| Literature DB >> 29169943 |
V Aparna1, Anu Rohit Melge1, V K Rajan1, Raja Biswas2, R Jayakumar3, C Gopi Mohan4.
Abstract
Intercellular Candida glabrata infections are difficult to treat due to poor penetration of drugs into the fungal niche. Delivering amphotericin B (Amp B) into the macrophages where the pathogen inhabits is an effective solution. We are studying the macrophage targeting proficiency of ɩ-carrageenan for the delivery of Amp B using gelatin A nanoparticles (GNPs). The choice of gelatin A was the outcome of in silico inspections where the amino functionalized polymer having the best docking score with Amp B was selected. We prepared a sustained release formulation of amp B loaded carboxymethyl ɩ-carrageenan conjugated gelatin nanoparticles (CMC-Amp B-GNPs) with size 343±12nm and -25±5.3mV zeta potential. The formulations were found to be stable, biocompatible and non-haemolytic. Flow cytometry analysis showed 3 fold higher uptake of CMC-GNPs compared to the GNPs by RAW 264.7 cells. CMC-Amp B-GNPs showed enhanced antifungal activity than bare Amp B and Amp B-GNPs.Entities:
Keywords: Amphotericin B; Candida glabrata; Carboxymethylated ɩ-carrageenan; Gelatin A; Macrophages; Targeted drug delivery
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Year: 2017 PMID: 29169943 DOI: 10.1016/j.ijbiomac.2017.11.126
Source DB: PubMed Journal: Int J Biol Macromol ISSN: 0141-8130 Impact factor: 6.953