Formulation of Kaempferol in Nanostructured Lipid Carriers (NLCs): A Delivery Platform to Sensitization of MDA-MB468 Breast Cancer Cells to Paclitaxel

被引:22
作者
Aghazadeh, Toofan [1 ]
Bakhtiari, Nuredin [1 ]
Rad, Isa Abdi [2 ]
Ramezani, Fatemeh [3 ]
机构
[1] Islamic Azad Univ, Fac Life Sci, Dept Biochem, Tehran North Branch, Tehran, Iran
[2] Urmia Univ Med Sci, Cellular & Mol Res Ctr, Cellular & Mol Med Inst, Orumiyeh, Iran
[3] Tabriz Univ Med Sci, Sch Adv Med Sci, Dept Mol Med, Tabriz, Iran
关键词
apoptosis; breast cancer; nanoparticle; Kaempferol; LOADED LECITHIN/CHITOSAN NANOPARTICLES; APOPTOSIS; MECHANISM;
D O I
10.33263/BRIAC116.1459114601
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Drug delivery-based nanoparticle has been developing as a widespread innovation in cancer treatment protocols. Here, we investigated the role of Kaempferol (KAE) loaded in nanostructured lipid carriers (NLCs) to promote cytotoxicity, efficacy, and paclitaxel-dependent apoptosis in MDA-MB 468 breast cancer cells. Particle size distribution, scanning electron microscopy (SEM), zeta potential, and cellular uptake were harnessed to optimize and characterize of KAE -loaded NLCs. MTT assay was used to measure the cellular proliferation of cancer cells. The clarification of early and late apoptosis and their gene expression patterns was assessed by Annexin V/PI staining and real-time PCR, respectively. SEM images offered us a nasty particle size of 80 +/- 3 nm to the Kaempferol formulated into NLCs. The IC50 values for KAE and paclitaxel determined 44 +/- 0.52 mu M and 1.75 +/- 0.36 nM, respectively. The moderated cell proliferation from 56 +/- 26.8% to 44 +/- 3.9% (p < 0.05) was demonstrated by KAE loaded NLCs. Co-administration of KAE-loaded nanoparticles and paclitaxel into cancer cells significantly strengthens the percentage of apoptosis (p < 0.05). Our results recommend that KAE incorporated into NLCs as an anti-cancer adjuvant is a powerful technique that may be a useful delivery system to enhance chemotherapy agents' effect on breast cancer cells.
引用
收藏
页码:14591 / 14601
页数:11
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