Albertini Beatrice, Passerini Nadia, Rodriguez Lorenzo
Department of Pharmaceutical Sciences, University of Bologna, V. S. Donato 19/2, 40127 Bologna, Italy.
J Pharm Pharmacol. 2005 Jul;57(7):821-9. doi: 10.1211/0022357056389.
Ultrasonic atomization was evaluated as a new approach for the preparation of ionically cross-linked controlled-release chitosan microparticles loaded with theophylline as the model drug, using tripolyphosphate (TPP) as counter-ion. It was possible to nebulize both 2% and 3% (w/v) chitosan solutions as a function of their viscosity, usually not processed by employing the conventional nebulizer. The results of the chitosan molecular characterization using the SEC-MALS analysis revealed that ultrasonic atomization caused a certain depolymerization, probably due to the main chain scission of the 1,4-glycosidic bond; however, Fourier transform-infrared spectroscopy revealed the absence of other chemical modifications. The ultrasonic atomization allowed preparation of TPP cross-linked chitosan microparticles mostly ranging between 50 and 200 mum. As regards manufacturing parameters, the linking time and washing medium were found to affect the properties of the microparticles, while the stirring rate of the TPP solution did not show any influence. The evaluation of the formulation variables revealed that chitosan concentration strongly affected both the feasibility of the ultrasonic atomization and the drug release. All the microparticles showed an encapsulation efficiency of > 50 % and, after an initial burst effect, a controlled release of drug for 48 h. In conclusion, the ultrasonic atomization could be proposed as a robust and innovative single-step procedure with scale-up potential to successfully prepare ionically cross-linked chitosan microparticles.
超声雾化被评估为一种制备载有茶碱作为模型药物的离子交联控释壳聚糖微粒的新方法,使用三聚磷酸钠(TPP)作为抗衡离子。根据壳聚糖溶液的粘度,能够雾化2%和3%(w/v)的壳聚糖溶液,而这些溶液通常无法用传统雾化器处理。使用SEC-MALS分析进行壳聚糖分子表征的结果表明,超声雾化导致了一定程度的解聚,这可能是由于1,4-糖苷键的主链断裂;然而,傅里叶变换红外光谱显示没有其他化学修饰。超声雾化使得能够制备出大多在50至200μm之间的TPP交联壳聚糖微粒。关于制造参数,发现交联时间和洗涤介质会影响微粒的性质,而TPP溶液的搅拌速率没有显示出任何影响。对配方变量的评估表明,壳聚糖浓度强烈影响超声雾化的可行性和药物释放。所有微粒的包封效率均>50%,并且在初始突释效应后,药物可控制释放48小时。总之,超声雾化可被提议作为一种强大且创新的单步程序,具有放大潜力,能够成功制备离子交联壳聚糖微粒。