Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Ain Shams University, African Union Organization Street, P.O. Box 11566, Abbassia, Cairo, Egypt.
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Ain Shams University, African Union Organization Street, P.O. Box 11566, Abbassia, Cairo, Egypt.
Int J Biol Macromol. 2014 Mar;64:334-40. doi: 10.1016/j.ijbiomac.2013.11.041. Epub 2013 Dec 16.
The aim of this study is to utilize statistical designs and mathematical modeling to end the continuous debate about the different variables that influence the production of nanoparticles using the ionic gelation method between the biopolymer chitosan (CS) and tripolyphosphate (TPP) ion. Preliminary experiments were adopted to extract the optimum conditions for the nanoparticles preparation and model construction. Critical process parameters were screened using the one-factor-at-a-time (OFAT) approach to select optimum experimental regions. Finally, these factors were optimized using two different methods of response surface modeling; the Box-Behnken and the D-optimal. The significant models showed excellent fitting of the data. The two methods were validated using a set of check points and were subsequently compared. Good agreement between actual and predicted values was obtained though the D-optimal model was more successful in predicting the particle size of the prepared nanoparticles with percentage bias as small as 1.49%. Nanoparticles were produced with diameters ranging from 52.21 nm to 400.30 nm, particle polydispersity from 0.06 to 0.40 and suitable morphology. This work provides an overview on the production of chitosan nanoparticles with desirable size enabling their successful use in drugs delivery and targeting or in any nanotechnology or interfacial application.
本研究旨在利用统计设计和数学建模来结束关于使用离子凝胶法制备壳聚糖(CS)和三聚磷酸(TPP)离子纳米颗粒的不同变量的连续争论。采用初步实验来提取纳米颗粒制备和模型构建的最佳条件。使用单因素实验(OFAT)方法筛选临界工艺参数,以选择最佳实验区域。最后,使用两种不同的响应面建模方法(Box-Behnken 和 D-最优)对这些因素进行优化。显著模型显示出对数据的出色拟合。通过一组检查点验证了这两种方法,随后进行了比较。尽管 D-最优模型在预测制备的纳米颗粒的粒径方面更为成功,百分比偏差仅为 1.49%,但实际值与预测值之间的吻合度较好。制备的纳米颗粒的粒径范围为 52.21nm 至 400.30nm,颗粒多分散性为 0.06 至 0.40,形态适宜。这项工作概述了具有理想尺寸的壳聚糖纳米颗粒的生产,使其能够成功用于药物输送和靶向或任何纳米技术或界面应用。