Halder A, Maiti S, Sa B
Division of Pharmaceutics, Centre for Advanced Research in Pharmaceutical Sciences, Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Int J Pharm. 2005 Sep 30;302(1-2):84-94. doi: 10.1016/j.ijpharm.2005.06.020.
Propranolol-HCl-loaded calcium alginate (ALG) beads, propranolol-resin complex (resinate)-loaded calcium alginate (RALG) beads and polyethyleneimine (PEI)-treated RALG (RALG-PEI) beads were prepared by ionotropic gelation/polyelectrolyte complexation method. The beads were evaluated and compared in respect of drug entrapment efficiency (DEE) and release characteristics in simulated gastric fluid (SGF, 0.1(N) HCl, pH 1.2) and simulated intestinal fluid (SIF, phosphate buffer, pH 6.8). DEE of RALG beads was considerably higher than that of ALG beads containing unresinated drug. However, DEE of RALG beads decreased with increase in both gelation time and concentration of the gel forming Ca2+ ions due to drug displacement from resinate. PEI treatment of RALG beads further decreased DEE as the polycation also displaced the drug from the resinate. The release of drug from all the beads was slow and incomplete in SGF owing to considerably less swelling of the beads and the decrease in drug release from the beads followed the order: RALG-PEI<RALG<ALG. In contrast to rapid discharge of the drug by ALG beads in SIF, RALG beads provided marginal prolongation in drug release as both ALG and RALG beads swelled and eroded rapidly although at different rates. On the other hand, drug release from RALG-PEI beads in SIF was considerably prolonged for different periods of time depending upon the conditions of PEI treatment. Interaction of the polycation with alginate resulted in the formation of polyelectrolyte complex membrane as evident from scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and fourier-transform infrared spectroscopy (FTIR) studies. The membrane having reduced swelling and erosion properties behaved as a physical barrier to drug release. Kinetics of the drug release also confirmed the formation of physical barrier as anomalous transport type of release associated with. RALG beads tended to shift towards Fickian transport in case of RALG-PEI beads.
采用离子凝胶化/聚电解质络合法制备了负载盐酸普萘洛尔的海藻酸钙(ALG)珠、负载普萘洛尔树脂复合物(树脂酸盐)的海藻酸钙(RALG)珠以及经聚乙烯亚胺(PEI)处理的RALG(RALG-PEI)珠。对这些珠子进行了评估,并比较了它们在模拟胃液(SGF,0.1(N) HCl,pH 1.2)和模拟肠液(SIF,磷酸盐缓冲液,pH 6.8)中的药物包封率(DEE)和释放特性。RALG珠的DEE显著高于含有未树脂化药物的ALG珠。然而,由于药物从树脂酸盐中被置换出来,RALG珠的DEE随着凝胶化时间和凝胶形成Ca2+离子浓度的增加而降低。RALG珠经PEI处理后,DEE进一步降低,因为聚阳离子也将药物从树脂酸盐中置换出来。由于珠子的溶胀程度相当小,所有珠子在SGF中的药物释放缓慢且不完全,珠子的药物释放减少顺序为:RALG-PEI<RALG<ALG。与ALG珠在SIF中药物快速释放相反,RALG珠使药物释放略有延长,因为ALG珠和RALG珠虽然速率不同,但都迅速溶胀和侵蚀。另一方面,RALG-PEI珠在SIF中的药物释放在不同时间段内显著延长,这取决于PEI处理条件。扫描电子显微镜(SEM)、差示扫描量热法(DSC)和傅里叶变换红外光谱(FTIR)研究表明,聚阳离子与海藻酸盐的相互作用导致形成了聚电解质复合膜。具有降低的溶胀和侵蚀性能的膜对药物释放起到了物理屏障作用。药物释放动力学也证实了物理屏障的形成,因为其与异常转运类型的释放相关。在RALG-PEI珠的情况下,RALG珠的药物释放倾向于向菲克扩散转运转变。