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基于N-三甲基壳聚糖的纳米颗粒:使用体外(Caco-2细胞)和体内(切除的大鼠空肠)模型评估吸收特性。

Nanoparticles based on N-trimethylchitosan: evaluation of absorption properties using in vitro (Caco-2 cells) and ex vivo (excised rat jejunum) models.

作者信息

Sandri Giuseppina, Bonferoni Maria Cristina, Rossi Silvia, Ferrari Franca, Gibin Sara, Zambito Ylenia, Di Colo Giacomo, Caramella Carla

机构信息

Department of Pharmaceutical Chemistry, University of Pavia, Pavia, Italy.

出版信息

Eur J Pharm Biopharm. 2007 Jan;65(1):68-77. doi: 10.1016/j.ejpb.2006.07.016. Epub 2006 Jul 27.

Abstract

Among the chitosan derivatives, trimethylchitosan (TMC) has been shown to have penetration enhancement properties also in intestinal environment. In addition, the use of nanoparticulate systems has the advantage of protecting peptidic drugs from intestinal degradations, due to internalisation behaviour. Therefore, the aim of this paper was to evaluate nanoparticulate systems based on TMC. In particular the mucoadhesive and absorption enhancement properties of nanoparticles based on TMC with different quaternization degree (QD) intended for the intestinal administration of macromolecules (peptides) have been evaluated. Comparison with chitosan (CS.HCl) nanoparticles was made. The nanoparticles were loaded with fluorescein isothiocyanate dextran (FD4, MW 4400 Da), used as the model macromolecule. The intestinal penetration enhancement properties of nanoparticles were investigated in an in vitro Caco-2 cell model and an ex vivo rat jejunum model. The mucoadhesion of the nanosystems was evaluated using excised rat jejunum. All of the nanoparticulate systems interacted with the Caco-2 cells decreasing the transepithelial electric resistance (TEER) and increasing Lucifer Yellow (LY) Papp (paracellular pathway marker). All the nanosystems improved FD4 Papp, with the exception of the nanoparticles based on TMC with the highest QD. In this case an entrapment of nanoparticles into Caco-2 cells was supposed. Analogous results were obtained using the excised rat jejunum model. The increase in QD of TMC was seen to favour the mucoadhesion, resulting in a prolonged residence time on intestinal mucosa. The nanoparticle penetration into excised rat jejunum tissue, observed by means of CLSM, suggested that the mucoadhesive properties delayed the absorption of nanoparticles, however they produced an increase in the contact time with intestinal epithelium, offering a better chance for internalisation. The improvement of mucoadhesion and of nanoparticle internalisation with respect to chitosan nanosystems makes the TMCs nanosystems suitable carriers for the intestinal absorption of peptides.

摘要

在壳聚糖衍生物中,三甲基壳聚糖(TMC)已被证明在肠道环境中也具有渗透增强特性。此外,由于纳米颗粒系统的内化行为,使用该系统具有保护肽类药物免受肠道降解的优势。因此,本文的目的是评估基于TMC的纳米颗粒系统。特别评估了不同季铵化度(QD)的基于TMC的纳米颗粒用于肠道给药大分子(肽)的粘膜粘附和吸收增强特性。并与壳聚糖(CS.HCl)纳米颗粒进行了比较。纳米颗粒负载了异硫氰酸荧光素葡聚糖(FD4,分子量4400 Da),用作模型大分子。在体外Caco-2细胞模型和离体大鼠空肠模型中研究了纳米颗粒的肠道渗透增强特性。使用离体大鼠空肠评估了纳米系统的粘膜粘附性。所有纳米颗粒系统均与Caco-2细胞相互作用,降低了跨上皮电阻(TEER)并增加了荧光素黄(LY)的表观渗透系数(Papp,细胞旁途径标志物)。除了基于最高QD的TMC的纳米颗粒外,所有纳米系统均改善了FD4的Papp。在这种情况下,推测纳米颗粒被Caco-2细胞截留。使用离体大鼠空肠模型获得了类似的结果。观察到TMC的QD增加有利于粘膜粘附,导致在肠粘膜上的停留时间延长。通过共聚焦激光扫描显微镜(CLSM)观察到纳米颗粒渗透到离体大鼠空肠组织中,表明粘膜粘附特性延迟了纳米颗粒的吸收,然而它们增加了与肠上皮的接触时间,为内化提供了更好的机会。相对于壳聚糖纳米系统,粘膜粘附性和纳米颗粒内化的改善使TMC纳米系统成为肽类肠道吸收的合适载体。

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