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氯化N-三甲基壳聚糖作为一种潜在的跨黏膜表面吸收增强剂:在肠上皮细胞(Caco-2)中的体外评价

N-trimethyl chitosan chloride as a potential absorption enhancer across mucosal surfaces: in vitro evaluation in intestinal epithelial cells (Caco-2).

作者信息

Kotzé A F, Luessen H L, de Leeuw B J, de Boer B G, Verhoef J C, Junginger H E

机构信息

Department of Pharmaceutics, Potchefstroom University for Christian Higher Education, Potchefstroom, Republic of South Africa.

出版信息

Pharm Res. 1997 Sep;14(9):1197-202. doi: 10.1023/a:1012106907708.

Abstract

PURPOSE

Previous studies have established that chitosan hydrochloride and glutamate are potent absorption enhancers for large hydrophilic compounds across mucosal surfaces. However, these compounds lack solubility at neutral pH values. A partially quaternized and well-soluble derivative of chitosan, N-trimethyl chitosan chloride, was synthesized and the effects of this polymer on the transepithelial electrical resistance and permeability of intestinal epithelial cells were investigated in vitro.

METHODS

N-trimethyl chitosan chloride was synthesized by reductive methylation and characterized with NMR. The effect of this polymer (1.0-2.5% w/v) on the transepithelial electrical resistance of intestinal epithelial cells, using Caco-2 cell monolayers, was investigated. Permeation of the hydrophilic model compounds [14C]-mannitol (MW 182.2), FITC-Dextran (MW 4400) and the peptide drug buserelin (MW 1299.5), in the presence of N-trimethyl chitosan chloride (1.5-2.5% w/v), was followed for 3 hours. The transport process of the fluorescent marker, FITC-Dextran 4400, across the cell monolayers was visualised with confocal laser scanning microscopy. Viability of the cells was checked with the trypan blue exclusion technique.

RESULTS

N-trimethyl chitosan chloride was found to be a perfectly water-soluble, partially quaternized (about 12%) derivative of chitosan. This polymer (1.5-2.5% w/v) caused a pronounced and immediate reduction (25-85%) in the transepithelial electrical resistance of Caco-2 cells. Large increases in the transport rate of [14C]-mannitol (32-60 fold), FITC-Dextran 4400 (167-373 fold) and buserelin (28-73 fold) were demonstrated. Confocal laser scanning microscopy confirmed that N-trimethyl chitosan chloride opens the tight junctions of intestinal epithelial cells to allow increased transport of hydrophilic compounds through the paracellular transport pathway. No deleterious effects to the cells could be demonstrated with trypan blue.

CONCLUSIONS

The potential use of N-trimethyl chitosan chloride as an absorption enhancer across mucosal surfaces could be an important contribution towards the development of effective delivery systems for hydrophilic drugs.

摘要

目的

先前的研究已证实,盐酸壳聚糖和谷氨酸是亲水性大分子化合物跨黏膜表面的有效吸收促进剂。然而,这些化合物在中性pH值下缺乏溶解性。合成了一种部分季铵化且溶解性良好的壳聚糖衍生物——氯化N-三甲基壳聚糖,并在体外研究了该聚合物对肠上皮细胞跨上皮电阻和通透性的影响。

方法

通过还原甲基化反应合成氯化N-三甲基壳聚糖,并用核磁共振对其进行表征。使用Caco-2细胞单层研究了该聚合物(1.0 - 2.5% w/v)对肠上皮细胞跨上皮电阻的影响。在存在氯化N-三甲基壳聚糖(1.5 - 2.5% w/v)的情况下,追踪亲水性模型化合物[¹⁴C]-甘露醇(分子量182.2)、异硫氰酸荧光素 - 葡聚糖(分子量4400)和肽类药物布舍瑞林(分子量1299.5)的渗透情况3小时。用共聚焦激光扫描显微镜观察荧光标记物异硫氰酸荧光素 - 葡聚糖4400跨细胞单层的转运过程。用台盼蓝排斥技术检查细胞活力。

结果

发现氯化N-三甲基壳聚糖是一种完全水溶性的、部分季铵化(约12%)的壳聚糖衍生物。该聚合物(1.5 - 2.5% w/v)使Caco-2细胞的跨上皮电阻显著且立即降低(25 - 85%)。[¹⁴C]-甘露醇(32 - 60倍)、异硫氰酸荧光素 - 葡聚糖4400(167 - 373倍)和布舍瑞林(28 - 73倍)的转运速率大幅增加。共聚焦激光扫描显微镜证实,氯化N-三甲基壳聚糖打开肠上皮细胞的紧密连接,使亲水性化合物通过细胞旁转运途径的转运增加。台盼蓝试验未显示对细胞有有害影响。

结论

氯化N-三甲基壳聚糖作为跨黏膜表面吸收促进剂的潜在用途,可能对亲水性药物有效递送系统的开发做出重要贡献。

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