Physical Stability of Sonicated Arsonoliposomes: Effect of Calcium Ions
The physical stability of sonicated arsonoliposomes in the absence and presence of Ca2+ ions is evaluated. Cholesterol‐containing arsonoliposomes composed of arsonolipids [having different acyl chains (C12-C18)], or mixtures of arsonolipids with phospholipids (phosphatidylcholine or distearoyl‐phosp...
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description | The physical stability of sonicated arsonoliposomes in the absence and presence of Ca2+ ions is evaluated. Cholesterol‐containing arsonoliposomes composed of arsonolipids [having different acyl chains (C12-C18)], or mixtures of arsonolipids with phospholipids (phosphatidylcholine or distearoyl‐phosphatidylcholine) were prepared, and physical stability was evaluated in the absence and presence of CaCl2, by vesicle dispersions turbidity measurements and cryo‐electron microscopy morphological assessment. In some cases, vesicle ζ‐potential was measured, under identical conditions. Results demonstrate that self‐aggregation of the vesicles studied is low and influenced by the acyl chain length of the arsonolipid used, whereas calcium‐induced aggregation is higher, correlating well with the decreased values of vesicle ζ‐potential in the presence of Ca2+ ions (weaker electrostatic repulsion). Acyl chain length of arsonolipids used has a significant quantitative effect on Ca2+‐induced vesicle aggregation mainly for arsonoliposomes that contain phospholipids (mixed), compared with the vesicles that consist of plain arsonolipids (significant effect only for initial aggregation at time 0). Another difference between plain and mixed arsonoliposomes is that for mixed arsonoliposomes Ca2+‐induced increases in turbidity are irreversible by ethylenediaminotetraacetic acid, suggesting that vesicle fusion is taking place. This was confirmed by cryo‐electron microscopy observations. Finally, when phosphatidylcholine is replaced by distearoyl‐phosphatidylcholine, arsonoliposomes are more stable in terms of self‐aggregation, but in the presence of calcium, the turbidity and morphology results are similar. |
doi_str_mv | 10.1002/jps.20221 |
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Cholesterol‐containing arsonoliposomes composed of arsonolipids [having different acyl chains (C12-C18)], or mixtures of arsonolipids with phospholipids (phosphatidylcholine or distearoyl‐phosphatidylcholine) were prepared, and physical stability was evaluated in the absence and presence of CaCl2, by vesicle dispersions turbidity measurements and cryo‐electron microscopy morphological assessment. In some cases, vesicle ζ‐potential was measured, under identical conditions. Results demonstrate that self‐aggregation of the vesicles studied is low and influenced by the acyl chain length of the arsonolipid used, whereas calcium‐induced aggregation is higher, correlating well with the decreased values of vesicle ζ‐potential in the presence of Ca2+ ions (weaker electrostatic repulsion). Acyl chain length of arsonolipids used has a significant quantitative effect on Ca2+‐induced vesicle aggregation mainly for arsonoliposomes that contain phospholipids (mixed), compared with the vesicles that consist of plain arsonolipids (significant effect only for initial aggregation at time 0). Another difference between plain and mixed arsonoliposomes is that for mixed arsonoliposomes Ca2+‐induced increases in turbidity are irreversible by ethylenediaminotetraacetic acid, suggesting that vesicle fusion is taking place. This was confirmed by cryo‐electron microscopy observations. Finally, when phosphatidylcholine is replaced by distearoyl‐phosphatidylcholine, arsonoliposomes are more stable in terms of self‐aggregation, but in the presence of calcium, the turbidity and morphology results are similar.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.20221</identifier><identifier>PMID: 15761929</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Hoboken: Elsevier Inc</publisher><subject>Arsenicals - chemistry ; Biological and medical sciences ; Calcium - chemistry ; Cholesterol - chemistry ; Cryoelectron Microscopy ; Drug Stability ; Edetic Acid ; Electrochemistry ; Excipients ; General pharmacology ; light scattering (dynamic) ; lipids ; liposomes ; Liposomes - chemistry ; Medical sciences ; microscopy ; morphology ; Nephelometry and Turbidimetry ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Phosphatidylcholines - chemistry ; physical stability ; Ultrasonics</subject><ispartof>Journal of pharmaceutical sciences, 2005-01, Vol.94 (1), p.46-55</ispartof><rights>2004 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 2004 Wiley‐Liss, Inc., A Wiley Company</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5321-d80ae2c67d517d8bf914c2a88470335808d15bb690600f2de1b8c191660900a23</citedby><cites>FETCH-LOGICAL-c5321-d80ae2c67d517d8bf914c2a88470335808d15bb690600f2de1b8c191660900a23</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.20221$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.20221$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16515594$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15761929$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fatouros, D.G.</creatorcontrib><creatorcontrib>Piperoudi, S.</creatorcontrib><creatorcontrib>Gortzi, O.</creatorcontrib><creatorcontrib>Ioannou, P.V.</creatorcontrib><creatorcontrib>Frederik, P.</creatorcontrib><creatorcontrib>Antimisiaris, S.G.</creatorcontrib><title>Physical Stability of Sonicated Arsonoliposomes: Effect of Calcium Ions</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>The physical stability of sonicated arsonoliposomes in the absence and presence of Ca2+ ions is evaluated. Cholesterol‐containing arsonoliposomes composed of arsonolipids [having different acyl chains (C12-C18)], or mixtures of arsonolipids with phospholipids (phosphatidylcholine or distearoyl‐phosphatidylcholine) were prepared, and physical stability was evaluated in the absence and presence of CaCl2, by vesicle dispersions turbidity measurements and cryo‐electron microscopy morphological assessment. In some cases, vesicle ζ‐potential was measured, under identical conditions. Results demonstrate that self‐aggregation of the vesicles studied is low and influenced by the acyl chain length of the arsonolipid used, whereas calcium‐induced aggregation is higher, correlating well with the decreased values of vesicle ζ‐potential in the presence of Ca2+ ions (weaker electrostatic repulsion). Acyl chain length of arsonolipids used has a significant quantitative effect on Ca2+‐induced vesicle aggregation mainly for arsonoliposomes that contain phospholipids (mixed), compared with the vesicles that consist of plain arsonolipids (significant effect only for initial aggregation at time 0). Another difference between plain and mixed arsonoliposomes is that for mixed arsonoliposomes Ca2+‐induced increases in turbidity are irreversible by ethylenediaminotetraacetic acid, suggesting that vesicle fusion is taking place. This was confirmed by cryo‐electron microscopy observations. Finally, when phosphatidylcholine is replaced by distearoyl‐phosphatidylcholine, arsonoliposomes are more stable in terms of self‐aggregation, but in the presence of calcium, the turbidity and morphology results are similar.</description><subject>Arsenicals - chemistry</subject><subject>Biological and medical sciences</subject><subject>Calcium - chemistry</subject><subject>Cholesterol - chemistry</subject><subject>Cryoelectron Microscopy</subject><subject>Drug Stability</subject><subject>Edetic Acid</subject><subject>Electrochemistry</subject><subject>Excipients</subject><subject>General pharmacology</subject><subject>light scattering (dynamic)</subject><subject>lipids</subject><subject>liposomes</subject><subject>Liposomes - chemistry</subject><subject>Medical sciences</subject><subject>microscopy</subject><subject>morphology</subject><subject>Nephelometry and Turbidimetry</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphatidylcholines - chemistry</subject><subject>physical stability</subject><subject>Ultrasonics</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UFvFCEUB3BiNHatHvwCZi6aeJj2PRhg8FY37VrTaOOu8UgYhonUmWGFWXW_vdRZ7UXjiQR-78H7Q8hThBMEoKc323RCgVK8RxbIKZQCUN4ni3xGS8YrdUQepXQDAAI4f0iOkEuBiqoFWV1_3idvTV-sJ9P43k_7InTFOox5c3JtcRZTGEPvtyGFwaVXxXnXOTvdoqXprd8NxWUY02PyoDN9ck8O6zH5eHG-Wb4pr96vLpdnV6XljGLZ1mActUK2HGVbN53CylJT15UExngNdYu8aYTKL4WOtg6b2qJCIUABGMqOyYu57zaGrzuXJj34ZF3fm9GFXdJCclCyUv-FKBkiFSzDlzO0MaQUXae30Q8m7jWCvo1X53j1r3izfXZoumsG197JQ54ZPD8Ak3KoXTSj9enOCY6cqyq709l9973b__tG_fZ6_fvqcq7waXI__lSY-CXPzCTXn96t9ObD5jVCfaFl9mz2Lv_GN--iTta70brWx_x_ug3-LwP-BLH7r2w</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Fatouros, D.G.</creator><creator>Piperoudi, S.</creator><creator>Gortzi, O.</creator><creator>Ioannou, P.V.</creator><creator>Frederik, P.</creator><creator>Antimisiaris, S.G.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>American Pharmaceutical Association</general><scope>BSCLL</scope><scope>IQODW</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>7QP</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Physical Stability of Sonicated Arsonoliposomes: Effect of Calcium Ions</title><author>Fatouros, D.G. ; Piperoudi, S. ; Gortzi, O. ; Ioannou, P.V. ; Frederik, P. ; Antimisiaris, S.G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5321-d80ae2c67d517d8bf914c2a88470335808d15bb690600f2de1b8c191660900a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Arsenicals - chemistry</topic><topic>Biological and medical sciences</topic><topic>Calcium - chemistry</topic><topic>Cholesterol - chemistry</topic><topic>Cryoelectron Microscopy</topic><topic>Drug Stability</topic><topic>Edetic Acid</topic><topic>Electrochemistry</topic><topic>Excipients</topic><topic>General pharmacology</topic><topic>light scattering (dynamic)</topic><topic>lipids</topic><topic>liposomes</topic><topic>Liposomes - chemistry</topic><topic>Medical sciences</topic><topic>microscopy</topic><topic>morphology</topic><topic>Nephelometry and Turbidimetry</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphatidylcholines - chemistry</topic><topic>physical stability</topic><topic>Ultrasonics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fatouros, D.G.</creatorcontrib><creatorcontrib>Piperoudi, S.</creatorcontrib><creatorcontrib>Gortzi, O.</creatorcontrib><creatorcontrib>Ioannou, P.V.</creatorcontrib><creatorcontrib>Frederik, P.</creatorcontrib><creatorcontrib>Antimisiaris, S.G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fatouros, D.G.</au><au>Piperoudi, S.</au><au>Gortzi, O.</au><au>Ioannou, P.V.</au><au>Frederik, P.</au><au>Antimisiaris, S.G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical Stability of Sonicated Arsonoliposomes: Effect of Calcium Ions</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>2005-01</date><risdate>2005</risdate><volume>94</volume><issue>1</issue><spage>46</spage><epage>55</epage><pages>46-55</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>The physical stability of sonicated arsonoliposomes in the absence and presence of Ca2+ ions is evaluated. Cholesterol‐containing arsonoliposomes composed of arsonolipids [having different acyl chains (C12-C18)], or mixtures of arsonolipids with phospholipids (phosphatidylcholine or distearoyl‐phosphatidylcholine) were prepared, and physical stability was evaluated in the absence and presence of CaCl2, by vesicle dispersions turbidity measurements and cryo‐electron microscopy morphological assessment. In some cases, vesicle ζ‐potential was measured, under identical conditions. Results demonstrate that self‐aggregation of the vesicles studied is low and influenced by the acyl chain length of the arsonolipid used, whereas calcium‐induced aggregation is higher, correlating well with the decreased values of vesicle ζ‐potential in the presence of Ca2+ ions (weaker electrostatic repulsion). Acyl chain length of arsonolipids used has a significant quantitative effect on Ca2+‐induced vesicle aggregation mainly for arsonoliposomes that contain phospholipids (mixed), compared with the vesicles that consist of plain arsonolipids (significant effect only for initial aggregation at time 0). Another difference between plain and mixed arsonoliposomes is that for mixed arsonoliposomes Ca2+‐induced increases in turbidity are irreversible by ethylenediaminotetraacetic acid, suggesting that vesicle fusion is taking place. This was confirmed by cryo‐electron microscopy observations. Finally, when phosphatidylcholine is replaced by distearoyl‐phosphatidylcholine, arsonoliposomes are more stable in terms of self‐aggregation, but in the presence of calcium, the turbidity and morphology results are similar.</abstract><cop>Hoboken</cop><pub>Elsevier Inc</pub><pmid>15761929</pmid><doi>10.1002/jps.20221</doi><tpages>10</tpages></addata></record> |
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subjects | Arsenicals - chemistry Biological and medical sciences Calcium - chemistry Cholesterol - chemistry Cryoelectron Microscopy Drug Stability Edetic Acid Electrochemistry Excipients General pharmacology light scattering (dynamic) lipids liposomes Liposomes - chemistry Medical sciences microscopy morphology Nephelometry and Turbidimetry Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Phosphatidylcholines - chemistry physical stability Ultrasonics |
title | Physical Stability of Sonicated Arsonoliposomes: Effect of Calcium Ions |
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