Developing Nanoceria‐Based pH‐Dependent Cancer‐Directed Drug Delivery System for Retinoblastoma. (12th November 2018)
- Record Type:
- Journal Article
- Title:
- Developing Nanoceria‐Based pH‐Dependent Cancer‐Directed Drug Delivery System for Retinoblastoma. (12th November 2018)
- Main Title:
- Developing Nanoceria‐Based pH‐Dependent Cancer‐Directed Drug Delivery System for Retinoblastoma
- Authors:
- Gao, Ruijuan
Mitra, Rajendra Narayan
Zheng, Min
Wang, Kai
Dahringer, Jesse Christine
Han, Zongchao - Abstract:
- Abstract: Development of a single combinatorial nanoplatform technology to target cancer cells has been an unprecedented reality in boosting synergistic antitumor activities and in reducing off‐target effects. An antitumor delivery system is designed using a chemotherapy drug and a tumor target molecule covalently linked to cerium oxide nanoparticles (nanoceria). Nanoceria have a unique redox activity in that they possess antioxidant activity at physiological pH but have an intrinsic oxidase activity at acidic pH. The system is integrated with 1) extracellular pH responsive functionality, 2) tumor cell targetable (CXC chemokine receptor 4, CXCR4 receptor specific) antagonist, 3) reactive oxygen species (ROS) inducible nanoceria, and 4) chemotherapeutic doxorubicin (DOX). These combinatorial nanoparticles (AMD–GCCNPs–DOX) are not only sensitive to the extracellular acidic pH conditions and targeted tumor cells but can also instantaneously induce ROS and release DOX intracellularly to enhance the chemotherapeutic activity in retinoblastoma cells (WERI‐Rb‐1 and Y79) and in xenograft (Y79/GFP‐luc grafted) and genetic p107s (Rb Lox/lox, p107 +/−, p130 −/− ) orthotopic mice models. A lucidly engineered combinatorial nanoconstruct is introduced that offers a viable and simple strategy for delivering a cocktail of therapeutics into tumor cells under acidosis, exhibiting a promising new future for clinical therapeutic opportunities. Abstract : Exploiting the pH differential of theAbstract: Development of a single combinatorial nanoplatform technology to target cancer cells has been an unprecedented reality in boosting synergistic antitumor activities and in reducing off‐target effects. An antitumor delivery system is designed using a chemotherapy drug and a tumor target molecule covalently linked to cerium oxide nanoparticles (nanoceria). Nanoceria have a unique redox activity in that they possess antioxidant activity at physiological pH but have an intrinsic oxidase activity at acidic pH. The system is integrated with 1) extracellular pH responsive functionality, 2) tumor cell targetable (CXC chemokine receptor 4, CXCR4 receptor specific) antagonist, 3) reactive oxygen species (ROS) inducible nanoceria, and 4) chemotherapeutic doxorubicin (DOX). These combinatorial nanoparticles (AMD–GCCNPs–DOX) are not only sensitive to the extracellular acidic pH conditions and targeted tumor cells but can also instantaneously induce ROS and release DOX intracellularly to enhance the chemotherapeutic activity in retinoblastoma cells (WERI‐Rb‐1 and Y79) and in xenograft (Y79/GFP‐luc grafted) and genetic p107s (Rb Lox/lox, p107 +/−, p130 −/− ) orthotopic mice models. A lucidly engineered combinatorial nanoconstruct is introduced that offers a viable and simple strategy for delivering a cocktail of therapeutics into tumor cells under acidosis, exhibiting a promising new future for clinical therapeutic opportunities. Abstract : Exploiting the pH differential of the tumor microenvironment versus the pH of nonmalignant tissue is potentially useful for cancer treatment. This study focuses on the treatment of retinoblastoma using the nanoceria as a base‐component due to its antioxidant activity at physiological pH but intrinsic oxidase activity at acidic pH. The development of a pH‐responsive nanoplatform is shown that can effectively deliver a combination of therapeutics to target tumor cells. … (more)
- Is Part Of:
- Advanced functional materials. Volume 28:Number 52(2018)
- Journal:
- Advanced functional materials
- Issue:
- Volume 28:Number 52(2018)
- Issue Display:
- Volume 28, Issue 52 (2018)
- Year:
- 2018
- Volume:
- 28
- Issue:
- 52
- Issue Sort Value:
- 2018-0028-0052-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-11-12
- Subjects:
- CXCR4 targeting -- doxorubicin -- nanoceria -- reactive oxygen species -- retinoblastoma
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.201806248 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9285.xml