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用于制备用于递送5-氟尿嘧啶的pH敏感纳米凝胶的丙烯酸和甲基丙烯酸琼脂接枝改性

Agar Graft Modification with Acrylic and Methacrylic Acid for the Preparation of pH-Sensitive Nanogels for 5-Fluorouracil Delivery.

作者信息

Ivanova Ivelina, Slavkova Marta, Popova Teodora, Tzankov Borislav, Stefanova Denitsa, Tzankova Virginia, Tzankova Diana, Spassova Ivanka, Kovacheva Daniela, Voycheva Christina

机构信息

Faculty of Pharmacy, Department Pharmaceutical Technology and Biopharmacy, Medical University-Sofia, 1000 Sofia, Bulgaria.

Faculty of Pharmacy, Department of Pharmacology, Pharmacotherapy and Toxicology, Medical University-Sofia, 1000 Sofia, Bulgaria.

出版信息

Gels. 2024 Feb 23;10(3):165. doi: 10.3390/gels10030165.

Abstract

Agar, a naturally occurring polysaccharide, has been modified by grafting it with acrylic (AcA) and methacrylic (McA) acid monomers, resulting in acrylic or methacrylic acid grafted polymer (AA-g-AcA or AA-g-McA) with pH-sensitive swelling behavior. Different ratios between agar, monomers, and initiator were applied. The synthesized grades of both new polymer series were characterized using FTIR spectroscopy, NMR, TGA, DSC, and XRD to ascertain the intended grafting. The percentage of grafting (% G), grafting efficiency (% GE), and % conversion (% C) were calculated, and models with optimal characteristics were further characterized. The swelling behavior of the newly synthesized polymers was studied over time and in solutions with different pH. These polymers were subsequently crosslinked with varying amounts of glutaraldehyde to obtain 5-fluorouracil-loaded nanogels. The optimal ratios of polymer, drug, and crosslinker resulted in nearly 80% loading efficiency. The performed physicochemical characterization (TEM and DLS) showed spherical nanogels with nanometer sizes (105.7-250 nm), negative zeta potentials, and narrow size distributions. According to FTIR analysis, 5-fluorouracil was physically incorporated. The swelling and release behavior of the prepared nanogels was pH-sensitive, favoring the delivery of the chemotherapeutic to tumor cells. The biocompatibility of the proposed nanocarrier was proven using an in vitro hemolysis assay.

摘要

琼脂是一种天然存在的多糖,已通过将其与丙烯酸(AcA)和甲基丙烯酸(McA)单体接枝进行改性,从而得到具有pH敏感溶胀行为的丙烯酸或甲基丙烯酸接枝聚合物(AA-g-AcA或AA-g-McA)。采用了琼脂、单体和引发剂之间的不同比例。使用傅里叶变换红外光谱(FTIR)、核磁共振(NMR)、热重分析(TGA)、差示扫描量热法(DSC)和X射线衍射(XRD)对两个新聚合物系列的合成产物进行表征,以确定预期的接枝情况。计算了接枝百分比(%G)、接枝效率(%GE)和转化率(%C),并对具有最佳特性的模型进行了进一步表征。研究了新合成聚合物在不同时间以及在不同pH溶液中的溶胀行为。随后,这些聚合物与不同量的戊二醛交联,以获得负载5-氟尿嘧啶的纳米凝胶。聚合物、药物和交联剂的最佳比例导致负载效率接近80%。所进行的物理化学表征(透射电子显微镜(TEM)和动态光散射(DLS))显示出具有纳米尺寸(105.7 - 250 nm)、负zeta电位和窄尺寸分布的球形纳米凝胶。根据FTIR分析,5-氟尿嘧啶是物理包埋的。所制备纳米凝胶的溶胀和释放行为对pH敏感,有利于将化疗药物递送至肿瘤细胞。使用体外溶血试验证明了所提出的纳米载体的生物相容性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d17/10970384/84cbcb42f3ce/gels-10-00165-g001.jpg

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