引卷765
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00535-7
{"title":"Author Index Vol. 765","authors":"","doi":"10.1016/S0378-4347(01)00535-7","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00535-7","url":null,"abstract":"","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00535-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136419945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preliminary application of liquid chromatography–electrospray-ionization mass spectrometry to the detection of 5-methyltetrahydrofolic acid monoglutamate in human plasma 液相色谱-电喷雾-电离质谱法检测人血浆中5-甲基四氢叶酸单谷氨酸的初步应用
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00412-1
Bryant C Nelson, Joseph J Dalluge, Sam A Margolis
{"title":"Preliminary application of liquid chromatography–electrospray-ionization mass spectrometry to the detection of 5-methyltetrahydrofolic acid monoglutamate in human plasma","authors":"Bryant C Nelson,&nbsp;Joseph J Dalluge,&nbsp;Sam A Margolis","doi":"10.1016/S0378-4347(01)00412-1","DOIUrl":"10.1016/S0378-4347(01)00412-1","url":null,"abstract":"<div><p>Liquid chromatography (LC) in direct combination with mass spectrometry (MS) has been shown to be a good analytical technique for the selective separation and detection of labile folate monoglutamates. Reversed-phase LC and electrospray-ionization MS conditions were developed and optimized for the separation and detection of 5-methyltetrahydrofolic acid, 5-formyl tetrahydrofolic acid, tetrahydrofolic acid, dihydrofolic acid and folic acid in aqueous samples. Representative and reproducible positive ion mass spectra were generated for each folate under mild MS conditions. The selective MS detection and identification of endogenous 5-methyltetrahydrofolic acid in human plasma was accomplished through the development of a straightforward C<sub>18</sub>-based solid-phase extraction procedure. This procedure allows for the qualitative assessment of 5-methyltetrahydrofolic acid in plasma. Based upon an isotope-dilution internal standard calibration study with standards, the LC–MS limit of quantitation for 5M-THF was estimated to be 0.39 ng/ml.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00412-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76425194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 31
Improved high-performance liquid chromatographic method to estimate aminosugars and its application to glycosaminoglycan determination in plasma and serum 改进高效液相色谱法测定氨基糖及其在血浆和血清中糖胺聚糖测定中的应用
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00427-3
Giuseppe M Campo , Salvatore Campo , Alida M Ferlazzo , Rosalia Vinci , Alberto Calatroni
{"title":"Improved high-performance liquid chromatographic method to estimate aminosugars and its application to glycosaminoglycan determination in plasma and serum","authors":"Giuseppe M Campo ,&nbsp;Salvatore Campo ,&nbsp;Alida M Ferlazzo ,&nbsp;Rosalia Vinci ,&nbsp;Alberto Calatroni","doi":"10.1016/S0378-4347(01)00427-3","DOIUrl":"10.1016/S0378-4347(01)00427-3","url":null,"abstract":"<div><p>An improved isocratic high-performance liquid chromatography (HPLC) method for the analysis of <span>l</span>-(−)-fucose, <span>d</span>-(+)-galactosamine, <span>d</span>-(+)-glucosamine, <span>d</span>-(+)-galactose, obtained by hydrolysis of glycosaminoglycans (GAGs) and <span>d</span>-(+)-glucose and <span>d</span>-(+)-mannose is described. The presence in circulation of GAGs, acid polysaccharide sequences of alternate monosaccharide units, aminosugar and uronic acid (galactose in keratan sulfate), has been measured in terms of their sugar components. To evaluate concentration of these circulating sugars we considered blood samples obtained from healthy humans. Plasma or serum was filtered through weak anion-exchange Ecteola-cellulose either untreated or after mild alkaline treatment. GAGs adhering to resin were recovered by salt elution, and desalted on Bio-Gel P-2 resin. GAG fractionation by charge was carried out on a strong anion exchanger. GAG composition was evaluated in terms of galactose and aminosugars, measured in HPLC by the proposed procedure using anion-exchange resin and pulsed amperometric detection. The mobile phase consisted of 0.02 <em>M</em> NaOH and elution was carried out at flow-rate of 1.0 ml/min. The amperometric detector was set as follows: <em>t</em><sub>1</sub> (0.5 s), <em>E</em><sub>1</sub> (+0.1 V); <em>t</em><sub>2</sub> (0.09 s), <em>E</em><sub>2</sub> (+0.6 V); <em>t</em><sub>3</sub> (0.05 s), <em>E</em><sub>3</sub> (−0.6 V). The analysis required 14 min. Calibration standard curves for the six analytes were linear from 0.25 to 40 μ<em>M</em>. RSD values for intra- and inter-day variabilities were ≤5.3% at concentrations between 0.25 and 40 μ<em>M</em>. Accuracy, expressed as percentage error, ranged from −16 to 14%. The method was specific and sensitive with quantitation limits of 1 pmol for <span>l</span>-(−)-fucose, <span>d</span>-galactosamine and <span>d</span>-glucosamine, 3 pmol for <span>d</span>-(+)-galactose and <span>d</span>-(+)-glucose and 5 pmol for <span>d</span>-(+)-mannose. The results of the assay showed higher GAG concentrations in serum than in plasma.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00427-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76837619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 42
Retention of bile salts in micellar electrokinetic chromatography: relation of capacity factor to octanol–water partition coefficient and critical micellar concentration 胶束电动色谱中胆盐的保留:容量因子与辛醇-水分配系数和临界胶束浓度的关系
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00417-0
Silvia E Lucangioli , Clyde N Carducci , Valeria P Tripodi , Ernst Kenndler
{"title":"Retention of bile salts in micellar electrokinetic chromatography: relation of capacity factor to octanol–water partition coefficient and critical micellar concentration","authors":"Silvia E Lucangioli ,&nbsp;Clyde N Carducci ,&nbsp;Valeria P Tripodi ,&nbsp;Ernst Kenndler","doi":"10.1016/S0378-4347(01)00417-0","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00417-0","url":null,"abstract":"<div><p>The capacity factors of 16 anionic cholates (from six bile salts, including their glyco- and tauro-conjugates) were determined in a micellar electrokinetic chromatography (MEKC) system consisting of buffer, pH 7.5 (phosphate–boric acid; 20 mmol/l) with 50 mmol/l sodium dodecyl sulfate (SDS) as micelle former and 10% acetonitrile as organic modifier. The capacity factors of the fully dissociated, negatively charged analytes (ranging between 0.2 and 60) were calculated from their mobilities, with a reference background electrolyte (BGE) without SDS representing “free” solution. For comparison, the capacity factors were derived for a second reference BGE where the SDS concentration (5 mmol/l) is close to the critical micellar concentration (CMC). The capacity factors are compared with the logarithm of the octanol–water partition coefficient, log <em>P</em><sub>OW</sub>, as measure for lipophilicity. Clear disagreement between these two parameters is found especially for epimeric cholates with the hydroxy group in position 7. In contrast, fair relation between the capacity factor of the analytes and their CMC is observed both depending strongly on the orientation of the OH groups, and tauro-conjugation as well. In this respect the retention behaviour of the bile salts in MEKC seems to reflect their role as detergents in living systems, and might serve as model parameter beyond lipophilicity.</p></div>","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0378-4347(01)00417-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91741844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 32
Highly sensitive analysis of the antifolate pemetrexed sodium, a new cancer agent, in human plasma and urine by high-performance liquid chromatography. 高效液相色谱法分析新型抗癌药物抗叶酸培美曲塞钠在人血浆和尿液中的高灵敏度。
Journal of Chromatography B: Biomedical Sciences and Applications Pub Date : 2001-12-25 DOI: 10.1016/S0378-4347(01)00406-6
L. Rivory, S. Clarke, M. Boyer, J. Bishop
{"title":"Highly sensitive analysis of the antifolate pemetrexed sodium, a new cancer agent, in human plasma and urine by high-performance liquid chromatography.","authors":"L. Rivory, S. Clarke, M. Boyer, J. Bishop","doi":"10.1016/S0378-4347(01)00406-6","DOIUrl":"https://doi.org/10.1016/S0378-4347(01)00406-6","url":null,"abstract":"","PeriodicalId":15463,"journal":{"name":"Journal of Chromatography B: Biomedical Sciences and Applications","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2001-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75764967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 21
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