Thermoresponsive and pH triggered drug release of cholate functionalized poly(organophosphazene) – polylactic acid co-polymeric nanostructure integrated with ICG
This study demonstrates the development of pH and thermosresponsive nanoparticles (NPs) composed via cholic acid, PCPP-PLA hybrid polymer integrated with indocyanine green (ICG) for site specific delivery hydrophobic drug (paclitaxel). Drug and ICG were physically encapsulated by poly (bis(carboxyph...
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Veröffentlicht in: | Polymer (Guilford) 2017-12, Vol.133, p.119-128 |
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creator | Mehnath, Sivaraj Rajan, Mariappan Sathishkumar, Gnanasekar Amarnath Praphakar, Rajendran Jeyaraj, Murugaraj |
description | This study demonstrates the development of pH and thermosresponsive nanoparticles (NPs) composed via cholic acid, PCPP-PLA hybrid polymer integrated with indocyanine green (ICG) for site specific delivery hydrophobic drug (paclitaxel). Drug and ICG were physically encapsulated by poly (bis(carboxyphenoxy)phosphazene) (PCPP)-poly lactic acid hybrid polymer. The hybrid polymer solution showed reversible gelation behaviour at the temperature between 37 °C and 20 °C and also it showed pH dependent drug release capability at acidic pH due to the pH responsive quenching effects of PCPP-PLA. The size (150–200 nm) and morphology of drug-loaded polymeric NPs were characterized using SEM and HR-TEM. Further, the release of loaded paclitaxel (PTX) from polymer was significantly sustained over 12 days. Drug release from the nanoparticles was effectively controlled by the mechanical strength of the polymer. All of these results demonstrate that pH triggered hybrid polymeric NPs are potential carriers for tumor-targeted drug delivery and also it exhibits great strength at 37 °C.
[Display omitted]
•Amphiphillic hybrid polymer were synthesized using poly (bis (carboxyphenoxy) phosphazene) -poly lactic acid.•Hybrid polymer showed reversible gelation behaviour at different temperature.•PCPP-PLA shows interesting pH responsive drug release behaviour.•Paclitaxel drug sustained released from polymer. |
doi_str_mv | 10.1016/j.polymer.2017.11.020 |
format | Article |
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[Display omitted]
•Amphiphillic hybrid polymer were synthesized using poly (bis (carboxyphenoxy) phosphazene) -poly lactic acid.•Hybrid polymer showed reversible gelation behaviour at different temperature.•PCPP-PLA shows interesting pH responsive drug release behaviour.•Paclitaxel drug sustained released from polymer.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2017.11.020</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Cholic acid ; Drug delivery ; Drug delivery systems ; Gelation ; Hybrid polymer ; Hydrogen ions ; Hydrophobicity ; Mechanical properties ; Nanoparticles ; Paclitaxel ; pH effects ; Phosphazene ; Poly(organophosphazene) ; Polylactic acid ; Polymers ; Quenching ; Thermoresponsive</subject><ispartof>Polymer (Guilford), 2017-12, Vol.133, p.119-128</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright Elsevier BV Dec 20, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c252t-e950738a2663af72c2181641ef0f0ca65d93f34161e6bfd9cd727fa5fab2a0443</citedby><cites>FETCH-LOGICAL-c252t-e950738a2663af72c2181641ef0f0ca65d93f34161e6bfd9cd727fa5fab2a0443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2017.11.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids></links><search><creatorcontrib>Mehnath, Sivaraj</creatorcontrib><creatorcontrib>Rajan, Mariappan</creatorcontrib><creatorcontrib>Sathishkumar, Gnanasekar</creatorcontrib><creatorcontrib>Amarnath Praphakar, Rajendran</creatorcontrib><creatorcontrib>Jeyaraj, Murugaraj</creatorcontrib><title>Thermoresponsive and pH triggered drug release of cholate functionalized poly(organophosphazene) – polylactic acid co-polymeric nanostructure integrated with ICG</title><title>Polymer (Guilford)</title><description>This study demonstrates the development of pH and thermosresponsive nanoparticles (NPs) composed via cholic acid, PCPP-PLA hybrid polymer integrated with indocyanine green (ICG) for site specific delivery hydrophobic drug (paclitaxel). Drug and ICG were physically encapsulated by poly (bis(carboxyphenoxy)phosphazene) (PCPP)-poly lactic acid hybrid polymer. The hybrid polymer solution showed reversible gelation behaviour at the temperature between 37 °C and 20 °C and also it showed pH dependent drug release capability at acidic pH due to the pH responsive quenching effects of PCPP-PLA. The size (150–200 nm) and morphology of drug-loaded polymeric NPs were characterized using SEM and HR-TEM. Further, the release of loaded paclitaxel (PTX) from polymer was significantly sustained over 12 days. Drug release from the nanoparticles was effectively controlled by the mechanical strength of the polymer. All of these results demonstrate that pH triggered hybrid polymeric NPs are potential carriers for tumor-targeted drug delivery and also it exhibits great strength at 37 °C.
[Display omitted]
•Amphiphillic hybrid polymer were synthesized using poly (bis (carboxyphenoxy) phosphazene) -poly lactic acid.•Hybrid polymer showed reversible gelation behaviour at different temperature.•PCPP-PLA shows interesting pH responsive drug release behaviour.•Paclitaxel drug sustained released from polymer.</description><subject>Cholic acid</subject><subject>Drug delivery</subject><subject>Drug delivery systems</subject><subject>Gelation</subject><subject>Hybrid polymer</subject><subject>Hydrogen ions</subject><subject>Hydrophobicity</subject><subject>Mechanical properties</subject><subject>Nanoparticles</subject><subject>Paclitaxel</subject><subject>pH effects</subject><subject>Phosphazene</subject><subject>Poly(organophosphazene)</subject><subject>Polylactic acid</subject><subject>Polymers</subject><subject>Quenching</subject><subject>Thermoresponsive</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFUctu1DAUjRBIDKWfgGSJDSwSbCdxkhVCo9JWqsSmXVuufZ14lLHDtVPUrvgHPoE_65fUw8ye1ZXueegcnaL4wGjFKBNfdtUS5sc9YMUp6yrGKsrpq2LD-q4uOR_Y62JDac3LuhfsbfEuxh2llLe82RR_byfAfUCIS_DRPQBR3pDliiR04wgIhhhcR4Iwg4pAgiV6CrNKQOzqdXLBq9k9Zdohw6eAo_JhmUJcJvUEHj6T599__mGzymxNlHaG6FCeIuePz4qYcNVpRSDOJxgx-xvyy6WJXG8v3xdvrJojnJ_uWXH3_eJ2e1Xe_Li83n67KXXukkoYWtrVveJC1Mp2XHPWM9EwsNRSrURrhtrWDRMMxL01gzYd76xqrbrnijZNfVZ8PPouGH6uEJPchRVzvyjZ0Le9EE0zZFZ7ZGkMMSJYuaDbK3yUjMrDHnInT-XkYQ_JmMx7ZN3Xow5yhQeX0agdeA3GIegkTXD_cXgBQFicTw</recordid><startdate>20171220</startdate><enddate>20171220</enddate><creator>Mehnath, Sivaraj</creator><creator>Rajan, Mariappan</creator><creator>Sathishkumar, Gnanasekar</creator><creator>Amarnath Praphakar, Rajendran</creator><creator>Jeyaraj, Murugaraj</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope></search><sort><creationdate>20171220</creationdate><title>Thermoresponsive and pH triggered drug release of cholate functionalized poly(organophosphazene) – polylactic acid co-polymeric nanostructure integrated with ICG</title><author>Mehnath, Sivaraj ; 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Drug and ICG were physically encapsulated by poly (bis(carboxyphenoxy)phosphazene) (PCPP)-poly lactic acid hybrid polymer. The hybrid polymer solution showed reversible gelation behaviour at the temperature between 37 °C and 20 °C and also it showed pH dependent drug release capability at acidic pH due to the pH responsive quenching effects of PCPP-PLA. The size (150–200 nm) and morphology of drug-loaded polymeric NPs were characterized using SEM and HR-TEM. Further, the release of loaded paclitaxel (PTX) from polymer was significantly sustained over 12 days. Drug release from the nanoparticles was effectively controlled by the mechanical strength of the polymer. All of these results demonstrate that pH triggered hybrid polymeric NPs are potential carriers for tumor-targeted drug delivery and also it exhibits great strength at 37 °C.
[Display omitted]
•Amphiphillic hybrid polymer were synthesized using poly (bis (carboxyphenoxy) phosphazene) -poly lactic acid.•Hybrid polymer showed reversible gelation behaviour at different temperature.•PCPP-PLA shows interesting pH responsive drug release behaviour.•Paclitaxel drug sustained released from polymer.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2017.11.020</doi><tpages>10</tpages></addata></record> |
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subjects | Cholic acid Drug delivery Drug delivery systems Gelation Hybrid polymer Hydrogen ions Hydrophobicity Mechanical properties Nanoparticles Paclitaxel pH effects Phosphazene Poly(organophosphazene) Polylactic acid Polymers Quenching Thermoresponsive |
title | Thermoresponsive and pH triggered drug release of cholate functionalized poly(organophosphazene) – polylactic acid co-polymeric nanostructure integrated with ICG |
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