Suppr超能文献

用于牙髓药物递送载体的光固化水凝胶的初步研究。

Preliminary study of light-cured hydrogel for endodontic drug delivery vehicle.

作者信息

Komabayashi Takashi, Wadajkar Aniket, Santimano Sonia, Ahn Chul, Zhu Qiang, Opperman Lynn A, Bellinger Larry L, Yang Jian, Nguyen Kytai T

机构信息

Department of Endodontics, West Virginia University School of Dentistry, Morgantown, WV, USA.

Department of Bioengineering, University of Texas, Arlington, TX, USA.

出版信息

J Investig Clin Dent. 2016 Feb;7(1):87-92. doi: 10.1111/jicd.12118. Epub 2014 Jul 22.

Abstract

AIM

Direct pulp capping is the treatment of an exposed vital pulp with a dental material to facilitate the formation of reparative dentin and maintenance of vital pulp. A bioengineered drug delivery vehicle has the potential to increase the success rate of pulp capping. The aim of this study was to develop an injectable and light-curing drug delivery vehicle for endodontic treatment including direct pulp capping.

METHODS

Polyethylene glycol-maleate-citrate (PEGMC) hydrogel was synthesized as a drug delivery vehicle that is composed of PEGMC (45% w/v), acrylic acid (AA) (5% w/v), 2,2'-azobis(2-methylpropionamidine) dihydrochloride (AAPH) (0.1% w/v), and deionized water. The association between prehydrogel-solution volume and visible light-curing was examined. The cytotoxicity of the hydrogel was tested using L929 cells in a cell culture system. Ca(2+) release from the hydrogel was determined using calcium hydroxide as the incorporated medicine.

RESULTS

The results showed that the light-curing time for hydrogel is comparable to composite resin. The hydrogel had cell toxicity similar to adhesive systems. Moreover, controlled Ca(2+) release was obtained from the calcium hydroxide incorporated hydrogel.

CONCLUSIONS

The data suggest that hydrogel should be explored further as a promising drug delivery vehicle for vital pulp therapy and regenerative endodontics.

摘要

目的

直接盖髓术是用牙科材料处理暴露的活髓,以促进修复性牙本质的形成并维持牙髓活力。一种生物工程药物递送载体有可能提高盖髓术的成功率。本研究的目的是开发一种用于牙髓治疗(包括直接盖髓术)的可注射且可光固化的药物递送载体。

方法

合成聚乙二醇 - 马来酸酯 - 柠檬酸盐(PEGMC)水凝胶作为药物递送载体,其由PEGMC(45% w/v)、丙烯酸(AA)(5% w/v)、2,2'-偶氮二异丁脒二盐酸盐(AAPH)(0.1% w/v)和去离子水组成。研究了预水凝胶溶液体积与可见光固化之间的关系。在细胞培养系统中使用L929细胞测试水凝胶的细胞毒性。以氢氧化钙作为掺入药物,测定水凝胶中Ca(2+)的释放情况。

结果

结果表明,水凝胶的光固化时间与复合树脂相当。该水凝胶具有与粘结系统相似的细胞毒性。此外,从掺入氢氧化钙的水凝胶中实现了Ca(2+)的可控释放。

结论

数据表明,水凝胶作为一种有前景的用于活髓治疗和再生牙髓病学的药物递送载体,应进一步探索。

相似文献

1
Preliminary study of light-cured hydrogel for endodontic drug delivery vehicle.
J Investig Clin Dent. 2016 Feb;7(1):87-92. doi: 10.1111/jicd.12118. Epub 2014 Jul 22.
4
Primate pulpal healing after exposure and TheraCal application.
J Clin Pediatr Dent. 2014 Summer;38(4):333-7. doi: 10.17796/jcpd.38.4.m585322121536q71.
8
Pulpal reactions to two experimental bonding systems for pulp capping procedures.
J Oral Sci. 2000 Jun;42(2):69-74. doi: 10.2334/josnusd.42.69.

引用本文的文献

3
4
Pivotal Local Drug Delivery Systems in Endodontics; A Review of Literature.
Iran Endod J. 2020 Spring;15(2):65-78. doi: 10.22037/iej.v15i2.30374.
5
Hydrogels and Dentin-Pulp Complex Regeneration: From the Benchtop to Clinical Translation.
Polymers (Basel). 2020 Dec 9;12(12):2935. doi: 10.3390/polym12122935.
6
Polymer-Based Instructive Scaffolds for Endodontic Regeneration.
Materials (Basel). 2019 Jul 24;12(15):2347. doi: 10.3390/ma12152347.
7
Citrate chemistry and biology for biomaterials design.
Biomaterials. 2018 Sep;178:383-400. doi: 10.1016/j.biomaterials.2018.05.003. Epub 2018 May 4.
8
Active Nanomaterials to Meet the Challenge of Dental Pulp Regeneration.
Materials (Basel). 2015 Nov 5;8(11):7461-7471. doi: 10.3390/ma8115387.
9
Injectable scaffolds: Preparation and application in dental and craniofacial regeneration.
Mater Sci Eng R Rep. 2017 Jan;111:1-26. doi: 10.1016/j.mser.2016.11.001.
10
Design Strategies and Applications of Biomaterials and Devices for Hernia Repair.
Bioact Mater. 2016 Sep;1(1):2-17. doi: 10.1016/j.bioactmat.2016.05.002. Epub 2016 May 30.

本文引用的文献

1
Citric acid-derived in situ crosslinkable biodegradable polymers for cell delivery.
Biomaterials. 2010 Dec;31(34):9092-105. doi: 10.1016/j.biomaterials.2010.08.022. Epub 2010 Aug 30.
2
Factorial analyses of photopolymerizable thermoresponsive composite hydrogels for protein delivery.
Nanomedicine. 2009 Sep;5(3):305-15. doi: 10.1016/j.nano.2008.11.003. Epub 2009 Feb 11.
3
Hydrogel nanoparticles in drug delivery.
Adv Drug Deliv Rev. 2008 Dec 14;60(15):1638-49. doi: 10.1016/j.addr.2008.08.002. Epub 2008 Sep 20.
5
The healing of phenolized pulp exposures.
Oral Surg Oral Med Oral Pathol. 1949 Jun;2(6):803-10. doi: 10.1016/0030-4220(49)90116-4.
7
The radiographic outcomes of direct pulp-capping procedures performed by dental students: a retrospective study.
J Am Dent Assoc. 2006 Dec;137(12):1699-705. doi: 10.14219/jada.archive.2006.0116.
8
Development of a temperature-sensitive composite hydrogel for drug delivery applications.
Biotechnol Prog. 2006 Jan-Feb;22(1):118-25. doi: 10.1021/bp0501367.
9
Advances since the paper by Zander and Glass (1949) on the pursuit of healing methods for pulpal exposures: historical perspectives.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005 Aug;100(2 Suppl):S102-8. doi: 10.1016/j.tripleo.2005.03.032.
10
DNA delivery from photocrosslinked PEG hydrogels: encapsulation efficiency, release profiles, and DNA quality.
J Control Release. 2004 Apr 28;96(2):341-51. doi: 10.1016/j.jconrel.2004.01.021.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验