Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells. / Stie, Mai Bay; Thoke, Henrik Seir; Issinger, Olaf Georg; Hochscherf, Jennifer; Guerra, Barbara; Olsen, Lars F.

In: Colloids and Surfaces B: Biointerfaces, Vol. 174, 01.02.2019, p. 216-223.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Stie, MB, Thoke, HS, Issinger, OG, Hochscherf, J, Guerra, B & Olsen, LF 2019, 'Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells', Colloids and Surfaces B: Biointerfaces, vol. 174, pp. 216-223. https://doi.org/10.1016/j.colsurfb.2018.11.005

APA

Stie, M. B., Thoke, H. S., Issinger, O. G., Hochscherf, J., Guerra, B., & Olsen, L. F. (2019). Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells. Colloids and Surfaces B: Biointerfaces, 174, 216-223. https://doi.org/10.1016/j.colsurfb.2018.11.005

Vancouver

Stie MB, Thoke HS, Issinger OG, Hochscherf J, Guerra B, Olsen LF. Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells. Colloids and Surfaces B: Biointerfaces. 2019 Feb 1;174:216-223. https://doi.org/10.1016/j.colsurfb.2018.11.005

Author

Stie, Mai Bay ; Thoke, Henrik Seir ; Issinger, Olaf Georg ; Hochscherf, Jennifer ; Guerra, Barbara ; Olsen, Lars F. / Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells. In: Colloids and Surfaces B: Biointerfaces. 2019 ; Vol. 174. pp. 216-223.

Bibtex

@article{0b9fcb67542b495c9624f5b5a3932215,
title = "Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells",
abstract = "We have successfully encapsulated two proteins, bovine serum albumin (BSA) and p53, in chitosan-tripolyphosphate (TPP) nanoparticles at various pH values from 5.5 to 6.5 and delivered the particles to human melanoma cells. The particles have diameters ranging from 180 nm to 280 nm and a zeta potential of +15 to + 40 mV. Cellular uptake of the particles by human skin melanoma cells was evaluated by: (i) fluorescence microscopy and (ii) gel electrophoresis showing that FITC-labeled BSA and p53 could be recovered in the soluble cell fraction after lysis of the cells. Our data also show that the highest cellular uptake takes place at the lowest pH as the particles have the highest positive charge under these conditions. The method we describe appears to be a general method for delivery of proteins to cells using chitosan-TPP nanoparticles as a drug delivery system, since structurally unrelated proteins such as BSA and p53 with different isoelectrical points can be encapsulated in the chitosan-TPP nanoparticles and be effectively internalized by the cells.",
keywords = "Chitosan, Nanoparticles, Protein, SK-mel 28, p53",
author = "Stie, {Mai Bay} and Thoke, {Henrik Seir} and Issinger, {Olaf Georg} and Jennifer Hochscherf and Barbara Guerra and Olsen, {Lars F.}",
year = "2019",
month = feb,
day = "1",
doi = "10.1016/j.colsurfb.2018.11.005",
language = "English",
volume = "174",
pages = "216--223",
journal = "Colloids and Surfaces B: Biointerfaces",
issn = "0927-7765",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Delivery of proteins encapsulated in chitosan-tripolyphosphate nanoparticles to human skin melanoma cells

AU - Stie, Mai Bay

AU - Thoke, Henrik Seir

AU - Issinger, Olaf Georg

AU - Hochscherf, Jennifer

AU - Guerra, Barbara

AU - Olsen, Lars F.

PY - 2019/2/1

Y1 - 2019/2/1

N2 - We have successfully encapsulated two proteins, bovine serum albumin (BSA) and p53, in chitosan-tripolyphosphate (TPP) nanoparticles at various pH values from 5.5 to 6.5 and delivered the particles to human melanoma cells. The particles have diameters ranging from 180 nm to 280 nm and a zeta potential of +15 to + 40 mV. Cellular uptake of the particles by human skin melanoma cells was evaluated by: (i) fluorescence microscopy and (ii) gel electrophoresis showing that FITC-labeled BSA and p53 could be recovered in the soluble cell fraction after lysis of the cells. Our data also show that the highest cellular uptake takes place at the lowest pH as the particles have the highest positive charge under these conditions. The method we describe appears to be a general method for delivery of proteins to cells using chitosan-TPP nanoparticles as a drug delivery system, since structurally unrelated proteins such as BSA and p53 with different isoelectrical points can be encapsulated in the chitosan-TPP nanoparticles and be effectively internalized by the cells.

AB - We have successfully encapsulated two proteins, bovine serum albumin (BSA) and p53, in chitosan-tripolyphosphate (TPP) nanoparticles at various pH values from 5.5 to 6.5 and delivered the particles to human melanoma cells. The particles have diameters ranging from 180 nm to 280 nm and a zeta potential of +15 to + 40 mV. Cellular uptake of the particles by human skin melanoma cells was evaluated by: (i) fluorescence microscopy and (ii) gel electrophoresis showing that FITC-labeled BSA and p53 could be recovered in the soluble cell fraction after lysis of the cells. Our data also show that the highest cellular uptake takes place at the lowest pH as the particles have the highest positive charge under these conditions. The method we describe appears to be a general method for delivery of proteins to cells using chitosan-TPP nanoparticles as a drug delivery system, since structurally unrelated proteins such as BSA and p53 with different isoelectrical points can be encapsulated in the chitosan-TPP nanoparticles and be effectively internalized by the cells.

KW - Chitosan

KW - Nanoparticles

KW - Protein

KW - SK-mel 28

KW - p53

U2 - 10.1016/j.colsurfb.2018.11.005

DO - 10.1016/j.colsurfb.2018.11.005

M3 - Journal article

C2 - 30465996

VL - 174

SP - 216

EP - 223

JO - Colloids and Surfaces B: Biointerfaces

JF - Colloids and Surfaces B: Biointerfaces

SN - 0927-7765

ER -

ID: 216311117