Diffusion, permeation, and solubility of selected agents in and through polyethylene
Even though polyethylene containers have and are being used with more frequency to package drug products, diagnostic agents, biological products, and cosmetic preparations, little emphasis apparently has been placed on the possible interactions between solute molecules in the product and the polyeth...
Gespeichert in:
Veröffentlicht in: | Journal of pharmaceutical sciences 1967-10, Vol.56 (10), p.1288-1293 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1293 |
---|---|
container_issue | 10 |
container_start_page | 1288 |
container_title | Journal of pharmaceutical sciences |
container_volume | 56 |
creator | Gonzales, M.A. Nematollahi, J. Guess, W.L. Autian, J. |
description | Even though polyethylene containers have and are being used with more frequency to package drug products, diagnostic agents, biological products, and cosmetic preparations, little emphasis apparently has been placed on the possible interactions between solute molecules in the product and the polyethylene. This report presents a study on the diffusion, permeation, and solubility of six compounds (acetophenone, benzaldehyde, benzoic acid, benzyl alcohol, 4-methylacetophenone, and 4-methylbenzaldehyde) in and through polyethylene. Results reveal that benzyl alcohol and benzoic acid had the lowest permeation (P) and diffusion (D) values as compared to the other compounds in the series. This was ascribed to the intermolecular hydrogen bonding potential of benzyl alcohol and benzoic acid; thus the formation of dimer or trimer whose permeation through the polymer is assumed to be restricted. In the case of 4-methylbenzaldehyde and 4-methylacetophenone, the D values obtained were similar to those of the parent compounds (benzaldehyde and acetophenone). Higher P values for the 4-methyl derivatives of benzaldehyde and acetophenone were related to the higher solubility of the molecules in the plastic. |
doi_str_mv | 10.1002/jps.2600561015 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_84593744</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022354915360160</els_id><sourcerecordid>84593744</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4275-44602d5a7fc537d3663238666164bc02acd4929d568fa010a2de312ee3bc2d743</originalsourceid><addsrcrecordid>eNqFkU1v1DAQhi0EKkvhyg0pJ05kGX9mc0QLXUAVVGIRR8trT7ou3ji1E9r8e9JmVcQBcRpL87yv5GcIeUlhSQHY26suL5kCkIoClY_IgkoGpQJaPSaLCWAll6J-Sp7lfAUACqQ8ISfTqIWEBdm-900zZB_bN0WH6YCmv3-b1hU5hmHng-_HIjZFxoC2R1eYS2z7XPj2Hur3KQ6X-6KLYcR-PwZs8Tl50piQ8cVxnpLvZx-264_l-dfNp_W789IKVslSCAXMSVM1VvLKcaU44yulFFViZ4EZ60TNaifVqjFAwTCHnDJEvrPMVYKfktdzb5fi9YC51wefLYZgWoxD1isha16JO3A5gzbFnBM2ukv-YNKoKeg7jXrSqP9onAKvjs3D7oDuAT96m_b1vL_xAcf_tOnPF9_-6i7nrM893j5kTfqpVcUrqX982WhZSbreXpzpzcSvZh4nlb88Jp2tx9ai82m6iHbR_-sbvwGCEZ_d</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>84593744</pqid></control><display><type>article</type><title>Diffusion, permeation, and solubility of selected agents in and through polyethylene</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Alma/SFX Local Collection</source><creator>Gonzales, M.A. ; Nematollahi, J. ; Guess, W.L. ; Autian, J.</creator><creatorcontrib>Gonzales, M.A. ; Nematollahi, J. ; Guess, W.L. ; Autian, J.</creatorcontrib><description>Even though polyethylene containers have and are being used with more frequency to package drug products, diagnostic agents, biological products, and cosmetic preparations, little emphasis apparently has been placed on the possible interactions between solute molecules in the product and the polyethylene. This report presents a study on the diffusion, permeation, and solubility of six compounds (acetophenone, benzaldehyde, benzoic acid, benzyl alcohol, 4-methylacetophenone, and 4-methylbenzaldehyde) in and through polyethylene. Results reveal that benzyl alcohol and benzoic acid had the lowest permeation (P) and diffusion (D) values as compared to the other compounds in the series. This was ascribed to the intermolecular hydrogen bonding potential of benzyl alcohol and benzoic acid; thus the formation of dimer or trimer whose permeation through the polymer is assumed to be restricted. In the case of 4-methylbenzaldehyde and 4-methylacetophenone, the D values obtained were similar to those of the parent compounds (benzaldehyde and acetophenone). Higher P values for the 4-methyl derivatives of benzaldehyde and acetophenone were related to the higher solubility of the molecules in the plastic.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600561015</identifier><identifier>PMID: 6059450</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Acetophenones ; Alcohols ; Aldehydes ; Benzoates ; Drug Packaging ; Permeability ; Polyethylenes ; Solubility</subject><ispartof>Journal of pharmaceutical sciences, 1967-10, Vol.56 (10), p.1288-1293</ispartof><rights>1967 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1967 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4275-44602d5a7fc537d3663238666164bc02acd4929d568fa010a2de312ee3bc2d743</citedby><cites>FETCH-LOGICAL-c4275-44602d5a7fc537d3663238666164bc02acd4929d568fa010a2de312ee3bc2d743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600561015$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600561015$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6059450$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonzales, M.A.</creatorcontrib><creatorcontrib>Nematollahi, J.</creatorcontrib><creatorcontrib>Guess, W.L.</creatorcontrib><creatorcontrib>Autian, J.</creatorcontrib><title>Diffusion, permeation, and solubility of selected agents in and through polyethylene</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>Even though polyethylene containers have and are being used with more frequency to package drug products, diagnostic agents, biological products, and cosmetic preparations, little emphasis apparently has been placed on the possible interactions between solute molecules in the product and the polyethylene. This report presents a study on the diffusion, permeation, and solubility of six compounds (acetophenone, benzaldehyde, benzoic acid, benzyl alcohol, 4-methylacetophenone, and 4-methylbenzaldehyde) in and through polyethylene. Results reveal that benzyl alcohol and benzoic acid had the lowest permeation (P) and diffusion (D) values as compared to the other compounds in the series. This was ascribed to the intermolecular hydrogen bonding potential of benzyl alcohol and benzoic acid; thus the formation of dimer or trimer whose permeation through the polymer is assumed to be restricted. In the case of 4-methylbenzaldehyde and 4-methylacetophenone, the D values obtained were similar to those of the parent compounds (benzaldehyde and acetophenone). Higher P values for the 4-methyl derivatives of benzaldehyde and acetophenone were related to the higher solubility of the molecules in the plastic.</description><subject>Acetophenones</subject><subject>Alcohols</subject><subject>Aldehydes</subject><subject>Benzoates</subject><subject>Drug Packaging</subject><subject>Permeability</subject><subject>Polyethylenes</subject><subject>Solubility</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1967</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EKkvhyg0pJ05kGX9mc0QLXUAVVGIRR8trT7ou3ji1E9r8e9JmVcQBcRpL87yv5GcIeUlhSQHY26suL5kCkIoClY_IgkoGpQJaPSaLCWAll6J-Sp7lfAUACqQ8ISfTqIWEBdm-900zZB_bN0WH6YCmv3-b1hU5hmHng-_HIjZFxoC2R1eYS2z7XPj2Hur3KQ6X-6KLYcR-PwZs8Tl50piQ8cVxnpLvZx-264_l-dfNp_W789IKVslSCAXMSVM1VvLKcaU44yulFFViZ4EZ60TNaifVqjFAwTCHnDJEvrPMVYKfktdzb5fi9YC51wefLYZgWoxD1isha16JO3A5gzbFnBM2ukv-YNKoKeg7jXrSqP9onAKvjs3D7oDuAT96m_b1vL_xAcf_tOnPF9_-6i7nrM893j5kTfqpVcUrqX982WhZSbreXpzpzcSvZh4nlb88Jp2tx9ai82m6iHbR_-sbvwGCEZ_d</recordid><startdate>196710</startdate><enddate>196710</enddate><creator>Gonzales, M.A.</creator><creator>Nematollahi, J.</creator><creator>Guess, W.L.</creator><creator>Autian, J.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>196710</creationdate><title>Diffusion, permeation, and solubility of selected agents in and through polyethylene</title><author>Gonzales, M.A. ; Nematollahi, J. ; Guess, W.L. ; Autian, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4275-44602d5a7fc537d3663238666164bc02acd4929d568fa010a2de312ee3bc2d743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1967</creationdate><topic>Acetophenones</topic><topic>Alcohols</topic><topic>Aldehydes</topic><topic>Benzoates</topic><topic>Drug Packaging</topic><topic>Permeability</topic><topic>Polyethylenes</topic><topic>Solubility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonzales, M.A.</creatorcontrib><creatorcontrib>Nematollahi, J.</creatorcontrib><creatorcontrib>Guess, W.L.</creatorcontrib><creatorcontrib>Autian, J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonzales, M.A.</au><au>Nematollahi, J.</au><au>Guess, W.L.</au><au>Autian, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffusion, permeation, and solubility of selected agents in and through polyethylene</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1967-10</date><risdate>1967</risdate><volume>56</volume><issue>10</issue><spage>1288</spage><epage>1293</epage><pages>1288-1293</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>Even though polyethylene containers have and are being used with more frequency to package drug products, diagnostic agents, biological products, and cosmetic preparations, little emphasis apparently has been placed on the possible interactions between solute molecules in the product and the polyethylene. This report presents a study on the diffusion, permeation, and solubility of six compounds (acetophenone, benzaldehyde, benzoic acid, benzyl alcohol, 4-methylacetophenone, and 4-methylbenzaldehyde) in and through polyethylene. Results reveal that benzyl alcohol and benzoic acid had the lowest permeation (P) and diffusion (D) values as compared to the other compounds in the series. This was ascribed to the intermolecular hydrogen bonding potential of benzyl alcohol and benzoic acid; thus the formation of dimer or trimer whose permeation through the polymer is assumed to be restricted. In the case of 4-methylbenzaldehyde and 4-methylacetophenone, the D values obtained were similar to those of the parent compounds (benzaldehyde and acetophenone). Higher P values for the 4-methyl derivatives of benzaldehyde and acetophenone were related to the higher solubility of the molecules in the plastic.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>6059450</pmid><doi>10.1002/jps.2600561015</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3549 |
ispartof | Journal of pharmaceutical sciences, 1967-10, Vol.56 (10), p.1288-1293 |
issn | 0022-3549 1520-6017 |
language | eng |
recordid | cdi_proquest_miscellaneous_84593744 |
source | MEDLINE; Access via Wiley Online Library; Alma/SFX Local Collection |
subjects | Acetophenones Alcohols Aldehydes Benzoates Drug Packaging Permeability Polyethylenes Solubility |
title | Diffusion, permeation, and solubility of selected agents in and through polyethylene |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T04%3A28%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diffusion,%20permeation,%20and%20solubility%20of%20selected%20agents%20in%20and%20through%20polyethylene&rft.jtitle=Journal%20of%20pharmaceutical%20sciences&rft.au=Gonzales,%20M.A.&rft.date=1967-10&rft.volume=56&rft.issue=10&rft.spage=1288&rft.epage=1293&rft.pages=1288-1293&rft.issn=0022-3549&rft.eissn=1520-6017&rft_id=info:doi/10.1002/jps.2600561015&rft_dat=%3Cproquest_cross%3E84593744%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=84593744&rft_id=info:pmid/6059450&rft_els_id=S0022354915360160&rfr_iscdi=true |