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Ultrasound responsive carbon monoxide releasing micelle

Carbon monoxide (CO), an endogenously produced gasotransmitter, has shown various therapeutic effects in previous studies. In this work, we developed an ultrasound responsive micelle for localized CO delivery. The micelle is composed of a pluronic shell and a core of a CO releasing molecule, CORM-2....

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Autores principales: Alghazwat, Osamah, Talebzadeh, Somayeh, Oyer, Jeremiah, Copik, Alicja, Liao, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803797/
https://www.ncbi.nlm.nih.gov/pubmed/33373872
http://dx.doi.org/10.1016/j.ultsonch.2020.105427
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author Alghazwat, Osamah
Talebzadeh, Somayeh
Oyer, Jeremiah
Copik, Alicja
Liao, Yi
author_facet Alghazwat, Osamah
Talebzadeh, Somayeh
Oyer, Jeremiah
Copik, Alicja
Liao, Yi
author_sort Alghazwat, Osamah
collection PubMed
description Carbon monoxide (CO), an endogenously produced gasotransmitter, has shown various therapeutic effects in previous studies. In this work, we developed an ultrasound responsive micelle for localized CO delivery. The micelle is composed of a pluronic shell and a core of a CO releasing molecule, CORM-2. The mechanism is based on the ultrasound response of pluronics, and the reaction between CORM-2 and certain biomolecules, e.g. cysteine. The latter allows CO release without significantly breaking the micelles. In a 3.5 mM cysteine solution, the micelles released low level of CO, indicating effective encapsulation of CORM-2. Treatment with a low intensity, non-focused ultrasound led to four times as much CO as the sample without ultrasonication, which is close to that of unencapsulated CORM-2. Significantly reduced proliferation of prostate cancer cells (PC-3) was observed 24 h after the PC-3 cells were treated with the CORM-2 micelles followed by ultrasound activation.
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spelling pubmed-78037972021-01-22 Ultrasound responsive carbon monoxide releasing micelle Alghazwat, Osamah Talebzadeh, Somayeh Oyer, Jeremiah Copik, Alicja Liao, Yi Ultrason Sonochem Original Research Article Carbon monoxide (CO), an endogenously produced gasotransmitter, has shown various therapeutic effects in previous studies. In this work, we developed an ultrasound responsive micelle for localized CO delivery. The micelle is composed of a pluronic shell and a core of a CO releasing molecule, CORM-2. The mechanism is based on the ultrasound response of pluronics, and the reaction between CORM-2 and certain biomolecules, e.g. cysteine. The latter allows CO release without significantly breaking the micelles. In a 3.5 mM cysteine solution, the micelles released low level of CO, indicating effective encapsulation of CORM-2. Treatment with a low intensity, non-focused ultrasound led to four times as much CO as the sample without ultrasonication, which is close to that of unencapsulated CORM-2. Significantly reduced proliferation of prostate cancer cells (PC-3) was observed 24 h after the PC-3 cells were treated with the CORM-2 micelles followed by ultrasound activation. Elsevier 2020-12-26 /pmc/articles/PMC7803797/ /pubmed/33373872 http://dx.doi.org/10.1016/j.ultsonch.2020.105427 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
Alghazwat, Osamah
Talebzadeh, Somayeh
Oyer, Jeremiah
Copik, Alicja
Liao, Yi
Ultrasound responsive carbon monoxide releasing micelle
title Ultrasound responsive carbon monoxide releasing micelle
title_full Ultrasound responsive carbon monoxide releasing micelle
title_fullStr Ultrasound responsive carbon monoxide releasing micelle
title_full_unstemmed Ultrasound responsive carbon monoxide releasing micelle
title_short Ultrasound responsive carbon monoxide releasing micelle
title_sort ultrasound responsive carbon monoxide releasing micelle
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803797/
https://www.ncbi.nlm.nih.gov/pubmed/33373872
http://dx.doi.org/10.1016/j.ultsonch.2020.105427
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