Bioinspired caffeic acid-laden milk protein-based nanoparticles targeting folate receptors for breast cancer treatment.

IF 3 Q2 PHARMACOLOGY & PHARMACY Therapeutic delivery Pub Date : 2024-11-26 DOI:10.1080/20415990.2024.2433938
Sally Safwat, Rania A H Ishak, Rania M Hathout, Nahed D Mortada
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Abstract

Aims: Breast cancer is the second leading cause of death worldwide. Conventional chemotherapeutic therapies lack the specific targeting effect toward the cancerous cells resulting in extensive side effects. Our current study endeavors to prepare novel bioinspired folic acid-functionalized caffeic acid (CA)-loaded casein nanoparticles (CS NPs) for curbing breast cancer.

Methods: CA-CS NPs were prepared by simple coacervation method followed by lyophilization. Functionalized CS NPs were achieved using folic acid as the targeting moiety. Entire comparative characterization between unconjugated and conjugated NPs were implemented in terms of size, polydispersity index, surface charge, 1H-NMR, surface morphology, in-vitro drug release, sterilization, cytotoxicity, and animal studies.

Results: Conjugated NPs attained PS = 157.23 ± 2.64 nm, PDI = 0.309 ± 0.199, ZP = -25.53 ± 2.31 mV and IC50 = 40 ± 2.9 µg/ml. Significant reduction in the biochemical marker levels of Carcino-embryonic antigen, carbohydrate antigen 15-3, and malondialdehyde while increased superoxide dismutase levels were achieved in the tumor -induced rats treated by the conjugated NPs. Histopathological examinations showed great improvement in the mammary and necrotic regions.

Conclusion: The present work paves the road of 'back to nature' approach in designing biocompatible bioinspired conjugated nanocarriers for the diagnosis and treatment of various diseases.

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基于生物启发的含咖啡酸牛奶蛋白的纳米颗粒,靶向叶酸受体治疗乳腺癌。
目的:乳腺癌是全球第二大死因。传统的化疗方法缺乏对癌细胞的特异性靶向作用,因此产生了广泛的副作用。我们目前的研究致力于制备新型的生物启发叶酸功能化咖啡酸(CA)负载酪蛋白纳米颗粒(CS NPs),用于遏制乳腺癌:方法:采用简单的共凝方法制备CA-CS NPs,然后进行冻干。采用叶酸作为靶向分子,制备了功能化 CS NPs。从尺寸、多分散指数、表面电荷、1H-NMR、表面形态、体外药物释放、灭菌、细胞毒性和动物实验等方面对未共轭和共轭 NPs 进行了全面的比较表征:共轭 NPs 的 PS = 157.23 ± 2.64 nm,PDI = 0.309 ± 0.199,ZP = -25.53 ± 2.31 mV,IC50 = 40 ± 2.9 µg/ml。经共轭 NPs 处理的肿瘤诱导大鼠的癌胚抗原、碳水化合物抗原 15-3 和丙二醛等生化标志物水平显著降低,而超氧化物歧化酶水平升高。组织病理学检查显示,乳腺和坏死区域的情况大有改善:本研究为设计用于诊断和治疗各种疾病的生物相容性生物启发共轭纳米载体铺平了 "回归自然 "之路。
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来源期刊
Therapeutic delivery
Therapeutic delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.50
自引率
0.00%
发文量
25
期刊介绍: Delivering therapeutics in a way that is right for the patient - safe, painless, reliable, targeted, efficient and cost effective - is the fundamental aim of scientists working in this area. Correspondingly, this evolving field has already yielded a diversity of delivery methods, including injectors, controlled release formulations, drug eluting implants and transdermal patches. Rapid technological advances and the desire to improve the efficacy and safety profile of existing medications by specific targeting to the site of action, combined with the drive to improve patient compliance, continue to fuel rapid research progress. Furthermore, the emergence of cell-based therapeutics and biopharmaceuticals such as proteins, peptides and nucleotides presents scientists with new and exciting challenges for the application of therapeutic delivery science and technology. Successful delivery strategies increasingly rely upon collaboration across a diversity of fields, including biology, chemistry, pharmacology, nanotechnology, physiology, materials science and engineering. Therapeutic Delivery recognizes the importance of this diverse research platform and encourages the publication of articles that reflect the highly interdisciplinary nature of the field. In a highly competitive industry, Therapeutic Delivery provides the busy researcher with a forum for the rapid publication of original research and critical reviews of all the latest relevant and significant developments, and focuses on how the technological, pharmacological, clinical and physiological aspects come together to successfully deliver modern therapeutics to patients. The journal delivers this essential information in concise, at-a-glance article formats that are readily accessible to the full spectrum of therapeutic delivery researchers.
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