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Synthesis and characterization of letrozole-loaded polymer based nanoparticulate formulations for treating breast cancer
被引:2
|作者:
Mandadi, Sandhya Rani
[1
,3
]
Srinivas, Lankalapalli
[2
]
机构:
[1] GITAM Inst Pharm GITAM Deemed Univ Univ, Dept Pharmaceut, Visakhapatnam 530045, Andhra Pradesh, India
[2] Vishnu Inst Pharmaceut Educ & Res, Ctr Mol Canc Res CMCR, Narsapur 502313, Telangana, India
[3] Vishnu Inst Pharmaceut Educ & Res Narsapur, Ctr Mol Canc Res CMCR, Narsapur 502313, Telangana, India
来源:
关键词:
Breast cancer;
Letrozole;
Nanoparticle;
MDA-MB-231;
PLGA NANOPARTICLES;
DRUG-DELIVERY;
DOXORUBICIN;
PLATFORM;
D O I:
10.54085/ap.2023.12.1.30
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Breast cancer (BC) is one of the most commonly diagnosed malignancies in the world. It is responsible for the majority of female mortality. Letrozole (LTZ) is an effective treatment for postmenopausal women whose BC responds positively to hormone receptors, but it has also been reported to have some unpleasant side effects. The inherent limitations of current anticancer drugs require the development of innovative technologies for more effective and safer cancer therapy. To address this problem, in this study, we fabricated unique PLGA nanoparticles loaded with LTZ. Optimized LTZ-PLGA nanoparticles (LTZ-PLGA NP) exhibited a particle size of 53.19 nm, with a polydispersity index (PDI) of 0.387 and a negative zeta potential of -10.9 mV. LTZ-PLGA NP also showed dose-dependent cell toxicity against MDA-MB-231 human breast cancer cell lines, with an inhibitory concentration (IC50) of 5.64 & PLUSMN; 0.346 mg/ml. The haemolytic properties indicate that LTZ-PLGA NPs are compatible with blood components. In general, the newly synthesized LTZ-PLGA NPs were in the nanosize range, had good entrapment efficiency and a slow drug release profile with good inhibitory concentrations against MDA-MB-231.
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页码:310 / 317
页数:8
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