Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells

Lijuan Zhang,1 Thomas J Webster21Department of Chemistry, 2School of Engineering, Brown University, Providence, RI, USABackground: The aim of this study was to investigate the effects of poly-lactic-co-glycolic acid (PLGA) nanotopographies with alginate or chitosan protein preadsorption on the funct...

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Autores principales: Zhang L, Webster TJ
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Publicado: Dove Medical Press 2013
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spelling oai:doaj.org-article:0d361680179f43c8b2b17f93f0b330a92021-12-02T01:13:35ZEffects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells1176-91141178-2013https://doaj.org/article/0d361680179f43c8b2b17f93f0b330a92013-05-01T00:00:00Zhttp://www.dovepress.com/effects-of-chemically-modified-nanostructured-plga-on-functioning-of-l-a13066https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Lijuan Zhang,1 Thomas J Webster21Department of Chemistry, 2School of Engineering, Brown University, Providence, RI, USABackground: The aim of this study was to investigate the effects of poly-lactic-co-glycolic acid (PLGA) nanotopographies with alginate or chitosan protein preadsorption on the functioning of healthy and cancerous lung and breast cells, including adhesion, proliferation, apoptosis, and release of vascular endothelial growth factor (VEGF), which promotes tumor angiogenesis and secretion.Methods: We used a well established cast-mold technique to create nanoscale surface features on PLGA. Some of the nanomodified PLGA films were then exposed to alginate and chitosan. Surface roughness and the presence of protein was confirmed by atomic force microscopy. Surface energy was quantified by contact angle measurement.Results: Nanostructured PLGA surfaces with 23 nm features decreased synthesis of VEGF in both lung and breast cancer cells compared with conventional PLGA. Preadsorbing alginate further decreased cancer cell function, with nanostructured PLGA preadsorbed with alginate achieving the greatest decrease in synthesis of VEGF in both lung and breast cancer cells. In contrast, compared with nonmodified smooth PLGA, healthy cell functions were either not altered (ie, breast) or were enhanced (ie, lung) by use of nanostructured features and alginate or chitosan protein preadsorption.Conclusion: Using this technique, we developed surface nanometric roughness and modification of surface chemistry that could selectively decrease breast and lung cancer cell functioning without the need for chemotherapeutics. This technique requires further study in a wide range of anticancer and regenerative medicine applications.Keywords: breast, lung, cancer, nanotechnology, alginate, chitosanZhang LWebster TJDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2013, Iss default, Pp 1907-1919 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Zhang L
Webster TJ
Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
description Lijuan Zhang,1 Thomas J Webster21Department of Chemistry, 2School of Engineering, Brown University, Providence, RI, USABackground: The aim of this study was to investigate the effects of poly-lactic-co-glycolic acid (PLGA) nanotopographies with alginate or chitosan protein preadsorption on the functioning of healthy and cancerous lung and breast cells, including adhesion, proliferation, apoptosis, and release of vascular endothelial growth factor (VEGF), which promotes tumor angiogenesis and secretion.Methods: We used a well established cast-mold technique to create nanoscale surface features on PLGA. Some of the nanomodified PLGA films were then exposed to alginate and chitosan. Surface roughness and the presence of protein was confirmed by atomic force microscopy. Surface energy was quantified by contact angle measurement.Results: Nanostructured PLGA surfaces with 23 nm features decreased synthesis of VEGF in both lung and breast cancer cells compared with conventional PLGA. Preadsorbing alginate further decreased cancer cell function, with nanostructured PLGA preadsorbed with alginate achieving the greatest decrease in synthesis of VEGF in both lung and breast cancer cells. In contrast, compared with nonmodified smooth PLGA, healthy cell functions were either not altered (ie, breast) or were enhanced (ie, lung) by use of nanostructured features and alginate or chitosan protein preadsorption.Conclusion: Using this technique, we developed surface nanometric roughness and modification of surface chemistry that could selectively decrease breast and lung cancer cell functioning without the need for chemotherapeutics. This technique requires further study in a wide range of anticancer and regenerative medicine applications.Keywords: breast, lung, cancer, nanotechnology, alginate, chitosan
format article
author Zhang L
Webster TJ
author_facet Zhang L
Webster TJ
author_sort Zhang L
title Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
title_short Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
title_full Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
title_fullStr Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
title_full_unstemmed Effects of chemically modified nanostructured PLGA on functioning of lung and breast cancer cells
title_sort effects of chemically modified nanostructured plga on functioning of lung and breast cancer cells
publisher Dove Medical Press
publishDate 2013
url https://doaj.org/article/0d361680179f43c8b2b17f93f0b330a9
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