Functionalized Nanoscale Micelles Improve Drug Delivery for Cancer Therapy in Vitro and in Vivo

Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic efficacy in vivo. In the study, we used a new tumor-penetrating peptide, CRGDK, to conjugate onto the surface of doxorubicin encapsulated nanoscale...

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Published inNano letters Vol. 13; no. 6; pp. 2528 - 2534
Main Authors Wei, Tuo, Liu, Juan, Ma, Huili, Cheng, Qiang, Huang, Yuanyu, Zhao, Jing, Huo, Shuaidong, Xue, Xiangdong, Liang, Zicai, Liang, Xing-Jie
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 12.06.2013
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Abstract Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic efficacy in vivo. In the study, we used a new tumor-penetrating peptide, CRGDK, to conjugate onto the surface of doxorubicin encapsulated nanoscale micelles. The CRGDK peptide triggered specific binding to neuropilin-1, leading to enhanced cellular uptake and cytotoxicity in vitro and highly accumulation and penetration in the tumors in vivo.
AbstractList Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic efficacy in vivo. In the study, we used a new tumor-penetrating peptide, CRGDK, to conjugate onto the surface of doxorubicin encapsulated nanoscale micelles. The CRGDK peptide triggered specific binding to neuropilin-1, leading to enhanced cellular uptake and cytotoxicity in vitro and highly accumulation and penetration in the tumors in vivo.Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic efficacy in vivo. In the study, we used a new tumor-penetrating peptide, CRGDK, to conjugate onto the surface of doxorubicin encapsulated nanoscale micelles. The CRGDK peptide triggered specific binding to neuropilin-1, leading to enhanced cellular uptake and cytotoxicity in vitro and highly accumulation and penetration in the tumors in vivo.
Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic efficacy in vivo. In the study, we used a new tumor-penetrating peptide, CRGDK, to conjugate onto the surface of doxorubicin encapsulated nanoscale micelles. The CRGDK peptide triggered specific binding to neuropilin-1, leading to enhanced cellular uptake and cytotoxicity in vitro and highly accumulation and penetration in the tumors in vivo.
Author Cheng, Qiang
Huo, Shuaidong
Xue, Xiangdong
Ma, Huili
Huang, Yuanyu
Liu, Juan
Liang, Xing-Jie
Zhao, Jing
Liang, Zicai
Wei, Tuo
AuthorAffiliation National Center for Nanoscience and Technology
Peking University
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  fullname: Liang, Xing-Jie
  email: liangxj@nanoctr.cn
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Keywords tumor-penetrating peptide
micelle
Targeted drug delivery
doxorubicin
neuropilin-1
Encapsulation
Drugs
Nanometer scale
In vivo
Antineoplastic drugs
Peptides
Tumours
Micelles
Cytotoxicity
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Snippet Poor penetration of therapeutic drugs into tumors is a major challenge in anticancer therapy, especially in solid tumors, leading to reduced therapeutic...
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SubjectTerms Biocompatibility
Biological and medical sciences
Biomedical materials
Biotechnology
Cell Line, Tumor
Condensed matter: structure, mechanical and thermal properties
Drug Delivery Systems
Exact sciences and technology
Fundamental and applied biological sciences. Psychology
Humans
In Vitro Techniques
In vivo testing
In vivo tests
Low-dimensional structures (superlattices, quantum well structures, multilayers): structure, and nonelectronic properties
Methods. Procedures. Technologies
Micelles
Nanostructure
Nanostructures
Neoplasms - drug therapy
Others
Peptides
Physics
Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties)
Surgical implants
Tumors
Various methods and equipments
Title Functionalized Nanoscale Micelles Improve Drug Delivery for Cancer Therapy in Vitro and in Vivo
URI http://dx.doi.org/10.1021/nl400586t
https://www.ncbi.nlm.nih.gov/pubmed/23634882
https://www.proquest.com/docview/1367881418
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https://www.proquest.com/docview/1753475595
Volume 13
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