Biomimetic Hybrid Nanozymes with Self-Supplied H+ and Accelerated O2 Generation for Enhanced Starvation and Photodynamic Therapy against Hypoxic Tumors

Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme acti...

Full description

Saved in:
Bibliographic Details
Published inNano letters Vol. 19; no. 7; pp. 4334 - 4342
Main Authors Yang, Xue, Yang, Ying, Gao, Fang, Wei, Jia-Jia, Qian, Cheng-Gen, Sun, Min-Jie
Format Journal Article
LanguageEnglish
Published American Chemical Society 10.07.2019
Subjects
Online AccessGet full text
ISSN1530-6984
1530-6992
1530-6992
DOI10.1021/acs.nanolett.9b00934

Cover

Abstract Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme activity in vivo. Here we report a biomimetic hybrid nanozyme (named rMGB) which integrates natural enzyme glucose oxidase (GOx) with nanozyme manganese dioxide (MnO2) by mutual promotion for maximizing the enzymatic activity of MnO2 and GOx. Under hypoxia environment, we observed that MnO2 could react with endogenous H2O2 to produce O2 for enhancing the catalytic efficiency of GOx for starvation therapy. Meanwhile, we confirmed that glucose oxidation generated gluconic acid and further improved the catalytic efficiency of MnO2 subsequently. The biochemical reaction cycle, consisting of MnO2, O2, GOx, and H+, was triggered by the tumor microenvironment and accelerated each other so as to achieve self-supplied H+ and accelerate O2 generation, enhancing the starvation therapy, alleviating tumor hypoxia and accelerating the reactive oxygen species generation in photodynamic therapy. This biomimetic hybrid nanozyme would further facilitate the development of biological nanozymes for cancer treatment.
AbstractList Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme activity in vivo. Here we report a biomimetic hybrid nanozyme (named rMGB) which integrates natural enzyme glucose oxidase (GOx) with nanozyme manganese dioxide (MnO2) by mutual promotion for maximizing the enzymatic activity of MnO2 and GOx. Under hypoxia environment, we observed that MnO2 could react with endogenous H2O2 to produce O2 for enhancing the catalytic efficiency of GOx for starvation therapy. Meanwhile, we confirmed that glucose oxidation generated gluconic acid and further improved the catalytic efficiency of MnO2 subsequently. The biochemical reaction cycle, consisting of MnO2, O2, GOx, and H+, was triggered by the tumor microenvironment and accelerated each other so as to achieve self-supplied H+ and accelerate O2 generation, enhancing the starvation therapy, alleviating tumor hypoxia and accelerating the reactive oxygen species generation in photodynamic therapy. This biomimetic hybrid nanozyme would further facilitate the development of biological nanozymes for cancer treatment.
Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme activity in vivo. Here we report a biomimetic hybrid nanozyme (named rMGB) which integrates natural enzyme glucose oxidase (GOx) with nanozyme manganese dioxide (MnO2) by mutual promotion for maximizing the enzymatic activity of MnO2 and GOx. Under hypoxia environment, we observed that MnO2 could react with endogenous H2O2 to produce O2 for enhancing the catalytic efficiency of GOx for starvation therapy. Meanwhile, we confirmed that glucose oxidation generated gluconic acid and further improved the catalytic efficiency of MnO2 subsequently. The biochemical reaction cycle, consisting of MnO2, O2, GOx, and H+, was triggered by the tumor microenvironment and accelerated each other so as to achieve self-supplied H+ and accelerate O2 generation, enhancing the starvation therapy, alleviating tumor hypoxia and accelerating the reactive oxygen species generation in photodynamic therapy. This biomimetic hybrid nanozyme would further facilitate the development of biological nanozymes for cancer treatment.Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic nanozymes require more consideration regarding complicated tumor microenvironments to mimic biological enzymes, thus achieving superior nanozyme activity in vivo. Here we report a biomimetic hybrid nanozyme (named rMGB) which integrates natural enzyme glucose oxidase (GOx) with nanozyme manganese dioxide (MnO2) by mutual promotion for maximizing the enzymatic activity of MnO2 and GOx. Under hypoxia environment, we observed that MnO2 could react with endogenous H2O2 to produce O2 for enhancing the catalytic efficiency of GOx for starvation therapy. Meanwhile, we confirmed that glucose oxidation generated gluconic acid and further improved the catalytic efficiency of MnO2 subsequently. The biochemical reaction cycle, consisting of MnO2, O2, GOx, and H+, was triggered by the tumor microenvironment and accelerated each other so as to achieve self-supplied H+ and accelerate O2 generation, enhancing the starvation therapy, alleviating tumor hypoxia and accelerating the reactive oxygen species generation in photodynamic therapy. This biomimetic hybrid nanozyme would further facilitate the development of biological nanozymes for cancer treatment.
Author Wei, Jia-Jia
Qian, Cheng-Gen
Yang, Xue
Gao, Fang
Yang, Ying
Sun, Min-Jie
AuthorAffiliation State Key Laboratory of Natural Medicines, Department of Pharmaceutics
AuthorAffiliation_xml – name: State Key Laboratory of Natural Medicines, Department of Pharmaceutics
Author_xml – sequence: 1
  givenname: Xue
  surname: Yang
  fullname: Yang, Xue
– sequence: 2
  givenname: Ying
  surname: Yang
  fullname: Yang, Ying
– sequence: 3
  givenname: Fang
  surname: Gao
  fullname: Gao, Fang
– sequence: 4
  givenname: Jia-Jia
  surname: Wei
  fullname: Wei, Jia-Jia
– sequence: 5
  givenname: Cheng-Gen
  surname: Qian
  fullname: Qian, Cheng-Gen
  email: cgqian@cpu.edu.cn
– sequence: 6
  givenname: Min-Jie
  orcidid: 0000-0003-0582-6189
  surname: Sun
  fullname: Sun, Min-Jie
  email: msun@cpu.edu.cn
BookMark eNo9UctOwzAQtFCRaAt_wMFHJJRiO06Ij6UqLVJFkVrOkZ04xFVih9gBwo_wuzhq4bS7s7PPmYCRNloCcI3RDCOC73hmZ5prU0nnZkwgxEJ6BsY4ClEQM0ZG_35CL8DE2gMaOBEag58HZWpVS6cyuO5Fq3L47Dt997W08FO5Eu5kVQS7rmkqJXO4voVc53CeZbKSLXce2hK4knoIlNGwMC1c6pLrzKd2jrcfR3yoeimNM3mvee2n7Utf0vSQv3GlrfPTG_M14F1tWnsJzgteWXl1slPw-rjcL9bBZrt6Wsw3ASeEuSDOY0pinmBGOMdFTrOEJpEQVERFyO4FoyEpKBKJpzEREczDJENMCpYRmRQ0nIKbY9-mNe-dtC6tlfW3VVxL09mUEEpwRChKPBUdqf7d6cF0rfaLpRilgwbpAP5pkJ40CH8BUGKB1A
ContentType Journal Article
DBID 7X8
DOI 10.1021/acs.nanolett.9b00934
DatabaseName MEDLINE - Academic
DatabaseTitle MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
EISSN 1530-6992
EndPage 4342
ExternalDocumentID c020840014
GroupedDBID -
.K2
123
55A
5VS
7~N
AABXI
ABMVS
ABPTK
ABUCX
ACGFS
ACS
AEESW
AENEX
AFEFF
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CS3
DU5
EBS
ED
ED~
EJD
F5P
GNL
IH9
IHE
JG
JG~
K2
PK8
RNS
ROL
TN5
UI2
VF5
VG9
W1F
X
---
-~X
4.4
6P2
7X8
AAHBH
ABBLG
ABJNI
ABLBI
ABQRX
ACBEA
ADHLV
AHGAQ
CUPRZ
GGK
ID FETCH-LOGICAL-a229t-6d6426a8192aa1fd4c8485bb4b5f397b9432f40b86429b521a38c09eb9c2e8f43
IEDL.DBID ACS
ISSN 1530-6984
1530-6992
IngestDate Fri Jul 11 14:56:32 EDT 2025
Thu Aug 27 13:44:20 EDT 2020
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords hypoxia
Nanozyme
oxygen generation
starvation therapy
photodynamic therapy
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a229t-6d6426a8192aa1fd4c8485bb4b5f397b9432f40b86429b521a38c09eb9c2e8f43
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-0582-6189
PQID 2242152408
PQPubID 23479
PageCount 9
ParticipantIDs proquest_miscellaneous_2242152408
acs_journals_10_1021_acs_nanolett_9b00934
ProviderPackageCode JG~
55A
AABXI
GNL
VF5
7~N
VG9
W1F
ACS
AEESW
AFEFF
.K2
ABMVS
ABUCX
IH9
BAANH
AQSVZ
ED~
UI2
PublicationCentury 2000
PublicationDate 2019-07-10
PublicationDateYYYYMMDD 2019-07-10
PublicationDate_xml – month: 07
  year: 2019
  text: 2019-07-10
  day: 10
PublicationDecade 2010
PublicationTitle Nano letters
PublicationTitleAlternate Nano Lett
PublicationYear 2019
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
SSID ssj0009350
Score 2.668256
Snippet Nanozymes as artificial enzymes that mimicked natural enzyme-like activities have received great attention in cancer diagnosis and therapy. Biomimetic...
SourceID proquest
acs
SourceType Aggregation Database
Publisher
StartPage 4334
Title Biomimetic Hybrid Nanozymes with Self-Supplied H+ and Accelerated O2 Generation for Enhanced Starvation and Photodynamic Therapy against Hypoxic Tumors
URI http://dx.doi.org/10.1021/acs.nanolett.9b00934
https://www.proquest.com/docview/2242152408
Volume 19
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1LS8QwEA4-LnrwLb6J4EWk626ahua4LsriQQVd2FtJ0lQXbSK2C65_xL_rTLfLiougtxLSpM1rvsnMfEPICSwLHelWFMg4BgVFhBbOQakCIRXSp4NAsZWD7I3o9vh1P-pPFcWfFnzWOlemaDjlPPxG2UAGPxnyebLIBIgahEKd-ynJblhlZIVNDCqRjPkkVO6XVlAgmWLmEK4ky9UquZ3E54wdSp4bw1I3zMcsXeMfP3qNrNQgk7bHq2KdzFm3QZa_UQ9uks-Lgc8HOYYw0u4Iw7YoHLT-Y5TbguLlLL23L1lQJf0ElEq7Z1S5lLaNATmF9BIpvWV0TFqNc0sB_NJL91Q5FFCAsPVdb_XW3ZMvfTpyKofeHsY8BlQ9qgFgU-j91b9j-TD3b8UW6V1dPnS6QZ2kIVCMyTIQKWgwQiGvmlKtLOUm5nGkNddRBlhHSx6yjDd1DNWkBrCgwtg0pdXSMBtnPNwmC847u0MoE6DcZKEQkTU8bEKVNINHADwak2qxXXIK45rUm6xIKvs5ayVYOBnspB7sXXI8mdUENgxaQZSzflgkDI3gETK77f2jvX2yBFAJ471AcB2QhfJtaA8BjpT6qFqDX-gF3bE
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwEB6V9gA9QHmJAi1G4oJQtruObcXHpWqVQilI3aLeIjtx6IrGRk1WYvtH-LvMeLNtVcSht8hy_LbnG4_nG4B3uCystCOZ6CxDBUWlDs9BbRKlDdGno0Bx8YHskcpPxKdTeboCcukLg41osaQ2GvGv2QVGO5TmjQ_Ym25ARH46FfdgTSqhKGLDePf4mms3jYFZcS-jZqQzsfSY-08pJJfK9p-zOAqY_Ufw_app8V3Jz8Gss4Py8hZr453bvgEPe8jJxos18hhWnH8C6zeICJ_Cn4_T0Ewbcmhk-ZycuBgeu-Fy3riW0VUtO3bndRJDgCJmZfkHZnzFxmWJUovIJir2lbMFhTXNNEMozPb8WXxewBDQ9je_8a9vZ6EL1dybBmubLFgNmPlhpohUsfZf4Telz5pw0T6Dk_29yW6e9CEbEsO57hJVoT6jDLGsGTOqK1FmIpPWCitrRD5Wi5TXYmgzzKYtQgeTZuVQO6tL7rJapM9h1QfvXgDjClWdOlVKulKkQ8xS1fiJ8MdSiC2-Ce9xXIt-y7VFtKbzUUGJy8Eu-sHehLfLyS1w-5BNxHgXZm3BySQuieft5R3KewP388mXw-Lw4OjzK3iAIIo8wVCkvYbV7mLmthCodHY7Lsu_4a_mEw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dT9swELegSNN4ADaGKF_zpL1MU0rjOFH8WEqr7kMMqSChvUR24tAKYiOSSrT_yP7d3bnpqEA8jLfISmzH9vl-5_P9jpDPsCxUqPzQE3EMBkoUaNgHhfQiIZE-HRSKdhdkz6LBJf9-FV4tpfqCTpRQU-mc-CjVd1leMwz4x1hupLHwR1ULyfxEwFfJGmASH7M2dLrDR77dwCVnBXkG60jEfBE190ItqJvS8tl-7JRMf5P8_tc9d7fkpjWpVCudPWFufFX_t8hGDT1pZ75W3pEVbd6T9SVCwm3y52Rsi3GBgY10MMVgLgrbr51NC11SPLKlQ32bey4VKGBXOvhKpcloJ01BeyHpREZ_MTqnssYZpwCJac-M3DUDCsC2PgF2X52PbGWzqZEFtHYxZzeg8lqOAbFC63f2Acsnhb0vP5DLfu-iO_Dq1A2eZExUXpSBXRNJZFuT0s8znsY8DpXiKswBASnBA5bztorhNaEAQsggTttCK5EyHec82CENY43eJZRFYPLkQRSFOuVBG17JcngEGKQw1RZrki8wrkktemXivOrMT7BwMdhJPdhN8mkxwQmIEfpGpNF2UiYMXeMh8r3t_Ud9H8mb89N-8vPb2Y998hawFAaEgWY7II3qfqIPAa9U6sitzL8z6-iN
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Biomimetic+Hybrid+Nanozymes+with+Self-Supplied+H%2B+and+Accelerated+O2+Generation+for+Enhanced+Starvation+and+Photodynamic+Therapy+against+Hypoxic+Tumors&rft.jtitle=Nano+letters&rft.au=Yang%2C+Xue&rft.au=Yang%2C+Ying&rft.au=Gao%2C+Fang&rft.au=Wei%2C+Jia-Jia&rft.date=2019-07-10&rft.pub=American+Chemical+Society&rft.issn=1530-6984&rft.eissn=1530-6992&rft.volume=19&rft.issue=7&rft.spage=4334&rft.epage=4342&rft_id=info:doi/10.1021%2Facs.nanolett.9b00934&rft.externalDocID=c020840014
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1530-6984&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1530-6984&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1530-6984&client=summon