Document Detail

Controlled Release of Fe(3) O(4) Nanoparticles in Encapsulated Microbubbles to Tumor Cells via Sonoporation and Associated Cellular Bioeffects.
MedLine Citation:
PMID:  21374806     Owner:  NLM     Status:  Publisher    
Fe(3) O(4) nanoparticles embedded in the shells of encapsulated microbubbles could be used therapeutically as in situ drug-delivery vehicles. Bioeffects on liver tumor cells SMMC-7721 due to the excitation of Fe(3) O(4) nanoparticles attached to microbubbles generated by ultrasound (US) are studied in an in vitro setting. The corresponding release phenomenon of Fe(3) O(4) nanoparticles from the shells of the microbubbles into the cells via sonoporation and related phenomena, including nanoparticle delivery efficiency, cell trafficking, cell apoptosis, cell cycle, and disturbed flow of intracellular calcium ions during this process, are also studied. Experimental observations show that Fe(3) O(4) nanoparticles embedded in the shells of microbubbles can be delivered into the tumor cells; the delivery rate can be controlled by adjusting the acoustic intensity. The living status or behavior of Fe(3) O(4) -tagged tumor cells can then be noninvasively tracked by magnetic resonance imaging (MRI). It is further demonstrated that the concentration of intracellular Ca(2+) in situ increases as a result of sonoporation. The elevated Ca(2+) is found to respond to the disrupted site in the cell membrane generated by sonoporation for the purpose of cell self-resealing. However, the excessive Ca(2+) accumulation on the membrane results in disruption of cellular Ca(2+) cycling that may be one of the reasons for the death of the cells at the G1 phase. The results also show that the Fe(3) O(4) -nanoparticle-embedded microbubbles have a lower effect on cell bioeffects compared with the non-Fe(3) O(4) -nanoparticle-embedded microbubbles under the same US intensity, which is beneficial for the delivery of nanoparticles and simultaneously maintains the cellular viability.
Fang Yang; Miao Zhang; Wen He; Ping Chen; Xiaowei Cai; Li Yang; Ning Gu; Junru Wu
Related Documents :
2254246 - The balance between different peptidoglycan precursors determines whether escherichia c...
15494366 - Variability and heritability of cell division pathways in toxoplasma gondii.
15225306 - The role of par proteins in the active segregation of the p1 plasmid.
2520196 - Effects of asymmetric division on a stochastic model of the cell division cycle.
20639436 - Phenotypic characterization of disseminated cells with tsc2 loss of heterozygosity in p...
15623776 - Soluble cd44 is cytotoxic to trabecular meshwork and retinal ganglion cells in vitro.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-2-25
Journal Detail:
Title:  Small (Weinheim an der Bergstrasse, Germany)     Volume:  -     ISSN:  1613-6829     ISO Abbreviation:  -     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-3-4     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101235338     Medline TA:  Small     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Jiangsu Key Laboratory for Biomaterials and Devices, Nanjing, 210009, China; State Key Laboratory of Bioeletronics, Nanjing, 210096, China; School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Surface-tension-driven gradient generation in a fluid stripe for bench-top and microwell application...
Next Document:  Characterization of protein hydrolysates of cosmetic use by CE-MS.