Torché A M, Jouan H, Le Corre P, Albina E, Primault R, Jestin A, Le Verge R
Laboratoire de Pharmacie Galénique, Biopharmacie et Pharmacie Clinique, Faculté des Sciences Pharmaceutiques et Biologiques, Université de Rennes I, 2, Avenue du Professeur Léon Bernard, 35043 cedex, Rennes, France.
Int J Pharm. 2000 May 15;201(1):15-27. doi: 10.1016/s0378-5173(00)00364-1.
We investigated the ability of pig ileal Peyer's patch segments to transport intestinal poly (D,L-lactide-co-glycolide) microspheres (PLGA MS) from intestinal lumen across the mucosae using in situ and ex vivo segments with confocal laser scanning microscopy (CLSM) and transmission electronic microscopy (TEM). From a global aspect, CLSM suggested that PLGA MS were translocated by M cells labelled with a FITC-conjugated anti-cytokeratin peptide 18, and transported through the follicle-associated epithelium (FAE) in the dome area in both types of experiments. At the ultrastructural level, TEM showed the traffic of PLGA MS throughout M cells, their transport into the basolateral invaginations of the M cells and their subsequent migration into the dome area and the follicular area in contact with macrophages and lymphatic vessels. Although in situ experiments allowed following the migration of PLGA MS until mesenteric lymph nodes, an ex vivo model could be used as a useful tool to study the targeting ability of PLGA MS formulations to the gut-associated lymphoid tissue (GALT).
我们使用原位和离体肠段,结合共聚焦激光扫描显微镜(CLSM)和透射电子显微镜(TEM),研究了猪回肠派尔集合淋巴结段将肠腔中的聚(D,L-丙交酯-共-乙交酯)微球(PLGA MS)跨黏膜转运的能力。从整体来看,CLSM显示PLGA MS被用异硫氰酸荧光素(FITC)偶联的抗细胞角蛋白肽18标记的M细胞转运,并且在两种实验类型中均通过圆顶区域的滤泡相关上皮(FAE)进行转运。在超微结构水平上,TEM显示PLGA MS在整个M细胞中的运输过程,它们进入M细胞的基底外侧内陷,随后迁移到圆顶区域以及与巨噬细胞和淋巴管接触的滤泡区域。尽管原位实验能够追踪PLGA MS迁移至肠系膜淋巴结的过程,但离体模型可作为研究PLGA MS制剂对肠道相关淋巴组织(GALT)靶向能力的有用工具。