Selective recognition of Triamterene in biological samples by molecularly imprinted monolithic column with a pseudo template employed
Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as func...
Saved in:
| Published in | Journal of separation science Vol. 36; no. 9-10; pp. 1501 - 1508 |
|---|---|
| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
Blackwell Publishing Ltd
01.05.2013
Wiley Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross‐linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 μmol/L and 132.28 μmol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples. |
|---|---|
| AbstractList | Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross-linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 μmol/L and 132.28 μmol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples.Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross-linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 μmol/L and 132.28 μmol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples. Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross-linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 µmol/L and 132.28 µmol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples. [PUBLICATION ABSTRACT] Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross-linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 μmol/L and 132.28 μmol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples. Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective recognition to Triamterene (TAT), whose structure was similar to that of MAM. Methacrylic acid and ethylene glycol dimethacrylate were applied as functional monomer and cross-linker, respectively, during the in situ polymerization process. Chromatographic behaviors were evaluated, the results indicated that the molecularly imprinted polymer monolithic column possessed excellent affinity and selectivity for TAT, and the imprinting factor was high up to 3.99 when 7:3 of ACN/water v/v was used as mobile phase. In addition, the dissociation constant and the binding sites were also determined by frontal chromatography as 134.31 mu mol/L and 132.28 mu mol/g, respectively, which demonstrated that the obtained molecularly imprinted polymer monolith had a high binding capacity and strong affinity ability to TAT. Furthermore, biological samples could be directly injected into the column and TAT was enriched with the optimized mobile phase. These assays gave recovery values higher than 91.60% with RSD values that were always less than 3.5%. The molecularly imprinted monolithic column greatly simplified experiment procedure and can be applied to preconcentration, purification, and analysis of TAT in biological samples. |
| Author | Shu, Ya-Ping Zhao, Xiao-Yun Zhang, Hong-Wu Liang, Zhen-Jie Liang, Yong |
| Author_xml | – sequence: 1 givenname: Xiao-Yun surname: Zhao fullname: Zhao, Xiao-Yun organization: School of Chemistry and Environment, South China Normal University, Guangzhou, P. R. China – sequence: 2 givenname: Hong-Wu surname: Zhang fullname: Zhang, Hong-Wu organization: School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, P. R. China – sequence: 3 givenname: Zhen-Jie surname: Liang fullname: Liang, Zhen-Jie organization: School of Chemistry and Environment, South China Normal University, Guangzhou, P. R. China – sequence: 4 givenname: Ya-Ping surname: Shu fullname: Shu, Ya-Ping organization: School of Chemistry and Environment, South China Normal University, Guangzhou, P. R. China – sequence: 5 givenname: Yong surname: Liang fullname: Liang, Yong email: liangy@scnu.edu.cn organization: School of Chemistry and Environment, South China Normal University, Guangzhou, P. R. China |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27382126$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/23424016$$D View this record in MEDLINE/PubMed |
| BookMark | eNqNkl2LEzEUhgdZcT_01ksJiLA3s-ZrMpNLqW5VyrrQlb0M6eRMTc0k3WTGdX6A_9uU1gpeCYGTkzzvC-fjvDjxwUNRvCT4imBM325Saq8oJvkQzJ8UZ0SQqpSM8JPjHYvT4jylDcakbiR-VpxSxinHRJwVv5bgoB3sD0AR2rD2drDBo9Chu2h1P0AED8h6tLLBhbVttUNJ91sHCa0m1IesHp2ObkK230brBzD51Qdnh2-2RW1wY-_RY86QRtsEowlogGygB0C7GCYwz4unnXYJXhziRfH1-sPd7GO5-DL_NHu3KNecUlY2VK8gV93xruOi67QESbkQlTTacKg7zMBwWhNNWGVA11gY3UjeGNlKbTC7KC73vtsYHkZIg-ptasE57SGMSRFOZSOqRvwHyipMKs65yOjrf9BNGKPPhWRDJiVt8mgy9epAjasejMrN6nWc1J9ZZODNAdApt7mL2rc2_eVq1lBCdxzfc4_WwXT8J1jtNkLtNkIdN0J9Xi5njDKWZeVeZtMAP48yHb8rUbO6Uvc3c7W4eX87F7dc3bPfwIi7bw |
| ContentType | Journal Article |
| Copyright | 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim 2014 INIST-CNRS 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| Copyright_xml | – notice: 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: 2014 INIST-CNRS – notice: 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. – notice: 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| DBID | BSCLL IQODW CGR CUY CVF ECM EIF NPM 7U5 8FD L7M 7X8 |
| DOI | 10.1002/jssc.201201104 |
| DatabaseName | Istex Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Solid State and Superconductivity Abstracts Technology Research Database Advanced Technologies Database with Aerospace MEDLINE - Academic |
| DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Technology Research Database Advanced Technologies Database with Aerospace Solid State and Superconductivity Abstracts MEDLINE - Academic |
| DatabaseTitleList | MEDLINE - Academic Technology Research Database MEDLINE Technology Research Database |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Engineering Chemistry |
| EISSN | 1615-9314 |
| EndPage | 1508 |
| ExternalDocumentID | 3091889001 23424016 27382126 JSSC3233 ark_67375_WNG_LNDPG6P4_W |
| Genre | article Evaluation Studies Journal Article |
| GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 1L6 1OC 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHBH AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCUV ABDBF ABIJN ABJNI ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACIWK ACPOU ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFZJQ AHBTC AI. AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BY8 CS3 D-E D-F DCZOG DPXWK DR2 DRFUL DRSTM DU5 EBD EJD F00 F01 F04 F5P FEDTE G-S G.N GNP GODZA H.T H.X HGLYW HHZ HVGLF HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TUS UB1 UPT VH1 W8V W99 WBFHL WBKPD WIH WIK WJL WOHZO WXSBR WYISQ XG1 XPP XV2 YQT ~IA ~KM ~WT AAHQN AAMNL AANHP AAYCA ACRPL ACUHS ACYXJ ADNMO AFWVQ ALVPJ AAMMB ADMLS AEFGJ AEYWJ AGHNM AGQPQ AGXDD AGYGG AIDQK AIDYY IQODW CGR CUY CVF ECM EIF NPM 1OB 7U5 8FD L7M 7X8 |
| ID | FETCH-LOGICAL-g4223-82abe002f4ff46ffa9e9246659dad4e7f03ed4271a135dea706da8948d9c9ad03 |
| IEDL.DBID | DR2 |
| ISSN | 1615-9306 1615-9314 |
| IngestDate | Sun Aug 24 04:03:31 EDT 2025 Fri Jul 11 12:33:03 EDT 2025 Wed Aug 13 06:19:25 EDT 2025 Mon Jul 21 05:53:46 EDT 2025 Mon Jul 21 09:13:59 EDT 2025 Wed Jan 22 16:52:13 EST 2025 Wed Oct 30 09:55:49 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 9-10 |
| Keywords | Biological fluid Chemical analysis Potassium sparing diuretic HPLC chromatography Selectivity Biological samples Blood Surface structure Affinity adsorbent Crosslinked copolymer Methacrylic acid copolymer Binding capacity Affinity chromatography Quantitative analysis Human Urine Scanning electron microscopy Healthy subject Characteristic Monolithic column Triamterene Ultraviolet detector Morphology Preparation Molecularly imprinted polymer Pseudo template Molecular recognition Radical copolymerization Blood serum Molecular imprinting |
| Language | English |
| License | CC BY 4.0 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-g4223-82abe002f4ff46ffa9e9246659dad4e7f03ed4271a135dea706da8948d9c9ad03 |
| Notes | ArticleID:JSSC3233 ark:/67375/WNG-LNDPG6P4-W istex:F9236569F33F9B4D238E6AFFD75A04ED9831D8F2 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Undefined-1 ObjectType-Feature-3 content type line 23 ObjectType-Feature-1 |
| PMID | 23424016 |
| PQID | 1439928104 |
| PQPubID | 105495 |
| PageCount | 8 |
| ParticipantIDs | proquest_miscellaneous_1429865860 proquest_miscellaneous_1350154446 proquest_journals_1439928104 pubmed_primary_23424016 pascalfrancis_primary_27382126 wiley_primary_10_1002_jssc_201201104_JSSC3233 istex_primary_ark_67375_WNG_LNDPG6P4_W |
| PublicationCentury | 2000 |
| PublicationDate | May 2013 |
| PublicationDateYYYYMMDD | 2013-05-01 |
| PublicationDate_xml | – month: 05 year: 2013 text: May 2013 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim – name: Germany |
| PublicationTitle | Journal of separation science |
| PublicationTitleAlternate | J. Sep. Science |
| PublicationYear | 2013 |
| Publisher | Blackwell Publishing Ltd Wiley Wiley Subscription Services, Inc |
| Publisher_xml | – name: Blackwell Publishing Ltd – name: Wiley – name: Wiley Subscription Services, Inc |
| References | Ventura, R., Segura, J., J. Chromatogr. B 1996, 687, 127-144. Lavignac, N., Allender, C. J., Brain, K. R., Anal. Chim. Acta 2004, 510, 139-145. Schweitz, L., Andersson, L. I., Nilsson, S., Anal. Chem. 1997, 69, 1179-1183. Watabe, Y., Kubo, T., Nishikawa, T., Fujita, T., Kaya, K., Hosoya, K., J. Chromatogr. A 2006, 1120, 252-259. Juana, R. F., Juan J. B. N., Isabel D. M., Maria J. R. G., J. Sep. Sci. 2005, 28, 658-664. Chen, Z. Y., Zhao, R., Shangguan, D. H., Liu, G. Q., Biomed. Chromatogr. 2005, 19, 533-538. Ensafi, A. A., Hajian, A., Anal. Sci. 2008, 24, 1449-1454. Mohammadpour, K., Sohrabi, M. R., Jourabchi, A., Talanta 2010, 81, 1821-1825. Watabe, Y., Kondo, T., Morita, M., Tanaka, N., Haginaka, J., Hosoya, K., J. Chromatogr. A 2004, 1032, 45-49. Yan, H. Y., Row, K. H., Int. J. Mol. Sci. 2006, 7, 155-178. Zarapkar, S.S., Athalye, K., Indian Drugs 1990, 28, 103-104. Sun, H. W., Qiao, F. X., J. Chromatogr. A 2008, 1212, 1-9. Ruiz-Angel, M. J., Torres-Lapasio, J. R., Garcia-Alvarez-Coque, M. C., J. Chromatogr. A 2004, 1022, 51-65. Matsui, J., Fujiwara, K., Takeuchi, T., Anal. Chem. 2000, 72, 1810-1813. Kubo, T., Hosoya, K., Watabe, Y., Ikegami, T., Tanaka, N., Sano, T., Kaya, K., J. Chromatogr. A 2003, 987, 389-394. Li, H., He, J. T., Liu, Q., Huo, Z. H., Liang, S., Liang, Y., J. Sep. Sci. 2011, 34, 542-547. Liu, H. Y., Row, K. H., Yang, G. L., J. Chromatogr. 2005, 61, 429-432. Arvand, M., Mousavi, M. F., Zanjanchi, M. A., Shamsipur, M., J. Pharm. Biomed. Anal. 2003, 33, 975-982. Wulff, G., Sarhan, A., Angew. Chem. Int. Ed. 1972, 11, 341. Yin, J. F., Yang, G. L., Chen, Y., J. Chromatogr. A 2005, 1090, 68-75. Martínez, E. J. L., Barrales, P. O., Díaz, A. M., Anal. Bioanal. Chem. 2005, 383, 797-803. Luis, M. L., Corujedo, S., Blanco, D., Fraga, J. M. G., Jimenez, A. I., Jimenez, F., Arias, J. J., Talanta 2002, 57, 223-231. Huang, X. D., Zou, H. F., Chen, X. M., Luo, Q. Z., Kong, L., J. Chromatogr. A 2003, 984, 273-282. Guchelaar, H. J., Chandi, L., Schouten, O., van den Brand, W. A., Anal. Chem. 1999, 363, 700-705. Matsui, J., Kato, T., Takeuchi, T., Suzuki, M., Yokoyama, K., Tamiya, E., Karube, I., Anal. Chem. 1993, 65, 2223-2224. Watanabe, F., Kubo, T., Kaya, K., Hosoya, K., J. Chromatogr. A 2009, 1216, 7402-7408 Ibanez, G. A., Escandar, G. M., Mansilla, A. E., Anal. Chim. Acta 2005, 538, 77-84. Hart, B. R., Rush, D. J., Shea, K. J., Am. Chem. Soc. 2000, 122, 460-465. Kempe, M., Mosbach, K., Anal. Lett. 1991, 24, 1137-1145. Andersson, L. I., Paprica, A., Arvidsson, T., Chromatographia 1997, 46, 57-62. Kempe, M., Mosbach, K., J. Chromatogr. A 1995, 694, 3-13. Sun, H. W., Qiao, F. X., Liu, G. Y., J. Chromatogr. A 2006, 1134, 194-200. Kargosha, K., Sarrafi, A. H. M., J. Pharm. Biomed. Anal. 2001, 26, 273-279. 2008; 1212 2002; 57 1993; 65 1997; 69 1997; 46 2006; 7 2000; 72 1999; 363 2005; 538 2001; 26 2011; 34 2004; 1022 1995; 694 2005; 61 1996; 687 2010; 81 2005; 28 2006; 1120 2003; 33 2009; 1216 2005; 19 2003; 987 2005; 383 2004; 510 2005; 1090 1991; 24 1990; 28 2008; 24 2004; 1032 2000; 122 2006; 1134 2003; 984 1972; 11 |
| References_xml | – reference: Liu, H. Y., Row, K. H., Yang, G. L., J. Chromatogr. 2005, 61, 429-432. – reference: Ruiz-Angel, M. J., Torres-Lapasio, J. R., Garcia-Alvarez-Coque, M. C., J. Chromatogr. A 2004, 1022, 51-65. – reference: Sun, H. W., Qiao, F. X., J. Chromatogr. A 2008, 1212, 1-9. – reference: Kargosha, K., Sarrafi, A. H. M., J. Pharm. Biomed. Anal. 2001, 26, 273-279. – reference: Watanabe, F., Kubo, T., Kaya, K., Hosoya, K., J. Chromatogr. A 2009, 1216, 7402-7408 – reference: Watabe, Y., Kondo, T., Morita, M., Tanaka, N., Haginaka, J., Hosoya, K., J. Chromatogr. A 2004, 1032, 45-49. – reference: Luis, M. L., Corujedo, S., Blanco, D., Fraga, J. M. G., Jimenez, A. I., Jimenez, F., Arias, J. J., Talanta 2002, 57, 223-231. – reference: Matsui, J., Kato, T., Takeuchi, T., Suzuki, M., Yokoyama, K., Tamiya, E., Karube, I., Anal. Chem. 1993, 65, 2223-2224. – reference: Guchelaar, H. J., Chandi, L., Schouten, O., van den Brand, W. A., Anal. Chem. 1999, 363, 700-705. – reference: Juana, R. F., Juan J. B. N., Isabel D. M., Maria J. R. G., J. Sep. Sci. 2005, 28, 658-664. – reference: Huang, X. D., Zou, H. F., Chen, X. M., Luo, Q. Z., Kong, L., J. Chromatogr. A 2003, 984, 273-282. – reference: Hart, B. R., Rush, D. J., Shea, K. J., Am. Chem. Soc. 2000, 122, 460-465. – reference: Martínez, E. J. L., Barrales, P. O., Díaz, A. M., Anal. Bioanal. Chem. 2005, 383, 797-803. – reference: Ensafi, A. A., Hajian, A., Anal. Sci. 2008, 24, 1449-1454. – reference: Yan, H. Y., Row, K. H., Int. J. Mol. Sci. 2006, 7, 155-178. – reference: Chen, Z. Y., Zhao, R., Shangguan, D. H., Liu, G. Q., Biomed. Chromatogr. 2005, 19, 533-538. – reference: Arvand, M., Mousavi, M. F., Zanjanchi, M. A., Shamsipur, M., J. Pharm. Biomed. Anal. 2003, 33, 975-982. – reference: Kubo, T., Hosoya, K., Watabe, Y., Ikegami, T., Tanaka, N., Sano, T., Kaya, K., J. Chromatogr. A 2003, 987, 389-394. – reference: Ventura, R., Segura, J., J. Chromatogr. B 1996, 687, 127-144. – reference: Matsui, J., Fujiwara, K., Takeuchi, T., Anal. Chem. 2000, 72, 1810-1813. – reference: Lavignac, N., Allender, C. J., Brain, K. R., Anal. Chim. Acta 2004, 510, 139-145. – reference: Sun, H. W., Qiao, F. X., Liu, G. Y., J. Chromatogr. A 2006, 1134, 194-200. – reference: Schweitz, L., Andersson, L. I., Nilsson, S., Anal. Chem. 1997, 69, 1179-1183. – reference: Andersson, L. I., Paprica, A., Arvidsson, T., Chromatographia 1997, 46, 57-62. – reference: Zarapkar, S.S., Athalye, K., Indian Drugs 1990, 28, 103-104. – reference: Kempe, M., Mosbach, K., Anal. Lett. 1991, 24, 1137-1145. – reference: Kempe, M., Mosbach, K., J. Chromatogr. A 1995, 694, 3-13. – reference: Watabe, Y., Kubo, T., Nishikawa, T., Fujita, T., Kaya, K., Hosoya, K., J. Chromatogr. A 2006, 1120, 252-259. – reference: Li, H., He, J. T., Liu, Q., Huo, Z. H., Liang, S., Liang, Y., J. Sep. Sci. 2011, 34, 542-547. – reference: Mohammadpour, K., Sohrabi, M. R., Jourabchi, A., Talanta 2010, 81, 1821-1825. – reference: Yin, J. F., Yang, G. L., Chen, Y., J. Chromatogr. A 2005, 1090, 68-75. – reference: Ibanez, G. A., Escandar, G. M., Mansilla, A. E., Anal. Chim. Acta 2005, 538, 77-84. – reference: Wulff, G., Sarhan, A., Angew. Chem. Int. Ed. 1972, 11, 341. – volume: 33 start-page: 975 year: 2003 end-page: 982 publication-title: J. Pharm. Biomed. Anal. – volume: 26 start-page: 273 year: 2001 end-page: 279 publication-title: J. Pharm. Biomed. Anal. – volume: 28 start-page: 103 year: 1990 end-page: 104 publication-title: Indian Drugs – volume: 987 start-page: 389 year: 2003 end-page: 394 publication-title: J. Chromatogr. A – volume: 383 start-page: 797 year: 2005 end-page: 803 publication-title: Anal. Bioanal. Chem. – volume: 24 start-page: 1137 year: 1991 end-page: 1145 publication-title: Anal. Lett. – volume: 1032 start-page: 45 year: 2004 end-page: 49 publication-title: J. Chromatogr. A – volume: 28 start-page: 658 year: 2005 end-page: 664 publication-title: J. Sep. Sci. – volume: 1212 start-page: 1 year: 2008 end-page: 9 publication-title: J. Chromatogr. A – volume: 1022 start-page: 51 year: 2004 end-page: 65 publication-title: J. Chromatogr. A – volume: 19 start-page: 533 year: 2005 end-page: 538 publication-title: Biomed. Chromatogr. – volume: 1120 start-page: 252 year: 2006 end-page: 259 publication-title: J. Chromatogr. A – volume: 61 start-page: 429 year: 2005 end-page: 432 publication-title: J. Chromatogr. – volume: 46 start-page: 57 year: 1997 end-page: 62 publication-title: Chromatographia – volume: 72 start-page: 1810 year: 2000 end-page: 1813 publication-title: Anal. Chem. – volume: 510 start-page: 139 year: 2004 end-page: 145 publication-title: Anal. Chim. Acta – volume: 538 start-page: 77 year: 2005 end-page: 84 publication-title: Anal. Chim. Acta – volume: 24 start-page: 1449 year: 2008 end-page: 1454 publication-title: Anal. Sci. – volume: 694 start-page: 3 year: 1995 end-page: 13 publication-title: J. Chromatogr. A – volume: 1216 start-page: 7402 year: 2009 end-page: 7408 publication-title: J. Chromatogr. A – volume: 7 start-page: 155 year: 2006 end-page: 178 publication-title: Int. J. Mol. Sci. – volume: 69 start-page: 1179 year: 1997 end-page: 1183 publication-title: Anal. Chem. – volume: 81 start-page: 1821 year: 2010 end-page: 1825 publication-title: Talanta – volume: 1090 start-page: 68 year: 2005 end-page: 75 publication-title: J. Chromatogr. A – volume: 363 start-page: 700 year: 1999 end-page: 705 publication-title: Anal. Chem. – volume: 11 start-page: 341 year: 1972 publication-title: Angew. Chem. Int. Ed. – volume: 65 start-page: 2223 year: 1993 end-page: 2224 publication-title: Anal. Chem. – volume: 34 start-page: 542 year: 2011 end-page: 547 publication-title: J. Sep. Sci. – volume: 122 start-page: 460 year: 2000 end-page: 465 publication-title: Am. Chem. Soc. – volume: 687 start-page: 127 year: 1996 end-page: 144 publication-title: J. Chromatogr. B – volume: 57 start-page: 223 year: 2002 end-page: 231 publication-title: Talanta – volume: 1134 start-page: 194 year: 2006 end-page: 200 publication-title: J. Chromatogr. A – volume: 984 start-page: 273 year: 2003 end-page: 282 publication-title: J. Chromatogr. A |
| SSID | ssj0017890 |
| Score | 2.1221511 |
| Snippet | Melamine (MAM) was employed as a pseudo template to prepare a molecularly imprinted polymer monolithic column which presents the ability of selective... |
| SourceID | proquest pubmed pascalfrancis wiley istex |
| SourceType | Aggregation Database Index Database Publisher |
| StartPage | 1501 |
| SubjectTerms | Affinity Analysis Analytical chemistry Biological Biological and medical sciences Biological samples Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography Chromatography - instrumentation Chromatography - methods Columns (process) Columns (structural) Exact sciences and technology General pharmacology Humans Imprinted polymers Medical sciences Molecular chemistry Molecular Imprinting Molecularly imprinted polymer Monolithic column Other chromatographic methods Pharmacology. Drug treatments Polymerization Polymers Polymers - chemical synthesis Polymers - chemistry Pseudo template Recognition Triamterene Triamterene - blood Triamterene - urine Triazines - chemistry |
| Title | Selective recognition of Triamterene in biological samples by molecularly imprinted monolithic column with a pseudo template employed |
| URI | https://api.istex.fr/ark:/67375/WNG-LNDPG6P4-W/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjssc.201201104 https://www.ncbi.nlm.nih.gov/pubmed/23424016 https://www.proquest.com/docview/1439928104 https://www.proquest.com/docview/1350154446 https://www.proquest.com/docview/1429865860 |
| Volume | 36 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Nb9QwELVQL8CBj_KVUiojIW5uHcdxkiNaaKsKVhXbqr1ZTmyXpd2kanalljv_mxlnk3YRQkJcEzuKPc_jZ3v8hpB3RnBV8VQwp0rBABScFaWsWGy8jS03lofNnC9jtX8sD07T0zu3-Dt9iGHDDUdG8Nc4wE3Z7tyKhn5vW5QgjMMMhoKgGLCFrOjroB8V4y1PXHHBtM0KIMe9aiMXO6vVgZpir15jaKRpoXd8l9biT7xzlcaGeWj3MTF9C7rwk_Ptxbzcrn78Ju74P018Qh4tSSr90KHqKbnn6nVyf9TnhlsnD-_IGD4jPychmQ74TTrEIzU1bTw9AnjP5iEBC53WtFN8QljQ1qAscUvLGzrrM_Re3NDpDDcagQXD0xpD875NK1qhB60pbhlTQy9bt7ANRU2tCyDK1HU5i-1zcrz76Wi0z5bpHdiZBFLCcmFKBw310nupvDeFg8WgUmlhjZUu8zxxVoosNnGSWmcyrqzJC5nboioARMkLslY3tXtFKHxKlEI4ayopXVoYcFuFlZWymSirPI3I-2BefdlJeGhzdY4RbVmqT8Z7-vP44-GeOpT6JCJbK_YfKuANJpjlVUQ2e0Do5WhvYfmE8r452Cgib4fXYBI8fDG1axZQBk9wUwmr77-UAXKQAyVUPCIvO7Dd_kAigXzFUJsFyAwvOt1poREsegCLPphMRolIko1_LP-aPBAh4wfGdG6StfnVwr0B3jUvt8LY-gUl-ilV |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3Pb9MwFH6CcRg78GOwERjDSIhbtsRxnOSIClsZXTXRTuNmObEDZWs6La3EuPN_857TZBQhJMQ1saPY_mx_7_n5ewCvNA9kEcTctzLnPoIi8LNcFH6oSxOaQJvAOXOOh7J_Ko4-xW00Id2FafQhOocbzQy3XtMEJ4f0_o1q6Ne6Jg3C0G1h4jbcobTezqr62ClIhXTPk2wu3Lj9DOlxq9sY8P3V-khOqV-_UXCkrrF_yiaxxZ-Y5yqRdTvRwX3I2zY0ASjne4t5vld8_03e8b8a-QDuLXkqe9MA6yHcstUmrPfa9HCbsPGLkuEj-DFy-XRw6WRdSNKsYrOSjRHh07nLwcImFWtEnwgZrNakTFyz_JpN2yS9F9dsMiVfIxJhfFpRdN6XScEKWkQrRl5jptllbRdmxkhW6wK5MrNN2mLzGE4P3o17fX-Z4cH_LJCX-CnXucWGlqIshSxLnVm0B6WMM6ONsEkZRNYInoQ6jGJjdRJIo9NMpCYrMsRRtAVr1ayyT4Dhp3jOuTW6EMLGmcaVKzOikCbheZHGHrx246suGxUPpa_OKagtidXZ8FANhm9PDuWJUGce7K4AoKtAl5hwo5ce7LSIUMsJX6MFRQq_KY6RBy-71zgkdP6iKztbYBk6xI0FGuB_KYP8IEVWKAMPthu03fxAJJB_hVjbd5jpXjTS01wRWFQHFnU0GvUiHkVP_7H8C1jvj48HavB--OEZ3OUuAQiFeO7A2vxqYZ8jDZvnu26i_QSX6C1w |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3Pb9MwFLZgSDAO_BgDAmMYCXHL5jiOkxxRSzfGqCq6abtZTmyzsjWpllZi3Pm_eS9pshUhJMQ1saPY7_PzZ_v5e4S81ZzJnEXctzLjPoCC-Wkmcj_QzgSGacPqzZzPQ7l_LA5Oo9Mbt_gbfYhuww1HRu2vcYDPjNu9Fg39VlUoQRjUM5i4Te4IyRLEdf9LJyAV4DVPXHLBvO2nwI5b2UbGd1frAzfFbv2OsZG6gu5xTV6LPxHPVR5bT0SDh0S3TWjiT853FvNsJ__xm7rj_7TxEXmwZKn0fQOrx-SWLTbIvV6bHG6D3L-hY_iE_BzX2XTAcdIuIKksaOnoEeB7Oq8zsNBJQRvJJ8QFrTTqElc0u6LTNkXvxRWdTHGnEWgwPC0wNu9sktMcXWhBcc-Yajqr7MKUFEW1LoApU9skLTab5Hjw4ai37y_zO_hfBbASP-E6s9BQJ5wT0jmdWlgNShmlRhthY8dCawSPAx2EkbE6ZtLoJBWJSfMUUBQ-JWtFWdjnhMKneMa5NToXwkapBr-VGpFLE_MsTyKPvKvNq2aNhofSl-cY0hZH6mS4pw6H_dGeHAl14pHtFft3FfAKE0zz0iNbLSDUcrhXsH5Cfd8EbOSRN91rMAmevujClgsog0e4kYDl91_KADtIgBNK5pFnDdiufyAUwL4CqO3XkOleNMLTXCFYVAcWdTAe90Iehi_-sfxrcnfUH6jDj8NPL8k6r7N_YHznFlmbXy7sK-Bg82y7Hma_ABK0LCg |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Selective+recognition+of+Triamterene+in+biological+samples+by+molecularly+imprinted+monolithic+column+with+a+pseudo+template+employed&rft.jtitle=Journal+of+separation+science&rft.au=Zhao%2C+Xiao-Yun&rft.au=Zhang%2C+Hong-Wu&rft.au=Liang%2C+Zhen-Jie&rft.au=Shu%2C+Ya-Ping&rft.date=2013-05-01&rft.eissn=1615-9314&rft.volume=36&rft.issue=9-10&rft.spage=1501&rft_id=info:doi/10.1002%2Fjssc.201201104&rft_id=info%3Apmid%2F23424016&rft.externalDocID=23424016 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1615-9306&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1615-9306&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1615-9306&client=summon |