Nanoengineering of Mesenchymal Stem Cells via Surface Modification for Efficient Cancer Therapy. Issue 9 (12th June 2019)
- Record Type:
- Journal Article
- Title:
- Nanoengineering of Mesenchymal Stem Cells via Surface Modification for Efficient Cancer Therapy. Issue 9 (12th June 2019)
- Main Title:
- Nanoengineering of Mesenchymal Stem Cells via Surface Modification for Efficient Cancer Therapy
- Authors:
- Layek, Buddhadev
Sehgal, Drishti
Argenta, Peter A.
Panyam, Jayanth
Prabha, Swayam - Abstract:
- Abstract: Mesenchymal stem cells (MSCs) can be used for tumor‐specific delivery of small molecular weight anticancer drugs by using nanoparticle‐encapsulated forms of the drugs. Current approaches to incorporate nanoparticles in MSCs rely on nonspecific endocytosis of nanoparticles or their conjugation to the cell surface via endogenous amines and thiols. These methods result in sub‐optimal drug loading, which hinders the widespread application of MSCs as drug carriers. An advanced nanoengineering strategy is reported here that involves generation of MSCs expressing azide functional groups on their surface and conjugation of dibenzyl cyclooctyne‐functionalized nanoparticles to the azide groups using copper‐free click chemistry. This novel strategy significantly improves the payload capacity of MSCs (≈48 pg of paclitaxel (PTX) per cell) relative to that reported previously (<1–20 pg per cell), without affecting their native phenotype. In vivo, the nanoengineered MSCs significantly inhibit tumor growth ( p < 0.05) and improve survival ( p < 0.0001) compared to free or nanoparticle encapsulated PTX and Abraxane in an orthotopic ovarian tumor model. In summary, the nanoengineering strategy reported here allows for improved delivery and anticancer efficacy of conventional chemotherapeutic agents using MSCs as drug carriers. Abstract : Nanoengineering via surface modification improves the drug loading and retention capacity of mesenchymal stem cells (MSCs). Nanoengineered MSCsAbstract: Mesenchymal stem cells (MSCs) can be used for tumor‐specific delivery of small molecular weight anticancer drugs by using nanoparticle‐encapsulated forms of the drugs. Current approaches to incorporate nanoparticles in MSCs rely on nonspecific endocytosis of nanoparticles or their conjugation to the cell surface via endogenous amines and thiols. These methods result in sub‐optimal drug loading, which hinders the widespread application of MSCs as drug carriers. An advanced nanoengineering strategy is reported here that involves generation of MSCs expressing azide functional groups on their surface and conjugation of dibenzyl cyclooctyne‐functionalized nanoparticles to the azide groups using copper‐free click chemistry. This novel strategy significantly improves the payload capacity of MSCs (≈48 pg of paclitaxel (PTX) per cell) relative to that reported previously (<1–20 pg per cell), without affecting their native phenotype. In vivo, the nanoengineered MSCs significantly inhibit tumor growth ( p < 0.05) and improve survival ( p < 0.0001) compared to free or nanoparticle encapsulated PTX and Abraxane in an orthotopic ovarian tumor model. In summary, the nanoengineering strategy reported here allows for improved delivery and anticancer efficacy of conventional chemotherapeutic agents using MSCs as drug carriers. Abstract : Nanoengineering via surface modification improves the drug loading and retention capacity of mesenchymal stem cells (MSCs). Nanoengineered MSCs improve tumor‐targeted drug delivery, resulting in effective inhibition of tumor growth and overall survival in a mouse orthotopic model of ovarian tumor. … (more)
- Is Part Of:
- Advanced therapeutics. Volume 2:Issue 9(2019)
- Journal:
- Advanced therapeutics
- Issue:
- Volume 2:Issue 9(2019)
- Issue Display:
- Volume 2, Issue 9 (2019)
- Year:
- 2019
- Volume:
- 2
- Issue:
- 9
- Issue Sort Value:
- 2019-0002-0009-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-06-12
- Subjects:
- cancer therapy -- mesenchymal stem cells -- nanoengineered mesenchymal stem cells -- nanoparticles -- targeted drug delivery
Therapeutics -- Periodicals
Pharmaceutical technology -- Periodicals
Pharmacogenetics -- Periodicals
615.5 - Journal URLs:
- https://onlinelibrary.wiley.com/loi/23663987 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adtp.201900043 ↗
- Languages:
- English
- ISSNs:
- 2366-3987
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.935580
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11694.xml