Vila Ana, Gill Howard, McCallion Orla, Alonso María José
Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Santiago de Compostel, 15782 Santiago de Compostela, Spain.
J Control Release. 2004 Aug 11;98(2):231-44. doi: 10.1016/j.jconrel.2004.04.026.
The aim of the study was to investigate the effect of the size and PEG coating density of Poly(lactic acid)-poly(ethylene glycol) (PLA-PEG) nano- and microparticles on their transport across the nasal mucosa. Particles were made of PLA-PEG copolymers of two different molecular weights (Mw: 37 and 28 kDa) and also PLA of Mw 28 kDa, and prepared using different techniques (simple emulsion (o/w), double emulsion (w/o/w), and nanoprecipitation techniques). The particles were characterized for their size, zeta potential, morphology [Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM)], and PEG coating efficiency. Additionally, the transport of rhodamine 6G-labelled PLA-PEG and PLA particles across the rat nasal mucosa was investigated by Confocal Laser Scanning Microscopy (CLSM). The results showed that the size of PLA-PEG nanoparticles varied between 150 and 300 nm and their zeta potential between -10 and -22 mV depending on both the polymer Mw and the preparation technique. Moreover, the PEG coating efficiency (amount of PEG on the surface with respect to the total amount of PEG in the particles) was high (between 75% and 92%) and affected by the PLA Mw and also by the particles preparation technique. The greatest PEG surface density was achieved for lowest Mw PLA-PEG, using the O/W emulsification technique. The CLSM images of nasal epithelia from rats showed the importance of the PEG coating density and the size on the transmucosal transport of the fluorescent nanoparticles. More specifically, PLA-PEG particles with a high PEG coating density and a small size were more significantly transported than noncoated PLA nanoparticles and also than PLA-PEG nanoparticles with a lower coating density. In conclusion, these results showed the important role that the PEG coating has on the efficacy of PLA-PEG nanoparticles as nasal drug carriers.
本研究的目的是调查聚乳酸-聚乙二醇(PLA-PEG)纳米和微粒的尺寸及聚乙二醇(PEG)包衣密度对其穿过鼻黏膜转运的影响。微粒由两种不同分子量(Mw:37 kDa和28 kDa)的PLA-PEG共聚物以及Mw为28 kDa的PLA制成,并采用不同技术(简单乳液法(o/w)、复乳法(w/o/w)和纳米沉淀技术)制备。对微粒的尺寸、zeta电位、形态[透射电子显微镜(TEM)和扫描电子显微镜(SEM)]以及PEG包衣效率进行了表征。此外,通过共聚焦激光扫描显微镜(CLSM)研究了罗丹明6G标记的PLA-PEG和PLA微粒穿过大鼠鼻黏膜的转运情况。结果表明,PLA-PEG纳米粒的尺寸在150至300 nm之间,其zeta电位在-10至-22 mV之间,这取决于聚合物的分子量和制备技术。此外,PEG包衣效率(颗粒表面PEG的量相对于颗粒中PEG总量)较高(在75%至92%之间),并受PLA分子量以及颗粒制备技术的影响。使用O/W乳化技术,对于最低分子量的PLA-PEG可实现最大的PEG表面密度。大鼠鼻上皮的CLSM图像显示了PEG包衣密度和尺寸对荧光纳米粒跨黏膜转运的重要性。更具体地说,具有高PEG包衣密度和小尺寸的PLA-PEG颗粒比未包衣的PLA纳米粒以及包衣密度较低的PLA-PEG纳米粒更易被转运。总之,这些结果表明PEG包衣在PLA-PEG纳米粒作为鼻用药物载体的功效中起着重要作用。