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
Hauptverfasser: Mehnath, Sivaraj, Rajan, Mariappan, Sathishkumar, Gnanasekar, Amarnath Praphakar, Rajendran, Jeyaraj, Murugaraj
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container_end_page 128
container_issue
container_start_page 119
container_title Polymer (Guilford)
container_volume 133
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
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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.</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). 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source Elsevier ScienceDirect Journals
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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