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Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells

[Image: see text] Extremely short half-life therapeutic molecule nitric oxide (NO) plays significant roles in the functioning of various physiological and pathological processes in the human body, whereas doxorubicin hydrochloride (DOX) is a clinically important anticancer drug widely used in cancer...

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Autores principales: Dutta, Bijaideep, Shelar, Sandeep B., Nirmalraj, Ananya, Gupta, Sonali, Barick, Kanhu C., Gupta, Jagriti, Hassan, Puthusserickal A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688159/
https://www.ncbi.nlm.nih.gov/pubmed/38046289
http://dx.doi.org/10.1021/acsomega.3c03734
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author Dutta, Bijaideep
Shelar, Sandeep B.
Nirmalraj, Ananya
Gupta, Sonali
Barick, Kanhu C.
Gupta, Jagriti
Hassan, Puthusserickal A.
author_facet Dutta, Bijaideep
Shelar, Sandeep B.
Nirmalraj, Ananya
Gupta, Sonali
Barick, Kanhu C.
Gupta, Jagriti
Hassan, Puthusserickal A.
author_sort Dutta, Bijaideep
collection PubMed
description [Image: see text] Extremely short half-life therapeutic molecule nitric oxide (NO) plays significant roles in the functioning of various physiological and pathological processes in the human body, whereas doxorubicin hydrochloride (DOX) is a clinically important anticancer drug widely used in cancer chemotherapy. Thus, the intracellular delivery of these therapeutic molecules is tremendously important to achieve their full potential. Herein, we report a novel approach for the development of highly water-dispersible magnetic nanocarriers for codelivery of NO and DOX. Primarily, bifunctional magnetic nanoparticles enriched with carboxyl and thiol groups were prepared by introducing cysteine onto the surface of citrate-functionalized Fe(3)O(4) nanoparticles. DOX was electrostatically conjugated onto the surface of bifunctional nanoparticles via carboxyl moieties, whereas the thiol group was further nitrosated to provide NO-releasing molecules. The developed magnetic nanocarrier exhibited good aqueous colloidal stability, protein resistance behavior, and high encapsulation efficacy for NO (65.5%) and DOX (85%), as well as sustained release characteristics. Moreover, they showed superior cytotoxicity toward cancer (A549 and MCF-7) cells via apoptosis induction over normal (WI26VA4) cells. Specifically, we have developed magnetic nanocarriers having the capability of dual delivery of NO and DOX, which holds great potential for combinatorial cancer treatment.
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spelling pubmed-106881592023-12-01 Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells Dutta, Bijaideep Shelar, Sandeep B. Nirmalraj, Ananya Gupta, Sonali Barick, Kanhu C. Gupta, Jagriti Hassan, Puthusserickal A. ACS Omega [Image: see text] Extremely short half-life therapeutic molecule nitric oxide (NO) plays significant roles in the functioning of various physiological and pathological processes in the human body, whereas doxorubicin hydrochloride (DOX) is a clinically important anticancer drug widely used in cancer chemotherapy. Thus, the intracellular delivery of these therapeutic molecules is tremendously important to achieve their full potential. Herein, we report a novel approach for the development of highly water-dispersible magnetic nanocarriers for codelivery of NO and DOX. Primarily, bifunctional magnetic nanoparticles enriched with carboxyl and thiol groups were prepared by introducing cysteine onto the surface of citrate-functionalized Fe(3)O(4) nanoparticles. DOX was electrostatically conjugated onto the surface of bifunctional nanoparticles via carboxyl moieties, whereas the thiol group was further nitrosated to provide NO-releasing molecules. The developed magnetic nanocarrier exhibited good aqueous colloidal stability, protein resistance behavior, and high encapsulation efficacy for NO (65.5%) and DOX (85%), as well as sustained release characteristics. Moreover, they showed superior cytotoxicity toward cancer (A549 and MCF-7) cells via apoptosis induction over normal (WI26VA4) cells. Specifically, we have developed magnetic nanocarriers having the capability of dual delivery of NO and DOX, which holds great potential for combinatorial cancer treatment. American Chemical Society 2023-11-15 /pmc/articles/PMC10688159/ /pubmed/38046289 http://dx.doi.org/10.1021/acsomega.3c03734 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Dutta, Bijaideep
Shelar, Sandeep B.
Nirmalraj, Ananya
Gupta, Sonali
Barick, Kanhu C.
Gupta, Jagriti
Hassan, Puthusserickal A.
Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title_full Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title_fullStr Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title_full_unstemmed Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title_short Smart Magnetic Nanocarriers for Codelivery of Nitric Oxide and Doxorubicin for Enhanced Apoptosis in Cancer Cells
title_sort smart magnetic nanocarriers for codelivery of nitric oxide and doxorubicin for enhanced apoptosis in cancer cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688159/
https://www.ncbi.nlm.nih.gov/pubmed/38046289
http://dx.doi.org/10.1021/acsomega.3c03734
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