Light-induced release of the cardioprotective peptide angiotensin-(1–9) from thermosensitive liposomes with gold nanoclusters

Angiotensin-(1-9), a component of the non-canonical renin-angiotensin system, has a short half-life in blood. This peptide has shown to prevent and/or attenuate hypertension and cardiovascular remodeling. A controlled release of angiotensin-(1-9) is needed for its delivery to the heart. Our aim was...

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Veröffentlicht in:Journal of controlled release 2020-12, Vol.328, p.859-872
Hauptverfasser: Bejarano, Julian, Rojas, Aldo, Ramírez-Sagredo, Andrea, Riveros, Ana L., Morales-Zavala, Francisco, Flores, Yvo, Riquelme, Jaime A., Guzman, Fanny, Araya, Eyleen, Chiong, Mario, Ocaranza, María Paz, Morales, Javier O., Villamizar Sarmiento, María Gabriela, Sanchez, Gina, Lavandero, Sergio, Kogan, Marcelo J.
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container_issue
container_start_page 859
container_title Journal of controlled release
container_volume 328
creator Bejarano, Julian
Rojas, Aldo
Ramírez-Sagredo, Andrea
Riveros, Ana L.
Morales-Zavala, Francisco
Flores, Yvo
Riquelme, Jaime A.
Guzman, Fanny
Araya, Eyleen
Chiong, Mario
Ocaranza, María Paz
Morales, Javier O.
Villamizar Sarmiento, María Gabriela
Sanchez, Gina
Lavandero, Sergio
Kogan, Marcelo J.
description Angiotensin-(1-9), a component of the non-canonical renin-angiotensin system, has a short half-life in blood. This peptide has shown to prevent and/or attenuate hypertension and cardiovascular remodeling. A controlled release of angiotensin-(1-9) is needed for its delivery to the heart. Our aim was to develop a drug delivery system for angiotensin-(1-9). Thermosensitive liposomes (LipoTherm) were prepared with gold nanoclusters (LipoTherm-AuNC) to increase the stability and reach a temporal and spatial control of angiotensin-(1-9) release. Encapsulation efficiencies of nearly 50% were achieved in LipoTherm, reaching a total angiotensin-(1-9) loading of around 180 μM. This angiotensin-(1–9)-loaded LipoTherm sized around 100 nm and exhibited a phase transition temperature of 43 °C. AuNC were grown on LipoTherm and the new hybrid nanosystem showed energy absorption in the near-infrared (NIR) wavelength range. By NIR laser irradiation, a controlled release of angiotensin-(1-9) was achieved from the LipoTherm-AuNC nanosystem. These nanosystems did not show any cytotoxic effect on cultured cardiomyocytes. Biological activity of angiotensin-(1-9) released from the LipoTherm-AuNC-based nanosystem was confirmed using an ex vivo Langendorff heart model. This graphical abstract was created using images from Servier medical art commons attribution 3.0 Unported license. (http://smart.servier.com). These images are licensed under a creative commons attribution 3.0 Unported license. [Display omitted]
doi_str_mv 10.1016/j.jconrel.2020.11.002
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This peptide has shown to prevent and/or attenuate hypertension and cardiovascular remodeling. A controlled release of angiotensin-(1-9) is needed for its delivery to the heart. Our aim was to develop a drug delivery system for angiotensin-(1-9). Thermosensitive liposomes (LipoTherm) were prepared with gold nanoclusters (LipoTherm-AuNC) to increase the stability and reach a temporal and spatial control of angiotensin-(1-9) release. Encapsulation efficiencies of nearly 50% were achieved in LipoTherm, reaching a total angiotensin-(1-9) loading of around 180 μM. This angiotensin-(1–9)-loaded LipoTherm sized around 100 nm and exhibited a phase transition temperature of 43 °C. AuNC were grown on LipoTherm and the new hybrid nanosystem showed energy absorption in the near-infrared (NIR) wavelength range. By NIR laser irradiation, a controlled release of angiotensin-(1-9) was achieved from the LipoTherm-AuNC nanosystem. 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subjects Angiotensin-(1-9)
Cardioprotection
Cardiovascular diseases
Nanoparticles
Thermosensitive liposomes
title Light-induced release of the cardioprotective peptide angiotensin-(1–9) from thermosensitive liposomes with gold nanoclusters
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