Triggered release of doxorubicin from temperature-sensitive poly(N-(2-hydroxypropyl)-methacrylamide mono/dilactate) grafted liposomes
| Autor: | Van Elk, Merel, Deckers, Roel, Oerlemans, Chris, Shi, Yang, Storm, Gert, Vermonden, Tina, Hennink, Wim E., Sub Drug delivery, UIPS - Utrecht Institute for Pharmaceutical Sciences, Sub Drug targeting, Sub General Pharmaceutics, Pharmaceutics |
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| Přispěvatelé: | Sub Drug delivery, UIPS - Utrecht Institute for Pharmaceutical Sciences, Sub Drug targeting, Sub General Pharmaceutics, Pharmaceutics, Biomaterials Science and Technology, Faculty of Science and Technology |
| Jazyk: | angličtina |
| Rok vydání: | 2014 |
| Předmět: |
Polymers and Plastics
Polymers Kinetics Bioengineering Biomaterials chemistry.chemical_compound Drug Delivery Systems Cell Line Tumor Polymer chemistry polycyclic compounds Materials Chemistry Humans Methacrylamide N-(2-Hydroxypropyl) methacrylamide chemistry.chemical_classification Acrylamides Liposome Chemistry METIS-309156 Temperature technology industry and agriculture Polymer Grafting Membrane Doxorubicin Liposomes Drug delivery IR-95134 Hydrophobic and Hydrophilic Interactions Nuclear chemistry |
| Zdroj: | Biomacromolecules, 15(3), 1002. American Chemical Society : Division of Carbohydrate Chemistry Biomacromolecules, 15(3), 1002-1009. American Chemical Society |
| ISSN: | 1525-7797 |
| Popis: | The objective of this study was to design temperature-sensitive liposomes with tunable release characteristics that release their content at an elevated temperature generated by high intensity focused ultrasound (HIFU) exposure. To this end, thermosensitive polymers of N-(2-hydroxypropyl)methacrylamide mono/dilactate of different molecular weights and composition with a cholesterol anchor (chol-pHPMAlac) were synthesized and grafted onto liposomes loaded with doxorubicin (DOX). The liposomes were incubated at different temperatures and their release kinetics were studied. A good correlation between the release-onset temperature of the liposomes and the cloud point (CP) of chol-pHPMAlac was found. However, release took place at significantly higher temperatures than the CP of chol-pHPMAlac, likely at the CP, the dehydration and thus hydrophobicity is insufficient to penetrate and permeabilize the liposomal membrane. Liposomes grafted with chol-pHPMAlac with a CP of 11.5 °C released 89% DOX within 5 min at 42 °C while for the liposomes grafted with a polymer with CP of 25.0 °C, a temperature of 52 °C was needed to obtain the same extent of DOX release. At a fixed copolymer composition, an increase in molecular weight from 6.5 to 14.5 kDa decreased the temperature at which DOX was released with a release-onset temperature from 52 to 42 °C. Liposomes grafted with 5% chol-pHPMAlac exhibited a rapid release to a temperature increase, while at a grafting density of 2 and 10%, the liposomes were less sensitive to an increase in temperature. Sequential release of DOX was obtained by mixing liposomes grafted with chol-pHPMAlac having different CPs. Chol-pHPMAlac grafted liposomes released DOX nearly quantitatively after pulsed wave HIFU. In conclusion, the release of DOX from liposomes grafted with thermosensitive polymers of N-(2-hydroxypropyl)methacrylamide mono/dilactate can be tuned to the characteristics and the grafting density of chol-pHPMAlac, making these liposomes attractive for local drug delivery using hyperthermia. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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