Carboxymethyl guar gum nanoparticles for drug delivery applications: Preparation and preliminary in-vitro investigations

被引:55
作者
Dodi, G. [1 ,2 ]
Pala, A. [3 ]
Barbu, E. [4 ]
Peptanariu, D. [5 ]
Hritcu, D. [1 ]
Popa, M. I. [1 ]
Tamba, B. I. [6 ]
机构
[1] Gheorghe Asachi Tech Univ Iasi, Iasi, Romania
[2] SCIENT Res Ctr Instrumental Anal, Bucharest, Romania
[3] Univ Sassari, I-07100 Sassari, Italy
[4] Univ Portsmouth, Portsmouth, Hants, England
[5] Petru Poni Inst Macromol Chem, R-6600 Iasi, Romania
[6] Gr T Popa Univ Med & Pharm, Iasi, Romania
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2016年 / 63卷
关键词
Carboxymethyl guar gum; Phosphate; Nanoparticles; Cytotoxicity; Drug delivery; REGIOSELECTIVE SYNTHESIS; HYDROGELS; MICROSPHERES;
D O I
10.1016/j.msec.2016.03.032
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Carboxymethyl guar gum (CMGG) synthesized from commercially available polysaccharide was formulated into nanoparticles via ionic gelation using trisodium trimetaphosphate (STMP) as cross-linking agent. Characterisation using a range of analytical techniques (FTIR, NMR, GPC, TGA and DLS) confirmed the CMGG structure and revealed the effect of the CMGG and STMP concentration on the main characteristics of the obtained nanoformulations. The average nanoparticle diameter was found to be around 208 nm, as determined by dynamic light scattering (DLS) and confirmed by scanning electron microscopy (SEM) and nanoparticle tracking analysis (NTA). Experiments using simulated gastric and intestinal fluids evidenced significant pH-dependent drug release behaviour of the nanoformulations loaded with Rhodamine B (RhB) as a model drug (loading capacity in excess of 83%), as monitored by UV-Vis. While dose-dependent cytotoxicity was observed, the nanoformulations appeared completely non-toxic at concentrations below 03 mg/mL. Results obtained so far suggest that carboxymethylated guar gum nanoparticles formulated with STMP warrant further investigations as polysaccharide based biocompatible drug nanocarriers. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:628 / 636
页数:9
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