Precipitation Profiles of Naproxen in Dissolution Media
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https://dataverse.rsu.lv/citation?persistentId=doi:10.48510/FK2/NQENJO
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This dataset contains raw UV absorbance values of naproxen at lambda max (330-334 nm, depending on the polymer), as well as normalised absorbance values (using readings at 850 nm for normalisation). UV spectra of naproxen was taken in a dissolution media consisting of HCl solution with pH 1.2 (prepared according to Ph. Eur.) supplemented with 2.4% acetonitrile (introduced with naproxen solution). The media additionally contained one of the following polymers: povidone (PVP K25), copovidone (Kollidon VA 64), poly (butyl methacrylateco-(2-dimethylaminoethyl) methacrylate-co-methyl methacrylate 1:2:1 (Eudragit E PO), polyacrylic acid (Apinovex LV), polyvinyl alcohol (PVAl; SRP, 4-88, and 3-82) at a concentration of 0.75 mg/ml (40:60 drug:polymer), and Soluplus at a concentration of 0.125 mg/ml (80:20 drug:polymer).
Method: A precipitation study was performed in 0.1 N HCl solution with pre-dissolved polymer (60, 40, and 20 wt. %). Naproxen solution in acetonitrile (20 mg/mL) to achieve the proportion of 500 mg of naproxen per 1 L of dissolution medium (0.5 mg/mL) was added. UV absorption was determined directly within 10 mm pathlength quartz cuvettes (at room temperature) with UV spectrophotometer (UV-1900i; Shimadzu Corp., Kyoto, Japan) Spectra were recorded at 5-minute intervals over a 2-hour period (n = 3), using the “Spectrum” or “Time Course” mode in LabSolutions software.
Data. The dataset contains a CSV file of naproxen UV-absorbance values in the presence of polymers. Picture “P1” provides a brief overview of data.
本数据集包含萘普生在其最大吸收波长(λmax,330~334 nm,具体取决于所用聚合物)下的原始紫外吸光度值,以及归一化吸光度值(以850 nm处的吸光度读数作为归一化基准)。萘普生的紫外光谱采集于下述溶出介质:以pH 1.2的盐酸溶液(依照欧洲药典Ph. Eur.制备)为基础溶剂,添加2.4%乙腈(由萘普生储备液引入)。该介质中额外添加以下聚合物之一:聚维酮(PVP K25)、共聚维酮(Kollidon VA 64)、聚(甲基丙烯酸丁酯-co-甲基丙烯酸二甲氨基乙酯-co-甲基甲酯)1:2:1共聚物(尤特奇Eudragit E PO)、聚丙烯酸(Apinovex LV)、聚乙烯醇(PVAl;涵盖SRP 4-88与3-82型号),浓度均为0.75 mg/ml,药物与聚合物质量比为40:60;以及索鲁普斯(Soluplus),浓度为0.125 mg/ml,药物与聚合物质量比为80:20。实验方法:以含预溶解聚合物(质量占比分别为60 wt%、40 wt%与20 wt%)的0.1 N盐酸溶液为介质开展沉淀实验。向介质中加入浓度为20 mg/mL的萘普生乙腈溶液,使最终溶出介质中萘普生浓度达到0.5 mg/mL(即每1升介质含500 mg萘普生)。采用光程10 mm的石英比色皿,于室温下通过紫外分光光度计(UV-1900i;岛津株式会社,日本京都)直接测定紫外吸光度。使用LabSolutions软件的"Spectrum"或"Time Course"模式,在2小时时长内以5分钟为间隔采集光谱,每组实验重复3次(n = 3)。本数据集包含一份记录聚合物存在下萘普生紫外吸光度值的CSV文件。附图"P1"简要概述了该数据集的内容。
提供机构:
Rīga Stradiņš University Institutional Repository Dataverse
创建时间:
2025-12-10



