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静电纺丝聚(丙烯酸-4-苯乙烯磺酸盐)作为用于胃癌(AGS)和乳腺癌(MDA-Mb-231)细胞系靶向化疗递送系统的潜在药物洗脱支架。

Electrospun Poly(acrylic acid--4-styrene sulfonate) as Potential Drug-Eluting Scaffolds for Targeted Chemotherapeutic Delivery Systems on Gastric (AGS) and Breast (MDA-Mb-231) Cancer Cell Lines.

作者信息

Neira-Carrillo Andrónico, Zárate Ignacio A, Nieto Eddie, Butto-Miranda Nicole, Lobos-González Lorena, Del Campo-Smith Matias, Palacio Daniel A, Urbano Bruno F

机构信息

Department of Biological and Animal Sciences, Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, La Pintana, Santiago 8820808, Chile.

Advanced Center for Chronic Diseases (ACCDIS), Santiago 380492, Chile.

出版信息

Nanomaterials (Basel). 2022 Nov 4;12(21):3903. doi: 10.3390/nano12213903.

Abstract

Potential drug-eluting scaffolds of electrospun poly(acrylic acid--styrene sulfonate) P(AA--SS) in clonogenic assays using tumorigenic gastric and ovarian cancer cells were tested in vitro. Electrospun polymer nanofiber (EPnF) meshes of PAA and PSSNa homo- and P(AA--SS) copolymer composed of 30:70, 50:50, 70:30 acrylic acid (AA) and sodium 4-styrene sulfonate (SSNa) units were performed by electrospinning (ES). The synthesis, structural and morphological characterization of all EPnF meshes were analyzed by optical and electron microscopy (SEM-EDS), infrared spectroscopy (FTIR), contact angle, and X-ray diffraction (XRD) measurements. This study shows that different ratio of AA and SSNa of monomers in P(AA--SS) EPnF play a crucial role in clonogenic in vitro assays. We found that 50:50 P(AA--SS) EPnF mesh loaded with antineoplastic drugs can be an excellent suppressor of growth-independent anchored capacities in vitro assays and a good subcutaneous drug delivery system for chemotherapeutic medication in vivo model for surgical resection procedures in cancer research.

摘要

在体外使用致瘤性胃癌和卵巢癌细胞的克隆形成试验中,测试了静电纺丝聚(丙烯酸 - 苯乙烯磺酸盐)P(AA - SS)潜在的药物洗脱支架。通过静电纺丝(ES)制备了由30:70、50:50、70:30的丙烯酸(AA)和对苯乙烯磺酸钠(SSNa)单元组成的PAA和PSSNa均聚物以及P(AA - SS)共聚物的静电纺丝聚合物纳米纤维(EPnF)网。通过光学和电子显微镜(SEM - EDS)、红外光谱(FTIR)、接触角和X射线衍射(XRD)测量对所有EPnF网进行了合成、结构和形态表征分析。本研究表明,P(AA - SS)EPnF中单体AA和SSNa的不同比例在体外克隆形成试验中起关键作用。我们发现,负载抗肿瘤药物的50:50 P(AA - SS)EPnF网在体外试验中可以成为生长非依赖性锚定能力的优异抑制剂,并且在癌症研究中用于手术切除程序的体内模型中是化疗药物的良好皮下给药系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a00f/9657868/1d4b28b3ef16/nanomaterials-12-03903-g001.jpg

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