Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy

Traditional cancer treatment modalities such as surgery, chemotherapy, and radiation therapy have seen significant advancements in the past. However, inherent drawbacks, including systemic toxicity and high recurrence rates. Consequently, The nanoparticles, with their targeting and multifunctionalit...

Full description

Bibliographic Details
Main Authors: Wei-wei Huan, Mengyang Dong, Ziling Chang, Huafei Li, Wei Liu, Yuxiang Yang, Hongmin Yuan, Yan Huang, Wenwen Liu, Riccardo Carlini, Mo Chen
Format: Article
Language:English
Published: Elsevier 2024-05-01
Series:Materials & Design
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0264127524002843
_version_ 1797214871138336768
author Wei-wei Huan
Mengyang Dong
Ziling Chang
Huafei Li
Wei Liu
Yuxiang Yang
Hongmin Yuan
Yan Huang
Wenwen Liu
Riccardo Carlini
Mo Chen
author_facet Wei-wei Huan
Mengyang Dong
Ziling Chang
Huafei Li
Wei Liu
Yuxiang Yang
Hongmin Yuan
Yan Huang
Wenwen Liu
Riccardo Carlini
Mo Chen
author_sort Wei-wei Huan
collection DOAJ
description Traditional cancer treatment modalities such as surgery, chemotherapy, and radiation therapy have seen significant advancements in the past. However, inherent drawbacks, including systemic toxicity and high recurrence rates. Consequently, The nanoparticles, with their targeting and multifunctionality, have captured significant attention. This work synthesizes HMNPs-C60-N-GQDs-SS-PEI (HMNPs:Fe3O4@SiO2@mSiO2-C18) nanoparticles, integrating diverse functionalities for enhanced cancer therapy. The inclusion of SiO2 and C60 significantly improves the loading efficiency of gallic acid (GA). The magnetic properties of HMNPs enable efficient targeting to cancer sites under external magnetic fields. The -SS- linkage ensures drug release exclusively in tumor cells over-expressing glutathione (GSH), minimizing adverse effects on normal tissues. Introduction of Polyethyleneimine (PEI) imparts positive charge to facilitate accumulation on negatively charged tumor surfaces and enhances biocompatibility. Additionally, the fluorescence properties of N-doped graphene quantum dots (N-GQDs) facilitate real-time monitoring of material distribution in vivo during mouse and clinical therapy. Furthermore, the nano-magnetic targeting material demonstrates efficient drug loading and precise control over drug release, addressing issues such as the poor biocompatibility and high biotoxicity associated with traditional materials. This study not only achieves effective tumor treatment but also offers a promising direction for developing efficient multifunctional nano-targeting materials.
first_indexed 2024-04-24T11:21:03Z
format Article
id doaj.art-1a517bb3901e442da8a104bc873fcb00
institution Directory Open Access Journal
issn 0264-1275
language English
last_indexed 2024-04-24T11:21:03Z
publishDate 2024-05-01
publisher Elsevier
record_format Article
series Materials & Design
spelling doaj.art-1a517bb3901e442da8a104bc873fcb002024-04-11T04:40:48ZengElsevierMaterials & Design0264-12752024-05-01241112911Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapyWei-wei Huan0Mengyang Dong1Ziling Chang2Huafei Li3Wei Liu4Yuxiang Yang5Hongmin Yuan6Yan Huang7Wenwen Liu8Riccardo Carlini9Mo Chen10College of Chemistry and Materials Engineering, Zhejiang A&F University, Hangzhou, Zhejiang 311300, ChinaSchool of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, ChinaSchool of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, ChinaSchool of Lifesciences, Shanghai University, 333 Nanchen Road, Shanghai, ChinaCollege of Chemistry and Materials Engineering, Zhejiang A&F University, Hangzhou, Zhejiang 311300, ChinaSchool of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China; Corresponding authors.State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, ChinaSchool of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, ChinaSchool of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, ChinaState Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, China; Chemistry and Material Chemistry Department, LAS Klee-Barabino, 16146 Genova, Italy; Corresponding authors.College of Chemistry and Materials Engineering, Zhejiang A&F University, Hangzhou, Zhejiang 311300, ChinaTraditional cancer treatment modalities such as surgery, chemotherapy, and radiation therapy have seen significant advancements in the past. However, inherent drawbacks, including systemic toxicity and high recurrence rates. Consequently, The nanoparticles, with their targeting and multifunctionality, have captured significant attention. This work synthesizes HMNPs-C60-N-GQDs-SS-PEI (HMNPs:Fe3O4@SiO2@mSiO2-C18) nanoparticles, integrating diverse functionalities for enhanced cancer therapy. The inclusion of SiO2 and C60 significantly improves the loading efficiency of gallic acid (GA). The magnetic properties of HMNPs enable efficient targeting to cancer sites under external magnetic fields. The -SS- linkage ensures drug release exclusively in tumor cells over-expressing glutathione (GSH), minimizing adverse effects on normal tissues. Introduction of Polyethyleneimine (PEI) imparts positive charge to facilitate accumulation on negatively charged tumor surfaces and enhances biocompatibility. Additionally, the fluorescence properties of N-doped graphene quantum dots (N-GQDs) facilitate real-time monitoring of material distribution in vivo during mouse and clinical therapy. Furthermore, the nano-magnetic targeting material demonstrates efficient drug loading and precise control over drug release, addressing issues such as the poor biocompatibility and high biotoxicity associated with traditional materials. This study not only achieves effective tumor treatment but also offers a promising direction for developing efficient multifunctional nano-targeting materials.http://www.sciencedirect.com/science/article/pii/S0264127524002843Spherical materialpH responseRedox responseMagnetic targeted therapyGambogic acid
spellingShingle Wei-wei Huan
Mengyang Dong
Ziling Chang
Huafei Li
Wei Liu
Yuxiang Yang
Hongmin Yuan
Yan Huang
Wenwen Liu
Riccardo Carlini
Mo Chen
Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
Materials & Design
Spherical material
pH response
Redox response
Magnetic targeted therapy
Gambogic acid
title Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
title_full Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
title_fullStr Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
title_full_unstemmed Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
title_short Sustainable gambogic acid release via pH/Redox Dual-Responsive C60-Modified magnetic mesoporous nanospheres for antitumor therapy
title_sort sustainable gambogic acid release via ph redox dual responsive c60 modified magnetic mesoporous nanospheres for antitumor therapy
topic Spherical material
pH response
Redox response
Magnetic targeted therapy
Gambogic acid
url http://www.sciencedirect.com/science/article/pii/S0264127524002843
work_keys_str_mv AT weiweihuan sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT mengyangdong sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT zilingchang sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT huafeili sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT weiliu sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT yuxiangyang sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT hongminyuan sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT yanhuang sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT wenwenliu sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT riccardocarlini sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy
AT mochen sustainablegambogicacidreleaseviaphredoxdualresponsivec60modifiedmagneticmesoporousnanospheresforantitumortherapy