title

فرمولاسیون و ارزیابی اسکفلد آهسته رهش تتراسایکلین در عفونت های پریودنتال

زیبانژاد, مهسا and رضایی شیرمرد, لیلا and دیده ور, آیناز (1398) فرمولاسیون و ارزیابی اسکفلد آهسته رهش تتراسایکلین در عفونت های پریودنتال. در: شانزدهمین همایش علوم دارویی, 15-17 سال 1398, ایران-کرمانشاه.

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Preparation and Characterization of Sustained Release Scaffold Containing Tetracycline in Periodontal Infections

English Abstract

Introduction Periodontitis is a chronic inflammatory disease that affects the integrity of the supporting tissues of the tooth, including the gingiva, periodontal ligament and alveolar bone, which are generally known as the periodontium. The local delivery of antibiotics offers the potential for reaching and maintaining the therapeutic concentration at the site of the infection; since in this method drug is directly applied to the site, the concentration of the drug can be significantly higher than the systemic ones. Several degradable and non- degradable devices were developed for the delivery of antimicrobial agents into the periodontal pocket. In recent years, functional biomaterial research has been directed towards the development of improved scaffolds and novel drug delivery systems. The aim of this study was to develop a local delivery device, Sodium Alginate/CMCNa/ Adipic acid dihydrazide (NaAlg/CMCNa/ADH) scaffold, which allows the sustained release of tetracycline to effectively control local infection in periodontitis. Methods In the present work, NaAlg/CMCNa/ADH scaffold synthesized by freeze-drying 2.5% polymer solution. Adipic acid dihydrazide (ADH) was added as crosslinker and N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC) and 1-Hydroxybenzotriazole hydrate (HOBt) were added as Carboxyl group activator. Then dialysis was performed for 3 days against distilled water. In order to drying, the gel was poured into plates and lyophilized at -45 ° C for 24 hours. Then Samples were immersed in tetracycline solution vials for 48 hours in dark condition. The scaffolds were then dried by freeze-drying method for 24 hours. Finally, the scaffolds were evaluated by SEM, FTIR, 1H NMR, Swelling test, and TG/DTA. The amount of tetracycline released from the scaffolds was analyzed by spectrophotometry in PBS solution. Triplicate experiments were performed for each sample and expressed as means± standard deviation. Results The synthesized scaffolds had porous structure according to SEM images and in the scaffolds containing tetracycline the porous macrostructure was intact. In the FTIR spectra of NaAlg/CMCNa/ADH scaffold, the shoulder was seen at 1645 cm-1 Which indicates the formation of amide bond. The average water uptake of scaffolds was 93.216% ± 4.419. Scaffolds loaded by tetracycline showed sustained release pattern and were able to release 68% of drug up to 72 hours (figure1). Conclusion The NaAlg/CMCNa/ADH scaffolds could be beneficial in the management of periodontal infections and were suitable as a slow‐release device for tetracycline.

Item Type:Conference or Workshop Item (Poster)
زبان سند : انگلیسی
نویسنده اول :مهسا زیبانژاد
نویسنده مسئول :لیلا رضایی شیرمرد
نویسنده :آیناز دیده ور
کلیدواژه ها (انگلیسی):Periodontitis, Scaffold, Sodium Alginate, Tetracycline, CMCNa, Local drug delivery
Subjects:QV pharmacology > QV 704 Pharmaceutics
Divisions:School of Pharmacy > Department of Pharmaceutics
ID Code:12644
Deposited By: دکتر لیلا رضائی
Deposited On:06 Nov 1398 14:48
Last Modified:06 Nov 1398 14:48

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