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半结晶共聚物水凝胶作为智能药物载体:萘普生体外热响应释放研究。

Semi-Crystalline Copolymer Hydrogels as Smart Drug Carriers: In Vitro Thermo-Responsive Naproxen Release Study.

作者信息

Ilić-Stojanović Snežana, Nikolić Ljubiša, Nikolić Vesna, Petrović Slobodan, Oro Violeta, Mitić Žarko, Najman Stevo

机构信息

Faculty of Technology, University of Niš, Bulevar oslobodjenja 124, 16000 Leskovac, Serbia.

Faculty of Technology and Metallurgy, University of Belgrade, 11000 Belgrade, Serbia.

出版信息

Pharmaceutics. 2021 Jan 26;13(2):158. doi: 10.3390/pharmaceutics13020158.

Abstract

In this study, poly(-isopropylacrylamide--2-hydroxypropyl methacrylate) hydrogels were synthesized using free radical initiated copolymerization method. Four hydrogels with different cross-linker concentrations were prepared. Semi-crystalline, cross-linked copolymer networks were confirmed by FTIR, SEM and XRD analysis. Variation of swelling behaviour was monitored gravimetrically and thermo-responsiveness has been noticed. An application of synthesized thermo-responsive hydrogels as carriers for the modulated release of anti-inflammatory model drug was investigated. Moreover, naproxen loading into these hydrogels was also determined using FTIR, SEM and XRD techniques and release was analyzed using HPLC method at simulated physiological conditions. Swelling kinetic and mechanism of water transport, as well as diffusion of naproxen through the hydrogels were analyzed. Thus, the aim of this work was to study various compositions of obtained hydrogels and their possibility of application as a thermo-responsive carrier for prolonged naproxen release in order to evaluate as a potential candidate for drug carrier in future pharmaceutical applications.

摘要

在本研究中,采用自由基引发共聚法合成了聚(-异丙基丙烯酰胺-甲基丙烯酸2-羟丙酯)水凝胶。制备了四种具有不同交联剂浓度的水凝胶。通过傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)和X射线衍射(XRD)分析证实了半结晶交联共聚物网络的形成。采用重量法监测溶胀行为的变化,并观察到了热响应性。研究了合成的热响应性水凝胶作为抗炎模型药物控释载体的应用。此外,还使用FTIR、SEM和XRD技术测定了萘普生在这些水凝胶中的负载量,并在模拟生理条件下使用高效液相色谱(HPLC)法分析了其释放情况。分析了溶胀动力学、水传输机制以及萘普生在水凝胶中的扩散情况。因此,本工作的目的是研究所得水凝胶的各种组成及其作为热响应载体用于萘普生长效释放的可能性,以便评估其在未来药物应用中作为药物载体的潜在候选性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb8/7911820/158db44d3302/pharmaceutics-13-00158-g001.jpg

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