Extraction, characterization and controlled release application of pectin-like/chitosan hydrogels system loaded Ciprofloxacin.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Amer Rashid Hameed, Zeineb Mzoughi, Mariem Itaimi Dammak, Fawzi Habeeb Jabrail, Didier Le Cerf, Hatem Majdoub
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引用次数: 0

Abstract

Introduction: In recent decades, drug delivery applications have extensively utilized hydrogel systems based on natural polymers. Among the numerous biopolymer-based hydrogel drug delivery systems reported, a novel pectin-like substance was extracted from fig leaves and copolymerized with chitosan.

Method: The hydrogel was reformed into microspheres using glutaraldehyde (chemical cross-linker) and sodium hexametaphosphate (physical cross-linker). The extracted polysaccharide and the prepared hydrogels were characterized by FTIR, GC/MS, SEC/MALS/DRI as well as XRD, SEM, BET, and thermal analysis. SEM images revealed the formation of porous microspheres with an average size of 50 μm in diameter. Degrees of swelling in pH7 at 35°C have shown the hydrogels reached two to three times their weights. This has been reflected in their ability to load drugs or any other chemicals. The loading formula shows that hydrogels have maximum loading efficiency more than one-third of the weight of hydrogel. The antimicrobial ciprofloxacin was used as a model for loading on prepared hydrogels. The loaded hydrogels were tested for their biological activities against staphylococcus aureus (S. aureus) bacteria. The antimicrobial growth inhibition zone of the cultured (S. aureus) by ciprofloxacin-loaded hydrogel was followed, which shows controlled growth in inhibition zone sizes and for long time intervals. Results showed that the pectin-chitosan hydrogels exhibited significant antibacterial activity against gram - positive bacteria (S. aureus), with an inhibition zone of 45 mm for (CH-co-FLP)/GLU hydrogel.

Result: In vitro, the ciprofloxacin-loaded hydrogels were studied and the cumulative release of ciprofloxacin under suitable conditions was found in a controlled manner and kept release for a long time interval. Data exhibited that the cumulative release profile of ciprofloxacin from the hydrogel demonstrated sustained release over 48 hours, with a value of 6.9% released within the first 24 hours and 7.0 and 6.9% % released at the end of the study for the (CH-co-FLP)/GLU and (CH-co-FLP)/SMP hydrogels, respectively.

Conclusion: The novel pectin-chitosan hydrogels hold the potential to enhance the quality of life for numerous patients by minimizing the need for frequent intake of chronic medications.

类果胶/壳聚糖水凝胶环丙沙星的提取、表征及控释应用。
近几十年来,药物递送应用广泛使用基于天然聚合物的水凝胶系统。在众多以生物聚合物为基础的水凝胶给药系统中,从无花果叶中提取了一种新型的类似果胶的物质,并与壳聚糖共聚。方法:用戊二醛(化学交联剂)和六偏磷酸钠(物理交联剂)将水凝胶改造成微球。通过FTIR、GC/MS、SEC/MALS/DRI、XRD、SEM、BET和热分析对提取的多糖和制备的水凝胶进行表征。SEM图像显示形成了平均直径为50 μm的多孔微球。在35°C下pH7的膨胀程度表明水凝胶达到其重量的两到三倍。这反映在它们装载药物或任何其他化学品的能力上。加载公式表明,水凝胶的最大加载效率大于水凝胶重量的三分之一。以抗菌药物环丙沙星为模型,在制备的水凝胶上进行负载。研究了负载水凝胶对金黄色葡萄球菌(S. aureus)细菌的生物活性。经环丙沙星负载水凝胶培养的金黄色葡萄球菌抗菌生长抑制带,抑制带大小和生长时间间隔均有控制。结果表明,果胶-壳聚糖水凝胶对革兰氏阳性菌(金黄色葡萄球菌)具有明显的抑菌活性,对(CH-co-FLP)/GLU水凝胶的抑菌带为45 mm。结果:体外对环丙沙星载水凝胶进行了研究,发现环丙沙星在适宜条件下的累积释放量可控,且缓释时间长。数据显示,环丙沙星在水凝胶中的累积释放量在48小时内持续释放,其中(CH-co-FLP)/GLU和(CH-co-FLP)/SMP水凝胶在研究结束时的释放量分别为7.0%和6.9%。结论:新型果胶-壳聚糖水凝胶通过减少频繁服用慢性药物的需要,有可能提高许多患者的生活质量。
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来源期刊
Current drug delivery
Current drug delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.20%
发文量
170
期刊介绍: Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase, however in many cases this idea cannot be met and the development of delivery systems becomes as important as the development of the drugs themselves. The journal aims to cover the latest outstanding developments in drug and vaccine delivery employing physical, physico-chemical and chemical methods. The drugs include a wide range of bioactive compounds from simple pharmaceuticals to peptides, proteins, nucleotides, nucleosides and sugars. The journal will also report progress in the fields of transport routes and mechanisms including efflux proteins and multi-drug resistance. The journal is essential for all pharmaceutical scientists involved in drug design, development and delivery.
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