Morin-Loaded Chitosan-Poloxamer Hydrogel as an Osteoinductive Delivery System for Endodontic Applications

被引:0
作者
Pereira, Jesse Augusto [1 ]
Martin, Victor [2 ,3 ]
Araujo, Rita [2 ,3 ]
Grenho, Liliana [2 ,3 ]
Gomes, Pedro [2 ,3 ]
Marto, Joana [4 ]
Fernandes, Maria Helena [2 ,3 ]
Santos, Catarina [5 ,6 ]
Duque, Cristiane [1 ,7 ]
机构
[1] Sao Paulo State Univ UNESP, Aracatuba Dent Sch, Dept Prevent & Restorat Dent, Sao Paulo, Brazil
[2] Univ Porto, Fac Med Dent, BoneLab, Porto, Portugal
[3] Univ Porto, Fac Med Dent, LAQV REQUIMTE, Porto, Portugal
[4] Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
[5] Inst Politecn Setubal, EST Setubal, CDP2T, Setubal, Portugal
[6] Univ Lisbon, Inst Super Tecn, CQE, Lisbon, Portugal
[7] Univ Catolica Portuguesa UCP, Fac Dent Med, Ctr Interdisciplinary Res Hlth CIIS, Viseu, Portugal
关键词
biocompatibility; chitosan; drug-delivery; Morin; Osteogenesis; Poloxamer; stem cells; DIFFERENTIATION; DISINFECTION; TOXICITY; CELLS;
D O I
10.1002/jbm.a.37895
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Considering the search for new biocompatible intracanal medicaments that can preserve remaining cells and stimulate bone tissue repair in the periapical region, this study aimed to synthesize and characterize the physicochemical properties of morin-loaded chitosan-poloxamer hydrogel (MCP) as well as to evaluate its osteogenic potential. Morin hydrate (M) was loaded into chitosan-poloxamer (CP) hydrogel and the resulting particles were characterized by infrared spectroscopy (FTIR), UV-vis spectrophotometer and scanning electron microscopy. Biological assays evaluated the metabolic activity, cell morphology and alkaline phosphatase (ALP) activity of human bone marrow stem cells (HBMSC) in three different settings, such as the exposure to dissolved morin, hydrogel's leachates and assembled particles by indirect contact. Cells cultured in standard culture conditions were used as control. The effect of CP and MCP particles on the formation of collagenous and mineralized tissues was also assessed within the organotypic model of segmented embryonic chick femora. Datasets were assessed for one-way analysis of variance (ANOVA), followed by Tukey's post hoc test (p < 0.05). Morin at 50 mu g/mL was cytocompatible and increased ALP activity. CP and MCP particles showed stability, and morin was entrapped in the hydrogel matrix without changing its chemical structure. Cultures treated with 30-min CP and MCP hydrogel leachates presented significantly higher metabolic activity compared to control. By indirect contact, CP particles increased metabolic activity, but only MCP particles induced an upregulation of ALP activity in comparison to control. The amount of collagenous tissue and mineralized area on the fractured embryonic chick femora was greater in MCP particles compared to CP counterparts. Chitosan-poloxamer platforms are suitable systems to delivery morin, enhancing cell proliferation and bone mineralization, which upholds its application as intracanal medication for endodontic purposes.
引用
收藏
页数:10
相关论文
共 47 条
[1]   Inhibitory Effect of Morin Against Candida albicans Pathogenicity and Virulence Factor Production: An in vitro and in vivo Approaches [J].
Abirami, Gurusamy ;
Alexpandi, Rajaiah ;
Durgadevi, Ravindran ;
Kannappan, Arunachalam ;
Ravi, Arumugam Veera .
FRONTIERS IN MICROBIOLOGY, 2020, 11
[2]   Chitosan Nanoparticles at the Biological Interface: Implications for Drug Delivery [J].
Aibani, Noorjahan ;
Rai, Raj ;
Patel, Parth ;
Cuddihy, Grace ;
Wasan, Ellen K. .
PHARMACEUTICS, 2021, 13 (10)
[3]   A new ex vivo model of the bone tissue response to the hyperglycemic environment - The embryonic chicken femur organotypic culture in high glucose conditions [J].
Araujo, Rita ;
Martin, Victor ;
Ferreira, Rita ;
Fernandes, Maria Helena ;
Gomes, Pedro Sousa .
BONE, 2022, 158
[4]   Role of odanacatib in reducing bone loss due to endodontic disease: An overview [J].
Bahuguna, Rachana ;
Jain, Atul ;
Khan, Suleman Abbas ;
Arvind, M. S. .
JOURNAL OF INTERNATIONAL SOCIETY OF PREVENTIVE AND COMMUNITY DENTISTRY, 2016, 6 :S175-S181
[5]   Morin: A Promising Natural Drug [J].
Caselli, Anna ;
Cirri, Paolo ;
Santi, Alice ;
Paoli, Paolo .
CURRENT MEDICINAL CHEMISTRY, 2016, 23 (08) :774-791
[6]   Exploring Morin as an anti-quorum sensing agent (anti-QSA) against resistant strains of Staphylococcus aureus [J].
Chemmugil, P. ;
Lakshmi, P. T. V. ;
Annamalai, A. .
MICROBIAL PATHOGENESIS, 2019, 127 :304-315
[7]   An Overview on Thermosensitive Oral Gel Based on Poloxamer 407 [J].
Chen, Yabing ;
Lee, Jeong-Ho ;
Meng, Mingyue ;
Cui, Naiyu ;
Dai, Chun-Yu ;
Jia, Qi ;
Lee, Eui-Seok ;
Jiang, Heng-Bo .
MATERIALS, 2021, 14 (16)
[8]   A 13-week subchronic toxicity study of dietary administered morin in F344 rats [J].
Cho, YM ;
Onodera, H ;
Ueda, M ;
Imai, T ;
Hirose, M .
FOOD AND CHEMICAL TOXICOLOGY, 2006, 44 (06) :891-897
[9]   Synthesis of Sr-morin complex and its in vitro response: decrease in osteoclast differentiation while sustaining osteoblast mineralization ability [J].
Cruz, Marcos A. E. ;
Tovani, Camila B. ;
Favarin, Bruno Z. ;
Soares, Mariana P. R. ;
Fukada, Sandra Y. ;
Ciancaglini, Pietro ;
Ramos, Ana P. .
JOURNAL OF MATERIALS CHEMISTRY B, 2019, 7 (05) :823-829
[10]   Morin Hydrate Encapsulation and Release from Mesoporous Silica Nanoparticles for Melanoma Therapy [J].
Cunha, Catarina ;
Marinheiro, Diogo ;
Ferreira, Barbara J. M. L. ;
Oliveira, Helena ;
Daniel-da-Silva, Ana L. .
MOLECULES, 2023, 28 (12)