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Comparison between the binding of chlorpheniramine maleate to poly(sodium 4-styrenesulfonate) and the binding to other polyelectrolytes
The interactions of the antihistaminic drug chlorpheniramine maleate (CPM) with the negatively charged polyelectrolytes poly(sodium 4-styrenesulfonate) (PSS) and poly(acrylic acid) (PAA) are studied by the washing method of the diafiltration technique at conditions simulating those of the small inte...
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Published in: | Polymer (Guilford) 2005-08, Vol.46 (18), p.7240-7245 |
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creator | Moreno-Villoslada, Ignacio Oyarzún, Felipe Miranda, Víctor Hess, Susan Rivas, Bernabé L. |
description | The interactions of the antihistaminic drug chlorpheniramine maleate (CPM) with the negatively charged polyelectrolytes poly(sodium 4-styrenesulfonate) (PSS) and poly(acrylic acid) (PAA) are studied by the washing method of the diafiltration technique at conditions simulating those of the small intestine such as pH 7.5 and 0.13
M NaCl. The results are compared with those already reported involving other pharmacologically important polyelectrolytes such as alginic acid (ALG), carboxymethylcellulose (CMC), and κ- and ι-carrageenan (κ- and ι-CAR). As in the case of ALG, CMC, and CAR, interactions of CPM with PAA appear to be electrostatic and are cleaved in the presence of 0.13
M NaCl. On the contrary, apart from electrostatic interactions, additional interactions are found with PSS and residual interactions are kept in the presence of 0.13
M NaCl, a fact that may be attributed to π–π interactions and hydrophobic forces. The effect of the addition of 4
M urea, branched poly(ethyleneimine) (BPEI), and poly(vinylpyrrolidone) (PVP) is also studied. The addition of urea 4
M or 0.001
M BPEI produces a decrease on the amounts of counterions bound to PSS at infinite elution, while the addition of PVP does not produce any change on the diafiltration profiles. |
doi_str_mv | 10.1016/j.polymer.2005.06.033 |
format | article |
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M NaCl. The results are compared with those already reported involving other pharmacologically important polyelectrolytes such as alginic acid (ALG), carboxymethylcellulose (CMC), and κ- and ι-carrageenan (κ- and ι-CAR). As in the case of ALG, CMC, and CAR, interactions of CPM with PAA appear to be electrostatic and are cleaved in the presence of 0.13
M NaCl. On the contrary, apart from electrostatic interactions, additional interactions are found with PSS and residual interactions are kept in the presence of 0.13
M NaCl, a fact that may be attributed to π–π interactions and hydrophobic forces. The effect of the addition of 4
M urea, branched poly(ethyleneimine) (BPEI), and poly(vinylpyrrolidone) (PVP) is also studied. The addition of urea 4
M or 0.001
M BPEI produces a decrease on the amounts of counterions bound to PSS at infinite elution, while the addition of PVP does not produce any change on the diafiltration profiles.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.06.033</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Biological and medical sciences ; Chlorpheniramine maleate ; Exact sciences and technology ; General pharmacology ; Medical sciences ; Organic polymers ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Physicochemistry of polymers ; Properties and characterization ; Solution and gel properties ; Ultrafiltration-diafiltration ; Water-soluble polymers</subject><ispartof>Polymer (Guilford), 2005-08, Vol.46 (18), p.7240-7245</ispartof><rights>2005 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-27ca4b60f1e8ed2c011958136e20c3e2cf1d51e87e5540aa0f0c3ae117eddbe33</citedby><cites>FETCH-LOGICAL-c432t-27ca4b60f1e8ed2c011958136e20c3e2cf1d51e87e5540aa0f0c3ae117eddbe33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16999737$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Moreno-Villoslada, Ignacio</creatorcontrib><creatorcontrib>Oyarzún, Felipe</creatorcontrib><creatorcontrib>Miranda, Víctor</creatorcontrib><creatorcontrib>Hess, Susan</creatorcontrib><creatorcontrib>Rivas, Bernabé L.</creatorcontrib><title>Comparison between the binding of chlorpheniramine maleate to poly(sodium 4-styrenesulfonate) and the binding to other polyelectrolytes</title><title>Polymer (Guilford)</title><description>The interactions of the antihistaminic drug chlorpheniramine maleate (CPM) with the negatively charged polyelectrolytes poly(sodium 4-styrenesulfonate) (PSS) and poly(acrylic acid) (PAA) are studied by the washing method of the diafiltration technique at conditions simulating those of the small intestine such as pH 7.5 and 0.13
M NaCl. The results are compared with those already reported involving other pharmacologically important polyelectrolytes such as alginic acid (ALG), carboxymethylcellulose (CMC), and κ- and ι-carrageenan (κ- and ι-CAR). As in the case of ALG, CMC, and CAR, interactions of CPM with PAA appear to be electrostatic and are cleaved in the presence of 0.13
M NaCl. On the contrary, apart from electrostatic interactions, additional interactions are found with PSS and residual interactions are kept in the presence of 0.13
M NaCl, a fact that may be attributed to π–π interactions and hydrophobic forces. The effect of the addition of 4
M urea, branched poly(ethyleneimine) (BPEI), and poly(vinylpyrrolidone) (PVP) is also studied. The addition of urea 4
M or 0.001
M BPEI produces a decrease on the amounts of counterions bound to PSS at infinite elution, while the addition of PVP does not produce any change on the diafiltration profiles.</description><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>Chlorpheniramine maleate</subject><subject>Exact sciences and technology</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Organic polymers</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Solution and gel properties</subject><subject>Ultrafiltration-diafiltration</subject><subject>Water-soluble polymers</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkc2KFDEUhYMo2I4-gpCNoosqb5KqStVKpPEPBtzoOqSTW3aaVFImaYd-Al_btN0grpxV_r5zTriHkOcMWgZseHNo1-hPC6aWA_QtDC0I8YBs2ChFw_nEHpINgOCNGAf2mDzJ-QAAvOfdhvzaxmXVyeUY6A7LHWKgZY9054J14TuNMzV7H9O6x-CSXlxAumiPuiAtkZ6DX-Vo3XGhXZPLKWHAfPRzDJV4TXWw_9hVSazn9EeIHk1JdVMwPyWPZu0zPruuN-Tbh_dft5-a2y8fP2_f3TamE7w0XBrd7QaYGY5ouQHGpn5kYkAORiA3M7N9fZPY9x1oDXO91siYRGt3KMQNeXnxXVP8ccRc1OKyQe91wHjMio9SjmLq7gH2IPtxvAfYDfUzZ7C_gCbFnBPOak1u0emkGKhzkeqgrkWqc5EKBlWLrLoX1wCdjfZz0sG4_Fc8TNMkhazc2wuHdX4_XXXJxmEwaF2qg1Y2uv8k_Qb4ebpX</recordid><startdate>20050823</startdate><enddate>20050823</enddate><creator>Moreno-Villoslada, Ignacio</creator><creator>Oyarzún, Felipe</creator><creator>Miranda, Víctor</creator><creator>Hess, Susan</creator><creator>Rivas, Bernabé L.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>7SR</scope><scope>JG9</scope></search><sort><creationdate>20050823</creationdate><title>Comparison between the binding of chlorpheniramine maleate to poly(sodium 4-styrenesulfonate) and the binding to other polyelectrolytes</title><author>Moreno-Villoslada, Ignacio ; Oyarzún, Felipe ; Miranda, Víctor ; Hess, Susan ; Rivas, Bernabé L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-27ca4b60f1e8ed2c011958136e20c3e2cf1d51e87e5540aa0f0c3ae117eddbe33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>Chlorpheniramine maleate</topic><topic>Exact sciences and technology</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Organic polymers</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Solution and gel properties</topic><topic>Ultrafiltration-diafiltration</topic><topic>Water-soluble polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moreno-Villoslada, Ignacio</creatorcontrib><creatorcontrib>Oyarzún, Felipe</creatorcontrib><creatorcontrib>Miranda, Víctor</creatorcontrib><creatorcontrib>Hess, Susan</creatorcontrib><creatorcontrib>Rivas, Bernabé L.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno-Villoslada, Ignacio</au><au>Oyarzún, Felipe</au><au>Miranda, Víctor</au><au>Hess, Susan</au><au>Rivas, Bernabé L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison between the binding of chlorpheniramine maleate to poly(sodium 4-styrenesulfonate) and the binding to other polyelectrolytes</atitle><jtitle>Polymer (Guilford)</jtitle><date>2005-08-23</date><risdate>2005</risdate><volume>46</volume><issue>18</issue><spage>7240</spage><epage>7245</epage><pages>7240-7245</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>The interactions of the antihistaminic drug chlorpheniramine maleate (CPM) with the negatively charged polyelectrolytes poly(sodium 4-styrenesulfonate) (PSS) and poly(acrylic acid) (PAA) are studied by the washing method of the diafiltration technique at conditions simulating those of the small intestine such as pH 7.5 and 0.13
M NaCl. The results are compared with those already reported involving other pharmacologically important polyelectrolytes such as alginic acid (ALG), carboxymethylcellulose (CMC), and κ- and ι-carrageenan (κ- and ι-CAR). As in the case of ALG, CMC, and CAR, interactions of CPM with PAA appear to be electrostatic and are cleaved in the presence of 0.13
M NaCl. On the contrary, apart from electrostatic interactions, additional interactions are found with PSS and residual interactions are kept in the presence of 0.13
M NaCl, a fact that may be attributed to π–π interactions and hydrophobic forces. The effect of the addition of 4
M urea, branched poly(ethyleneimine) (BPEI), and poly(vinylpyrrolidone) (PVP) is also studied. The addition of urea 4
M or 0.001
M BPEI produces a decrease on the amounts of counterions bound to PSS at infinite elution, while the addition of PVP does not produce any change on the diafiltration profiles.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.06.033</doi><tpages>6</tpages></addata></record> |
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subjects | Applied sciences Biological and medical sciences Chlorpheniramine maleate Exact sciences and technology General pharmacology Medical sciences Organic polymers Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Physicochemistry of polymers Properties and characterization Solution and gel properties Ultrafiltration-diafiltration Water-soluble polymers |
title | Comparison between the binding of chlorpheniramine maleate to poly(sodium 4-styrenesulfonate) and the binding to other polyelectrolytes |
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