Cook Thomas J, Edwards Shanya, Gyemah Charlene, Shah Manoj, Shah Indu, Fox Tiziana
Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.
J Am Pharm Assoc (2003). 2004 Sep-Oct;44(5):583-6. doi: 10.1331/1544-3191.44.5.583.cook.
To determine the weight variation and calculated dosing variability of tablet fragments upon splitting unscored cyclobenzaprine hydrochloride 10 mg tablets using two common tablet splitting devices.
Comparative pharmaceutics study.
Pharmacy school laboratory.
Not applicable.
Unscored cyclobenzaprine hydrochloride 10 mg tablets from one generic manufacturer were split with a tablet splitter or a kitchen knife by a licensed pharmacist and two doctor of pharmacy students (n = 15 tablets for each method per participant).
Fragment weights (FWs) were compared with the theoretical weights (TWs), which were calculated as one half of the mean weight of the tablets used in each part of the experiment; means, relative standard deviations (RSDs), and percentages of TW were also calculated.
The mean weight before splitting the 45 tablets with the tablet splitter was 136.6 +/- 2.1 mg (TW = 68.3 mg). The mean FW after splitting was 67.9 +/- 7.9 mg. The RSD of 11.6% corresponded to a range of 69.4% to 130.2% of the TW and an estimated drug content of the split fragments between 3.47 mg and 6.51 mg. The mean weight before splitting the 45 tablets cut with a kitchen knife was 136.6 +/- 2.0 mg (TW = 68.3 mg). The mean FW was 68.0 +/- 15.7 mg with a RSD of 23.2%, corresponding to a range of 49.9% to 149.5% of the TW and an estimated drug content of the split fragments between 2.49 mg and 7.48
Tablet fragments obtained after splitting this generic cyclobenzaprine 10 mg product varied considerably in weight and estimated drug content. Accordingly, splitting cyclobenzaprine 10 mg tablets to achieve 5 mg doses could result in unpredictable dosing and therapeutic response.
使用两种常见的片剂分割装置,确定未刻痕的10毫克盐酸环苯扎林片剂分割后的重量变化及计算剂量的变异性。
比较药剂学研究。
药学院实验室。
不适用。
由一名持证药剂师和两名药学博士学生,使用片剂分割器或菜刀将来自同一普通制造商的未刻痕10毫克盐酸环苯扎林片剂进行分割(每位参与者每种方法分割15片)。
将分割后的碎片重量(FWs)与理论重量(TWs)进行比较,理论重量计算为实验各部分所用片剂平均重量的一半;还计算了平均值、相对标准偏差(RSDs)以及TW的百分比。
用片剂分割器分割45片片剂前的平均重量为136.6±2.1毫克(TW = 68.3毫克)。分割后的平均FW为67.9±7.9毫克。11.6%的RSD对应于TW的69.4%至130.2%的范围,以及分割碎片的估计药物含量在3.47毫克至6.51毫克之间。用菜刀切割45片片剂前的平均重量为136.6±2.0毫克(TW = 68.3毫克)。平均FW为68.0±15.7毫克,RSD为23.2%,对应于TW的49.9%至149.5%的范围,以及分割碎片的估计药物含量在2.49毫克至7.48毫克之间。
分割这种普通的10毫克盐酸环苯扎林产品后得到的片剂碎片在重量和估计药物含量方面差异很大。因此,分割10毫克盐酸环苯扎林片剂以获得5毫克剂量可能导致不可预测的给药和治疗反应。