Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells

Research output: Contribution to journalJournal articlepeer-review

Standard

Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells. / Pitaksuteepong, T.; Davies, N. M.; Baird, M.; Rades, T.

In: Pharmazie, Vol. 59, No. 2, 02.2004, p. 134-142.

Research output: Contribution to journalJournal articlepeer-review

Harvard

Pitaksuteepong, T, Davies, NM, Baird, M & Rades, T 2004, 'Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells', Pharmazie, vol. 59, no. 2, pp. 134-142.

APA

Pitaksuteepong, T., Davies, N. M., Baird, M., & Rades, T. (2004). Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells. Pharmazie, 59(2), 134-142.

Vancouver

Pitaksuteepong T, Davies NM, Baird M, Rades T. Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells. Pharmazie. 2004 Feb;59(2):134-142.

Author

Pitaksuteepong, T. ; Davies, N. M. ; Baird, M. ; Rades, T. / Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells. In: Pharmazie. 2004 ; Vol. 59, No. 2. pp. 134-142.

Bibtex

@article{0a801dc4fde54ee8926934b9770ddb57,
title = "Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells",
abstract = "Polyethylcyanoacrylate (PECA) nanoparticles were prepared by interfacial polymerization of a water-in-oil microemulsion. Nanoparticles were isolated from the polymerization template by sequential ethanol washing and centrifugation. A nanocapsule preparation yielding the original particle size and distribution following redispersion in an aqueous solution was achieved by freeze-drying the isolated nanoparticles in a solution of 5% w/v sugar. The cytotoxicity and uptake of nanocapsules by dendritic cells was investigated using a murine-derived cell line (D1). PECA nanoparticles were found to adversely effect cell viability at concentrations greater than 10 μg/ml of polymer in the culture medium. In comparison to antigen in solution, cell uptake of antigen encapsulated within nanoparticles was significantly higher at both 4 and 37 °C. Following a 24 h incubation period, the percentage of cells taking-up antigen was also increased when antigen was encapsulated in nanoparticles as compared to antigen in solution. The uptake of nanoparticles and the effect of antigen formulation on morphological cell changes indicative of cell maturation were also investigated by scanning electron microscopy (SEM). SEM clearly demonstrated the adherence of nanoparticles to the cell surface. Incubation of D1 dendritic cells with nanoparticles containing antigen also resulted in morphological changes indicative of cell maturation similar to that observed when the cells were incubated with lipopolysaccharide. In contrast, cells incubated with antigen solution did not demonstrate such morphological changes and appeared similar to immature cells that had not been exposed to antigen.",
author = "T. Pitaksuteepong and Davies, {N. M.} and M. Baird and T. Rades",
year = "2004",
month = feb,
language = "English",
volume = "59",
pages = "134--142",
journal = "Die Pharmazie",
issn = "0031-7144",
publisher = "Govi-Verlag Pharmazeutischer Verlag GmbH",
number = "2",

}

RIS

TY - JOUR

T1 - Uptake of antigen encapsulated in polyethylcyanoacrylate nanoparticles by D1-dendritic cells

AU - Pitaksuteepong, T.

AU - Davies, N. M.

AU - Baird, M.

AU - Rades, T.

PY - 2004/2

Y1 - 2004/2

N2 - Polyethylcyanoacrylate (PECA) nanoparticles were prepared by interfacial polymerization of a water-in-oil microemulsion. Nanoparticles were isolated from the polymerization template by sequential ethanol washing and centrifugation. A nanocapsule preparation yielding the original particle size and distribution following redispersion in an aqueous solution was achieved by freeze-drying the isolated nanoparticles in a solution of 5% w/v sugar. The cytotoxicity and uptake of nanocapsules by dendritic cells was investigated using a murine-derived cell line (D1). PECA nanoparticles were found to adversely effect cell viability at concentrations greater than 10 μg/ml of polymer in the culture medium. In comparison to antigen in solution, cell uptake of antigen encapsulated within nanoparticles was significantly higher at both 4 and 37 °C. Following a 24 h incubation period, the percentage of cells taking-up antigen was also increased when antigen was encapsulated in nanoparticles as compared to antigen in solution. The uptake of nanoparticles and the effect of antigen formulation on morphological cell changes indicative of cell maturation were also investigated by scanning electron microscopy (SEM). SEM clearly demonstrated the adherence of nanoparticles to the cell surface. Incubation of D1 dendritic cells with nanoparticles containing antigen also resulted in morphological changes indicative of cell maturation similar to that observed when the cells were incubated with lipopolysaccharide. In contrast, cells incubated with antigen solution did not demonstrate such morphological changes and appeared similar to immature cells that had not been exposed to antigen.

AB - Polyethylcyanoacrylate (PECA) nanoparticles were prepared by interfacial polymerization of a water-in-oil microemulsion. Nanoparticles were isolated from the polymerization template by sequential ethanol washing and centrifugation. A nanocapsule preparation yielding the original particle size and distribution following redispersion in an aqueous solution was achieved by freeze-drying the isolated nanoparticles in a solution of 5% w/v sugar. The cytotoxicity and uptake of nanocapsules by dendritic cells was investigated using a murine-derived cell line (D1). PECA nanoparticles were found to adversely effect cell viability at concentrations greater than 10 μg/ml of polymer in the culture medium. In comparison to antigen in solution, cell uptake of antigen encapsulated within nanoparticles was significantly higher at both 4 and 37 °C. Following a 24 h incubation period, the percentage of cells taking-up antigen was also increased when antigen was encapsulated in nanoparticles as compared to antigen in solution. The uptake of nanoparticles and the effect of antigen formulation on morphological cell changes indicative of cell maturation were also investigated by scanning electron microscopy (SEM). SEM clearly demonstrated the adherence of nanoparticles to the cell surface. Incubation of D1 dendritic cells with nanoparticles containing antigen also resulted in morphological changes indicative of cell maturation similar to that observed when the cells were incubated with lipopolysaccharide. In contrast, cells incubated with antigen solution did not demonstrate such morphological changes and appeared similar to immature cells that had not been exposed to antigen.

UR - http://www.scopus.com/inward/record.url?scp=1242291860&partnerID=8YFLogxK

M3 - Journal article

C2 - 15025183

AN - SCOPUS:1242291860

VL - 59

SP - 134

EP - 142

JO - Die Pharmazie

JF - Die Pharmazie

SN - 0031-7144

IS - 2

ER -

ID: 299428982