Université de Lyon, Institut des Sciences Analytiques, UMR 5280, CNRS, Université Lyon 1, ENS Lyon - 5, rue de la Doua, F-69100 Villeurbanne, France; Université de Lyon, Laboratoire d'Automatique et de Génie des Procédés, UMR CNRS 5007, Université Lyon 1, F-69622 Villeurbanne, France.
Université de Lyon, Laboratoire d'Automatique et de Génie des Procédés, UMR CNRS 5007, Université Lyon 1, F-69622 Villeurbanne, France; Université de Lyon, Université Lyon 1, ISPB-School of Pharmacy, F-69008 Lyon, France.
Int J Pharm. 2018 May 5;542(1-2):205-212. doi: 10.1016/j.ijpharm.2018.03.011. Epub 2018 Mar 8.
Having previously highlighted the gelation of pectin with chlorhexidine (CX), pectinate microparticles were prepared here by vibrational prilling using CX, not only as an active ingredient encapsulated but also as a cross-linking agent. CX amount required for pectin gelation was smaller than usual dications (Ca, Zn) used as cross-linking agent for pectin ionotropic gelation: CX seemed to bind more easily to pectin chains that could be explained by its large molecular size. Three batches of CX microparticles with different mean size were prepared. Whatever the droplet mean diameter, similar particle characteristics in terms of encapsulation efficiency, CX encapsulation yield and drug release were observed. The encapsulation efficiency was about 5.5%, the CX encapsulation yield was approximately 44% and the maximal amount of CX released after 6 h was about 7%. Finally, zinc diacetate was added to the formulation as a competitive pectin cross-linking agent in order to limit CX binding to pectin and to improve CX release. The influence of CX and Zn concentrations on the particles properties was studied by the means of a Doehlert design. Results showed the interest of such a mixture since the competition between both cations led to more or less structured and large microparticles, some of them having promoted the quantity of CX released.
先前已经强调了果胶与洗必泰(CX)的胶凝作用,这里通过振动造粒制备了以 CX 作为包封的活性成分和交联剂的果胶定形微球。用于果胶离子凝胶交联的常规二价阳离子(Ca、Zn)所需的 CX 量小于通常所需的量:CX 似乎更容易与果胶链结合,这可以用其较大的分子量来解释。制备了三批具有不同平均粒径的 CX 微球。无论液滴的平均直径如何,在包封效率、CX 包封产率和药物释放方面观察到相似的颗粒特性。包封效率约为 5.5%,CX 包封产率约为 44%,6 小时后释放的最大 CX 量约为 7%。最后,向制剂中添加了二乙酸锌作为竞争性果胶交联剂,以限制 CX 与果胶的结合并改善 CX 的释放。通过 Doehlert 设计研究了 CX 和 Zn 浓度对颗粒特性的影响。结果表明,这种混合物很有意义,因为两种阳离子之间的竞争导致了或多或少结构复杂和较大的微球,其中一些微球促进了 CX 的释放量。