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DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy

Cisplatin is the most widely used anticancer drug, but its side effects limit the maximum systemic dose. To circumvent the side effects, a DNA tetrahedron–affibody nanoparticle was prepared by combination of a DNA chain with cisplatin via interstrand crosslinks or adducts. Each nanocarrier can bind...

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Detalles Bibliográficos
Autores principales: Zhang, Chao, Zhang, HongLei, Han, MengNan, Yang, XueLi, Pei, ChaoHong, Xu, ZhiDong, Du, Jie, Li, Wei, Chen, Shengxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059769/
https://www.ncbi.nlm.nih.gov/pubmed/35516156
http://dx.doi.org/10.1039/c8ra08735k
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author Zhang, Chao
Zhang, HongLei
Han, MengNan
Yang, XueLi
Pei, ChaoHong
Xu, ZhiDong
Du, Jie
Li, Wei
Chen, Shengxi
author_facet Zhang, Chao
Zhang, HongLei
Han, MengNan
Yang, XueLi
Pei, ChaoHong
Xu, ZhiDong
Du, Jie
Li, Wei
Chen, Shengxi
author_sort Zhang, Chao
collection PubMed
description Cisplatin is the most widely used anticancer drug, but its side effects limit the maximum systemic dose. To circumvent the side effects, a DNA tetrahedron–affibody nanoparticle was prepared by combination of a DNA chain with cisplatin via interstrand crosslinks or adducts. Each nanocarrier can bind ∼68 molecules of cisplatin. This cisplatin nanoparticle exhibited high selectivity and inhibition for breast cancer HER2 overexpressing cells BT474 and lower toxicity in MCF-7 cells with low HER2 expression. The nano-drug inhibited the growth of BT474 cells by 94.57% at 512 nM (containing 33.3 μM cisplatin), which was higher than that of cisplatin (82.9%, 33.3 μM).
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spelling pubmed-90597692022-05-04 DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy Zhang, Chao Zhang, HongLei Han, MengNan Yang, XueLi Pei, ChaoHong Xu, ZhiDong Du, Jie Li, Wei Chen, Shengxi RSC Adv Chemistry Cisplatin is the most widely used anticancer drug, but its side effects limit the maximum systemic dose. To circumvent the side effects, a DNA tetrahedron–affibody nanoparticle was prepared by combination of a DNA chain with cisplatin via interstrand crosslinks or adducts. Each nanocarrier can bind ∼68 molecules of cisplatin. This cisplatin nanoparticle exhibited high selectivity and inhibition for breast cancer HER2 overexpressing cells BT474 and lower toxicity in MCF-7 cells with low HER2 expression. The nano-drug inhibited the growth of BT474 cells by 94.57% at 512 nM (containing 33.3 μM cisplatin), which was higher than that of cisplatin (82.9%, 33.3 μM). The Royal Society of Chemistry 2019-01-15 /pmc/articles/PMC9059769/ /pubmed/35516156 http://dx.doi.org/10.1039/c8ra08735k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Chao
Zhang, HongLei
Han, MengNan
Yang, XueLi
Pei, ChaoHong
Xu, ZhiDong
Du, Jie
Li, Wei
Chen, Shengxi
DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title_full DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title_fullStr DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title_full_unstemmed DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title_short DNA–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
title_sort dna–affibody nanoparticle delivery system for cisplatin-based breast cancer chemotherapy
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059769/
https://www.ncbi.nlm.nih.gov/pubmed/35516156
http://dx.doi.org/10.1039/c8ra08735k
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