Chimie ParisTech, PSL Research University, Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), F-75005 Paris, France; CNRS, UTCBS UMR 8258, F-75006 Paris, France; Université Paris Descartes, Sorbonne-Paris-Cité, F-75006 Paris, France; INSERM, UTCBS U 1022, F-75006 Paris, France; Unither Pharmaceuticals, 41, rue de la chaussée d'Antin, F-75009 Paris, France.
Chimie ParisTech, PSL Research University, Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), F-75005 Paris, France; CNRS, UTCBS UMR 8258, F-75006 Paris, France; Université Paris Descartes, Sorbonne-Paris-Cité, F-75006 Paris, France; INSERM, UTCBS U 1022, F-75006 Paris, France.
Int J Pharm. 2017 Dec 20;534(1-2):128-135. doi: 10.1016/j.ijpharm.2017.09.073. Epub 2017 Oct 2.
Buccal administration route is a promising way for a large number of drugs exhibiting a low oral bioavailability. The present work describes the formulation and evaluation of a mucoadhesive and thermosensitive in situ gelling delivery system based on poloxamer 407, poloxamer 188 and xanthan gum for buccal drug delivery. First, the mucoadhesion properties were evaluated using a tensile test. The effect of xanthan gum on the mucoadhesion force was demonstrated. Then, to assess the buccal residence time which reflects the mucoadhesion properties, the validation of a fluorescence probe for in vivo optical imaging experiment was conducted. Methyl-Cyanine 5 derivative (Me-Cy5) was used to label the hydrogels, dissolution tests and permeation studies through buccal epithelium cells showed that Me-Cy5 release from hydrogels was mainly due to an erosion mechanism and presented a limited penetration across epithelium cells. These results suggest that, Me-Cy5 is a suitable marker for thermosensitive in situ gelling delivery systems as the probe mostly stays entrapped in the hydrogel and do not cross the epithelial barrier. Buccal residence performance of the hydrogel was evaluated for the first time by non-invasive optical imaging after administration to mice. This technique is an interesting alternative compared to visual observations and sacrifice involved experiments, which could also be exploited to various administration routes.
颊黏膜给药途径是许多口服生物利用度低的药物的一种很有前途的给药方式。本工作描述了基于泊洛沙姆 407、泊洛沙姆 188 和黄原胶的用于颊部给药的粘膜粘附性和温敏原位凝胶递送系统的制剂和评价。首先,使用拉伸试验评估粘膜粘附性。证明了黄原胶对粘膜粘附力的影响。然后,为了评估反映粘膜粘附特性的颊部滞留时间,进行了荧光探针用于体内光学成像实验的验证。甲基花青 5 衍生物(Me-Cy5)被用来标记水凝胶,溶出试验和通过颊上皮细胞的渗透研究表明,Me-Cy5 从水凝胶中的释放主要是由于侵蚀机制,并呈现出有限的穿透上皮细胞。这些结果表明,Me-Cy5 是热敏原位凝胶递送系统的合适标记物,因为探针主要困在水凝胶中,不会穿过上皮屏障。首次通过给予小鼠后的非侵入性光学成像来评估水凝胶的颊部滞留性能。与涉及视觉观察和牺牲的实验相比,这种技术是一种有趣的替代方法,也可以用于各种给药途径。