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用于药物释放和磁热疗应用的含超顺磁性纳米粒子的可注射热响应性微粒/水凝胶系统

Injectable Thermoresponsive Microparticle/Hydrogel System with Superparamagnetic Nanoparticles for Drug Release and Magnetic Hyperthermia Applications.

作者信息

Carrelo Henrique, Escoval André R, Vieira Tânia, Jiménez-Rosado Mercedes, Silva Jorge Carvalho, Romero Alberto, Soares Paula Isabel P, Borges João Paulo

机构信息

CENIMAT/i3N, Department of Materials Science, NOVA School of Science and Technology (FCT NOVA), Campus de Caparica, 2829-516 Caparica, Portugal.

CENIMAT/i3N, Department of Physics, NOVA School of Science and Technology (FCT NOVA), Campus de Caparica, 2829-516 Caparica, Portugal.

出版信息

Gels. 2023 Dec 15;9(12):982. doi: 10.3390/gels9120982.


DOI:10.3390/gels9120982
PMID:38131968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10742759/
Abstract

Cancer is a disease that continues to greatly impact our society. Developing new and more personalized treatment options is crucial to decreasing the cancer burden. In this study, we combined magnetic polysaccharide microparticles with a Pluronic thermoresponsive hydrogel to develop a multifunctional, injectable drug delivery system (DDS) for magnetic hyperthermia applications. Gellan gum and alginate microparticles were loaded with superparamagnetic iron oxide nanoparticles (SPIONs) with and without coating. The magnetic microparticles' registered temperature increases up to 4 °C upon the application of an alternating magnetic field. These magnetic microparticles were mixed with drug-loaded microparticles, and, subsequently, this mixture was embedded within a Pluronic thermoresponsive hydrogel that is capable of being in the gel state at 37 °C. The proposed DDS was capable of slowly releasing methylene blue, used as a model drug, for up to 9 days. The developed hydrogel/microparticle system had a smaller rate of drug release compared with microparticles alone. This system proved to be a potential thermoresponsive DDS suitable for magnetic hyperthermia applications, thus enabling a synergistic treatment for cancer.

摘要

癌症是一种持续对我们社会产生重大影响的疾病。开发新的、更具个性化的治疗方案对于减轻癌症负担至关重要。在本研究中,我们将磁性多糖微粒与普朗尼克热响应水凝胶相结合,开发了一种用于磁热疗应用的多功能可注射药物递送系统(DDS)。结冷胶和海藻酸盐微粒分别负载有有无涂层的超顺磁性氧化铁纳米颗粒(SPIONs)。施加交变磁场时,磁性微粒记录到的温度升高可达4°C。这些磁性微粒与载药微粒混合,随后将该混合物包埋于在37°C时能够呈凝胶状态的普朗尼克热响应水凝胶中。所提出的DDS能够将用作模型药物的亚甲蓝缓慢释放长达9天。与单独的微粒相比,所开发的水凝胶/微粒系统具有更低的药物释放速率。该系统被证明是一种适用于磁热疗应用的潜在热响应DDS,从而能够实现癌症的协同治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/496a48e89edc/gels-09-00982-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/e7214a04b45f/gels-09-00982-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/29bf6014e049/gels-09-00982-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/4ae892afadff/gels-09-00982-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/496a48e89edc/gels-09-00982-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/e7214a04b45f/gels-09-00982-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/29bf6014e049/gels-09-00982-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/4ae892afadff/gels-09-00982-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b598/10742759/496a48e89edc/gels-09-00982-g007.jpg

相似文献

[1]
Injectable Thermoresponsive Microparticle/Hydrogel System with Superparamagnetic Nanoparticles for Drug Release and Magnetic Hyperthermia Applications.

Gels. 2023-12-15

[2]
Injectable Hydrogels Based on Pluronic/Water Systems Filled with Alginate Microparticles for Biomedical Applications.

Materials (Basel). 2019-4-2

[3]
A Thermoresponsive injectable drug delivery system of chitosan/β-glycerophosphate with gellan gum/alginate microparticles.

Int J Biol Macromol. 2024-6

[4]
Simultaneous Release of Aflibercept and Dexamethasone from an Ocular Drug Delivery System.

Curr Eye Res. 2022-7

[5]
The in vivo performance of magnetic particle-loaded injectable, in situ gelling, carriers for the delivery of local hyperthermia.

Biomaterials. 2009-10-29

[6]
Ca:Mg:Zn:CO and Ca:Mg:CO-tri- and bi-elemental carbonate microparticles for novel injectable self-gelling hydrogel-microparticle composites for tissue regeneration.

Biomed Mater. 2017-3-24

[7]
Synthesis and characterization of an injectable microparticles integrated hydrogel composite biomaterial: In-vivo biocompatibility and inflammatory arthritis treatment.

Colloids Surf B Biointerfaces. 2021-5

[8]
Cartilage regeneration with dual-drug-releasing injectable hydrogel/microparticle system: In vitro and in vivo study.

J Cell Physiol. 2021-3

[9]
Injectable and thermoresponsive self-assembled nanocomposite hydrogel for long-term anticancer drug delivery.

Langmuir. 2013-3-7

[10]
Novel injectable, self-gelling hydrogel-microparticle composites for bone regeneration consisting of gellan gum and calcium and magnesium carbonate microparticles.

Biomed Mater. 2016-11-21

本文引用的文献

[1]
Switching it Up: The Promise of Stimuli-Responsive Polymer Systems in Biomedical Science.

Chem Rec. 2024-2

[2]
Gellan Gum/Alginate Microparticles as Drug Delivery Vehicles: DOE Production Optimization and Drug Delivery.

Pharmaceuticals (Basel). 2023-7-19

[3]
Cytotoxicity towards Breast Cancer Cells of Pluronic F-127/Hyaluronic Acid Hydrogel Containing Nitric Oxide Donor and Silica Nanoparticles Loaded with Cisplatin.

Pharmaceutics. 2022-12-17

[4]
Mesoporous Bioactive Glasses Incorporated into an Injectable Thermosensitive Hydrogel for Sustained Co-Release of Sr Ions and -Acetylcysteine.

Pharmaceutics. 2022-9-7

[5]
Sequential Drug Delivery in Targeted Cancer Therapy.

Pharmaceutics. 2022-3-5

[6]
Biomedical Applications of Iron Oxide Nanoparticles: Current Insights Progress and Perspectives.

Pharmaceutics. 2022-1-16

[7]
Biocompatible and Thermoresistant Hydrogels Based on Collagen and Chitosan.

Polymers (Basel). 2022-1-10

[8]
Chitosan/Pluronic F127 Thermosensitive Hydrogel as an Injectable Dexamethasone Delivery Carrier.

Gels. 2022-1-7

[9]
Injectable Composite Systems Based on Microparticles in Hydrogels for Bioactive Cargo Controlled Delivery.

Gels. 2021-9-18

[10]
Incorporation of Dual-Stimuli Responsive Microgels in Nanofibrous Membranes for Cancer Treatment by Magnetic Hyperthermia.

Gels. 2021-3-5

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