A Combined Self-Assembled Drug Delivery for Effective Anti-Breast Cancer Therapy

Autor: Xiu Wang, Xiangle Zeng, Yawen Zhang, Jianchun Li, Yu-shuai Wang, Hairong Wang, Ranran Fan, Wenjun Pei
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Proton Magnetic Resonance Spectroscopy
Dasatinib
Pharmaceutical Science
02 engineering and technology
01 natural sciences
Metastasis
Rats
Sprague-Dawley

chemistry.chemical_compound
Drug Delivery Systems
inhibiting metastasis
Cell Movement
International Journal of Nanomedicine
Drug Discovery
Hyaluronic acid
Tissue Distribution
Hyaluronic Acid
Cytotoxicity
Micelles
Original Research
Drug Carriers
Mice
Inbred BALB C

Cell Death
Chemistry
General Medicine
021001 nanoscience & nanotechnology
Endocytosis
Tumor Burden
Drug delivery
Female
0210 nano-technology
HA targeting
medicine.drug
polymer
Static Electricity
Biophysics
Mice
Nude

Breast Neoplasms
Bioengineering
010402 general chemistry
Hemolysis
Rosiglitazone
Biomaterials
Breast cancer
In vivo
Cell Line
Tumor

micelle
medicine
Animals
Humans
Particle Size
Body Weight
Organic Chemistry
technology
industry
and agriculture

medicine.disease
In vitro
0104 chemical sciences
Drug Liberation
Cancer research
Nanoparticles
Zdroj: International Journal of Nanomedicine
ISSN: 1178-2013
Popis: Hairong Wang, Yawen Zhang, Xiangle Zeng, Wenjun Pei, Ranran Fan, Yushuai Wang, Xiu Wang, Jianchun Li School of Pharmacy, Bengbu Medical College, Bengbu, 233030, People’s Republic of ChinaCorrespondence: Jianchun LiSchool of Pharmacy, Bengbu Medical College, Bengbu, 233030, People’s Republic of ChinaTel +86 552-3175066Email Lijc66577@sohu.comAim: The metastasis of breast cancer is an important cause of tumor recurrence. This study highlights that tyrosine kinase inhibitors dasatinib (DAS) and rosiglitazone (ROZ) inhibit tumor growth and reduce the occurrence of tumor cell metastasis. Due to the poor water solubility, short half-time in the body of DAS and ROZ, which increases the difficulty of tumor treatment, as well as the demand for nano-drug delivery systems for organ-specific therapies.Methods: Hyaluronic acid (HA) and DAS are bonded by a pH-sensitive ester bond to form an HA-DAS polymer. Then, ROZ was added as the core, D-A-tocopherol polydiethylene glycol isosuccinate (TPGS) and HA-DAS were used as carriers to form HA-DAS and TPGS mixed micelle system loaded with ROZ (THDR-NPs). The size and structure of THDR-NPs were characterized, the drug release, stability and biosafety of THDR-NPs were studied. In vitro, the cytotoxicity, targeting effect and tumor metastasis inhibition of THDR-NPs were evaluated in human breast cancer cell lines. In addition, the selective potency of designed THDR-NPs in depleting was further verified in vivo in the tumor-bearing nude mice model.Results: The designed THDR-NPs have a particle size of less than 100 nm, good stability, biological safety and sustained release, and showed strong therapeutic effects on breast cancer models in vitro and in vivo. Moreover, it has been proved that THDR-NPs have the ability to inhibit tumor metastasis.Conclusion: DAS and ROZ were designed into micelles, the efficacy of THDR-NPs was higher than that of free drugs. These results indicate that nanoparticles have a good application prospect in the treatment of tumor metastasis.Keywords: HA targeting, inhibiting metastasis, polymer, micelle
Databáze: OpenAIRE