Yong Jing M, Mantaj Julia, Cheng Yiyi, Vllasaliu Driton
School of Cancer and Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 9NH, UK.
Pharmaceutics. 2019 Jun 26;11(7):298. doi: 10.3390/pharmaceutics11070298.
The aim of this study was to probe whether the transferrin (Tf) transport pathway can be exploited for intestinal delivery of nanoparticles. Tf was adsorbed on 100 nm model polystyrene nanoparticles (NP), followed by size characterisation of these systems. Cell uptake of Tf and Tf-adsorbed NP was investigated in intestinal epithelial Caco-2 cells cultured on multi-well plates and as differentiated polarised monolayers. Tf-NP demonstrated a remarkably higher cell uptake compared to unmodified NP in both non-polarised (5-fold) and polarised cell monolayers (16-fold difference). Application of soluble Tf significantly attenuated the uptake of Tf-NP. Notably, Tf-NP displayed remarkably higher rate (23-fold) of epithelial transport across Caco-2 monolayers compared to unmodified NP. This study therefore strongly suggests that the Tf transport pathway should be considered as a candidate biological transport route for orally-administered nanomedicines and drugs with poor oral bioavailability.
本研究的目的是探究转铁蛋白(Tf)转运途径是否可用于纳米颗粒的肠道递送。将Tf吸附在100 nm的模型聚苯乙烯纳米颗粒(NP)上,随后对这些体系进行尺寸表征。在多孔板上培养的以及分化为极化单层的肠上皮Caco-2细胞中研究了Tf和吸附Tf的NP的细胞摄取情况。在非极化(5倍)和极化细胞单层中,Tf-NP的细胞摄取量均显著高于未修饰的NP(相差16倍)。加入可溶性Tf可显著减弱Tf-NP的摄取。值得注意的是,与未修饰的NP相比,Tf-NP跨Caco-2单层的上皮转运速率显著更高(23倍)。因此,本研究强烈表明,Tf转运途径应被视为口服纳米药物和口服生物利用度差的药物的候选生物转运途径。