Assessing the anticancer potential of Bergenia ciliata conjugated silk fibroin nanoparticles through histopathological and biomarkers study.

IF 2.9 4区 生物学 Q3 CELL BIOLOGY
Faiza, Shaukat Ali, Muhammad Summer, Faiza Sharif
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引用次数: 0

Abstract

The present research has aimed to formulate fibroin nanoparticles (FNPs) and Bergenia ciliata-loaded fibroin nanoparticles (BCFNPs) to investigate their antitumor activity against breast cancer in mice. The prepared FNPs and BCFNPs characterized by Ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), Dynamic light scattering (DLS), Zeta potential measurement, Fourier-transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). UV-Vis spectroscopy revealed characteristic peak at 282 nm for FNPs and 285 nm for BCFNPs, indicating the successful development of fibroin nanoparticles (FNPs) and Bergenia ciliata-loaded fibroin nanoparticles (BCFNPs). FT-IR analysis identified characteristic absorption bands in the FNPs spectrum at 3350 cm-1, 1654 cm-1, 1587 cm-1, and 1087 cm-1, indicating the preserved secondary structure of fibroin. In the BCFNPs spectrum, peak shifts and intensity variations were observed at 3338 cm-1 and 1180 cm-1 due to the loading of the bioactive compound, indicating successful incorporation of B. ciliata. The DLS analysis confirmed that the FNPs were within the nanometer size range, while the zeta potential measurements indicated that FNPs and BCFNPs have slightly negative surface charge. The SEM analysis assessed the shapes of nanoparticles ranging from round, triangular, and hexagonal shapes and XRD peaks at 2ϴ (20-80) confirmed crystalline nature of FNPs and BCFNPs. In the present study, we established a mice model (Swiss albino) of breast cancer induced by CdCl2 and treated with tamoxifen, Bergenia ciliata, FNP, and BCFNP to access their antitumor activity. During breast cancer induction, CdCl2 treated groups experienced weight loss, dropping from 30.2 to 18.0 g. After two months, administration of BCFNP significantly inversed the alteration of body weight. At the end of the trial, levels of blood serum biomarkers analyzed. All treatment groups showed better results but BCFNPs treated group exhibited significant reduction (P < 0.0001) in TNF-α (31.7 ± 1.4 pg/ml), IL-6 (20.2 ± 0.9 pg/mL), IL-10 (25.4 ± 1.9 pg/mL), LDH (481.0 ± 7.5 μmol/ml), ASAT (179.0 ± 7.3 μmol/ml), ALAT (532.8 ± 13.4 μmol/ml), and ALP (164.8 ± 5.9 μmol/ml) along with reduced tumor volume. Moreover, Significant (P < 0.0001) improvements in GSH and MDA (248.6 ± 7.9 μmol/ml) serum biomarkers also found. Histological analysis of the BCFNPs treated group revealed a significant reduction in ductal carcinoma. In conclusion, Bergenia ciliata loaded fibroin nanoparticles have potent potential to treat tumors by targeted drug delivery.

通过组织病理学和生物标志物研究评估纤毛草偶联丝素纳米颗粒的抗癌潜力。
本研究旨在制备纤维蛋白纳米颗粒(FNPs)和纤毛菌负载的纤维蛋白纳米颗粒(BCFNPs),研究其对小鼠乳腺癌的抗肿瘤活性。采用紫外可见光谱、傅里叶红外光谱(FTIR)、扫描电镜(SEM)、动态光散射(DLS)、Zeta电位测量、傅里叶红外光谱(FT-IR)和x射线衍射(XRD)对制备的FNPs和BCFNPs进行了表征。紫外可见光谱显示,FNPs和BCFNPs的特征峰分别在282 nm和285 nm处,表明成功制备了丝素纳米粒子(FNPs)和纤毛卑根菌负载的丝素纳米粒子(BCFNPs)。FT-IR分析在3350 cm-1、1654 cm-1、1587 cm-1和1087 cm-1的FNPs光谱中发现了特征吸收带,表明保留了丝蛋白的二级结构。在BCFNPs光谱中,由于生物活性化合物的负载,在3338 cm-1和1180 cm-1处观察到峰移和强度变化,表明纤毛杆菌成功掺入。DLS分析证实了FNPs在纳米尺寸范围内,而zeta电位测量表明FNPs和BCFNPs具有轻微的表面负电荷。SEM分析了纳米颗粒的形状,包括圆形、三角形和六边形,XRD峰在2ϴ(20-80)处证实了FNPs和BCFNPs的晶体性质。在本研究中,我们建立了CdCl2诱导的乳腺癌小鼠模型(瑞士白化病),并用他莫昔芬、毛癣菌、FNP和BCFNP治疗,以获得它们的抗肿瘤活性。在乳腺癌诱导过程中,CdCl2治疗组体重下降,从30.2 g降至18.0 g。2个月后,服用BCFNP显著逆转了体重的变化。在试验结束时,分析了血清生物标志物的水平。各治疗组疗效均较好,但BCFNPs治疗组疗效显著降低(P
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来源期刊
Journal of Molecular Histology
Journal of Molecular Histology 生物-细胞生物学
CiteScore
5.90
自引率
0.00%
发文量
68
审稿时长
1 months
期刊介绍: The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes. Major research themes of particular interest include: - Cell-Cell and Cell-Matrix Interactions; - Connective Tissues; - Development and Disease; - Neuroscience. Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance. The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.
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