Abstract

The therapeutic effectiveness of chemotherapy is optimal only when tumor cells are subjected to a maximum drug exposure. To increase the intratumoral drug concentration and thus the efficacy of chemotherapy, a thermoresponsive bubble-generating liposomal system is proposed for triggering localized extracellular drug delivery. The key component of this liposomal formulation is the encapsulated ammonium bicarbonate (ABC), which is used to create the transmembrane gradient needed for a highly efficient encapsulation of doxorubicin (DOX). At an elevated temperature (42 °C), decomposition of ABC generates CO(2) bubbles, creating permeable defects in the lipid bilayer that rapidly release DOX and instantly increase the drug concentration locally. Because the generated CO(2) bubbles are hyperechogenic, they also enhance ultrasound imaging. Consequently, this new liposomal system encapsulated with ABC may also provide an ability to monitor a temperature-controlled drug delivery process.

Keywords

Drug deliveryLiposomeDoxorubicinDrugLipid bilayerMaterials scienceBilayerNanotechnologyAmmonium bicarbonateBiomedical engineeringBiophysicsMembraneChemistryChemotherapyPharmacologyMedicineBiochemistrySurgeryOrganic chemistry

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Publication Info

Year
2012
Type
article
Volume
7
Issue
1
Pages
438-446
Citations
267
Access
Closed

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Ko‐Jie Chen, Hsiang‐Fa Liang, Hsin‐Lung Chen et al. (2012). A Thermoresponsive Bubble-Generating Liposomal System for Triggering Localized Extracellular Drug Delivery. ACS Nano , 7 (1) , 438-446. https://doi.org/10.1021/nn304474j

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DOI
10.1021/nn304474j