Carboplatin Niosomal Nanoplatform for Potentiated Chemotherapy
Carboplatin Niosomal Nanoplatform for Potentiated Chemotherapy
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DOI:
10.1016/j.xphs.2022.06.002
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发表时间:
2022-10-13
影响因子:
3.8
通讯作者:
Shahmabadi, Hasan Ebrahimi
中科院分区:
文献类型:
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作者:
Alavi, Seyed Ebrahim;Raza, Aun;Shahmabadi, Hasan Ebrahimi
This study aimed to characterize a stable nano-niosome formulation, which could reduce the adverse effects of carboplatin (CB) and improve its therapeutic efficacy in the treatment of breast cancer. For this purpose, CB-loaded polyethylene glycol (PEG)ylated niosome nanoparticles (PEG-NS-CB) were synthesized using the reverse-phase evaporation method. PEG-NS-CB (226.0 10.6 nm) could release CB in a controlled manner and, compared to CB and CB-loaded non-PEGylated niosome (NS-CB), caused higher cytotoxicity effects against mouse breast cancer 4T1 cells (IC50: 83.4, 26.6, and 22.5 mM for CB, NS-CB, and PEG-NS-CB, respec-tively). Also, PEG-NS-CB demonstrated higher stability, in which its profile of drug release, cytotoxicity, and LE% did not change significantly three months after preparation compared to those at the production time. In addition, the in vivo results demonstrated that PEG-NS-CB caused higher therapeutic (the number of alive mice: 12, 15, and 17 out of 20 in CB, NS-CB, and PEG-NS-CB receiver groups, respectively) and less toxicity effects (weight loss of 17, 12.5, and 10% in CB, NS-CB, and PEG-NS-CB receiver groups, respectively), com-pared to NS-CB and CB in breast cancer-bearing mice. Overall, the results of this study suggest that PEG-NS -CB could be a promising formulation for the treatment of breast cancer. (C) 2022 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.