Mohanta Vaishakhi, Madras Giridhar, Patil Satish
Solid State and Structural Chemistry Unit, ‡Department of Chemical Engineering, Indian Institute of Science , Bangalore 560012, India.
ACS Appl Mater Interfaces. 2014 Nov 26;6(22):20093-101. doi: 10.1021/am505681e. Epub 2014 Oct 23.
A layer-by-layer (LbL) approach has been employed for the fabrication of multilayer thin films and microcapsules having nanofibrous morphology using nanocrystalline cellulose (NCC) as one of the components of the assembly. The applicability of these nanoassemblies as drug delivery carriers has been explored by the loading of an anticancer drug, doxorubicin hydrochloride, and a water-insoluble drug, curcumin. Doxorubicin hydrochloride, having a good water solubility, is postloaded in the assembly. In the case of curcumin, which is very hydrophobic and has limited solubility in water, a stable dispersion is prepared via noncovalent interaction with NCC prior to incorporation in the LbL assembly. The interaction of various other lipophilic drugs with NCC was analyzed theoretically by molecular docking in consideration of NCC as a general carrier for hydrophobic drugs.
采用逐层(LbL)方法,以纳米晶纤维素(NCC)作为组装组件之一,制备具有纳米纤维形态的多层薄膜和微胶囊。通过负载抗癌药物盐酸多柔比星和水不溶性药物姜黄素,探索了这些纳米组装体作为药物递送载体的适用性。盐酸多柔比星具有良好的水溶性,后负载于组装体中。对于非常疏水且在水中溶解度有限的姜黄素,在将其掺入LbL组装体之前,通过与NCC的非共价相互作用制备稳定的分散体。考虑到NCC作为疏水药物的通用载体,通过分子对接从理论上分析了各种其他亲脂性药物与NCC的相互作用。