Carboplatin loaded protein nanoparticles exhibit improve anti-proliferative activity in retinoblastoma cells

被引:46
作者
Ahmed, Farhan [1 ]
Ali, Mohammad Javed [2 ]
Kondapi, Anand K. [1 ]
机构
[1] Univ Hyderabad, Sch Life Sci, Dept Biotechnol & Bioinformat, Hyderabad 500046, Andhra Pradesh, India
[2] LV Prasad Eye Inst, Hyderabad, Andhra Pradesh, India
关键词
Protein nanoparticle; Carboplatin; Retinoblastoma; TARGETED DRUG-DELIVERY; SUBCONJUNCTIVAL CARBOPLATIN; INVOLVEMENT; LACTOFERRIN; MANAGEMENT; INDUCTION; APOPTOSIS; THERAPY; TISSUES;
D O I
10.1016/j.ijbiomac.2014.07.041
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
Retinoblastoma, a common neoplasm of eye in children accounts about 9-10% of all paediatric cancer. Carboplatin (carbo) is preferred chemotherapeutic regimen. In this study the prospective of carboplatin loaded apotranferrin (Apo-nano-carbo) and lactoferrin (Lacto-nano-carbo) nanoparticles have been demonstrated for the treatment of retinoblastoma. Apo-nano-carbo and Lacto-nano-carbo were prepared by sal-oil method (as a patented formula) with size of 82-92 nm and 68-81 nm, hydrodynamic size were 142+/-15 nm and 263+/-20 nm, encapsulation efficiency were 50%+/-2.3 and 52%+/-3.9 respectively. Results of pH dependent-drug release and receptor-blocking assay showed that nanoparticles may deliver drug through receptor mediated endocytosis. The carboplatin loaded nanoparticles shows greater intracellular uptake, sustained retention and thus, high anti-proliferative activity (Apo-nano-carbo IC50 = 4.31 mu g ml(-1), Lacto-nano-carbo IC50 = 4.16 mu g ml(-1), Sol-carbo IC50 = 13.498 mu g ml(-1)) into the retinoblastoma cells compared to their soluble counterpart. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:572 / 582
页数:11
相关论文
共 42 条
[1]   A phase I/II study of subconjunctival carboplatin for intraocular retinoblastoma [J].
Abramson, DH ;
Frank, CM ;
Dunkel, IJ .
OPHTHALMOLOGY, 1999, 106 (10) :1947-1950
[2]   The effects of chemotherapeutic drugs on viabilty, apoptosis, and survivin expression in MCF-7 cells [J].
Al-Joudi, FS ;
Alias, IZ ;
Samsudin, AR .
ACTA HISTOCHEMICA ET CYTOCHEMICA, 2005, 38 (05) :323-330
[3]   ANALYSIS OF TREATMENT RESULTS IN 36 CHILDREN WITH RETINOBLASTOMA TREATED BY SCLERAL PLAQUE IRRADIATION [J].
AMENDOLA, BE ;
MARKOE, AM ;
AUGSBURGER, JJ ;
KARLSSON, UL ;
GIBLIN, M ;
SHIELDS, JA ;
BRADY, LW ;
WOODLEIGH, R .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1989, 17 (01) :63-70
[4]  
Ashwin N., 2008, J BIOMED NANOTECHNOL, V4, P410
[5]  
Chaleawlert-umpon S., 2009, J MICROSCOPY SOC THA, V223, P62
[6]  
CHAN HSL, 1989, ANTICANCER RES, V9, P469
[7]   PREPARATION AND PROPERTIES OF SERUM AND PLASMA PROTEINS .4. A SYSTEM FOR THE SEPARATION INTO FRACTIONS OF THE PROTEIN AND LIPOPROTEIN COMPONENTS OF BIOLOGICAL TISSUES AND FLUIDS [J].
COHN, EJ ;
STRONG, LE ;
HUGHES, WL ;
MULFORD, DJ ;
ASHWORTH, JN ;
MELIN, M ;
TAYLOR, HL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (03) :459-475
[8]   Solid lipid nanoparticles for retinal gene therapy:: Transfection and intracellular trafficking in RPE cells [J].
del Pozo-Rodriguez, A. ;
Delgado, D. ;
Solinis, M. A. ;
Gascon, A. R. ;
Pedraz, J. L. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 360 (1-2) :177-183
[9]  
Di Felice V, 1998, INT J ONCOL, V13, P225
[10]  
DOZ F, 1994, CANCER, V74, P722, DOI 10.1002/1097-0142(19940715)74:2<722::AID-CNCR2820740228>3.0.CO