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. 2023 Nov 1;24(11):3985-3991.
doi: 10.31557/APJCP.2023.24.11.3985.

Toxicity of Carboplatin-Niosomal Nanoparticles in a Brain Cancer Cell Line

Affiliations

Toxicity of Carboplatin-Niosomal Nanoparticles in a Brain Cancer Cell Line

Mohadeseh Abbasi et al. Asian Pac J Cancer Prev. .

Abstract

Objective: Cancer poses a significant challenge in modern medicine, standing as the primary cause of death in many countries, second only to cardiovascular diseases. Among the various treatments available, carboplatin, a chemotherapy drug, is employed for specific cancer types, including brain carcinoma. The main objective of this investigation is to enhance the therapeutic efficacy of carboplatin by utilizing niosomal nanocarriers.

Methods: We synthesized nanoniosomal carboplatin using the reverse-phase evaporation technique and conducted an assessment of its particle size, zeta potential, and drug-release properties. Subsequently, we evaluated the cytotoxicity of nanoniosomal carboplatin using the C6 rat glioma cell line.

Results: Our research revealed that these niosomal nanoparticles possessed a particle size of 290.5±5.5 nm and a zeta potential of -21.7±7.4 mV. The amount of encapsulated drug and drug loading level were found to be 60.2±2.3% and 2.5±1.1%, respectively. Importantly, the cytotoxic impact of these nanoniosomes on the C6 rat glioma cell line exhibited a significant increase compared to the free drug (P<0.05).

Conclusion: Based on our discoveries, it is evident that carboplatin niosomal nanocarriers hold potential as an innovative approach to chemotherapy for brain cancer therapy.

Keywords: Brain cancer; Carboplatin; Nanoniosome; Nanoparticle.

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Conflict of interest statement

The authors declare no potential conflict of interest.

Figures

Figure 1
Figure 1
The Mean Size of Nanoniosomal Carboplatin
Figure 2
Figure 2
A Standard Carboplatin Curve was Generated by Measuring the Absorbance (optical density; OD) of Various Dilutions of Carboplatin Concentrations
Figure 3
Figure 3
The Graph Illustrates How Carboplatin is Released in Vitro from the Carboplatin Nanoniosomes into a PBS Buffer. The information is depicted as the mean value along with the standard deviation (SD), and it originates from three distinct experiments, with each experiment conducted twice
Figure 4.
Figure 4.
Viability Effects of Carboplatin-loaded Nanoparticles Compared to the Standard Drug (carboplatin) on C6 Rat Glioma Cell Line after 48-h Incubation. (Graph represents mean ± SD; n= 3 independent experiments, ***p = 0.0002, two-way ANOVA with Šidák test)

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