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Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy and has a 5-year survival rate of <35%. ACC cells require cholesterol for steroid hormone production, and this requirement is met via expression on the cell surface of a high level of SRB1, responsible for the uptake of high-density li...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593402/ https://www.ncbi.nlm.nih.gov/pubmed/28919755 http://dx.doi.org/10.2147/IJN.S140591 |
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author | Kuai, Rui Subramanian, Chitra White, Peter T Timmermann, Barbara N Moon, James J Cohen, Mark S Schwendeman, Anna |
author_facet | Kuai, Rui Subramanian, Chitra White, Peter T Timmermann, Barbara N Moon, James J Cohen, Mark S Schwendeman, Anna |
author_sort | Kuai, Rui |
collection | PubMed |
description | Adrenocortical carcinoma (ACC) is a rare endocrine malignancy and has a 5-year survival rate of <35%. ACC cells require cholesterol for steroid hormone production, and this requirement is met via expression on the cell surface of a high level of SRB1, responsible for the uptake of high-density lipoproteins (HDLs), which carry and transport cholesterol in vivo. Here, we describe how this natural lipid carrier function of SRB1 can be utilized to improve the tumor-targeted delivery of a novel natural product derivative – withalongolide A 4,19,27-triacetate (WGA-TA) – which has shown potent antitumor efficacy, but poor aqueous solubility. Our strategy was to use synthetic HDL (sHDL) nanodisks, which are effective in tumor-targeted delivery due to their smallness, long circulation half-life, documented safety, and ability to bind to SRB1. In this study, we prepared sHDL nanodisks using an optimized phospholipid composition combined with ApoA(1) mimetic peptide (22A), which has previously been tested in clinical trials, to load WGA-TA. Following optimization, WGA-TA nanodisks showed drug encapsulation efficiency of 78%, a narrow particle size distribution (9.81±0.41 nm), discoid shape, and sustained drug release in phosphate buffered saline. WGA-TA-sHDL nanodisks exhibited higher cytotoxicity in the ACC cell line H295R half maximal inhibitory concentration ([IC(50)] 0.26±0.045 μM) than free WGA-TA (IC(50) 0.492±0.115 μM, P<0.05). Fluorescent dye-loaded sHDL nanodisks efficiently accumulated in H295R adrenal carcinoma xenografts 24 hours following dosing. Moreover, daily intraperitoneal administration of 7 mg/kg WGA-TA-loaded sHDL nanodisks significantly inhibited tumor growth during 21-day administration to H295R xenograft-bearing mice compared to placebo (P<0.01). Collectively, these results suggest that WGA-TA-loaded nanodisks may represent a novel and beneficial therapeutic strategy for the treatment of ACC. |
format | Online Article Text |
id | pubmed-5593402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55934022017-09-15 Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma Kuai, Rui Subramanian, Chitra White, Peter T Timmermann, Barbara N Moon, James J Cohen, Mark S Schwendeman, Anna Int J Nanomedicine Original Research Adrenocortical carcinoma (ACC) is a rare endocrine malignancy and has a 5-year survival rate of <35%. ACC cells require cholesterol for steroid hormone production, and this requirement is met via expression on the cell surface of a high level of SRB1, responsible for the uptake of high-density lipoproteins (HDLs), which carry and transport cholesterol in vivo. Here, we describe how this natural lipid carrier function of SRB1 can be utilized to improve the tumor-targeted delivery of a novel natural product derivative – withalongolide A 4,19,27-triacetate (WGA-TA) – which has shown potent antitumor efficacy, but poor aqueous solubility. Our strategy was to use synthetic HDL (sHDL) nanodisks, which are effective in tumor-targeted delivery due to their smallness, long circulation half-life, documented safety, and ability to bind to SRB1. In this study, we prepared sHDL nanodisks using an optimized phospholipid composition combined with ApoA(1) mimetic peptide (22A), which has previously been tested in clinical trials, to load WGA-TA. Following optimization, WGA-TA nanodisks showed drug encapsulation efficiency of 78%, a narrow particle size distribution (9.81±0.41 nm), discoid shape, and sustained drug release in phosphate buffered saline. WGA-TA-sHDL nanodisks exhibited higher cytotoxicity in the ACC cell line H295R half maximal inhibitory concentration ([IC(50)] 0.26±0.045 μM) than free WGA-TA (IC(50) 0.492±0.115 μM, P<0.05). Fluorescent dye-loaded sHDL nanodisks efficiently accumulated in H295R adrenal carcinoma xenografts 24 hours following dosing. Moreover, daily intraperitoneal administration of 7 mg/kg WGA-TA-loaded sHDL nanodisks significantly inhibited tumor growth during 21-day administration to H295R xenograft-bearing mice compared to placebo (P<0.01). Collectively, these results suggest that WGA-TA-loaded nanodisks may represent a novel and beneficial therapeutic strategy for the treatment of ACC. Dove Medical Press 2017-09-06 /pmc/articles/PMC5593402/ /pubmed/28919755 http://dx.doi.org/10.2147/IJN.S140591 Text en © 2017 Kuai et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kuai, Rui Subramanian, Chitra White, Peter T Timmermann, Barbara N Moon, James J Cohen, Mark S Schwendeman, Anna Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title | Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title_full | Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title_fullStr | Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title_full_unstemmed | Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title_short | Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
title_sort | synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593402/ https://www.ncbi.nlm.nih.gov/pubmed/28919755 http://dx.doi.org/10.2147/IJN.S140591 |
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