A tumor-sensitive biological metal–organic complex for drug delivery and cancer therapy. Issue 32 (3rd July 2020)
- Record Type:
- Journal Article
- Title:
- A tumor-sensitive biological metal–organic complex for drug delivery and cancer therapy. Issue 32 (3rd July 2020)
- Main Title:
- A tumor-sensitive biological metal–organic complex for drug delivery and cancer therapy
- Authors:
- Jiang, Zelei
Wang, Tong
Yuan, Shuai
Wang, Mengfan
Qi, Wei
Su, Rongxin
He, Zhimin - Abstract:
- Abstract : Tumor-sensitive bioMOC-Zn(Cys) was developed using an endogenous Zn 2+ ion and l -cystine for the delivery of anti-cancer drug DOX. In vivo application of DOX@bioMOC-Zn(Cys) shows the increased inhibition of tumor growth and prevented side effects. Abstract : Metal–organic complexes (MOCs) or metal–organic frameworks (MOFs) have attracted increasing interest for constructing nanoscale drug delivery systems for cancer therapy. However, conventional MOC/MOF materials usually contain toxic metals or low-biocompatible organic ligands. Also, current approaches for creating tumor-sensitive nanocarriers are always based on the instability of coordination bonds under acidic conditions, or through post-synthetic modification with sensitive molecules. As a matter of fact, it is more facile to fabricate tumor-sensitive MOCs/MOFs based on the stimuli-responsiveness of organic ligands. In this study, a novel tumor-sensitive biological MOC (bioMOC-Zn(Cys)) was created through the assembly of endogenous Zn 2+ ions and the small biological molecule (l -cystine, Cys). The disulfide bond in l -cystine is cleavable by the overexpressed GSH in tumor cells, thus achieving rapid release of drugs from nanocarriers. By encapsulating doxorubicin (DOX) in bioMOC-Zn(Cys), DOX@bioMOC-Zn(Cys) displayed higher cellular uptake and cytotoxicity in cancer cells than free DOX. In vivo investigations indicated that DOX@bioMOC-Zn(Cys) largely inhibited tumor growth and reduced side effects.Abstract : Tumor-sensitive bioMOC-Zn(Cys) was developed using an endogenous Zn 2+ ion and l -cystine for the delivery of anti-cancer drug DOX. In vivo application of DOX@bioMOC-Zn(Cys) shows the increased inhibition of tumor growth and prevented side effects. Abstract : Metal–organic complexes (MOCs) or metal–organic frameworks (MOFs) have attracted increasing interest for constructing nanoscale drug delivery systems for cancer therapy. However, conventional MOC/MOF materials usually contain toxic metals or low-biocompatible organic ligands. Also, current approaches for creating tumor-sensitive nanocarriers are always based on the instability of coordination bonds under acidic conditions, or through post-synthetic modification with sensitive molecules. As a matter of fact, it is more facile to fabricate tumor-sensitive MOCs/MOFs based on the stimuli-responsiveness of organic ligands. In this study, a novel tumor-sensitive biological MOC (bioMOC-Zn(Cys)) was created through the assembly of endogenous Zn 2+ ions and the small biological molecule (l -cystine, Cys). The disulfide bond in l -cystine is cleavable by the overexpressed GSH in tumor cells, thus achieving rapid release of drugs from nanocarriers. By encapsulating doxorubicin (DOX) in bioMOC-Zn(Cys), DOX@bioMOC-Zn(Cys) displayed higher cellular uptake and cytotoxicity in cancer cells than free DOX. In vivo investigations indicated that DOX@bioMOC-Zn(Cys) largely inhibited tumor growth and reduced side effects. Remarkably, since both metal ions and organic ligands were obtained from biological sources, bioMOC-Zn(Cys) exhibited superior biocompatibility. This study presents a new method for fabricating MOC-based nanodrugs with high tumor-sensitivity and low toxicity. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 8:Issue 32(2020)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 8:Issue 32(2020)
- Issue Display:
- Volume 8, Issue 32 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 32
- Issue Sort Value:
- 2020-0008-0032-0000
- Page Start:
- 7189
- Page End:
- 7196
- Publication Date:
- 2020-07-03
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0tb00599a ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13823.xml