In Vitro Evaluation of the Safety and Antineoplastic Effects in Gastrointestinal Tumors of Nanostructured Lipid Carriers Loaded with Berberine.

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Denitsa Stefanova, Yordan Yordanov, Radostina Bogdanova, Christina Voycheva, Borislav Tzankov, Teodora Popova, Magdalena Kondeva-Burdina, Virginia Tzankova, Natalia Toncheva-Moncheva, Diana Tzankova, Marta Slavkova
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引用次数: 0

Abstract

Background/Objectives: Natural substances have been a widely studied source of both pharmaceutical excipients and drugs. Berberine (BRB) is a benzylisoquinoline alkaloid isolated from different plant sources. It possesses various pharmacological properties including antibacterial, antitumor, antidiabetic, neuroprotective, hepatoprotective, anti-inflammatory, antioxidant, etc. However, the limited aqueous solubility hinders its application. Nanosized drug delivery systems are an innovative approach for addressing various challenges regarding drug delivery via different routes of administration. Their utilization could improve the solubility of active constituents. Methods: A melt-emulsification and ultrasonication technique was applied for the preparation of nanostructured lipid carriers (NLCs). They were thoroughly physicochemically characterized by the means of Dynamic Light Scattering, TEM, FTIR, DSC, TGA, and In Vitro release. The In Vitro efficacy and safety were evaluated on cholangiocarcinoma, colorectal adenocarcinoma, hepatocellular carcinoma, lymphoma, fibroblast, and cardioblast cells, as well as rat liver microsomes by means of cytotoxicity assays and the comet assay. Results: The obtained nanoparticles had a spherical shape and size around 158.2 ± 1.8 nm with negative zeta potential. They revealed successful drug loading and improved dissolution of berberine in physiological conditions. The In Vitro safety studies showed that loading BRB in NLCs resulted in improved or retained cytotoxicity to tumor cell lines and reduced cytotoxicity to normal cell lines and liver microsomes. The NLC itself increased microsomal malondialdehyde (MDA) and comet formation. Conclusions: A successful preparation of NLCs with berberine is presented. The nanocarriers show favorable physicochemical and biopharmaceutical properties. The cellular experiments show that the NLC loading of berberine could improve its anticancer efficacy and safety. These findings highlight the potential applicability of berberine in gastrointestinal neoplasms and build the foundation for future practical translation.

载小檗碱的纳米结构脂质载体在胃肠道肿瘤中的安全性和抗肿瘤作用的体外评价。
背景/目的:天然物质已成为广泛研究的药用辅料和药物来源。小檗碱(Berberine, BRB)是一种从不同植物中分离得到的苯基异喹啉类生物碱。具有抗菌、抗肿瘤、抗糖尿病、保护神经、保护肝脏、抗炎、抗氧化等药理作用。然而,有限的水溶性阻碍了它的应用。纳米给药系统是解决通过不同给药途径给药的各种挑战的一种创新方法。利用它们可以提高活性成分的溶解度。方法:采用熔融乳化超声技术制备纳米脂质载体。采用动态光散射、透射电镜(TEM)、红外光谱(FTIR)、差热分析(DSC)、热重分析(TGA)和体外释放度等手段对其进行了全面的理化表征。通过细胞毒性试验和彗星试验,评价其对胆管癌、结直肠腺癌、肝细胞癌、淋巴瘤、成纤维细胞、成心细胞及大鼠肝微粒体的体外疗效和安全性。结果:所制得的纳米颗粒呈球形,尺寸约为158.2±1.8 nm, zeta电位为负。他们揭示了在生理条件下成功的药物装载和改善小檗碱的溶解。体外安全性研究表明,在NLCs中加载BRB可改善或保留对肿瘤细胞系的细胞毒性,并降低对正常细胞系和肝微粒体的细胞毒性。NLC本身增加微粒体丙二醛(MDA)和彗星形成。结论:用小檗碱成功制备了nclc。纳米载体表现出良好的物理化学和生物制药性能。细胞实验表明,NLC负载小檗碱可以提高其抗癌效果和安全性。这些发现突出了小檗碱在胃肠道肿瘤中的潜在适用性,并为未来的实际转化奠定了基础。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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