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叶酸偶联凹凸棒石/金杂化微凝胶:温、pH 值和光三重响应及其在药物传递中的应用。

Folic acid conjugated palygorskite/Au hybrid microgels: Temperature, pH and light triple-responsive and its application in drug delivery.

机构信息

College of Materials Science and Engineering, Nanjing Tech University, Nanjing 210000, PR China; Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials, School of Chemistry & Chemical Engineering, Huaiyin Normal University, Huaian 223300, PR China.

Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials, School of Chemistry & Chemical Engineering, Huaiyin Normal University, Huaian 223300, PR China.

出版信息

Colloids Surf B Biointerfaces. 2023 Sep;229:113432. doi: 10.1016/j.colsurfb.2023.113432. Epub 2023 Jun 28.

Abstract

Herein, folic acid conjugated poly (NIPAM-co-functional palygorskite-Au-co-acrylic acid) (FA-PNFA) hybrid microgels were fabricated by emulsion polymerization. The introduction of acrylic acid can increase the low critical solution temperature (LCST) of FA-PNFA from 36 °C at pH 5.5-42 °C at pH 7.4. Doxorubicin hydrochloride (DOX) was chosen as the load drug, the results show that the DOX release behavior is driven by temperature, pH and light. Cumulative drug release rate can reach 74 % at 37 °C and pH 5.5 while only 20 % at 37 °C and pH 7.4, which effectively avoided the early leakage of the drug. In addition, by exposing FA-PNFA hybrid microgels to laser irradiation, the cumulative release rate was increased by 5 % compared to the release rate under dark conditions. Functional palygorskite-Au as physical crosslinkers not only improves the drug loading content of microgels but also promotes the release of DOX through light drive. Methyl thiazolyl tetrazolium bromide (MTT) assay demonstrated that the FA-PNFA are nontoxic up to 200 μg mL towards 4T1 breast cancer cell. Meanwhile, DOX-loaded FA-PNFA show more significant cytotoxicity than the free DOX. Confocal laser scanning microscope (CLSM) revealed that the DOX-loaded FA-PNFA could be efficiently taken by 4T1 breast cancer cells. FA-PNFA hybrid microgels not only improve the LCST of PNIPAM, but also endow the microgels with photostimulation responsiveness, which can release drugs in response to the triple stimulation response of temperature, pH and light, thus effectively reducing the activity of cancer cells, making them more promising for wider medical applications.

摘要

本文通过乳液聚合制备了叶酸偶联聚(NIPAM-co-功能化坡缕石-Au-co-丙烯酸)(FA-PNFA)杂化微凝胶。引入丙烯酸可以将 FA-PNFA 的低临界溶液温度(LCST)从 pH5.5 时的 36°C 提高到 pH7.4 时的 42°C。盐酸阿霉素(DOX)被选为负载药物,结果表明 DOX 的释放行为受温度、pH 值和光照的驱动。在 37°C 和 pH5.5 时,累积药物释放率可达 74%,而在 37°C 和 pH7.4 时仅为 20%,有效避免了药物的早期泄漏。此外,通过将 FA-PNFA 杂化微凝胶暴露于激光照射下,与黑暗条件下的释放率相比,累积释放率增加了 5%。功能化坡缕石-Au 作为物理交联剂,不仅提高了微凝胶的载药含量,而且通过光驱动促进了 DOX 的释放。噻唑蓝(MTT)测定表明,FA-PNFA 对 4T1 乳腺癌细胞的毒性在 200μg·mL-1 以下。同时,载 DOX 的 FA-PNFA 比游离 DOX 具有更显著的细胞毒性。共聚焦激光扫描显微镜(CLSM)显示,载 DOX 的 FA-PNFA 可以被 4T1 乳腺癌细胞有效摄取。FA-PNFA 杂化微凝胶不仅提高了 PNIPAM 的 LCST,而且赋予微凝胶光刺激响应性,可响应温度、pH 值和光的三重刺激释放药物,从而有效降低癌细胞的活性,使其更有希望在更广泛的医学应用中得到应用。

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