Investigating the Properties and Cytotoxicity of Cisplatin-Loaded Nano-Polybutylcyanoacrylate on Breast Cancer Cells

Amirsasan Gorgzadeh, Ali Hheidari, Parizad Ghanbarikondori, Mahshid Arastonejad, Tayebeh Ghasemi Goki, Mehrad Aria, Ahmadreza Allahyartorkaman, Farimah Moazzam
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Abstract

Background: This study aimed to develop a novel drug formulation using polybutylcyanoacrylate (PBCA) nanoparticles to deliver cisplatin, a commonly used chemotherapeutic agent for breast cancer treatment.Materials and Methods: PBCA nanoparticles were synthesized using a mini-emulsion polymerization method, and the resulting NPs were comprehensively characterized for their physical properties, such as size, size distribution, zeta potential, drug loading, and encapsulation efficiency. In addition, the cytotoxicity of the NPs was assessed, along with their ability to release the entrapped drugs over time. Results: The results showed that the PBCA nanoparticles had a mean size of 457 ± 7.4 nm, a size distribution of 0.253±0.011 and a negative zeta potential of -12.3 ± 1.3 mV. The drug encapsulation efficiency and loading capacity of cisplatin-PBCA were found to be 45.6 ± 2.7% and 3.5 ±0.8%, respectively; The release of the drug from the PBCA was estimated to be approximately 12.2±1.1% after 45 hours. The cytotoxic effects of the nanoparticle formulation were significantly enhanced compared to the free drug. The cytotoxicity of cisplatin-PBCA was evaluated in the T-47D breast cancer cell line, showing promising results as a potential drug formulation for breast cancer therapy. Conclusions: These findings suggest that cisplatin-PBCA may offer advantages over traditional cisplatin formulations, potentially improving the efficacy and reducing the toxicity of breast cancer treatment.
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研究顺铂负载纳米聚丁基氰基丙烯酸酯对乳腺癌细胞的特性和细胞毒性
背景:本研究旨在利用聚丁基氰基丙烯酸酯(PBCA)纳米粒子开发一种新型药物制剂,用于递送顺铂(一种常用的乳腺癌化疗药物):采用微型乳液聚合法合成了 PBCA 纳米粒子,并对所得纳米粒子的物理性质(如尺寸、尺寸分布、zeta 电位、载药量和包封效率)进行了全面表征。此外,还评估了 NPs 的细胞毒性及其随时间释放所含药物的能力。结果显示结果表明,PBCA 纳米粒子的平均尺寸为 457 ± 7.4 nm,尺寸分布为 0.253±0.011,负 zeta 电位为 -12.3 ± 1.3 mV。顺铂-PBCA的药物包封效率和负载能力分别为45.6±2.7%和3.5±0.8%;估计45小时后药物从PBCA中的释放量约为12.2±1.1%。与游离药物相比,纳米颗粒制剂的细胞毒性作用明显增强。在 T-47D 乳腺癌细胞系中对顺铂-PBCA 的细胞毒性进行了评估,结果表明该制剂有望成为治疗乳腺癌的潜在药物。结论这些研究结果表明,顺铂-PBCA 与传统的顺铂制剂相比具有优势,有可能提高乳腺癌治疗的疗效并降低毒性。
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