TY - JOUR
T1 - Teaching an Old Dog New Tricks
T2 - A Global Approach to Enhancing the Cytotoxicity of Drug-Loaded, Non-responsive Micelles Using Oligoelectrolytes
AU - Saddam Hussain, Md
AU - Khetan, Riya
AU - Clulow, Andrew J.
AU - Ganesan, Raja
AU - MacMillan, Alexander
AU - Robinson, Nirmal
AU - Ahmed-Cox, Aria
AU - Krasowska, Marta
AU - Albrecht, Hugo
AU - Blencowe, Anton
N1 - Funding Information:
M.S.H. thanks the University of South Australia for scholarship support. SAXS experiments on the micelles were undertaken at the SAXS/WAXS beamline at the Australian Synchrotron, part of the Australian Nuclear Science and Technology Organisation (ANSTO); the authors thank the Australian Synchrotron for providing facilities, expertise, and support (Project M18270). The authors also acknowledge the SasView application originally developed under NSF award DMR-0520547. SasView contains code developed within the framework of the SINE2020 project funded by the EU research and innovation program “Horizon 2020”, grant agreement No. 654000. A.M. and A.A.-C. acknowledge the Katharina Gaus Light Microscopy Facility, University of New South Wales, Sydney, and thank the Cancer Institute of New South Wales for funding that enabled the acquisition of a PicoQuant Microtime 200 RapidFLIM STED used in this work. The authors thank Prof. Richard D’Andrea (UniSA) for kindly providing the NIH 3T3 fibroblast cell lines. The graphical abstract accompanying this manuscript was created using Biorender.com.
Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/2/28
Y1 - 2024/2/28
N2 - Polymeric micelles have been extensively studied as vectors for the delivery of hydrophobic drugs for the treatment of cancers and other diseases. Despite intensive research, few formulations provide significant benefits, and even fewer have been clinically approved. While many traditional non-responsive micelles have excellent safety profiles, they lack the ability to respond to the intracellular environment and release their cargo in a spatiotemporally defined manner to effectively deliver large doses of cytotoxic drugs into the cytosol of cells that overwhelm efflux pumps. As a novel and adaptable strategy, we hypothesized that well-established non-responsive polymeric micelles could be augmented with a pH-trigger via the co-encapsulation of cytocompatible oligoelectrolytes, which would allow rapid cargo release in the endosome, leading to increased cytotoxicity. Herein, we demonstrate how this strategy can be applied to render non-responsive micelles pH-responsive, resulting in abrupt cargo release at specific and tunable pH values compatible with endosomal delivery, which significantly increased their cytotoxicity up to 3-fold in an ovarian adenocarcinoma (SKOV-3) cell line compared to non-responsive micelles. In comparison, the oligoelectrolyte-loaded micelles were significantly less toxic to healthy 3T3 fibroblasts, indicating a selective cargo release in cancer cell lines. Oligoelectrolytes can be co-encapsulated in the micelles along with drugs at high encapsulation efficiency percentages, which are both ejected from the micelle core upon oligoelectrolyte ionization. Mechanistically, the increase in cytotoxicity appears to also result from the accelerated endosomal escape of the cargo caused by disruption of the endosomal membrane by the simultaneous release of the oligoelectrolytes from the micelles. Furthermore, we show how this approach is broadly applicable to non-responsive micelles regardless of their composition and various classes of hydrophobic chemotherapeutics. The preliminary studies presented here reveal the versatility and wide scope of oligoelectrolyte-mediated, pH-triggered drug release as a compelling and powerful strategy to enhance the cytotoxicity of non-responsive polymeric micelles.
AB - Polymeric micelles have been extensively studied as vectors for the delivery of hydrophobic drugs for the treatment of cancers and other diseases. Despite intensive research, few formulations provide significant benefits, and even fewer have been clinically approved. While many traditional non-responsive micelles have excellent safety profiles, they lack the ability to respond to the intracellular environment and release their cargo in a spatiotemporally defined manner to effectively deliver large doses of cytotoxic drugs into the cytosol of cells that overwhelm efflux pumps. As a novel and adaptable strategy, we hypothesized that well-established non-responsive polymeric micelles could be augmented with a pH-trigger via the co-encapsulation of cytocompatible oligoelectrolytes, which would allow rapid cargo release in the endosome, leading to increased cytotoxicity. Herein, we demonstrate how this strategy can be applied to render non-responsive micelles pH-responsive, resulting in abrupt cargo release at specific and tunable pH values compatible with endosomal delivery, which significantly increased their cytotoxicity up to 3-fold in an ovarian adenocarcinoma (SKOV-3) cell line compared to non-responsive micelles. In comparison, the oligoelectrolyte-loaded micelles were significantly less toxic to healthy 3T3 fibroblasts, indicating a selective cargo release in cancer cell lines. Oligoelectrolytes can be co-encapsulated in the micelles along with drugs at high encapsulation efficiency percentages, which are both ejected from the micelle core upon oligoelectrolyte ionization. Mechanistically, the increase in cytotoxicity appears to also result from the accelerated endosomal escape of the cargo caused by disruption of the endosomal membrane by the simultaneous release of the oligoelectrolytes from the micelles. Furthermore, we show how this approach is broadly applicable to non-responsive micelles regardless of their composition and various classes of hydrophobic chemotherapeutics. The preliminary studies presented here reveal the versatility and wide scope of oligoelectrolyte-mediated, pH-triggered drug release as a compelling and powerful strategy to enhance the cytotoxicity of non-responsive polymeric micelles.
KW - co-encapsulation
KW - cytotoxicity
KW - drug release
KW - oligoelectrolyte
KW - pH-triggered
KW - polymeric micelle
UR - http://www.scopus.com/inward/record.url?scp=85185614071&partnerID=8YFLogxK
U2 - 10.1021/acsami.3c16551
DO - 10.1021/acsami.3c16551
M3 - Article
C2 - 38349780
AN - SCOPUS:85185614071
SN - 1944-8244
VL - 16
SP - 9736
EP - 9748
JO - ACS Applied Materials & Interfaces
JF - ACS Applied Materials & Interfaces
IS - 8
ER -