Carboxymethylated ι-carrageenan conjugated amphotericin B loaded gelatin nanoparticles for treating intracellular Candida glabrata infections

被引:34
作者
Aparna, V. [1 ]
Melge, Anu Rohit [1 ]
Rajan, V. K. [1 ]
Biswas, Raja [1 ]
Jayakumar, R. [1 ]
Mohan, C. Gopi [1 ]
机构
[1] Amrita Vishwa Vidyapeetham, Amrita Inst Med Sci & Res Ctr, Ctr Nanosci & Mol Med, Kochi 682041, Kerala, India
关键词
Amphotericin B; Carboxymethylated iota-carrageenan; Macrophages; Gelatin A; Targeted drug delivery; Candida glabrata; CYSTEINE-RICH DOMAIN; MANNOSE RECEPTOR; DRUG-DELIVERY; DOCKING; BINDING; CANCER; MICE;
D O I
10.1016/j.ijbiomac.2017.11.126
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 L-carrageenan for the delivery of Amp B using gelatin A nanoparticles (GNPs). The choice of gelatin A was the outcome of in silica 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 L-carrageenan conjugated gelatin nanoparticles (CMC-Amp B-GNPs) with size 343 +/- 12 nm and -25 +/- 5.3 mV 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. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 149
页数:10
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