Lecomte Florence, Siepmann Juergen, Walther Mathias, MacRae Ross J, Bodmeier Roland
College of Pharmacy, Freie Universitaet Berlin, Kelchstrasse 31, 12169, Berlin, Germany.
Pharm Res. 2005 Jul;22(7):1129-41. doi: 10.1007/s11095-005-5421-2. Epub 2005 Jul 22.
To elucidate the drug release mechanisms from pellets coated with pH-sensitive polymer blends.
Verapamil hydrochloride-loaded beads were coated with various blends of a water-insoluble and an enteric polymer, ethylcellulose:Eudragit L and Eudragit NE:Eudragit L, respectively. Both experimental and theoretical techniques were used to characterize the systems before and upon exposure to 0.1 M HCl and phosphate buffer (pH 7.4).
Using analytical solutions of Fick's second law of diffusion, optical and scanning electron microscopy, and mechanical and gravimetric analysis, new insight into the underlying drug release mechanisms could be gained. More importantly, the latter can be effectively altered by varying the type of polymer blend and blend ratio. For example, at low pH drug release is primarily controlled by diffusion through the intact film coatings in Eudragit NE:Eudragit L blends, whereas crack formation is of major importance in ethylcellulose:Eudragit L-coated systems. At high pH, the (partial) leaching of the enteric polymer out of the coatings plays an important role. In all cases, the observed drug release profiles could be explained based on the occurring mass transport processes.
The obtained new knowledge can be used to effectively adjust desired drug release mechanisms and, thus, release patterns.
阐明药物从涂覆有pH敏感聚合物共混物的微丸中的释放机制。
分别用乙基纤维素与尤特奇L、尤特奇NE与尤特奇L的各种共混物对载有盐酸维拉帕米的微球进行包衣。在暴露于0.1 M盐酸和磷酸盐缓冲液(pH 7.4)之前和之后,采用实验和理论技术对系统进行表征。
利用菲克第二扩散定律的解析解、光学和扫描电子显微镜以及力学和重量分析,可以对潜在的药物释放机制有新的认识。更重要的是,通过改变聚合物共混物的类型和共混比例可以有效地改变后者。例如,在低pH值下,药物释放主要受通过尤特奇NE:尤特奇L共混物中完整膜包衣的扩散控制,而在乙基纤维素:尤特奇L包衣系统中,裂缝形成起主要作用。在高pH值下,肠溶聚合物从包衣中的(部分)浸出起重要作用。在所有情况下,观察到的药物释放曲线都可以根据发生的传质过程来解释。
所获得的新知识可用于有效地调整所需的药物释放机制,从而调整释放模式。