Rao Monica R P, Ranpise Anuradha A, Thanki K C, Borate S G, Parikh G N
AISSMS College of Pharmacy, Kennedy Road, Near RTO, Pune-411 001, India.
Indian J Pharm Sci. 2009 Sep;71(5):538-44. doi: 10.4103/0250-474X.58188.
The objective of present study was to evaluate the effect of processing methods and sintering condition on matrix formation and subsequent drug release from wax matrix tablets for controlled release. Ketorolac tromethamine and compritol were processed with appropriate diluent using either dry blending, spray drying, partial melt granulation or melt granulation.The tablets were then sintered at 80 degrees . The sintered tablets were characterized by their physical parameters and in vitro dissolution tests. The micro-morphology and wettability of the tablets was also investigated. It was evident that different processing methods for identical formulation significant impact the release profile of drug. Sintering further retarded drug release and its effect was related to the manufacturing processes. Scanning electron microscopy showed that heat treatment redistributed the wax and formed a film-like structure covering drug and excipient particle. The contact angle of tablets made by dry blending, spray drying and partial melt granulation methods increased after sintering, while that of tablets made by melt granulation remained constant. Drug release from the wax tablets with or without heat treatment was best described by the Higuchi equation. Different processing methods produced different matrix structures that resulted in different drug release rates. Sintering retarded drug release mainly by decreasing the porosity of the matrix. Contact angle measurement and SEM analysis indicated that heat treatment caused the wax to melt, redistribute, coat the drug and diluents and form a network structure. Differential scanning calorimetry studies ruled out the occurrence of solid solution of the drug during sintering condition.
本研究的目的是评估加工方法和烧结条件对蜡基质控释片的基质形成及随后药物释放的影响。将酮咯酸氨丁三醇和康普立脂与合适的稀释剂一起,采用干混、喷雾干燥、部分熔融制粒或熔融制粒的方法进行加工。然后将片剂在80摄氏度下烧结。对烧结后的片剂进行物理参数表征和体外溶出试验。还研究了片剂的微观形态和润湿性。显然,相同配方的不同加工方法对药物的释放曲线有显著影响。烧结进一步延缓了药物释放,其效果与制造工艺有关。扫描电子显微镜显示,热处理使蜡重新分布,并形成覆盖药物和辅料颗粒的膜状结构。采用干混、喷雾干燥和部分熔融制粒方法制备的片剂烧结后的接触角增大,而采用熔融制粒方法制备的片剂接触角保持不变。含或不含热处理的蜡片的药物释放最适合用Higuchi方程描述。不同的加工方法产生了不同的基质结构,导致不同的药物释放速率。烧结主要通过降低基质的孔隙率来延缓药物释放。接触角测量和扫描电子显微镜分析表明,热处理使蜡熔化、重新分布、包裹药物和稀释剂并形成网络结构。差示扫描量热法研究排除了在烧结条件下药物形成固溶体的情况。