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A green organic-solvent-free route to prepare nanostructured zinc oxide carriers of clotrimazole for pharmaceutical applications

机译:一种绿色无有机溶剂的途径,用于制备克霉唑的纳米结构氧化锌载体,用于制药应用

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摘要

In the context of proposing cleaner production strategies for the pharmaceutical industry, an organicsolvent-free route to prepare nanostructured zinc oxide (NsZnO) reservoirs of clotrimazole (CTZ) was studied. Two different NsZnO materials were synthesized, selecting wet chemical approaches without any organic solvents: chemical bath deposition and a soft-template sol-gel method. Both materials showed a pure crystalline wurzite structure with two different morphologies: aggregates of nanosheets or interconnected nanoparticles. For the former material the specific surface area and the pore volume reached the values of 66 m2/g and 0,230 cm3/g, respectively, which were higher than those of the latter (19 m2/g and 0,050 cm3/g). For the first time, the loading of CTZ in a ZnO carrier was performed using supercritical CO2 as a solvent. The NsZnO materials were characterized, before and after the drug loading, by FESEM, EDS, XRD, nitrogen adsorption isotherms, TGA, DSC. CTZ was dispersed in the NsZnO carrier in amorphous form, with a maximum loading of 17% w/w. The decrease of specific surface area and pore volume upon drug loading for both samples is ascribed to the adsorption of CTZ molecules on the surface of the NsZnO materials. This confirms the feasibility of using the NsZnO as a CTZ carrier. In vitro drug-release was investigated and revealed that the NsZnO carrier can deliver CTZ with a faster release of a larger drug amount when compared to the solid crystalline drug. The novel clean preparation route of a ZnO carrier for CTZ delivery herein presented is easily adabtable to batch small-scale pharmaceutical industrial process.
机译:在提出制药工业的清洁生产策略的背景下,研究了制备纳米结构氧化锌(NSZNO)克拉咪唑(CTZ)的无器材无人驾驶途径。合成了两种不同的NSZNO材料,选择没有任何有机溶剂的湿化学方法:化学浴沉积和软模板溶胶 - 凝胶法。两种材料显示出具有两种不同形态的纯结晶紫颗结构:纳米片或互连纳米颗粒的聚集体。对于前一种材料,比表面积和孔体积分别达到66m 2 / g和0,230cm 3 / g的值,其高于后者(19m 2 / g和0.050cm 3 / g)。首次使用超临界CO 2作为溶剂进行ZnO载体中CTZ的加载。在药物载荷之前和之后,通过FeSem,EDS,XRD,氮吸附等温线,TGA,DSC,在药物载荷之前和之后的表征。 CTZ以无定形形式分散在NSZNO载体中,最大负载为17%w / w。对于两个样品的药物负载时,比表面积和孔体积的降低均匀地归因于NSZNO材料表面上的CTZ分子的吸附。这证实了使用NSZNO作为CTZ载体的可行性。研究了体外药物释放,并揭示了与固体结晶药物相比,NsZnO载体可以递送CTZ的较快释放较大的药物量。本文的CTZ递送的ZnO载体的新型清洁制剂途径易于达到批量小规模药业工艺。

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