Gum tragacanth-based hemostatic sponge for enhanced hemostasis in dental surgery.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Mirmousa Mousavai, Ramin Khajavi, Mohammadreza Kalaee, Mohammad Karim Rahimi
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Abstract

Regulating hemorrhage is crucial during dental procedures, particularly surgical interventions where substantial blood loss may occur. Hemostatic sponges are effective instruments for controlling hemorrhage, facilitating hemostasis, preparing the surgical area, and enhancing the healing of injuries. This work aimed to present a novel hemostatic sponge created by integrating antihemorrhagic chemicals with the natural polysaccharide tragacanth. Gum tragacanth (GT) (derived from the species Astragalus gossypinus) was solubilized in water and combined with nanoclay (NC) and tranexamic acid (TXA) at varying doses. Subsequently, they were freeze-dried in cubic silicone molds. Scanning electron micrographs revealed that the incorporation of TXA and NC significantly increased the porosity of the sponges. No evidence of chemical bonding was present in our converted infrared spectra. Prothrombin time (PT), activated partial thromboplastin time (aPTT), and whole blood coagulation index showed improvement with the administration of hemostatics, with TXA demonstrating a more pronounced impact. The cytotoxicity assay of the hemostatic GT exhibited no notable difference from the control sample. The hemostatic GT has demonstrated significant potential for medical applications, particularly in dentistry, and applies to procedures such as endodontics and prosthesis placement.

牙龈黄芪止血海绵在牙科手术中的止血作用。
在牙科手术过程中,尤其是可能发生大量失血的外科手术中,调节出血是至关重要的。止血海绵是控制出血、促进止血、准备手术区域、促进伤口愈合的有效工具。本工作旨在提出一种新型止血海绵,将抗出血化学物质与天然多糖黄芪多糖结合制成。将黄芪胶(GT)溶于水,并与纳米粘土(NC)和氨甲环酸(TXA)以不同剂量混合。随后,它们在立方硅胶模具中被冷冻干燥。扫描电镜显示,TXA和NC的掺入显著增加了海绵的孔隙率。在我们转换的红外光谱中没有化学键的证据。凝血酶原时间(PT)、活化的部分凝血活素时间(aPTT)和全血凝指数均随止血药的使用而改善,其中TXA的影响更为明显。止血药GT的细胞毒性实验结果与对照样品无显著差异。止血GT已显示出巨大的医学应用潜力,特别是在牙科领域,并适用于牙髓学和假体植入等手术。
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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