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利用牛角瓜制备多功能乳胶基混合纳米载体以实现阿霉素(DOX)的持续释放。

Assembling of multifunctional latex-based hybrid nanocarriers from Calotropis gigantea for sustained (doxorubicin) DOX releases.

作者信息

Pradeepkumar Periyakaruppan, Govindaraj Dharman, Jeyaraj Murugaraj, Munusamy Murugan A, Rajan Mariappan

机构信息

Biomaterials in Medicinal Chemistry Laboratory, Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai, 625021, Tamil Nadu, India.

National Centre for Nanoscience and Nanotechnology, University of Madras, Guindy campus, Chennai, 25, India.

出版信息

Biomed Pharmacother. 2017 Mar;87:461-470. doi: 10.1016/j.biopha.2016.12.133. Epub 2017 Jan 6.

Abstract

Natural rubber Latex (Lax) is a colloidal dispersion of polymer particles in liquid and shows good biodegradable, biocompatibility, and non-toxicity. Natural polymers are the most important materials used in food packaging, micro/nano-drug delivery, tissue engineering, agriculture, and coating. In the present study, natural compounds extracted from plant Lax were designed to function as drug carriers using various surfactants via emulation and solvent evaporation method. Calotropis gigantea belongs to the family Apocynaceae and has received considerable attention in modern medicine, ayurvedeic, siddha, and traditional medicine. Since, we were isolated biodegradable, non-toxic, and biocompatible materials as latex from Calotropis gigantea plant. The Lax was separated as per their solubility nature and it was designed as a carrier using surfactant namely; Sorbitanmonolaurate (Span-20), sodium lauryl sulfate (SLS), and cetyltrimethylammonium bromide (CTAB). The isolated compounds from Lax of Calotropis gigantea were analyzed using high-performance liquid chromatography. To confirm the encapsulation efficiency and in vitro drug release of the carriers, doxorubicin (DOX) was used as a model natural drug. The hybrid nanocarriers were successfully synthesized through simple solvent evaporation using three surfactants, and the morphology was characterized by SEM and TEM technique. The functionality and crystalline nature of the nanocarriers were confirmed using FTIR and XRD, respectively. Within 90min, the maximum amount of DOX was encapsulated in the carriers, and prolonged cumulative drug release by the nanocarriers was observed. The formulated natural carriers were found to have potentially effective cytotoxic effects on lung cancer cells.

摘要

天然橡胶胶乳(Lax)是聚合物颗粒在液体中的胶体分散体,具有良好的生物可降解性、生物相容性和无毒特性。天然聚合物是食品包装、微/纳米药物递送、组织工程、农业和涂料中使用的最重要材料。在本研究中,从植物Lax中提取的天然化合物通过乳化和溶剂蒸发法,使用各种表面活性剂设计用作药物载体。牛角瓜属于夹竹桃科,在现代医学、阿育吠陀医学、悉达医学和传统医学中受到了相当大的关注。因为,我们从牛角瓜植物中分离出了可生物降解、无毒且具有生物相容性的材料作为胶乳。根据其溶解性对Lax进行分离,并使用表面活性剂山梨醇单月桂酸酯(司盘-20)、十二烷基硫酸钠(SLS)和十六烷基三甲基溴化铵(CTAB)将其设计为载体。使用高效液相色谱法分析从牛角瓜Lax中分离出的化合物。为了确认载体的包封效率和体外药物释放,使用阿霉素(DOX)作为模型天然药物。通过简单的溶剂蒸发使用三种表面活性剂成功合成了杂化纳米载体,并通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)技术对其形态进行了表征。分别使用傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)确认了纳米载体的功能和晶体性质。在90分钟内,DOX的最大量被包封在载体中,并且观察到纳米载体延长了药物的累积释放。发现所制备的天然载体对肺癌细胞具有潜在有效的细胞毒性作用。

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