Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light

Drug resistance is accountable for the inadequate outcome of chemotherapy in clinics. The newly emerging role of nitric oxide (NO) to conquer drug resistance has been recognized as a potential strategy. However, it remains a great challenge to realize targeted delivery as well as accurate release of...

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Main Authors: Linping Jiang, Kesi Wang, Liyan Qiu
Format: Article
Language:English
Published: Elsevier 2022-11-01
Series:Asian Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1818087622001039
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author Linping Jiang
Kesi Wang
Liyan Qiu
author_facet Linping Jiang
Kesi Wang
Liyan Qiu
author_sort Linping Jiang
collection DOAJ
description Drug resistance is accountable for the inadequate outcome of chemotherapy in clinics. The newly emerging role of nitric oxide (NO) to conquer drug resistance has been recognized as a potential strategy. However, it remains a great challenge to realize targeted delivery as well as accurate release of NO at desired sites. Herein, we developed a PEGylated indocyanine green (mPEG-ICG) integrated nanovesicle system (PIDA) to simultaneously load doxorubicin hydrochloride (DOX⋅HCl) and the NO donor L-arginine (L-Arg), which can produce NO triggered by NIR light irradiation and exert multimodal therapy to sensitize drug-resistant cancers. Upon 808 nm irradiation, the NO released from PIDA led to a decrease in mitochondrial membrane potential, an increase in ROS and significant ATP depletion in K562/ADR cells, thus inhibiting cell growth and resolving the problem of drug resistance. Consequently, the in vivo experiment on K562/ADR-bearing nude mice indicated that PIDA nanovesicles achieved significant anticancer efficacy with a tumor inhibition rate of 80.8%. Above all, PIDA nanovesicles offer guidance for designing nanoplatforms for drug-resistant cancer treatment.
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spelling doaj.art-1eceeb444ce64c31b3be35ef11e1aa702022-12-22T04:41:42ZengElsevierAsian Journal of Pharmaceutical Sciences1818-08762022-11-01176924937Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared lightLinping Jiang0Kesi Wang1Liyan Qiu2Ministry of Educational (MOE) Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, ChinaMinistry of Educational (MOE) Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, ChinaCorresponding author.; Ministry of Educational (MOE) Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, ChinaDrug resistance is accountable for the inadequate outcome of chemotherapy in clinics. The newly emerging role of nitric oxide (NO) to conquer drug resistance has been recognized as a potential strategy. However, it remains a great challenge to realize targeted delivery as well as accurate release of NO at desired sites. Herein, we developed a PEGylated indocyanine green (mPEG-ICG) integrated nanovesicle system (PIDA) to simultaneously load doxorubicin hydrochloride (DOX⋅HCl) and the NO donor L-arginine (L-Arg), which can produce NO triggered by NIR light irradiation and exert multimodal therapy to sensitize drug-resistant cancers. Upon 808 nm irradiation, the NO released from PIDA led to a decrease in mitochondrial membrane potential, an increase in ROS and significant ATP depletion in K562/ADR cells, thus inhibiting cell growth and resolving the problem of drug resistance. Consequently, the in vivo experiment on K562/ADR-bearing nude mice indicated that PIDA nanovesicles achieved significant anticancer efficacy with a tumor inhibition rate of 80.8%. Above all, PIDA nanovesicles offer guidance for designing nanoplatforms for drug-resistant cancer treatment.http://www.sciencedirect.com/science/article/pii/S1818087622001039Nitric oxideL-arginineDoxorubicinIndocyanine greenDrug resistanceNanovesicle
spellingShingle Linping Jiang
Kesi Wang
Liyan Qiu
Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
Asian Journal of Pharmaceutical Sciences
Nitric oxide
L-arginine
Doxorubicin
Indocyanine green
Drug resistance
Nanovesicle
title Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
title_full Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
title_fullStr Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
title_full_unstemmed Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
title_short Doxorubicin hydrochloride and L-arginine co-loaded nanovesicle for drug resistance reversal stimulated by near-infrared light
title_sort doxorubicin hydrochloride and l arginine co loaded nanovesicle for drug resistance reversal stimulated by near infrared light
topic Nitric oxide
L-arginine
Doxorubicin
Indocyanine green
Drug resistance
Nanovesicle
url http://www.sciencedirect.com/science/article/pii/S1818087622001039
work_keys_str_mv AT linpingjiang doxorubicinhydrochlorideandlargininecoloadednanovesiclefordrugresistancereversalstimulatedbynearinfraredlight
AT kesiwang doxorubicinhydrochlorideandlargininecoloadednanovesiclefordrugresistancereversalstimulatedbynearinfraredlight
AT liyanqiu doxorubicinhydrochlorideandlargininecoloadednanovesiclefordrugresistancereversalstimulatedbynearinfraredlight