Nasti Alessandro, Zaki Noha M, de Leonardis Piero, Ungphaiboon Suwipa, Sansongsak Proramate, Rimoli Maria Grazia, Tirelli Nicola
School of Pharmacy, University of Manchester, Stopford Building, Oxford Road, Manchester, M13 9PT, UK.
Pharm Res. 2009 Aug;26(8):1918-30. doi: 10.1007/s11095-009-9908-0. Epub 2009 Jun 9.
Chitosan is one of the most sought-after components for designing nanoparticles for drug delivery applications. However, despite the large number of studies, reproducibility is often an issue; generally more attention should be focused on purity and precise characterization of the starting material, as well as on the development of robust preparative procedures.
Using a rational experimental design, we have studied the influence of a number of orthogonal factors (pH, concentrations, ratios of components, different methods of mixing) in the preparation of chitosan/triphosphate (TPP) nanoparticles and in their coating with hyaluronic acid (HA), aiming at the minimisation of size polydispersity, the maximisation of zeta potential and long-term stability, and at the control over average nanoparticle size.
Three optimised nanoparticles have been developed (two uncoated and one HA-coated) and their toxicity on fibroblasts and macrophages has been evaluated: experiments showed the beneficial character of HA-coating in the reduction of toxicity (IC50 raised from 0.7-0.8 mg/mL to 1.8 mg/mL) and suggested that the uncoated chitosan/TPP nanoparticles had toxic effects following internalisation rather than membrane disruption.
壳聚糖是药物递送应用中设计纳米颗粒最受追捧的成分之一。然而,尽管有大量研究,但可重复性往往是个问题;一般来说,应更多地关注起始材料的纯度和精确表征,以及稳健制备程序的开发。
通过合理的实验设计,我们研究了壳聚糖/三磷酸(TPP)纳米颗粒制备过程中以及用透明质酸(HA)包被过程中多个正交因素(pH值、浓度、组分比例、不同混合方法)的影响,旨在使粒径多分散性最小化、zeta电位最大化以及长期稳定性最大化,并控制纳米颗粒的平均粒径。
已开发出三种优化的纳米颗粒(两种未包被的和一种HA包被的),并评估了它们对成纤维细胞和巨噬细胞的毒性:实验表明HA包被在降低毒性方面具有有益作用(IC50从0.7 - 0.8 mg/mL提高到1.8 mg/mL),并表明未包被的壳聚糖/TPP纳米颗粒在内化后具有毒性作用,而非膜破坏作用。