4.8 Article

Dual pH-Mediated Mechanized Hollow Zirconia Nanospheres

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 35, Pages 23289-23301

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b07603

Keywords

hollow mesoporous zirconia nanospheres; supramolecular switches; mechanized hollow zirconia nanospheres; dual pH-stimuli-responsive controlled release; targeted drug delivery

Funding

  1. Fundamental Research Funds for the Central University [30915011312, 30915012207]
  2. QingLan Project, Jiangsu Province, China
  3. National Science Foundation of Jiangsu Province [BK20161496]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Science and Technology Bureau of Lianyungang City [CG1421]
  6. Prospective Joint Research Project, Jiangsu Province [BY2015050-01]

Ask authors/readers for more resources

We demonstrate for the first time how to assemble mechanized hollow zirconia nanospheres (MHzNs), consisting of hollow mesoporous zirconia nanospheres. (HMZNs) as nanoscaffolds and supramolecular switches anchored on the exterior surface of HMZNs. The remarkable advantage of substitution of HMZNs for conventional mesoporous silica nanoscaffolds is that HMZNs can suffer the hot alkaline reaction environment, which provides a novel strategy for functionalization and thus achieve dual pH mediated controlled release functions by simple and practicable assembly procedure. Under neutral solution, cucurbituril[7] (CB[7]) macrocycles complexed with propanone bis(2-aminoethyl)ketal (PBAEK) to form [2]pseudorotaxanes as supramolecular switches, blocking the pore orifices and preventing the undesirable leakage of cargoes. When solution pH was adjusted to alkaline range, CB [7] macrocycles, acting as caps, disassociated from PBAEK stalks and opened the switches due to the dramatic decrease of ion dipole interactions. While under acidic conditions, PBAEK stalks were broken on account of the cleavage of ketal groups, resulting in the collapse of supramolecular switches and subsequent release of encapsulated cargoes. MHzNs owning dual pH-mediated controlled release characteristic are expected to apply in many fields. In this work, the feasibility of doxorubicin (DOX)-loaded MHzNs as targeted drug delivery systems was evaluated. In vitro cellular studies demonstrate that DOX-loaded MHzNs can be easily taken up by SMMC-7721 cells, can rapidly release DOX intracellularly, and can enhance cytotoxicity against tumor cells, proving their potential for chemotherapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available