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首页> 外文期刊>Bulletin of materials science >Characterization and in vitro and in vivo evaluation of cross-linked chitosan films as implant for controlled release of citalopram
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Characterization and in vitro and in vivo evaluation of cross-linked chitosan films as implant for controlled release of citalopram

机译:表征和体外和体内交联壳聚糖薄膜的植入物,用于植入西酞普兰的控制释放

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摘要

The aim of the present study is to develop cross-linked chitosan (CH) films that can release drug over an extended period of time and that too in a controlled manner. A solution of different percentages of CH, is prepared in 1% lactic acid, followed by addition of citalopram (CTP) and then reacted with increasing amounts of glutaraldehyde (GL) to obtain films with different cross-linking densities. Prepared films are characterized for their physical and mechanical properties. The films are then subjected to in vitro drug release studies using pH 7.4 phosphate buffer saline (PBS) as dissolution medium and cumulative amount of drug released is calculated. Kinetic analysis of drug release is performed using Power law model and Higuchia€?s model.With increase in concentration of CH, water absorption capacity and mechanical strength are increased; whereas, water vapour permeability and elasticity of the films are decreased. The effect of cross-linking agent, GL, is such that with an increase in the amount of GL, water vapour permeability, water absorption capacity and elasticity of the films are decreased; whereas, mechanical strength increased to some extent and then decreased. In vitro release studies indicate that films containing 3% CH, cross-linked with 2a€“3% GL and films containing 4%CH, cross-linked 1%GL are able to sustain the drug release for a prolonged time along with releasing almost complete drug in a desired period. Out of these batches, films containing 3% CH, cross-linked with 2a€“3% GL are having sufficient strength, water vapour permeation, water absorption capacity and elongation at break for implantation purpose. The in vitro degradation studies and histopathological studies were carried out with a sample film (batch C3 as in table 1) in rabbit model. In vitro degradation study indicates that the films maintained their integrity for desired implantation. The histopathological studies under optical microscope indicates that on implanting, there is no evidence of any inflammation, any foreign body granuloma or any necrosis or hemorrhage. Tissue configuration remains unaltered after 30 days of implantation. So, it can be suggested that cross-linked CH films of above said composition can be used as implant for long term application in depression and related disorders.
机译:本研究的目的是开发可以长时间释放药物的交联壳聚糖(CH)膜,并且也可以以受控方式释放。在1%的乳酸中制备了不同百分比的CH溶液,然后添加西酞普兰(CTP),然后与增加量的戊二醛(GL)反应以获得具有不同交联密度的薄膜。所制备的薄膜的物理和机械性能得以表征。然后使用pH 7.4磷酸盐缓冲盐水(PBS)作为溶出介质对膜进行体外药物释放研究,并计算累积的药物释放量。药物释放的动力学分析采用幂律模型和Higuchia模型进行。随着CH浓度的增加,吸水能力和机械强度提高。相反,膜的透湿性和弹性降低。交联剂GL的作用是,随着GL含量的增加,薄膜的水蒸气渗透性,吸水能力和弹性会降低。而机械强度在一定程度上先增大后减小。 体外释放研究表明,含2%3%GL交联的含3%CH的薄膜和含1%GL交联的含4%CH的薄膜能够维持药物的释放。延长时间,并在所需时间内释放几乎完整的药物。在这些批次中,含2%3%GL的3%CH交联的薄膜具有足够的强度,水蒸气渗透性,吸水能力和断裂伸长率,可用于植入目的。在兔模型中用样品膜(表1中的批次C3)进行了体外降解研究和组织病理学研究。 体外降解研究表明,该膜可保持其完整性,以实现所需的植入。光学显微镜下的组织病理学研究表明,植入后没有任何炎症,异物肉芽肿或任何坏死或出血的迹象。植入30天后,组织构型保持不变。因此,可以建议将上述组成的交联的CH膜用作长期用于抑郁症和相关疾病的植入物。

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