Irma Lerma Rangel College of Pharmacy, Texas A&M Health Science Center, Texas A&M University, Reynolds Medical Building, Suite 159, College Station, Texas, 77843-1114, USA.
AAPS PharmSciTech. 2021 Jan 18;22(1):51. doi: 10.1208/s12249-020-01894-8.
The focus of the study was to develop discriminatory dissolution methods for portioned snus and moist snuff sub-categories of smokeless tobacco products (STPs) using USP basket and paddle apparatuses. Skoal Classic Wintergreen (SCW) and CORESTA CRP1.1 pouches were used as test products. The dissolution was performed at 10, 20, 30, 40, and 50 rpm basket or paddle speed in 500 ml artificial saliva pH 6.8. The products were also characterized for assay, pH, particle size, and loss on drying. The dissolution profiles were evaluated for amount/% of nicotine dissolved, time to reach plateau, and profiles comparison by f2 and f1 factors. The nicotine assay was 13.3 ± 0.2 and 7.6 ± 0.1 mg/pouch for SCW and CRP1.1, respectively. The nicotine dissolved in 30 min from SCW and CRP1.1 were 38.4-81.8 and 37.6-88.1, and 50.5-64.9 and 72.3-92.1% by paddle and basket methods, respectively. The f2 and f1 values were ≤ 39.2 and ≥ 42.1 and ≤ 43.2 and ≥ 34.1 for basket methods and paddle methods. RSD were less than 20% at all points of dissolution profiles, and dissolution plateau were achieved in 30 min at some of the tested conditions. In summary, dissolution methods based on basket and paddle can be used as a performance test for STPs.
本研究的重点是使用 USP 篮筐和桨式装置为部分鼻烟和湿鼻烟等无烟烟草制品 (STP) 开发区分性溶解方法。使用 Skoal Classic Wintergreen (SCW) 和 CORESTA CRP1.1 小袋作为测试产品。在 10、20、30、40 和 50 rpm 篮筐或桨速下,在 500ml 人工唾液 pH6.8 中进行溶解。还对产品进行了含量/尼古丁溶解百分比、达到平台所需时间以及通过 f2 和 f1 因子进行的图谱比较的测定、pH、粒度和干燥失重等特性进行了评价。通过 f2 和 f1 因子评价了尼古丁溶解量/溶解百分比、达到平台所需时间以及图谱比较。SCW 和 CRP1.1 的尼古丁含量分别为 13.3 ± 0.2 和 7.6 ± 0.1 mg/袋。SCW 和 CRP1.1 在 30 分钟内溶解的尼古丁量分别为 38.4-81.8%和 37.6-88.1%,通过桨式和篮筐方法分别为 50.5-64.9%和 72.3-92.1%。对于篮筐方法和桨方法,f2 和 f1 值分别为≤39.2 和≥42.1,≤43.2 和≥34.1。在所有溶解曲线的所有点,RSD 均小于 20%,并且在一些测试条件下,在 30 分钟内达到了溶解平台。总之,基于篮筐和桨的溶解方法可作为 STP 的性能测试方法。