Development and Characterization of Core-Shell Nanoparticles for Anticancer Therapy

被引:1
作者
Ganesh, G. N. K. [1 ]
Chopra, Vianni [1 ]
Karri, Veera Venkata Satyanarayana Reddy [1 ]
Koundinya, S. Kiran [1 ]
Kumar, R. Suresh [1 ]
Arun, R. [1 ]
机构
[1] JSS Univ, Ootacamund, JSS Coll Pharm, Dept Pharmaceut, Mysuru, India
关键词
Gemcitabine; FDA; Cytidine-Deaminase; Core-Shell Nanoparticle; Double Emulsion-Solvent Diffusion Evaporation Method; BSA-PLGA; TPGS; MIA-PaCa2 Cell Lines; DRUG MICROENCAPSULATION; PLA/PLGA COACERVATION; CANCER-THERAPY; RELEASE; MICROSPHERES; DELIVERY; POLY(D; L-LACTIDE-CO-GLYCOLIDE); PROTEIN; THERMODYNAMICS; MICROCAPSULES;
D O I
10.1166/asl.2018.12194
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gemcitabine hydrophilic used for the treatment of solid tumours like ovarian, breast, bladder and small-cell lung cancer, pancreatic cancer. In year 1996 FDA approved it for breast cancer treatment but it has a drawback of rapid body clearance by kidney and metabolism by the plasmatic enzyme cytidine-deaminase. The aim of the study is to entrap gemcitabine in Core-Shell nanoparticles which acts an efficient carrier system for increasing drug's efficacy. Gemcitabine loaded with BSA-PLGA core shell Nanoparticle prepared by double emulsion-solvent diffusion evaporation method using a ratio optimized to 1: 4 respectively. The particle size was found to be 237.6 nm and high encapsulation efficiency was achieved with a concentration of 1.5% TPGS as a primary stabilizer and 3% PVA as a secondary stabilizer. The drug loading and encapsulation efficiency of the Nanoparticles was 18 mu g/mg and 35.1% w/w. IC-50 value of the formulation was found to be (10 mu M) in MIA-PaCA 2 cell line.
引用
收藏
页码:5768 / 5777
页数:10
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