{"title":"合成纳米沸石在给药中的应用","authors":"Shaghayegh Rahmani, S. N. Azizi, N. Asemi","doi":"10.3329/ICPJ.V5I6.27710","DOIUrl":null,"url":null,"abstract":"In this study nanozeolite sodalite was synthesized from natural volcanic glass (perlite) as silica (Si) source and sodium aluminate as aluminium (Al) source without using any organic template. We use perlite as Si source because it is cost-effective and available source. These nanoparticles of synthesized zeolite were prepared at 170°C in stainless steel reactor with hydrothermal method. The synthesized nanozeolite was characterized by X-ray diffraction (XRD), fourier transform infrared (FTIR) and scanning electron microscopy (SEM) techniques. Chemical composition of perlite was determined by X-ray fluorescence (XRF).This nanozeolite was modified with cationic surfactant, hexadecyltrimethylammonium bromide (HDTMAB). In this study adsorption of cetirizine (Cet) as a model drug onto nanozeolite sodalite as a carrier of drug was investigated and Ultra Violet-Visible (UV-Vis) spectrophotometry was used for determination of concentrations of Cet at 230 nm. Adsorption characteristics of Cet on nanozeolite sodalite were examined at different times (0-6 h) and also the analysis was carried at three pH levels 4, 5 and 6. Finally three buffered solutions with different pH (1.2, 6.8 and 7.2) were selected for release medium and the temperature was precisely controlled at 37 ± 0.1°C. Rahmani et al., International Current Pharmaceutical Journal, May 2016, 5(6): 55-58","PeriodicalId":13811,"journal":{"name":"International Current Pharmaceutical Journal","volume":"83 1","pages":"55-58"},"PeriodicalIF":0.0000,"publicationDate":"2016-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"Application of Synthetic Nanozeolite Sodalite in Drug Delivery\",\"authors\":\"Shaghayegh Rahmani, S. N. Azizi, N. Asemi\",\"doi\":\"10.3329/ICPJ.V5I6.27710\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study nanozeolite sodalite was synthesized from natural volcanic glass (perlite) as silica (Si) source and sodium aluminate as aluminium (Al) source without using any organic template. We use perlite as Si source because it is cost-effective and available source. These nanoparticles of synthesized zeolite were prepared at 170°C in stainless steel reactor with hydrothermal method. The synthesized nanozeolite was characterized by X-ray diffraction (XRD), fourier transform infrared (FTIR) and scanning electron microscopy (SEM) techniques. Chemical composition of perlite was determined by X-ray fluorescence (XRF).This nanozeolite was modified with cationic surfactant, hexadecyltrimethylammonium bromide (HDTMAB). In this study adsorption of cetirizine (Cet) as a model drug onto nanozeolite sodalite as a carrier of drug was investigated and Ultra Violet-Visible (UV-Vis) spectrophotometry was used for determination of concentrations of Cet at 230 nm. Adsorption characteristics of Cet on nanozeolite sodalite were examined at different times (0-6 h) and also the analysis was carried at three pH levels 4, 5 and 6. Finally three buffered solutions with different pH (1.2, 6.8 and 7.2) were selected for release medium and the temperature was precisely controlled at 37 ± 0.1°C. Rahmani et al., International Current Pharmaceutical Journal, May 2016, 5(6): 55-58\",\"PeriodicalId\":13811,\"journal\":{\"name\":\"International Current Pharmaceutical Journal\",\"volume\":\"83 1\",\"pages\":\"55-58\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-05-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Current Pharmaceutical Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/ICPJ.V5I6.27710\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Current Pharmaceutical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/ICPJ.V5I6.27710","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
摘要
本研究以天然火山玻璃(珍珠岩)为硅(Si)源,铝酸钠为铝(Al)源,不使用任何有机模板合成纳米沸石。我们使用珍珠岩作为硅源,因为它是经济有效的来源。在不锈钢反应器中,用水热法在170℃下制备了这些合成的纳米沸石。采用x射线衍射(XRD)、红外傅立叶变换(FTIR)和扫描电镜(SEM)对合成的纳米沸石进行了表征。用x射线荧光(XRF)测定了珍珠岩的化学成分。采用阳离子表面活性剂十六烷基三甲基溴化铵(HDTMAB)对纳米沸石进行了改性。本文研究了西替利嗪(Cet)作为模型药物在纳米沸石钠石上作为药物载体的吸附,并采用紫外-可见分光光度法在230 nm处测定了Cet的浓度。研究了不同时间(0 ~ 6 h)纳米沸石钠石对Cet的吸附特性,并在4、5、6 3种pH水平下进行了分析。最后选择pH值分别为1.2、6.8和7.2的3种缓冲溶液作为释放介质,温度精确控制在37±0.1℃。Rahmani et al.,国际药学杂志,2016,5(6):55-58
Application of Synthetic Nanozeolite Sodalite in Drug Delivery
In this study nanozeolite sodalite was synthesized from natural volcanic glass (perlite) as silica (Si) source and sodium aluminate as aluminium (Al) source without using any organic template. We use perlite as Si source because it is cost-effective and available source. These nanoparticles of synthesized zeolite were prepared at 170°C in stainless steel reactor with hydrothermal method. The synthesized nanozeolite was characterized by X-ray diffraction (XRD), fourier transform infrared (FTIR) and scanning electron microscopy (SEM) techniques. Chemical composition of perlite was determined by X-ray fluorescence (XRF).This nanozeolite was modified with cationic surfactant, hexadecyltrimethylammonium bromide (HDTMAB). In this study adsorption of cetirizine (Cet) as a model drug onto nanozeolite sodalite as a carrier of drug was investigated and Ultra Violet-Visible (UV-Vis) spectrophotometry was used for determination of concentrations of Cet at 230 nm. Adsorption characteristics of Cet on nanozeolite sodalite were examined at different times (0-6 h) and also the analysis was carried at three pH levels 4, 5 and 6. Finally three buffered solutions with different pH (1.2, 6.8 and 7.2) were selected for release medium and the temperature was precisely controlled at 37 ± 0.1°C. Rahmani et al., International Current Pharmaceutical Journal, May 2016, 5(6): 55-58