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基于海藻酸钠和石墨烯纳米片的白藜芦醇递送高效材料。

Natrium Alginate and Graphene Nanoplatelets-Based Efficient Material for Resveratrol Delivery.

作者信息

Mormile Cristina, Opriș Ocsana, Bellucci Stefano, Lung Ildiko, Kacso Irina, Turza Alexandru, Stegarescu Adina, Tripon Septimiu, Soran Maria-Loredana, Bâldea Ioana

机构信息

National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat, 400293 Cluj-Napoca, Romania.

R.A.I.T. 88 S.R.L, Via Pieve Torina 64/66, 00156 Rome, Italy.

出版信息

Gels. 2024 Dec 27;11(1):15. doi: 10.3390/gels11010015.

DOI:10.3390/gels11010015
PMID:39851987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11765397/
Abstract

In this study, alginate-based composite beads were developed for the delivery of resveratrol, a compound with therapeutic potential. Two formulations were prepared: one with sodium alginate and resveratrol (AR) and another incorporating graphene nanoplatelets (AGR) to improve drug release control. The beads were formed by exploiting alginate's ability to gel via ionic cross-linking. For the AGR formulation, sodium alginate was dissolved in water, and graphene was dispersed in isopropyl alcohol to achieve smaller flakes. Resveratrol was dissolved in an ethanol/water mixture and added to the graphene dispersion; the resulting solution was mixed with the alginate one. For the AR formulation, the resveratrol solution was mixed directly with the alginate solution. Both formulations were introduced into a calcium chloride solution to form the beads. The release of resveratrol was studied in phosphate-buffered saline at different pH values. Results showed that the presence of graphene in the AGR sample increased drug release, particularly at pH 6.8, indicating a pH-driven release mechanism. Kinetic analysis revealed that the Higuchi model best describes the release mechanism. Finally, cytotoxicity tests showed the biocompatibility of the system in normal human cells. These findings suggest that graphene-enhanced alginate matrices have significant potential for controlled drug delivery applications.

摘要

在本研究中,开发了基于藻酸盐的复合珠用于递送白藜芦醇,这是一种具有治疗潜力的化合物。制备了两种配方:一种是含有海藻酸钠和白藜芦醇的(AR),另一种加入了石墨烯纳米片(AGR)以改善药物释放控制。通过利用藻酸盐通过离子交联形成凝胶的能力来形成珠子。对于AGR配方,将海藻酸钠溶解在水中,并将石墨烯分散在异丙醇中以获得更小的薄片。将白藜芦醇溶解在乙醇/水混合物中并添加到石墨烯分散体中;将所得溶液与藻酸盐溶液混合。对于AR配方,将白藜芦醇溶液直接与藻酸盐溶液混合。将两种配方都引入氯化钙溶液中以形成珠子。在不同pH值的磷酸盐缓冲盐水中研究了白藜芦醇的释放。结果表明,AGR样品中石墨烯的存在增加了药物释放,特别是在pH 6.8时,表明存在pH驱动的释放机制。动力学分析表明,Higuchi模型最能描述释放机制。最后,细胞毒性测试表明该系统在正常人细胞中具有生物相容性。这些发现表明,石墨烯增强的藻酸盐基质在控释药物应用方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/cb9c6ceb1e4c/gels-11-00015-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/20a61f917305/gels-11-00015-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/d03ae7f4406a/gels-11-00015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/a3dbee5826fa/gels-11-00015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/4f0b3e9166e6/gels-11-00015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/e31fa56165e5/gels-11-00015-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/5b784756e1b6/gels-11-00015-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/24a415ce3918/gels-11-00015-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/cb9c6ceb1e4c/gels-11-00015-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/20a61f917305/gels-11-00015-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/d03ae7f4406a/gels-11-00015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/a3dbee5826fa/gels-11-00015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/4f0b3e9166e6/gels-11-00015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/e31fa56165e5/gels-11-00015-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/5b784756e1b6/gels-11-00015-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/24a415ce3918/gels-11-00015-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7085/11765397/cb9c6ceb1e4c/gels-11-00015-g008.jpg

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