Wheatley Thomas A
FMC BioPolymer, PO Box 8, Princeton, NJ 08543, USA.
Drug Dev Ind Pharm. 2007 Mar;33(3):281-90. doi: 10.1080/03639040600683469.
The objective of this study was to investigate the use of water soluble cellulose acetate (WSCA) as a film coating material for tablets. Aspirin (ASA) tablets were prepared by direct compression and coated with either WSCA or HPMC (hydroxypropyl methylcellulose) dispersions. Coatings of 1-3%, depending on the intended application, were applied to the model drug (ASA) tablets employing a side-vented coating pan. Free films of WSCA, prepared by cast method, are crystal clear and, depending on the viscosity grade, are flexible, strong and durable. WSCA has the capability of forming free films without plasticizers and the films dry at room temperature. Glass transition temperature, Tg, was determined by differential scanning calorimetry. The Tg of WSCA is significantly higher relative to HPMC. Inclusion of plasticizer lowers the Tg of WSCA and effective plasticizers were PEG 400 and glycerin. Low viscosity WSCA was more soluble in water (25-30%) relative to medium viscosity WSCA (10-15%). WSCA solutions exhibited no increase in viscosity with an increase in temperature. Samples of coated (WSCA and HPMC) tablets and uncoated ASA cores were packaged for stability studies at room and elevated temperature storage. Physical stability of ASA tablets coated with 2:1 LV: MV (low viscosity: medium viscosity) WSCA formulations was better when compared to tablets coated with HPMC. Dissolution stability of WSCA coated ASA was similar to the physical stability results. After three months at elevated temperature (35 and 45 degrees C), the WSCA coated tablets complied with USP dissolution requirements for ASA, while the HPMC coated tablets did not. There was no difference in moisture (weight) gain of ASA tablets coated with either WSCA or HPMC. The WSCA coated tablets were not sticky or tacky, while the HPMC coated tablets were tacky and stuck together.
本研究的目的是考察水溶性醋酸纤维素(WSCA)作为片剂薄膜包衣材料的应用。通过直接压片法制备阿司匹林(ASA)片剂,并用WSCA或羟丙基甲基纤维素(HPMC)分散体进行包衣。根据预期用途,使用侧通风包衣锅将1%-3%的包衣材料施用于模型药物(ASA)片剂上。通过流延法制备的WSCA游离膜清澈透明,根据粘度等级不同,具有柔韧性、强度和耐久性。WSCA能够在不添加增塑剂的情况下形成游离膜,且薄膜在室温下干燥。通过差示扫描量热法测定玻璃化转变温度Tg。WSCA的Tg相对于HPMC显著更高。添加增塑剂会降低WSCA的Tg,有效的增塑剂为聚乙二醇400和甘油。低粘度WSCA在水中的溶解度(25%-30%)高于中粘度WSCA(10%-15%)。WSCA溶液的粘度不会随温度升高而增加。将包衣(WSCA和HPMC)片剂和未包衣的ASA片芯样品进行包装,在室温和高温储存条件下进行稳定性研究。与用HPMC包衣的片剂相比,用2:1低粘度:中粘度(LV:MV)WSCA配方包衣的ASA片剂的物理稳定性更好。WSCA包衣的ASA的溶出稳定性与物理稳定性结果相似。在高温(35℃和45℃)下放置三个月后,WSCA包衣片剂符合美国药典对ASA的溶出要求,而HPMC包衣片剂则不符合。用WSCA或HPMC包衣的ASA片剂的水分(重量)增加没有差异。WSCA包衣片剂不发粘或发 tacky,而HPMC包衣片剂发 tacky 且会粘在一起。 (注:原文中“tacky”未给出准确中文释义,可根据语境理解为发粘等类似意思)